Changes in cellular metabolism are associated with the activation of diverse immune subsets. These changes are fuelled by nutrients including glucose, amino acids and fatty acids, and are closely linked to immune cell fate and function. An emerging concept is that nutrients are not equally available to all immune cells, suggesting that the regulation of nutrient utility through competitive uptake and use is important for controlling immune responses. This review considers immune microenvironments where nutrients become limiting, the signalling alterations caused by insufficient nutrients, and the importance of nutrient availability in the regulation of immune responses.
Immune responses involve rapid and extensive changes in the activities of immune cells with concomitant alterations in cellular metabolism. Immune cells have various demands for nutrients, including glucose, glutamine and fatty acids, which are metabolised to generate ATP for energy expenditure. Meanwhile, these nutrients are also used to generate cellular building blocks for the biosynthesis of cellular components, including protein, nucleic acids and lipids (Fig. 1). Indeed, diverse metabolic configurations supported by a number of different nutrients have been described for immune subsets, which facilitate the specialised immune functions of individual cells1. To understand how distinct immune cells are affected by immune microenvironments where nutrient levels are limited, it is important to first appreciate the nutrient demands and metabolic configurations of different immune cells, as briefly outlined in the first section of this review [reviewed in detail elsewhere1,2,3]. We then discuss the circumstances in which nutrients might become limiting within different types of immune microenvironment, including the tumour microenvironment and sites of infection. Finally, we consider the consequences of nutrient deprivation on nutrient-sensitive signalling pathways and its impact for immune function.
Nutrient demands and metabolic configurations
Cellular metabolism is a key factor in determining the fate and functions of immune cells. Studies have shown that disrupting metabolic signalling pathways can result in the loss of normal immune function or altered immune cell differentiation. Immune cells have diverse functions, so it is perhaps unsurprising that they have different nutrient and energy demands. As T cells differentiate into memory, regulatory and effector T cell subsets, the nutrients they use and the metabolic configurations they adopt adjust to match their respective metabolic demands. A good example is the different metabolic requirements of naive and effector T cell subsets (Fig. 2)4. Naive T cells have low metabolic rates and minimal biosynthetic requirements when compared to activated T cell subsets, which is due to their relative inactivity. Naive T cells take up small amounts of fuels such as glucose, glutamine and fatty acids, which they metabolise through oxidative phosphorylation (OXPHOS), primarily for the purpose of making energy (Figs. 1 and 2)4. Metabolic rates significantly increase in T cells following immune activation due to proliferative expansion and the induction of a range of effector functions including the production of large amounts of cytokines, