The immune response comprises not only pro-inflammatory and anti-inflammatory pathways but also pro-resolution mechanisms that serve to balance the need of the host to target microbial pathogens while preventing excess inflammation and bystander tissue damage.
Specialized pro-resolving mediators (SPMs) are enzymatically derived from essential fatty acids to serve as a novel class of immunoresolvents that limit acute responses and orchestrate the clearance of tissue pathogens, dying cells and debris from the battlefield of infectious inflammation.
SPMs are composed of lipoxins, E-series and D-series resolvins, protectins and maresins. Individual members of the SPM family serve as agonists at cognate receptors to induce cell-type specific responses.
Important regulatory roles for SPMs have been uncovered in host responses to several microorganisms, including bacterial, viral, fungal and parasitic pathogens.
SPMs also promote the resolution of non-infectious inflammation and tissue injury. Defects in host SPM pathways contribute to the development of chronic inflammatory diseases.
With the capacity to enhance host defence and modulate inflammation, SPMs represent a promising translational approach to enlist host resolution programmes for the treatment of infection and excess inflammation.
Specialized pro-resolving mediators (SPMs) are enzymatically derived from essential fatty acids and have important roles in orchestrating the resolution of tissue inflammation — that is, catabasis. Host responses to tissue infection elicit acute inflammation in an attempt to control invading pathogens. SPMs are lipid mediators that are part of a larger family of pro-resolving molecules, which includes proteins and gases, that together restrain inflammation and resolve the infection. These immunoresolvents are distinct from immunosuppressive molecules as they not only dampen inflammation but also promote host defence. Here, we focus primarily on SPMs and their roles in lung infection and inflammation to illustrate the potent actions these mediators play in restoring tissue homeostasis after an infection.
Acute inflammation is a vital response to infection that is initiated within seconds of pathogen detection1. Granulocytes are rapidly recruited to sites of infection2, where they become activated and augment the resident capacity of infected tissue to kill and ultimately clear the pathogen3. These early events in the host response to infection are essential for survival and are coordinated by several families of pro-inflammatory mediators, including lipid mediators (such as prostaglandins and leukotrienes), cytokines and chemokines. These pro-inflammatory mediators have overlapping and distinct functions and ultimately induce an increase in vascular permeability and orchestrate leukocyte recruitment. This leads to the cardinal signs of tissue inflammation — namely calor, rubor, tumor, dolor and potentially functio laesa (Fig. 1).
Recently, a new array of molecules that function in the resolution of inflammation were elucidated and named specialized pro-resolving mediators (SPMs)4,5. Many of these SPMs are produced during the acute inflammatory response6, and their structure, biosynthesis and organic synthesis have been recently reviewed (see Ref. 5). Typically, acute inflammatory responses to pathogens are self-limiting, and there is a growing appreciation that SPMs have pivotal anti-inflammatory and anti-infective roles in tissue catabasis4. For effective resolution of inflammation to occur in tissues, cessation of granulocyte recruitment is required in conjunction with the recruitment and differentiation of macrophages, which help clear inflammatory cells and tissue debris to restore tissue homeostasis7. Granulocytes in the tissue undergo apoptosis during the resolution of inflammation to prevent bystander tissue injury occurring from the release of potentially toxic cellular contents8. Removal of apoptotic neutrophils prompts a switch from a pro- to an anti-inflammatory macrophage phenotype, which is a prerequisite for macrophage efferocytosis and egress via the lymphatic vessels9. Efferocytosis also leads to further production of additional SPMs that signal for restoration of vascular integrity, regeneration and/or repair of injured tissues, remission of fever by inhibition of pro-inflammatory lipid mediators and cytokines, and relief of inflammatory pain10. Together, the SPMs and these cellular events in resolution can be summarized as the newly recognized five cardinal signs of resolution (Fig. 1).
In this Review, we address the functions of SPMs in infectious immunity and chronic inflammatory diseases, with a focus on how SPMs affect lung physiology and pathology in these diseases. Recent discoveries11,12,13,14,15 regarding anti-inflammatory, anti-infective and pro-resolving roles for SPMs point to their potential translational applications in harnessing endogenous resolution responses for novel host-directed therapeutic strategies in sterile and infectious inflammation. Additional roles in these homeostatic processes for non-lipid mediators of resolution will not be covered in detail here but have been recently reviewed (see Refs 16,17,18). Cellular and molecular mechanisms for catabasis have now been determined in multiple organ systems and diseases. Here, we will primarily focus on lung infection and inflammation. The resolution responses that occur in non-pulmonary sites of infection and inflammation have recently been reviewed (see Refs 7,19,20,21). Finally, we consider how new therapeutic strategies that incorporate immunoresolvents may have the potential to synergize with antibiotics and to mitigate the growing problem of antibiotic resistance.
In response to pathogen invasion or tissue injury, polyunsaturated fatty acids are released locally from membrane phospholipids or delivered to sites of inflammation by tissue oedema for subsequent conversion to specialized mediators by cells in the exudates22. Within minutes, the generation of eicosanoids (that is, prostaglandins and cysteinyl leukotrienes) from arachidonic acid (C20:4n-6) metabolism helps to direct peripheral blood neutrophils to infected sites. Prostaglandin E2 (PGE2) and PGI2 regulate blood flow, whereas leukotriene C4 (LTC4) and LTD4 regulate vascular permeability1,23. Furthermore, neutrophils transmigrate towards chemotactic gradients of LTB4 (Ref. 24). With selected cytokines, chemokines and complement components (namely C5a and C3b), these eicosanoids induce neutrophil entry into the tissue to engulf and kill invading pathogens3,25. Early in the acute inflammatory response, the origins are laid for biosynthesis of resolution-phase mediators through lipid mediator class-switching, in which arachidonic acid metabolism switches from the production of leukotrienes to the production of lipoxins — the lead family of pro-resolving mediators26. Disruption of lipoxin formation or lipoxin receptor availability delays the resolution response27,28,29,30.
As a class, the SPMs are enzymatically derived from essential fatty acids, including arachidonic acid, eicosapentaenoic acid (EPA; C20:5n-3) and docosahexaenoic acid (DHA; C22:6n-3) in a lipoxygenase (LOX)-dependent manner (Fig. 2). SPMs are stereoselective, and complete stereochemical assignment for the majority of the SPMs has been established (reviewed in Ref. 31). Lipoxins are formed by transcellular biosynthesis via multiple distinct pathways. One pathway involves leukocyte-derived 5-LOX and platelet-derived 12-LOX in the vasculature32. A second pathway involves the conversion of arachidonic acid by epithelial cell-, eosinophil- or monocyte-derived 15-LOX and leukocyte-derived 5-LOX33,34. Although aspirin inhibits prostaglandin production, aspirin-mediated acetylation of cyclooxygenase 2 (COX2; also known as PTGS2) leads to the conversion of arachidonic acid to 15(R)-hydroxyeicosatetraenoic acid (15(R)-HETE), which can serve as a substrate for 5-LOX-mediated conversion to 15-epi-lipoxins (also known as aspirin-triggered (AT) lipoxins)35. Of note, in the absence of aspirin, 15(R)-HETE can also be produced by cytochrome P450 enzymes to act as a substrate for 15-epi-lipoxin transcellular biosynthesis36,37.
In addition to lipoxins, resolving exudates also contain pro-resolving mediators derived from omega-3 fatty acids. These include resolvins, protectins and maresins (reviewed in Ref. 38) (Fig. 2). E-series and D-series resolvins are enzymatically derived from EPA and DHA, respectively. Similarly to 15-epi-lipoxins, resolvins are generated through interactions between aspirin-acetylated COX2 and LOX activities39. For example, in the vasculature, resolvin E1 (RvE1) transcellular synthesis in the presence of aspirin is notable for transformation of EPA to 18(R)-hydroxyEPA (18(R)-HEPE) by aspirin-acetylated COX2 in endothelial cells and 18(R)-HEPE conversion to RvE1 by leukocyte 5-LOX40,41. There are two major series of resolvins that are derived from DHA, namely D-series resolvins (RvD1–RvD6) and their positional AT isomers (AT-RvD1–RvD6)42. The D-series resolvins are enzymatically generated by 15-LOX-mediated conversion of DHA to 17(S)-hydroperoxyDHA (17(S)-HpDHA) and subsequent transformation by 5-LOX. For the AT-resolvins, DHA is initially converted by aspirin-acetylated COX2 to 17(R)-HpDHA that can also serve as a substrate for 5-LOX-mediated transformation to epimeric resolvins. Additional families of pro-resolution mediators derived from DHA have also been identified in resolving inflammatory exudates that display protective bioactivities, namely protectins and maresins43,44. At sites of inflammation, 15-LOX-derived 17(S)-HpDHA can be converted to protectin D1 (Ref. 45), and 12-LOX-derived 14(S)-HpDHA can be converted to maresin 1 (MaR1) (for a detailed review, see Ref. 31). The respiratory tract mucosa in health is enriched with DHA46, and both 17(S)-hydroxy-DHA and protectin D1 are generated in human airways47.
These SPMs exert their bioactions as molecular signals via agonist properties at cognate receptors (Fig. 2). The lipoxin A4 (LXA4) receptor ALX (also known as FPR2) is a G protein-coupled receptor that binds LXA4 and 15-epi-LXA4 with high affinity. High-affinity receptors have also been identified for RvE1 (namely, chemokine-like receptor 1 (CMKLR1; also known as CHEMR23))41, for RvD1 (namely, the probable G protein-coupled receptor GPR32) and for RvD2 (namely, the N-arachidonyl glycine receptor GPR18)48,49. Of interest, RvD1 can also activate ALX with high affinity and is equipotent to LXA4 in binding and activating this receptor49. In addition to RvD1, AT-RvD1 and RvD3 bind to GPR32 with high affinity49,50,51. These SPMs display potent receptor-mediated cell-specific actions (Table 1). Pharmacological structure activity relationships support receptor-dependent signalling mechanisms for the remaining SPMs; however, the molecular identity of their cognate receptors is still to be determined.
As is the case with lipoxins, defects in these SPM pathways can undermine resolution and contribute to chronic inflammation27,30,52,53,54,55. Failure of the resolution response may occur as a result of defects in receptor expression, enzyme synthesis, intracellular signalling or nutritional deficiencies in essential polyunsaturated fatty acids. Functional roles bring these structurally distinct families of lipoxins, resolvins, protectins and maresins together as SPMs — a genus of endogenous molecules that pharmacologically act as immunoresolvents4.
Pro-resolving mediators are active in the picogram to nanogram dose range, whereby they are able to control inflammation, limit tissue damage, shorten resolution intervals, promote healing and alleviate pain in experimental models of inflammation and resolution. These fatty acid-derived mediators are part of a larger resolution programme that includes annexin A1 protein16, several cytokines (for example, transforming growth factor-β (TGFβ) and interleukin-10 (IL-10))11, microRNAs51 and carbon monoxide56. Inhibitors of cyclin-dependent kinases can also pharmacologically promote resolution57.
Cellular targets of SPMs
Counter-regulation of the acute inflammatory response evolved to neutralize and eliminate pathogens and enable repair of inflamed or injured tissues. The main cellular events of resolution are the cessation of neutrophil influx and activation, in conjunction with macrophage recruitment, efferocytosis and phagocytosis of microorganisms and debris6,58. As a class of mediators, SPMs are partly defined by their overlapping function to limit neutrophil tissue accumulation, counter-regulate pro-inflammatory cytokines and encourage macrophage phagocytosis (Fig. 3). During efferocytosis, phagocytes generate SPMs that serve as autacoids to inhibit neutrophil activation, increase apoptotic cell expression of CC-chemokine receptor 5 (CCR5) for chemokine clearance and promote bacterial killing and efferocytosis by macrophages (Table 1). In addition to phagocytes, lymphoid cells have vital roles in host defence, express SPM receptors and can serve as cellular effectors for SPMs. In this section, we highlight selected cell types with important functions in resolution and host defence that respond to SPMs.
Neutrophils. For tissue resolution of inflammation, it is essential to prevent further neutrophil entry, inhibit tissue neutrophil activation and promote the clearance of apoptotic neutrophils. All of these cellular actions are mediated by SPMs. Of particular note, SPMs initiate leukocyte shape changes that limit neutrophil migration in vitro22, diapedesis in vivo and reduce tissue inflammation and damage29,47,59,60,61. For neutrophils, SPMs have potent anti-inflammatory actions, including decreased cell activation, adhesion and reactive oxygen species generation and increased microbial clearance (reviewed in Ref. 4).
Macrophages. Both tissue-resident and recruited inflammatory macrophages serve pivotal roles in responses to infection and inflammation. SPMs augment macrophage functions to clear microorganisms, tissue debris and apoptotic cells (reviewed in Ref. 6). In contrast to neutrophils, SPMs lead to macrophage shape changes that prepare the cells for phagocytosis of microorganisms, apoptotic cells and debris9,12,62,63. Key macrophage actions for SPMs include increased phagocytosis and IL-10 production and decreased pro-inflammatory cytokine production9,64,65.
Natural killer cells. Natural killer (NK) cells can help promote the resolution of an inflammatory response by inducing neutrophil66 and eosinophil apoptosis67, which is a non-inflammatory mechanism for cell removal from tissues and has a crucial role in successful resolution of the inflammatory response8. Apoptotic granulocytes can subsequently be removed by tissue macrophage efferocytosis before tissues are exposed to their potentially toxic contents. By accelerating granulocyte apoptosis, NK cells can limit pathogen-mediated inflammatory responses. NK cells express ALX67, and LXA4 increases NK cell-mediated apoptosis of eosinophils and neutrophils67. NK cells also express CMKLR1, which is the receptor for RvE1 (Ref. 67), and NK cell depletion markedly impairs the protective actions of RvE1 in vivo68.
Innate lymphoid cells. Group 2 innate lymphoid cells (ILC2s) are members of the family of innate-like leukocytes. ILC2s do not express T cell or B cell antigen receptors, or markers of other leukocyte lineages, but they serve important roles for host defence against helminth infections69. In response to epithelial-derived cytokines, such as IL-25, IL-33, thymic stromal lymphopoietin and mast cell-derived prostanoids (that is, PGD2), ILC2s generate type 2 cytokines — IL-5 and IL-13 — in an antigen-independent manner67. Similarly to NK cells, ILC2s express receptors for pro-resolving mediators, including LXA4 and RvE1 (Ref. 67). LXA4 and MaR1 can potently inhibit ILC2 release of pro-inflammatory cytokines67,70. MaR1 also promotes amphiregulin release by ILC2s70, a protective response for restoring lung mucosal homeostasis after influenza infection71.
Lymphocytes. Adaptive immune cells also have important roles in the active resolution of inflammation. CCR5 expression on apoptotic, activated T cells acts to sequester pro-inflammatory cytokines and terminate inflammation; a mechanism that is augmented by SPMs72. RvE1 decreases the production of pro-inflammatory cytokines, such as IL-23 and IL-17, to dampen the adaptive immune response, particularly T helper 17 (TH17) cell responses73. Regulatory T cells are pivotal to controlling effector T cell proliferation and activation. Of note, MaR1 was recently identified as a potent inducer for the formation of regulatory T cells in vivo and in vitro in combination with TGFβ70. Only limited information is available on SPM actions on B cells, but RvD1 was recently shown to augment B cell antibody production and increase the number of antibody-producing B cells in a mouse influenza vaccination model74. These emerging data on the regulation of adaptive immunity by SPMs extend their range of actions and suggest a pivotal role for these imunoresolvents in the transition from innate to adaptive inflammation.
Mucosal epithelial cells. In mucosal host defence, transmigrating neutrophils initiate a respiratory burst and degranulation response to invading pathogens; however, excessive neutrophil activation can cause 'bystander' tissue damage and contribute to pathobiology of mucosal inflammatory disease75. During resolution, the activated neutrophils are cleared apically from the intestinal lumin by decay accelerating factor (also known as CD55), which is an anti-adhesive molecule76. SPMs potently inhibit neutrophil trans-epithelial migration and the production of pro-inflammatory cytokines by epithelial cells77. In addition, SPMs promote decay accelerating factor expression in mucosal epithelia as well as expression of the anti-infective peptide bactericidal permeability-increasing protein and the lipopolysaccharide (LPS) detoxification enzyme alkaline phosphatase78,79.
SPMs in infection
Although the role of SPMs has only recently been uncovered in tissue homeostasis, there is already a push to understand the functions of SPMs in infections. Studies on the role of SPMs in the modulation of host responses to various infectious diseases have highlighted a new therapeutic opportunity for targeting the host in infectious inflammation to complement antibiotic therapy. Some recent examples are provided in Table 2 and the following sections, in which we consider the roles of SPMs in bacterial, viral and fungal diseases.
SPMs in bacterial infection
Pneumonia. Although pneumonia typically initiates a self-limiting acute inflammatory response, in some individuals the inflammation is so severe that it leads to life-threatening hypoxaemia and respiratory failure — namely, the acute respiratory distress syndrome (ARDS) — which is discussed in greater detail in the next section. In Escherichia coli-induced pneumonia, the SPM LXA4 promotes neutrophil apoptosis by inducing the phosphorylation of BCL-2-associated death promoter (BAD) and reducing the expression of the anti-apoptotic protein myeloid cell leukaemia sequence 1 (MCL1)80, whereas RvE1 promotes neutrophil apoptosis through activation of caspases81. In both cases, promotion of neutrophil death leads to a reduction in the severity of acute lung inflammation81,82. These findings highlight a direct interaction between the SPMs and apoptotic pathways in immune cells. In addition, RvE1 enhances bacterial clearance and reduces local production of pro-inflammatory cytokines in E. coli aspiration pneumonia, which results in enhanced survival of mice13.
Periodontitis. Bacterial periodontitis is a well-established experimental model that has been used to elucidate the role of SPMs in controlling localized bacterial infection, its associated tissue damage and systemic effects. Periodontitis is generally caused by a polymicrobial insult, resulting in the generation of biofilms, overgrowth of resident Gram-negative bacteria in the oral cavity and mucosal inflammation. The disease process is thought to be mediated by an overly robust immune response to the bacteria, including to Porphyromonas gingivalis in chronic infection and Actinobacillus spp. in the localized aggressive form of the disease. Periodontitis also carries a more generalized implication to human health, as localized periodontitis elicits a systemic response, increasing systemic inflammation and risk for accelerated atherosclerosis82,83.
In localized P. gingivalis infection models, introduction of stable analogues of lipoxins and AT-lipoxins results in a reduction of neutrophil recruitment to the site of infection84. In a rabbit model of the same infection, rabbits that either transgenically overexpress 15-LOX, the enzyme responsible for production of lipoxins and protectins, or are treated with a topical formulation of LXA4 had a reduction in leukocyte infiltration in inflammation at the site of injury and a reduction in bone loss85, highlighting a suppressive role for the lipoxins in the control of localized inflammation in this chronic infection. Furthermore, the systemic response to infection is attenuated, resulting in a decrease in neutrophil–platelet interactions86 and limiting generalized systemic inflammation, as indicated by a reduction in biomarkers such as C-reactive protein61.
Resolvins also have a role in promoting protection against bacterial periodontitis. In localized aggressive periodontitis (LAP), RvE1 suppresses neutrophil superoxide generation87, neutrophil infiltration88 and the production of pro-inflammatory cytokines88, and enhances macrophage activity89. At least some of its actions are mediated through its interaction with CMKLR1, which is highly expressed on macrophages and dendritic cells (DCs)41. In models of LAP, treatment of animals with topical RvE1 results in a decrease in localized and systemic inflammation and allows the host to regenerate lost tissue and bone mass61. The ability of RvE1 to re-establish homeostasis at the local tissue level proceeds in part through its ability to restore phagocyte activity of macrophages, which is impaired in LAP90. Lipoxin analogues or AT-lipoxins have no significant effect on neutrophil activity in LAP, which is in contrast to chronic periodontitis, in which LXA4 has a regulatory role, highlighting a context-specific mechanism for the pro-resolving mediators.
Lyme disease. In a similar manner to periodontitis, a pattern of localized and systemic control of inflammation is seen in mouse models of Lyme disease. In 5-LOX-deficient mice, which have a defect in SPM production, the development of arthritis in animals infected with Borrelia burgdorferi is similar to that in wild-type animals; however, the absence of lipoxins and resolvins impairs the host ability to resolve arthritis, resulting in chronic disease91 and a lack of control of the chronic systemic inflammatory response long after the triggering infectious agent has been cleared.
Tuberculosis. The protective roles for SPMs in acute infections, such as pneumonia, are also integral to the host immune response to Mycobacterium tuberculosis. In this host response, there is a delicate balance between pro-inflammatory mediators, such as PGE2 and LTB4, and pro-resolving mediators, such as LXA4, that can dictate the intensity of the pathogen-mediated inflammation as well as microbial clearance. In a mouse model of M. tuberculosis infection, there is a rise in the levels of both the pro-inflammatory LTB4 and the pro-resolving LXA4 after infection, with LXA4 high levels persisting throughout the chronic infection92. In animals deficient in 5-LOX (a deficiency that leads to defective leukotriene and lipoxin production), M. tuberculosis infection is associated with enhanced survival92. Host lipoxin generation is related to M. tuberculosis strain virulence, suggesting a vital role for SPMs in modulating the host inflammatory responses to M. tuberculosis. Excessive production of either LTB4 or LXA4 can result in aberrant host responses to M. tuberculosis infection that, intriguingly, converge on dysregulated expression of TNF15. This accentuates the importance of both pro-inflammatory and pro-resolving responses for host defence and regulation of pathogen-mediated inflammation. Crucial roles for arachidonic acid metabolism in immune responses may be linked to the different infectious rates observed with human variants in the ALOX5 (encoding 5-LOX) locus93 and the LTA4H (which encodes LTA4 hydrolase, an enzyme involved in the final step of LTB4 production) locus94, which both appear to disrupt LTB4 and LXA4 production as well as altering protection against naturally occurring M. tuberculosis infection. Together, these findings suggest that a combinatorial approach to tuberculosis therapy would be most effective, including antibiotics to help endogenous mechanisms kill the microorganism and SPMs to control the host immune response.
Sepsis. Sepsis is the most serious complication of acute bacterial infection. The host response in sepsis leads to diffuse systemic immune dysregulation that progresses rapidly, frequently resulting in shock. In Gram-negative bacteria-initiated sepsis, there appears to be a protective and potentially therapeutic role for lipid mediators. In mice with sepsis after caecal ligation and puncture, treatment with LXA4 reduced the production of pro-inflammatory cytokines, while simultaneously promoting a reduction in Gram-negative bacteria loads that improved survival95,96. Resolvins also have an important protective role in sepsis models. RvD2 serves as a potent regulator of the systemic inflammatory response in sepsis14. This reduction in pro-inflammatory signals is a consequence, in part, of reduction in nuclear factor-κB (NF-κB) activity13,60,96. Treatment of septic mice with RvD2 leads to a profound reduction in the production of cytokines, including IL-6, IL-10 and interferon-α (IFNα), and leukocyte infiltration to the site of infection is reduced. Of interest, control of the inflammatory response leads to an overall reduction in bacterial loads, both at the local site of insult and systemically within the blood, and an improvement in overall animal survival14. Sepsis is a disease of overwhelming infectious insult, compounded by an overly robust inflammatory response, whereby treatment with anti-inflammatory therapies potentially subjects the host to further harm. Modulation of pro-resolution responses appears to promote dampening of the inflammatory response while still allowing for adequate, and possibly improved, clearance of the bacterial infection. The ability to clear the source of infection while still limiting the immune response provides an attractive therapeutic paradigm for this disease of substantial health-care burden.
The biological demand for an initial robust response against a bacterial insult is juxtaposed against the need to control prolonged and overly exuberant inflammatory responses that are potentially harmful, raising potential challenges for the therapeutic use of pro-resolving mediators. For example, in a pneumosepsis model, early treatment with LXA4 appears to limit the immune response by decreasing leukocyte infiltration, reducing bacterial clearance and worsening the survival rate97. By contrast, in the same model, later treatment with LXA4 had positive effects, allowing for adequate clearance of infection but dampening the protracted and pathological immune response, therefore enhancing survival97. In the future, timing and dosing considerations and concomitant antibiotic use will be important for developing SPM therapeutic strategies in sepsis.
Overall, in bacterial infection, SPMs have significant therapeutic potential with ongoing research focused on their anti-infective mechanisms and optimal dose and timing strategies to harness their beneficial actions. In animal models, the augmentation of resolution also appears to reduce the needed dosage for antibiotics in the clearance of bacterial infections12,95. Given the worldwide crisis of emerging antibiotic resistance, therapies that could reduce antibiotic usage provide an attractive alternative in the quest to develop new and enhanced antimicrobial therapeutic approaches.
SPMs in viral infections
Influenza. Viral pathogens also appear to interact with the host in a way that is modifiable by pro-resolving factors. Influenza viruses are a well-suited model to understand the role of resolution mediators and the mechanisms in viral infections, as different strains of the virus elicit varied host immune responses and outcomes. In studies that compare more virulent strains of the influenza virus to less virulent strains, pro-resolving mediators inversely correlated with biological activity of the virus. More virulent strains of influenza led to suppression of lipoxins98, which is associated with enhanced viral dissemination. Protectin D1 has pivotal and multiple roles in regulating viral pathogenicity. More virulent influenza strains, such as H5N1, downregulate protectin D1 levels, and the pathogenicity of various isolates correlates inversely with levels of protectins99. In addition to host inflammatory responses, protectin D1 has direct antiviral actions on influenza; both protectin D1 and its isomer protectin DX (which is formed by LOX-mediated double oxygenation) interfere with viral RNA nuclear export machinery, thereby limiting viral replication100,101,102. Treatment of infected mice with protectin D1 improves survival (Fig. 4) even when administered as late as 48 hours after infection102, at a time when current antiviral therapies are no longer significantly effective103.
Respiratory syncytial virus. Respiratory syncytial virus (RSV) infection results in a bronchiolitis that is driven by classically activated macrophages and eventually resolved by alternatively activated macrophages104. Promotion of these two alternative macrophage fates appears related to RSV-induced COX2 (Ref. 105) and LXA4- and RvE1-mediated protective actions106. Host responses to RSV again highlight roles for SPMs and lipid mediator class-switching in the initial control and eventual clearance of infection.
Herpes simplex virus. Herpes simplex virus (HSV) ocular infection represents another example in which local control of the virus results from a robust inflammatory response, with long-term consequences of chronic inflammation that persists after clearance of the virus, including the potential for eventual blindness from stromal keratitis. In animals with HSV, topical administration of RvE1 results in decreased influx of effector CD4+ T cells (both TH1 cells and TH17 cells) and neutrophils, reduced production of pro-inflammatory cytokines, including IFNγ and IL-6, increased levels of the anti-inflammatory cytokine IL-10 and decreased pro-angiogenic factors107. Overall, RvE1 significantly decreased stromal keratitis. Similar results have been demonstrated for protectin D1 (Ref. 108), further illustrating the potential therapeutic benefits of SPM control of pathogen-mediated inflammation to lessen injury to bystander tissues.
The interaction of the host immune system with infectious insults from viruses represents a novel opportunity for exploitation of SPMs. Finding the delicate balance between the need for a sufficient immune response to clear infection and rapid dampening of that response to prevent host damage is a well-suited target for SPMs, and further research is needed to identify opportunities for optimizing this balance in human viral infectious disease.
SPMs in parasitic infections
Responses to parasitic infections also appear to engage SPMs in host defence. With Toxoplasma gondii, there is a robust DC response with production of IL-12 (Ref. 109). Lipoxins are generated in vivo during toxoplasmosis and act in an autacoid mechanism on DCs via ALX leading to reduction of CCR5 expression and diminished IL-12 production110. In animal models, 5-LOX deficiency results in the production of significantly more IL-2 and IFNγ compared with wild-type animals, as well as severe encephalitis and increased mortality, all of which can be reversed by administration of LXA4 analogues111. Similar protective roles for lipoxins have been suggested for other intracellular and extracellular parasites, including Angiostrongylus costaricensi s112, Plasmodium spp.113 and Trypanosoma cruz i114.
Pathogen–host interactions for SPM biosynthesis
The generation of SPMs may not always be beneficial to the host. As discussed previously in M. tuberculosis infections, experimental models that strongly favour the generation of lipoxins over leukotrienes can have detrimental effects on pathogen clearance. If given early in pharmacologically large amounts, SPM regulation of the pathogen-mediated immune response may impair microbial clearance. In addition, there are now examples identified of select pathogens using local SPM production as an immune evasion and survival strategy. T. gondii is able to generate components of SPM biosynthetic pathways, resulting in local collaboration with host cells to increase lipoxin production with the consequence of a dampened immune response to T. gondi i115. Recruitment of neutrophils, lymphocytes and eosinophils to the site of infection are all decreased by this mechanism115. In addition to T. gondii, the opportunistic bacteria Pseudomonas aeruginosa can express a secreted LOX that can augment SPM production in the local milieu to modulate host defence116. Similarly, Candida albicans can biosynthesize RvE1 that limits IL-8-mediated neutrophil infiltration in the host, enabling colonization117. These examples further illustrate the delicate balance between the pathogen and the host in SPM production and control of host immune responses.
SPMs in chronic inflammatory diseases
Non-infectious inflammation is a common and often devastating cause of human disease. Most current therapies rely on blunting the inappropriate immune response through the use of anti-inflammatory medications, all of which have significant undesirable side effects, including increasing the host susceptibility to infection. Although the roles of SPMs have been investigated in many inflammatory diseases (Table 3), below we focus on the role of SPMs in inflammation of the lung by highlighting data from preclinical animal models.
Asthma and allergic inflammation. Asthma is a disease of excessive airway inflammation and hyperresponsiveness induced by irritant triggers and subsequently driven by a multitude of factors, including the trafficking of neutrophils, eosinophils and the generation of type 2 inflammatory responses in many cases. Severe asthma is poorly responsive to existing therapies, and it is characterized by increased oxidative stress and decreased lipoxin production in the airways55,118,119. Recently, the increased oxidative stress in uncontrolled asthma was linked to decreased lipoxin levels through a compensatory increase in soluble epoxide hydrolase activity118. As a consequence of the soluble epoxide hydrolase activity, levels of 14,15-epoxyeicosatrienoic acid levels were decreased, which adversely impacted lipoxin production118, providing a biochemical mechanism for oxidative insults to disrupt lung resolution programmes. Low SPM levels in severe asthma are likely to have the functional consequence of chronic inflammation and airway hyperreactivity because airway LXA4 blunts leukotriene-mediated bronchoprovocation in humans120, and in mice stable analogues of LXA4 block airway hyperresponsiveness, mucus metaplasia and type 2 lung inflammation121,122, and accelerate resolution of the inflammatory response73.
RvE1 has protective effects in preclinical models of allergic lung inflammation; it decreases eosinophil recruitment, type 2 cytokine production and airway hyperresponsiveness73,123. RvE1 targets NK cells in mouse models of asthma through the RvE1 receptor CMKLR1, promoting NK cell migration and cytotoxicity. With NK cell depletion, the pro-resolving function of RvE1 is partially impaired68. In allergic inflammation, RvE1 increases lipoxin formation, suggesting the possibility of redundant pathway effects to limit chronic inflammation. RvE1 inhibits IL-6, IL-23 and IL-17 release, thereby dampening the development and activation of TH17 cells. Similarly to RvE1, lipoxins can inhibit IL-17 production but do not inhibit IL-23, which is indicative of convergent but not overlapping signalling pathways. Of note, as mentioned above, RvE1 and LXA4 also engage distinct receptors, namely CMKLR1 and ALX, respectively73. RvD1 acts in a complementary manner, similarly promoting the resolution of eosinophil tissue accumulation and pro-inflammatory responses with a macrophage directed action to enhance allergen phagocytosis and clearance63. Similarly, protectin D1 has been shown to promote resolution of the lung inflammatory response and block airway hyperresponsiveness47. Of interest, protectin D1 regulates IL-5 and IL-13 but not IL-4 levels, suggesting that ILC2s rather than TH2 cells are likely to be a principal cellular target for protectin D1. It is notable that protectin D1 levels are decreased in exhaled breath condensates during asthma exacerbations47.
Recently, lung sensory neurons were identified as early inducers of ILC2 activation in type 2 lung inflammation124. These activated neurons express transient receptor potential (TRP) channels, which can serve as SPM targets. Of note, mouse models have suggested a role for RvD1, RvE1, neuroprotectin D1 (NPD1) and MaR1 in attenuating pain by inhibition of TRP channels125,126,127,128. Because SPMs act at these pain receptors in the nervous system and on inflammatory pathways, these findings suggest that regulation of sensory neuron activation could be a crucial mechanism for SPM inhibition of both pain and lung inflammation. Together, these findings highlight an integrated network of pro-resolving mediators in asthma and allergic inflammation and suggest several potential therapeutic targets.
Chronic obstructive pulmonary disease. Chronic obstructive pulmonary disease (COPD) is a pulmonary inflammatory disease most often triggered by cigarette smoke and propagated through maladaptive and prolonged pro-inflammatory responses, predisposing the host to recurrent infections. Pro-inflammatory lipid mediators, including leukotrienes, have been observed at elevated levels in patients with COPD119. Roles for SPMs remain to be determined in these individuals. In addition to LXA4, the acute phase reactant serum amyloid A (SAA) can also interact with ALX, and it is increased in COPD exacerbations27, which are largely caused by viral and bacterial respiratory tract infections. In acute exacerbations of COPD, levels of SAA are more than 2 log orders higher than LXA4 (Ref. 27). In sharp contrast to LXA4, when SAA engages ALX, it triggers a pro-inflammatory, neutrophil driven response. Although SAA-mediated inflammation is glucocorticoid-resistant, it can be regulated by pharmacological dosing of lipoxins27, suggesting a new therapeutic approach for steroid-resistant lung inflammation.
The role of resolvins in COPD is a subject of active investigation. Cigarette smoke exposure results in the development of classically activated macrophages, which produce a pro-inflammatory response. Alternatively activated, or M2, macrophages also play a part in the clearance of inhaled particles and quelling of the initial response to the cigarette smoke. RvD1 polarizes cigarette smoke-exposed macrophages towards the M2 pathway, resulting in enhanced phagocytosis as well as upregulated production of IL-10 (Ref. 64). RvE1 also acts on cigarette smoke-activated macrophages, reducing superoxide production and limiting inflammation129. The ability of resolvins to polarize the macrophage population towards the M2 phenotype suggests a novel mechanism for SPM control in this chronic inflammatory disorder.
Cystic fibrosis. Cystic fibrosis is a genetic disorder with multi-organ defects caused by a single mutation. Patients with cystic fibrosis have viscous respiratory tract secretions, recurrent airway infections and an over-exuberant immune response, eventually resulting in the deterioration of lung function. Genetic modifier analysis suggests that patients with cystic fibrosis who carry a polymorphism in PTGS2 (encoding COX2) that leads to reduced production of pro-inflammatory mediators have improved clinical status130. Profiling of lipid mediators in the airways of patients with cystic fibrosis showed that lipoxin levels may be lower in these patients compared with healthy control subjects54. Moreover, patients with cystic fibrosis who had detectable levels of RvE1 in the airways showed improved lung function compared with patients without any detectable RvE1 (Ref. 131). Furthermore, in animal models of cystic fibrosis, lipoxin administration suppresses neutrophil infiltration and reduces bacterial burden, resulting in an overall reduction in disease severity54.
Fibrotic lung disease. Multiple pulmonary injurious exposures have a unifying endpoint in the development of extensive tissue scarring, resulting in poor gas exchange, air movement and demise of the host. These fibrotic lung diseases can be mediated by a poorly controlled inflammatory response that triggers a fibrotic response in a maladaptive attempt to heal the damaged lung parenchyma. These diseases represent a devastating human burden, as very few treatments exist to slow or reverse this fibrotic process. Pro-resolving mediators could represent a novel strategy in a sparse arsenal. Bleomycin is an important chemotherapeutic agent but carries a known risk of pulmonary fibrosis. Treatment with LXA4 or 15-epi-LXA4 results in an attenuation of pulmonary fibrosis in animals exposed to bleomycin through reduction of the pro-fibrotic cytokine TGFβ132, as well as an increase in the prevalence of M2 macrophages133, both resulting in decrease fibrotic matrix and improved pulmonary function. In humans, scleroderma lung disease is characterized by idiopathic progressive lung inflammation and fibrosis and, of interest, patients with scleroderma lung disease underproduce pro-resolving mediators, in comparison to their pro-inflammatory counterparts134.
Acute respiratory distress syndrome. ARDS is a prevalent condition with high rates of morbidity and mortality. It is characterized by an overly robust inflammatory response to infection (for example, pneumonia and sepsis) or injury that fills the alveoli with oedema and pus, resulting in life-threatening respiratory failure. Many unsuccessful attempts have been made to therapeutically target an inflammatory pathway to limit this over-exuberant host response. In contrast to these anti-inflammatory strategies, a pro-resolving therapeutic strategy directed at harnessing host pro-resolving mechanisms is showing promise in preclinical model systems. Using a sterile model of ARDS from gastric acid aspiration, an important clinical risk factor for ARDS, several SPMs, including LXA4, 15-epi-LXA4, RvE1, RvD1 and MaR1, have proven effective as pharmacological agents in limiting acute lung inflammation and injury, and accelerating lung tissue catabasis13,29,59,60,135. Because SPMs engage endogenous resolution pathways, these mediators have the potential to both decrease pathogen-mediated inflammation and enhance host defence, which distinguishes SPMs from immunosuppressive agents. Early inflammation in ARDS is mediated by platelet–neutrophil interactions59,136, and this interaction can lead to transcellular production of lipoxins or of the most recently discovered member of the SPM family, MaR1 (Ref. 59). Treatment with MaR1 is organ protective and limits the extent of lung inflammation. Furthermore, the timing of MaR1 production appears specific and regulated, as does the production of RvD1 (Ref. 137). Together, these findings highlight the potential roles SPMs could have in decreasing the severity and duration of ARDS and, more generally, the data support a targeted pro-resolving approach as a new therapeutic strategy for this devastating condition that is currently without available medical treatment.
As momentum grows to leverage these natural resolution pathways for rational new therapeutic strategies for diseases of acute and chronic inflammation, it is essential to clarify the roles of SPMs in human host defence and in the regulation of pathogen-mediated inflammation. As discussed above, preclinical data for bacterial infection points to important and pivotal roles for lipid mediators, in particular SPMs, in the regulation of host responses to infection12,13 with the potential for host SPM-directed interventions to decrease antibiotic requirements12,95. In addition, for viral host responses, SPMs lessened the severity of influenza and HSV infections102,107,108. Several lines of evidence have suggested dysregulation of SPM pathways in several human diseases27,47,55.
Clinical trials with SPM analogues that resist metabolic inactivation are still in early phases. A recent study of children with infantile eczema compared a topical stable LXA4 analogue (15-(R/S)-methyl-LXA4) to the current clinical approach of topical corticosteroids (specifically, mometasone). 15-(R/S)-methyl-LXA4 was well tolerated and controlled clinical symptoms and disease as effectively as topical steroids138. This trial is the first to report successful treatment with an SPM in humans. Moreover, for allergic diseases, inhaled LXA4 decreases LTC4-initiated bronchoprovocation in patients with asthma120. Several clinical trials using a topical formulation of an RvE1 analogue for ocular conditions are also underway (NCT01639846, NCT01675570, NCT00799552 and NCT02329743).
Host responses to infection naturally trigger both an acute inflammatory response and its resolution. Counter-regulation of pathogen-mediated inflammation is an active process with specific cellular and biochemical events that are tightly regulated in health. With the identification of several families of endogenous pro-resolving mediators, their potent anti-inflammatory properties are now being determined. Distinct from immunosuppressive agents, these endogenous pro-resolving mediators generally display protective actions in host defence, including direct antimicrobial actions. There is still much to be done to more fully understand the intersection of these novel endogenous pathways in control of pathogen-mediated inflammation and the diversity of their mechanisms in microbial pathogenesis. The abundant presence of SPMs in human healthy breast milk139 suggests important protective actions for these mediators. Clinically, acute infections are principally treated with antibiotics with current approaches devoid of host-directed therapy. In light of the current serious threat of emerging pathogens, in particular those that display antibiotic resistance, the development of therapies to augment host anti-infective mechanisms are needed. Members of the growing new genus of SPMs or their bioactive stable analogues represent potential candidates to harness endogenous anti-inflammatory resolution mechanisms to limit overly exuberant pathogen-mediated inflammation in future therapeutic strategies.
Nathan, C. Points of control in inflammation. Nature 420, 846–852 (2002).
Vaporciyan, A. A. et al. Involvement of platelet-endothelial cell adhesion molecule-1 in neutrophil recruitment in vivo. Science 262, 1580–1582 (1993).
Mizgerd, J. P. Acute lower respiratory tract infection. New Engl. J. Med. 358, 716–727 (2008).
Serhan, C. N. Pro-resolving lipid mediators are leads for resolution physiology. Nature 510, 92–101 (2014).
Serhan, C. N., Dalli, J., Colas, R. A., Winkler, J. W. & Chiang, N. Protectins and maresins: new pro-resolving families of mediators in acute inflammation and resolution bioactive metabolome. Biochim. Biophys. Acta 1851, 397–413 (2015).
Serhan, C. N. & Savill, J. Resolution of inflammation: the beginning programs the end. Nat. Immunol. 6, 1191–1197 (2005).
Buckley, C. D., Gilroy, D. W. & Serhan, C. N. Proresolving lipid mediators and mechanisms in the resolution of acute inflammation. Immunity 40, 315–327 (2014).
Savill, J. Apoptosis. Phagocytic docking without shocking. Nature 392, 442–443 (1998).
Dalli, J. & Serhan, C. N. Specific lipid mediator signatures of human phagocytes: microparticles stimulate macrophage efferocytosis and pro-resolving mediators. Blood 120, e60–e72 (2012).
Freire-de-Lima, C. G. et al. Apoptotic cells, through transforming growth factor-β, coordinately induce anti-inflammatory and suppress pro-inflammatory eicosanoid and NO synthesis in murine macrophages. J. Biol. Chem. 281, 38376–38384 (2006).
Bannenberg, G. L. et al. Molecular circuits of resolution: formation and actions of resolvins and protectins. J. Immunol. 174, 4345–4355 (2005).
Chiang, N. et al. Infection regulates pro-resolving mediators that lower antibiotic requirements. Nature 484, 524–528 (2012). This report illustrates that SPMs can enhance the antimicrobial actions of ciprofloxacin and vancomycin to promote bacterial clearance.
Seki, H. et al. The anti-inflammatory and proresolving mediator resolvin E1 protects mice from bacterial pneumonia and acute lung injury. J. Immunol. 184, 836–843 (2010). This study shows that SPM actions increase clearance of E. coli and decrease host inflammation to enhance survival.
Spite, M. et al. Resolvin D2 is a potent regulator of leukocytes and controls microbial sepsis. Nature 461, 1287–1291 (2009). This study highlights the role of resolvins in a complex bacterial infection with suppression of both local bacterial and systemic inflammatory responses.
Tobin, D. M. et al. Host genotype-specific therapies can optimize the inflammatory response to mycobacterial infections. Cell 148, 434–446 (2012). This report highlights the balance between pro-inflammatory and pro-resolving mediators in the clearance of M. tuberculosis infection.
Perretti, M. & D'Acquisto, F. Annexin A1 and glucocorticoids as effectors of the resolution of inflammation. Nat. Rev. Immunol. 9, 62–70 (2009).
Savill, J., Dransfield, I., Gregory, C. & Haslett, C. A blast from the past: clearance of apoptotic cells regulates immune responses. Nat. Rev. Immunol. 2, 965–975 (2002).
Wallace, J. L., Ianaro, A., Flannigan, K. L. & Cirino, G. Gaseous mediators in resolution of inflammation. Semin. Immunol. 3, 227–233 (2015).
Gilroy, D. W. & De Maeyer, R. New insights into the resolution of inflammation. Semin. Immunol. 3, 161–168 (2015).
Romano, M., Cianci, E., Simiele, F. & Recchiuti, A. Lipoxins and aspirin-triggered lipoxins in resolution of inflammation. Eur. J. Pharmacol. 760, 49–63 (2015).
Viola, J. & Soehnlein, O. Atherosclerosis – a matter of unresolved inflammation. Semin. Immunol. 3, 184–193 (2015).
Kasuga, K. et al. Rapid appearance of resolvin precursors in inflammatory exudates: novel mechanisms in resolution. J. Immunol. 181, 8677–8687 (2008).
Badr, K. F., DeBoer, D. K., Schwartzberg, M. & Serhan, C. N. Lipoxin A4 antagonizes cellular and in vivo actions of leukotriene D4 in rat glomerular mesangial cells: evidence for competition at a common receptor. Proc. Natl Acad. Sci. USA 86, 3438–3442 (1989).
Malawista, S. E., de Boisfleury Chevance, A., van Damme, J. & Serhan, C. N. Tonic inhibition of chemotaxis in human plasma. Proc. Natl Acad. Sci. USA 105, 17949–17954 (2008).
Dinarello, C. A., Simon, A. & van der Meer, J. W. Treating inflammation by blocking interleukin-1 in a broad spectrum of diseases. Nat. Rev. Drug Discov. 11, 633–652 (2012).
Levy, B. D., Clish, C. B., Schmidt, B., Gronert, K. & Serhan, C. N. Lipid mediator class switching during acute inflammation: signals in resolution. Nat. Immunol. 2, 612–619 (2001).
Bozinovski, S. et al. Serum amyloid A opposes lipoxin A4 to mediate glucocorticoid refractory lung inflammation in chronic obstructive pulmonary disease. Proc. Natl Acad. Sci. USA 109, 935–940 (2012).
Dufton, N. et al. Anti-inflammatory role of the murine formyl-peptide receptor 2: ligand-specific effects on leukocyte responses and experimental inflammation. J. Immunol. 184, 2611–2619 (2010).
Fukunaga, K., Kohli, P., Bonnans, C., Fredenburgh, L. E. & Levy, B. D. Cyclooxygenase 2 plays a pivotal role in the resolution of acute lung injury. J. Immunol. 174, 5033–5039 (2005).
Schwab, J. M., Chiang, N., Arita, M. & Serhan, C. N. Resolvin E1 and protectin D1 activate inflammation-resolution programmes. Nature 447, 869–874 (2007). This study provides crucial evidence that resolution is an active process and inhibiting SPM formation leads to a 'toxic' resolution.
Serhan, C. N. & Petasis, N. A. Resolvins and protectins in inflammation resolution. Chem. Rev. 111, 5922–5943 (2011).
Serhan, C. N. & Sheppard, K. A. Lipoxin formation during human neutrophil-platelet interactions. Evidence for the transformation of leukotriene A4 by platelet 12-lipoxygenase in vitro. J. Clin. Invest. 85, 772–780 (1990).
Levy, B. D. et al. Human alveolar macrophages have 15-lipoxygenase and generate 15(S)-hydroxy-5,8,11-cis-13-trans-eicosatetraenoic acid and lipoxins. J. Clin. Invest. 92, 1572–1579 (1993).
Serhan, C. N., Hamberg, M. & Samuelsson, B. Lipoxins: novel series of biologically active compounds formed from arachidonic acid in human leukocytes. Proc. Natl Acad. Sci. USA 81, 5335–5339 (1984).
Claria, J. & Serhan, C. N. Aspirin triggers previously undescribed bioactive eicosanoids by human endothelial cell-leukocyte interactions. Proc. Natl Acad. Sci. USA 92, 9475–9479 (1995).
Claria, J., Lee, M. H. & Serhan, C. N. Aspirin-triggered lipoxins (15-epi-LX) are generated by the human lung adenocarcinoma cell line (A549)-neutrophil interactions and are potent inhibitors of cell proliferation. Mol. Med. 2, 583–596 (1996).
Chiang, N. et al. Aspirin-triggered 15-epi-lipoxin A4 (ATL) generation by human leukocytes and murine peritonitis exudates: development of a specific 15-epi-LXA4 ELISA. J. Pharmacol. Exp. Ther. 287, 779–790 (1998).
Serhan, C. N. The resolution of inflammation: the devil in the flask and in the details. FASEB J. 25, 1441–1448 (2011).
Serhan, C. N. et al. Resolvins: a family of bioactive products of omega-3 fatty acid transformation circuits initiated by aspirin treatment that counter proinflammation signals. J. Exp. Med. 196, 1025–1037 (2002).
Serhan, C. N. et al. Novel functional sets of lipid-derived mediators with antiinflammatory actions generated from omega-3 fatty acids via cyclooxygenase 2-nonsteroidal anti-inflammatory drugs and transcellular processing. J. Exp. Med. 192, 1197–1204 (2000).
Arita, M. et al. Stereochemical assignment, antiinflammatory properties, and receptor for the omega-3 lipid mediator resolvin E1. J. Exp. Med. 201, 713–722 (2005).
Serhan, C. N., Arita, M., Hong, S. & Gotlinger, K. Resolvins, docosatrienes, and neuroprotectins, novel omega-3-derived mediators, and their endogenous aspirin-triggered epimers. Lipids 39, 1125–1132 (2004).
Hong, S., Gronert, K., Devchand, P. R., Moussignac, R. L. & Serhan, C. N. Novel docosatrienes and 17S-resolvins generated from docosahexaenoic acid in murine brain, human blood, and glial cells. Autacoids in anti-inflammation. J. Biol. Chem. 278, 14677–14687 (2003).
Serhan, C. N. et al. Maresins: novel macrophage mediators with potent antiinflammatory and proresolving actions. J. Exp. Med. 206, 15–23 (2009).
Serhan, C. N. et al. Anti-inflammatory actions of neuroprotectin D1/protectin D1 and its natural stereoisomers: assignments of dihydroxy-containing docosatrienes. J. Immunol. 176, 1848–1859 (2006).
Freedman, S. D. et al. Association of cystic fibrosis with abnormalities in fatty acid metabolism. N. Engl. J. Med. 350, 560–569 (2004).
Levy, B. D. et al. Protectin D1 is generated in asthma and dampens airway inflammation and hyperresponsiveness. J. Immunol. 178, 496–502 (2007).
Chiang, N., Dalli, J., Colas, R. A. & Serhan, C. N. Identification of resolvin D2 receptor mediating resolution of infections and organ protection. J. Exp. Med. 212, 1203–1217 (2015).
Krishnamoorthy, S. et al. Resolvin D1 binds human phagocytes with evidence for proresolving receptors. Proc. Natl Acad. Sci. USA 107, 1660–1665 (2010).
Krishnamoorthy, S., Recchiuti, A., Chiang, N., Fredman, G. & Serhan, C. N. Resolvin D1 receptor stereoselectivity and regulation of inflammation and proresolving microRNAs. Am. J. Pathol. 180, 2018–2027 (2012).
Recchiuti, A., Krishnamoorthy, S., Fredman, G., Chiang, N. & Serhan, C. N. MicroRNAs in resolution of acute inflammation: identification of novel resolvin D1-miRNA circuits. FASEB J. 25, 544–560 (2011).
Chan, M. M. & Moore, A. R. Resolution of inflammation in murine autoimmune arthritis is disrupted by cyclooxygenase-2 inhibition and restored by prostaglandin E2-mediated lipoxin A4 production. J. Immunol. 184, 6418–6426 (2010).
Gilroy, D. W. et al. Inducible cyclooxygenase may have anti-inflammatory properties. Nat. Med. 5, 698–701 (1999).
Karp, C. L. et al. Defective lipoxin-mediated anti-inflammatory activity in the cystic fibrosis airway. Nat. Immunol. 5, 388–392 (2004).
Levy, B. D. et al. Diminished lipoxin biosynthesis in severe asthma. Am. J. Respir. Crit. Care Med. 172, 824–830 (2005).
Shinohara, M. et al. Cell-cell interactions and bronchoconstrictor eicosanoid reduction with inhaled carbon monoxide and resolvin D1. Am. J. Physiol. Lung Cell. Mol. Physiol. 307, L746–L757 (2014).
Leitch, A. E. et al. Cyclin-dependent kinases 7 and 9 specifically regulate neutrophil transcription and their inhibition drives apoptosis to promote resolution of inflammation. Cell Death Differ. 19, 1950–1961 (2012).
Maderna, P. & Godson, C. Lipoxins: resolutionary road. Br. J. Pharmacol. 158, 947–959 (2009).
Abdulnour, R. E. et al. Maresin 1 biosynthesis during platelet-neutrophil interactions is organ-protective. Proc. Natl Acad. Sci. USA 111, 16526–16531 (2014).
Eickmeier, O. et al. Aspirin-triggered resolvin D1 reduces mucosal inflammation and promotes resolution in a murine model of acute lung injury. Mucosal Immunol. 6, 256–266 (2013).
Hasturk, H. et al. Resolvin E1 regulates inflammation at the cellular and tissue level and restores tissue homeostasis in vivo. J. Immunol. 179, 7021–7029 (2007).
Godson, C. et al. Cutting edge: lipoxins rapidly stimulate nonphlogistic phagocytosis of apoptotic neutrophils by monocyte-derived macrophages. J. Immunol. 164, 1663–1667 (2000).
Rogerio, A. P. et al. Resolvin D1 and aspirin-triggered resolvin D1 promote resolution of allergic airways responses. J. Immunol. 189, 1983–1991 (2012).
Hsiao, H. M. et al. A novel anti-inflammatory and pro-resolving role for resolvin D1 in acute cigarette smoke-induced lung inflammation. PLoS ONE 8, e58258 (2013).
Palmer, C. D. et al. 17(R)-Resolvin D1 differentially regulates TLR4-mediated responses of primary human macrophages to purified LPS and live E. coli. J. Leukocyte Biol. 90, 459–470 (2011).
Thoren, F. B. et al. Human NK Cells induce neutrophil apoptosis via an NKp46- and Fas-dependent mechanism. J. Immunol. 188, 1668–1674 (2012).
Barnig, C. et al. Lipoxin A4 regulates natural killer cell and type 2 innate lymphoid cell activation in asthma. Sci. Transl Med. 5, 174ra26 (2013). This study identifies new cellular mechanisms for SPMs to regulate innate lymphoid cell responses, such as NK cell-mediated granulocyte apoptosis and regulation of ILC2 cytokine release.
Haworth, O., Cernadas, M. & Levy, B. D. NK cells are effectors for resolvin E1 in the timely resolution of allergic airway inflammation. J. Immunol. 186, 6129–6135 (2011).
Molofsky, A. B. et al. Innate lymphoid type 2 cells sustain visceral adipose tissue eosinophils and alternatively activated macrophages. J. Exp. Med. 210, 535–549 (2013).
Krishnamoorthy, N. et al. Cutting edge: maresin-1 engages regulatory T cells to limit type 2 innate lymphoid cell activation and promote resolution of lung inflammation. J. Immunol. 194, 863–867 (2015).
Monticelli, L. A. et al. Innate lymphoid cells promote lung-tissue homeostasis after infection with influenza virus. Nat. Immunol. 12, 1045–1054 (2011).
Ariel, A. et al. Apoptotic neutrophils and T cells sequester chemokines during immune response resolution through modulation of CCR5 expression. Nat. Immunol. 7, 1209–1216 (2006).
Haworth, O., Cernadas, M., Yang, R., Serhan, C. N. & Levy, B. D. Resolvin E1 regulates interleukin 23, interferon-γ and lipoxin A4 to promote the resolution of allergic airway inflammation. Nat. Immunol. 9, 873–879 (2008).
Ramon, S. et al. The specialized proresolving mediator 17-HDHA enhances the antibody-mediated immune response against influenza virus: a new class of adjuvant? J. Immunol. 193, 6031–6040 (2014).
Colgan, S. P., Serhan, C. N., Parkos, C. A., Delp-Archer, C. & Madara, J. L. Lipoxin A4 modulates transmigration of human neutrophils across intestinal epithelial monolayers. J. Clin. Invest. 92, 75–82 (1993).
Lawrence, D. W. et al. Antiadhesive role of apical decay-accelerating factor (CD55) in human neutrophil transmigration across mucosal epithelia. J. Exp. Med. 198, 999–1010 (2003).
Bonnans, C., Fukunaga, K., Levy, M. A. & Levy, B. D. Lipoxin A4 regulates bronchial epithelial cell responses to acid injury. Am. J. Pathol. 168, 1064–1072 (2006).
Campbell, E. L. et al. Resolvin E1-induced intestinal alkaline phosphatase promotes resolution of inflammation through LPS detoxification. Proc. Natl Acad. Sci. USA 107, 14298–14303 (2010).
Canny, G. et al. Lipid mediator-induced expression of bactericidal permeability-increasing protein (BPI) in human mucosal epithelia. Proc. Natl Acad. Sci. USA 99, 3902–3907 (2002).
El Kebir, D. et al. 15-epi-lipoxin A4 inhibits myeloperoxidase signaling and enhances resolution of acute lung injury. Am. J. Respir. Crit. Care Med. 180, 311–319 (2009).
El Kebir, D., Gjorstrup, P. & Filep, J. G. Resolvin E1 promotes phagocytosis-induced neutrophil apoptosis and accelerates resolution of pulmonary inflammation. Proc. Natl Acad. Sci. USA 109, 14983–14988 (2012).
Amar, S. et al. Periodontal disease is associated with brachial artery endothelial dysfunction and systemic inflammation. Arterioscler. Thromb. Vasc. Biol. 23, 1245–1249 (2003).
Jain, A. et al. Role for periodontitis in the progression of lipid deposition in an animal model. Infect. Immun. 71, 6012–6018 (2003).
Pouliot, M., Clish, C. B., Petasis, N. A., Van Dyke, T. E. & Serhan, C. N. Lipoxin A4 analogues inhibit leukocyte recruitment to Porphyromonas gingivalis: a role for cyclooxygenase-2 and lipoxins in periodontal disease. Biochemistry 39, 4761–4768 (2000).
Serhan, C. N. et al. Reduced inflammation and tissue damage in transgenic rabbits overexpressing 15-lipoxygenase and endogenous anti-inflammatory lipid mediators. J. Immunol. 171, 6856–6865 (2003).
Borgeson, E. et al. Lipoxin A4 inhibits Porphyromonas gingivalis-induced aggregation and reactive oxygen species production by modulating neutrophil-platelet interaction and CD11b expression. Infect. Immun. 79, 1489–1497 (2011).
Hasturk, H. et al. RvE1 protects from local inflammation and osteoclast- mediated bone destruction in periodontitis. FASEB J. 20, 401–403 (2006).
Oh, S. F., Pillai, P. S., Recchiuti, A., Yang, R. & Serhan, C. N. Pro-resolving actions and stereoselective biosynthesis of 18S E-series resolvins in human leukocytes and murine inflammation. J. Clin. Invest. 121, 569–581 (2011).
Hong, S. et al. Resolvin E1 metabolome in local inactivation during inflammation-resolution. J. Immunol. 180, 3512–3519 (2008).
Fredman, G. et al. Impaired phagocytosis in localized aggressive periodontitis: rescue by Resolvin E1. PLoS ONE 6, e24422 (2011).
Blaho, V. A., Zhang, Y., Hughes-Hanks, J. M. & Brown, C. R. 5-Lipoxygenase-deficient mice infected with Borrelia burgdorferi develop persistent arthritis. J. Immunol. 186, 3076–3084 (2011).
Bafica, A. et al. Host control of Mycobacterium tuberculosis is regulated by 5-lipoxygenase-dependent lipoxin production. J. Clin. Invest. 115, 1601–1606 (2005).
Herb, F. et al. ALOX5 variants associated with susceptibility to human pulmonary tuberculosis. Hum. Mol. Genet. 17, 1052–1060 (2008).
Tobin, D. M. et al. The lta4h locus modulates susceptibility to mycobacterial infection in zebrafish and humans. Cell 140, 717–730 (2010).
Ueda, T. et al. Combination therapy of 15-epi-lipoxin A4 with antibiotics protects mice from Escherichia coli-induced sepsis*. Crit. Care Med. 42, e288–e295 (2014).
Walker, J. et al. Lipoxin a4 increases survival by decreasing systemic inflammation and bacterial load in sepsis. Shock 36, 410–416 (2011).
Sordi, R. et al. Dual role of lipoxin A4 in pneumosepsis pathogenesis. Int. Immunopharmacol. 17, 283–292 (2013).
Cilloniz, C. et al. Lethal dissemination of H5N1 influenza virus is associated with dysregulation of inflammation and lipoxin signaling in a mouse model of infection. J. Virol. 84, 7613–7624 (2010).
Tam, V. C. et al. Lipidomic profiling of influenza infection identifies mediators that induce and resolve inflammation. Cell 154, 213–227 (2013).
Baillie, J. K. & Digard, P. Influenza—time to target the host? New Engl. J. Med. 369, 191–193 (2013).
Imai, Y. Role of omega-3 PUFA-derived mediators, the protectins, in influenza virus infection. Biochim. Biophys. Acta 1851, 496–502 (2015).
Morita, M. et al. The lipid mediator protectin D1 inhibits influenza virus replication and improves severe influenza. Cell 153, 112–125 (2013). This study demonstrates a new role for SPMs, whereby protectin exerts a direct antiviral effect on influenza virus and improves clinical outcomes.
Ng, S. et al. Effects of oseltamivir treatment on duration of clinical illness and viral shedding and household transmission of influenza virus. Clin. Infect. Dis. 50, 707–714 (2010).
Shirey, K. A. et al. Control of RSV-induced lung injury by alternatively activated macrophages is IL-4Rα-, TLR4-, and IFN-β-dependent. Mucosal Immunol. 3, 291–300 (2010).
Richardson, J. Y. et al. Respiratory syncytial virus (RSV) infection induces cyclooxygenase 2: a potential target for RSV therapy. J. Immunol. 174, 4356–4364 (2005).
Shirey, K. A. et al. Role of the lipoxygenase pathway in RSV-induced alternatively activated macrophages leading to resolution of lung pathology. Mucosal Immunol. 7, 549–557 (2014).
Rajasagi, N. K. et al. Controlling herpes simplex virus-induced ocular inflammatory lesions with the lipid-derived mediator resolvin E1. J. Immunol. 186, 1735–1746 (2011).
Rajasagi, N. K., Reddy, P. B., Mulik, S., Gjorstrup, P. & Rouse, B. T. Neuroprotectin D1 reduces the severity of herpes simplex virus-induced corneal immunopathology. Invest. Ophthalmol. Visual Sci. 54, 6269–6279 (2013).
Reis e Sousa, C. et al. In vivo microbial stimulation induces rapid CD40 ligand-independent production of interleukin 12 by dendritic cells and their redistribution to T cell areas. J. Exp. Med. 186, 1819–1829 (1997).
Aliberti, J., Hieny, S., Reis e Sousa, C., Serhan, C. N. & Sher, A. Lipoxin-mediated inhibition of IL-12 production by DCs: a mechanism for regulation of microbial immunity. Nat. Immunol. 3, 76–82 (2002).
Aliberti, J., Serhan, C. & Sher, A. Parasite-induced lipoxin A4 is an endogenous regulator of IL-12 production and immunopathology in Toxoplasma gondii infection. J. Exp. Med. 196, 1253–1262 (2002).
Bandeira-Melo, C. et al. Cyclooxygenase-2-derived prostaglandin E2 and lipoxin A4 accelerate resolution of allergic edema in Angiostrongylus costaricensis-infected rats: relationship with concurrent eosinophilia. J. Immunol. 164, 1029–1036 (2000).
Shryock, N. et al. Lipoxin A4 and 15-epi-lipoxin A4 protect against experimental cerebral malaria by inhibiting IL-12/IFN-γ in the brain. PLoS ONE 8, e61882 (2013).
Molina-Berrios, A. et al. Protective role of acetylsalicylic acid in experimental Trypanosoma cruzi infection: evidence of a 15-epi-lipoxin A4-mediated effect. PLoS Negl Trop. Dis. 7, e2173 (2013).
Bannenberg, G. L., Aliberti, J., Hong, S., Sher, A. & Serhan, C. Exogenous pathogen and plant 15-lipoxygenase initiate endogenous lipoxin A4 biosynthesis. J. Exp. Med. 199, 515–523 (2004).
Vance, R. E., Hong, S., Gronert, K., Serhan, C. N. & Mekalanos, J. J. The opportunistic pathogen Pseudomonas aeruginosa carries a secretable arachidonate 15-lipoxygenase. Proc. Natl Acad. Sci. USA 101, 2135–2139 (2004).
Haas-Stapleton, E. J. et al. Candida albicans modulates host defense by biosynthesizing the pro-resolving mediator resolvin E1. PLoS ONE 2, e1316 (2007).
Ono, E. et al. Lipoxin generation is related to soluble epoxide hydrolase activity in severe asthma. Am. J. Respir. Crit. Care Med. 190, 886–897 (2014).
Vachier, I. et al. Severe asthma is associated with a loss of LX4, an endogenous anti-inflammatory compound. J. Allergy Clin. Immunol. 115, 55–60 (2005).
Christie, P. E., Spur, B. W. & Lee, T. H. The effects of lipoxin A4 on airway responses in asthmatic subjects. Am. Rev. Respir. Dis. 145, 1281–1284 (1992).
Levy, B. D. et al. Multi-pronged inhibition of airway hyper-responsiveness and inflammation by lipoxin A4 . Nat. Med. 8, 1018–1023 (2002).
Levy, B. D. et al. Lipoxin A4 stable analogs reduce allergic airway responses via mechanisms distinct from CysLT1 receptor antagonism. FASEB J. 21, 3877–3884 (2007).
Aoki, H. et al. Resolvin E1 dampens airway inflammation and hyperresponsiveness in a murine model of asthma. Biochem. Biophys. Res. Commun. 367, 509–515 (2008).
Talbot, S. et al. silencing nociceptor neurons reduces allergic airway inflammation. Neuron 87, 341–354 (2015).
Park, C. K. et al. Resolving TRPV1- and TNF-α-mediated spinal cord synaptic plasticity and inflammatory pain with neuroprotectin D1. J. Neurosci. 31, 15072–15085 (2011).
Park, C. K. et al. Resolvin D2 is a potent endogenous inhibitor for transient receptor potential subtype V1/A1, inflammatory pain, and spinal cord synaptic plasticity in mice: distinct roles of resolvin D1, D2, and E1. J. Neurosci. 31, 18433–18438 (2011).
Serhan, C. N. et al. Macrophage proresolving mediator maresin 1 stimulates tissue regeneration and controls pain. FASEB J. 26, 1755–1765 (2012).
Xu, Z. Z. et al. Resolvins RvE1 and RvD1 attenuate inflammatory pain via central and peripheral actions. Nat. Med. 16, 592–597 (2010).
Takamiya, R. et al. Resolvin E1 maintains macrophage function under cigarette smoke-induced oxidative stress. FEBS Open Bio 2, 328–333 (2012).
Czerska, K. et al. Prostaglandin-endoperoxide synthase genes COX1 and COX2 - novel modifiers of disease severity in cystic fibrosis patients. J. Appl. Genet. 51, 323–330 (2010).
Yang, J., Eiserich, J. P., Cross, C. E., Morrissey, B. M. & Hammock, B. D. Metabolomic profiling of regulatory lipid mediators in sputum from adult cystic fibrosis patients. Free Radic. Biol. Med. 53, 160–171 (2012).
Martins, V. et al. ATLa, an aspirin-triggered lipoxin A4 synthetic analog, prevents the inflammatory and fibrotic effects of bleomycin-induced pulmonary fibrosis. J. Immunol. 182, 5374–5381 (2009).
Guilherme, R. F. et al. Pulmonary antifibrotic mechanisms aspirin-triggered lipoxin A4 synthetic analog. Am. J. Respir. Cell Mol. Biol. 49, 1029–1037 (2013).
Kowal-Bielecka, O. et al. Cyclooxygenase- and lipoxygenase-derived eicosanoids in bronchoalveolar lavage fluid from patients with scleroderma lung disease: an imbalance between proinflammatory and anti-inflammatory lipid mediators. Arthritis Rheum. 52, 3783–3791 (2005).
Planaguma, A. et al. Lovastatin decreases acute mucosal inflammation via 15-epi-lipoxin A4. Mucosal Immunol. 3, 270–279 (2010).
Zarbock, A., Singbartl, K. & Ley, K. Complete reversal of acid-induced acute lung injury by blocking of platelet-neutrophil aggregation. J. Clin. Invest. 116, 3211–3219 (2006).
Sun, W. et al. Endogenous expression pattern of resolvin D1 in a rat model of self-resolution of lipopolysaccharide-induced acute respiratory distress syndrome and inflammation. Int. Immunopharmacol. 23, 247–253 (2014).
Wu, S. H., Chen, X. Q., Liu, B., Wu, H. J. & Dong, L. Efficacy and safety of 15(R/S)-methyl-lipoxin A4 in topical treatment of infantile eczema. Br. J. Dermatol. 168, 172–178 (2013). This study reports the first randomized control trial of a SPM in the treatment of human disease; the use of lipoxin in eczema was associated with excellent clinical outcomes.
Weiss, G. A. et al. High levels of anti-inflammatory and pro-resolving lipid mediators lipoxins and resolvins and declining docosahexaenoic acid levels in human milk during the first month of lactation. Lipids Health Dis. 12, 89 (2013).
Serhan, C. N. et al. Design of lipoxin A4 stable analogs that block transmigration and adhesion of human neutrophils. Biochemistry 34, 14609–14615 (1995).
Papayianni, A., Serhan, C. N. & Brady, H. R. Lipoxin A4 and B4 inhibit leukotriene-stimulated interactions of human neutrophils and endothelial cells. J. Immunol. 156, 2264–2272 (1996).
Levy, B. D. et al. Polyisoprenyl phosphate (PIPP) signaling regulates phospholipase D activity: a 'stop' signaling switch for aspirin-triggered lipoxin A4. FASEB J. 13, 903–911 (1999).
Lee, T. H. et al. Lipoxin A4 and lipoxin B4 inhibit chemotactic responses of human neutrophils stimulated by leukotriene B4 and N-formyl-L-methionyl-L-leucyl-L-phenylalanine. Clin. Sci. 77, 195–203 (1989).
Gewirtz, A. T., Fokin, V. V., Petasis, N. A., Serhan, C. N. & Madara, J. L. LXA4, aspirin-triggered 15-epi-LXA4, and their analogs selectively downregulate PMN azurophilic degranulation. Am. J. Physiol. 276, C988–C994 (1999).
Maddox, J. F. & Serhan, C. N. Lipoxin A4 and B4 are potent stimuli for human monocyte migration and adhesion: selective inactivation by dehydrogenation and reduction. J. Exp. Med. 183, 137–146 (1996).
Jozsef, L., Zouki, C., Petasis, N. A., Serhan, C. N. & Filep, J. G. Lipoxin A4 and aspirin-triggered 15-epi-lipoxin A4 inhibit peroxynitrite formation, NF-κB and AP-1 activation, and IL-8 gene expression in human leukocytes. Proc. Natl Acad. Sci. USA 99, 13266–13271 (2002).
Bonnans, C. et al. Lipoxins are potential endogenous anti-inflammatory mediators in asthma. Am. J. Respir. Crit. Care Med. 165, 1531–1535 (2002).
Soyombo, O., Spur, B. W. & Lee, T. H. Effects of lipoxin A4 on chemotaxis and degranulation of human eosinophils stimulated by platelet-activating factor and N-formyl-L-methionyl-L-leucyl-L-phenylalanine. Allergy 49, 230–234 (1994).
Ramstedt, U. et al. Lipoxin A-induced inhibition of human natural killer cell cytotoxicity: studies on stereospecificity of inhibition and mode of action. J. Immunol. 138, 266–270 (1987).
Brezinski, M. E., Gimbrone, M. A. Jr, Nicolaou, K. C. & Serhan, C. N. Lipoxins stimulate prostacyclin generation by human endothelial cells. FEBS Lett. 245, 167–172 (1989).
Nascimento-Silva, V., Arruda, M. A., Barja-Fidalgo, C. & Fierro, I. M. Aspirin-triggered lipoxin A4 blocks reactive oxygen species generation in endothelial cells: a novel antioxidative mechanism. Thromb. Haemostasis 97, 88–98 (2007).
Cezar- de-Mello, P. F., Nascimento-Silva, V., Villela, C. G. & Fierro, I. M. Aspirin-triggered Lipoxin A4 inhibition of VEGF-induced endothelial cell migration involves actin polymerization and focal adhesion assembly. Oncogene 25, 122–129 (2006).
Sodin-Semrl, S., Taddeo, B., Tseng, D., Varga, J. & Fiore, S. Lipoxin A4 inhibits IL-1β-induced IL-6, IL-8, and matrix metalloproteinase-3 production in human synovial fibroblasts and enhances synthesis of tissue inhibitors of metalloproteinases. J. Immunol. 164, 2660–2666 (2000).
Wu, S. H., Wu, X. H., Lu, C., Dong, L. & Chen, Z. Q. Lipoxin A4 inhibits proliferation of human lung fibroblasts induced by connective tissue growth factor. Am. J. Respir. Cell Mol. Biol. 34, 65–72 (2006).
Parameswaran, K. et al. Modulation of human airway smooth muscle migration by lipid mediators and Th-2 cytokines. Am. J. Respir. Cell Mol. Biol. 37, 240–247 (2007).
Campbell, E. L. et al. Resolvin E1 promotes mucosal surface clearance of neutrophils: a new paradigm for inflammatory resolution. FASEB J. 21, 3162–3170 (2007).
Arita, M. et al. Resolvin E1, an endogenous lipid mediator derived from omega-3 eicosapentaenoic acid, protects against 2,4,6-trinitrobenzene sulfonic acid-induced colitis. Proc. Natl Acad. Sci. USA 102, 7671–7676 (2005).
Isobe, Y. et al. Identification and structure determination of novel anti-inflammatory mediator resolvin E3, 17,18-dihydroxyeicosapentaenoic acid. J. Biol. Chem. 287, 10525–10534 (2012).
Sun, Y. P. et al. Resolvin D1 and its aspirin-triggered 17R epimer. Stereochemical assignments, anti-inflammatory properties, and enzymatic inactivation. J. Biol. Chem. 282, 9323–9334 (2007).
Duffield, J. S. et al. Resolvin D series and protectin D1 mitigate acute kidney injury. J. Immunol. 177, 5902–5911 (2006).
Ariel, A. et al. The docosatriene protectin D1 is produced by TH2 skewing and promotes human T cell apoptosis via lipid raft clustering. J. Biol. Chem. 280, 43079–43086 (2005).
Nordgren, T. M. et al. Maresin-1 reduces the pro-inflammatory response of bronchial epithelial cells to organic dust. Respir. Res. 14, 51 (2013).
Genis, P. et al. Cytokines and arachidonic metabolites produced during human immunodeficiency virus (HIV)-infected macrophage-astroglia interactions: implications for the neuropathogenesis of HIV disease. J. Exp. Med. 176, 1703–1718 (1992).
Chen, M. et al. Lipid mediators in innate immunity against tuberculosis: opposing roles of PGE2 and LXA4 in the induction of macrophage death. J. Exp. Med. 205, 2791–2801 (2008).
Divangahi, M. et al. Mycobacterium tuberculosis evades macrophage defenses by inhibiting plasma membrane repair. Nat. Immunol. 10, 899–906 (2009).
Van Dyke, T. E. et al. Proresolving nanomedicines activate bone regeneration in periodontitis. J. Dent. Res. 94, 148–156 (2015).
Gao, L. et al. Resolvin E1 and chemokine-like receptor 1 mediate bone preservation. J. Immunol. 190, 689–694 (2013).
Kurihara, T. et al. Resolvin D2 restores neutrophil directionality and improves survival after burns. FASEB J. 27, 2270–2281 (2013).
Levy, B. D. et al. The endogenous pro-resolving mediators lipoxin A4 and resolvin E1 preserve organ function in allograft rejection. Prostaglandins Leukot. Essent. Fatty Acids 84, 43–50 (2011).
Liao, W. et al. Lipoxin A4 attenuates acute rejection via shifting TH1/TH2 cytokine balance in rat liver transplantation. Transplant. Proc. 45, 2451–2454 (2013).
Hua, J. et al. The resolvin D1 analogue controls maturation of dendritic cells and suppresses alloimmunity in corneal transplantation. Invest. Ophthalmol. Vis. Sci. 55, 5944–5951 (2014).
Devchand, P. R. et al. A synthetic eicosanoid LX-mimetic unravels host-donor interactions in allogeneic BMT-induced GvHD to reveal an early protective role for host neutrophils. FASEB J. 19, 203–210 (2005).
Medeiros, R. et al. Aspirin-triggered lipoxin A4 stimulates alternative activation of microglia and reduces Alzheimer disease-like pathology in mice. Am. J. Pathol. 182, 1780–1789 (2013).
Lukiw, W. J. et al. A role for docosahexaenoic acid-derived neuroprotectin D1 in neural cell survival and Alzheimer disease. J. Clin. Invest. 115, 2774–2783 (2005).
Mizwicki, M. T. et al. 1α, 25-dihydroxyvitamin D3 and resolvin D1 retune the balance between amyloid- β phagocytosis and inflammation in Alzheimer's disease patients. J. Alzheimer's Dis. 34, 155–170 (2013).
Liu, G. et al. Neuronal phagocytosis by inflammatory macrophages in ALS spinal cord: inhibition of inflammation by resolvin D1. Am. J. Neurodegener. Dis. 1, 60–74 (2012).
Prescott, D. & McKay, D. M. Aspirin-triggered lipoxin enhances macrophage phagocytosis of bacteria while inhibiting inflammatory cytokine production. Am. J. Physiol. Gastrointestinal Liver Physiol. 301, G487–G497 (2011).
Gewirtz, A. T. et al. Lipoxin a4 analogs attenuate induction of intestinal epithelial proinflammatory gene expression and reduce the severity of dextran sodium sulfate-induced colitis. J. Immunol. 168, 5260–5267 (2002).
Ishida, T. et al. Resolvin E1, an endogenous lipid mediator derived from eicosapentaenoic acid, prevents dextran sulfate sodium-induced colitis. Inflamm. Bowel Dis. 16, 87–95 (2010).
Bento, A. F., Claudino, R. F., Dutra, R. C., Marcon, R. & Calixto, J. B. Omega-3 fatty acid-derived mediators 17(R)-hydroxy docosahexaenoic acid, aspirin-triggered resolvin D1 and resolvin D2 prevent experimental colitis in mice. J. Immunol. 187, 1957–1969 (2011).
Hellmann, J., Tang, Y., Kosuri, M., Bhatnagar, A. & Spite, M. Resolvin D1 decreases adipose tissue macrophage accumulation and improves insulin sensitivity in obese-diabetic mice. FASEB J. 25, 2399–2407 (2011).
Neuhofer, A. et al. Impaired local production of proresolving lipid mediators in obesity and 17-HDHA as a potential treatment for obesity-associated inflammation. Diabetes 62, 1945–1956 (2013).
Quan-Xin, F. et al. Resolvin D1 reverses chronic pancreatitis-induced mechanical allodynia, phosphorylation of NMDA receptors, and cytokines expression in the thoracic spinal dorsal horn. BMC Gastroenterol. 12, 148 (2012).
Gronert, K. et al. A role for the mouse 12/15-lipoxygenase pathway in promoting epithelial wound healing and host defense. J. Biol. Chem. 280, 15267–15278 (2005).
de Paiva, C. S., Schwartz, C. E., Gjorstrup, P. & Pflugfelder, S. C. Resolvin E1 (RX-10001) reduces corneal epithelial barrier disruption and protects against goblet cell loss in a murine model of dry eye. Cornea 31, 1299–1303 (2012).
Dartt, D. A. et al. Conjunctival goblet cell secretion stimulated by leukotrienes is reduced by resolvins D1 and E1 to promote resolution of inflammation. J. Immunol. 186, 4455–4466 (2011).
Li, D. et al. Resolvin D1 and aspirin-triggered resolvin D1 regulate histamine-stimulated conjunctival goblet cell secretion. Mucosal Immunol. 6, 1119–1130 (2013).
Li, N., He, J., Schwartz, C. E., Gjorstrup, P. & Bazan, H. E. Resolvin E1 improves tear production and decreases inflammation in a dry eye mouse model. J. Ocular Pharmacol. Ther. 26, 431–439 (2010).
Connor, K. M. et al. Increased dietary intake of omega-3-polyunsaturated fatty acids reduces pathological retinal angiogenesis. Nat. Med. 13, 868–873 (2007).
Munger, K. A. et al. Transfection of rat kidney with human 15-lipoxygenase suppresses inflammation and preserves function in experimental glomerulonephritis. Proc. Natl Acad. Sci. USA 96, 13375–13380 (1999).
Borgeson, E. et al. Lipoxin A4 and benzo-lipoxin A4 attenuate experimental renal fibrosis. FASEB J. 25, 2967–2979 (2011).
Qu, X. et al. Resolvins E1 and D1 inhibit interstitial fibrosis in the obstructed kidney via inhibition of local fibroblast proliferation. J. Pathol. 228, 506–519 (2012).
Zhang, L. et al. BML-111, a lipoxin receptor agonist, modulates the immune response and reduces the severity of collagen-induced arthritis. Inflamm. Res. 57, 157–162 (2008).
Lima-Garcia, J. F. et al. The precursor of resolvin D series and aspirin-triggered resolvin D1 display anti-hyperalgesic properties in adjuvant-induced arthritis in rats. Br. J. Pharmacol. 164, 278–293 (2011).
Keyes, K. T. et al. Resolvin E1 protects the rat heart against reperfusion injury. Am. J. Physiol. Heart Circ. Physiol. 299, H153–H164 (2010).
Shen, J. et al. Macrophage-mediated 15-lipoxygenase expression protects against atherosclerosis development. J. Clin. Invest. 98, 2201–2208 (1996).
Marcheselli, V. L. et al. Novel docosanoids inhibit brain ischemia-reperfusion-mediated leukocyte infiltration and pro-inflammatory gene expression. J. Biol. Chem. 278, 43807–43817 (2003).
Kim, T. H., Kim, G. D., Jin, Y. H., Park, Y. S. & Park, C. S. Omega-3 fatty acid-derived mediator, Resolvin E1, ameliorates 2,4-dinitrofluorobenzene-induced atopic dermatitis in NC/Nga mice. Int. Immunopharmacol. 14, 384–391 (2012).
Klein, C. P. et al. Effects of D-series resolvins on behavioral and neurochemical changes in a fibromyalgia-like model in mice. Neuropharmacology 86, 57–66 (2014).
Bang, S. et al. Resolvin D1 attenuates activation of sensory transient receptor potential channels leading to multiple anti-nociception. Br. J. Pharmacol. 161, 707–720 (2010).
he authors wish to acknowledge C. N. Serhan for his helpful advice in the preparation of this manuscript. This work was funded in part by US National Institutes of Health grants HL122531, U10HL109172, U01HL108712 and P01GM095467.
B.D.L. is a co-inventor on patents assigned to Brigham and Women's Hospital; some of these patents (those pertaining to resolvins) are licensed to Resolvyx Pharmaceuticals. The interests of B.D.L. were reviewed and are managed by the Brigham and Women's Hospital and Partners HealthCare in accordance with their conflict-of-interest policies.
An active process at the cellular and tissue level governed by specific mediators that promote a return to tissue homeostasis.
The cellular process by which phagocytes engulf dying and dead cells (for example, apoptotic or necrotic) for removal from tissues. It is part of the resolution programme to restore tissue homeostasis.
Rights and permissions
About this article
Cite this article
Basil, M., Levy, B. Specialized pro-resolving mediators: endogenous regulators of infection and inflammation. Nat Rev Immunol 16, 51–67 (2016). https://doi.org/10.1038/nri.2015.4
This article is cited by
Cystathionine gamma-lyase (Cth) induces efferocytosis in macrophages via ERK1/2 to modulate intestinal barrier repair
Cell Communication and Signaling (2023)
Pain-resolving immune mechanisms in neuropathic pain
Nature Reviews Neurology (2023)
Protectin DX as a therapeutic strategy against frailty in mice
In vitro phenotypic effects of Lipoxin A4 on M1 and M2 polarized macrophages derived from THP-1
Molecular Biology Reports (2023)
Revealing concealed cardioprotection by platelet Mfsd2b-released S1P in human and murine myocardial infarction
Nature Communications (2023)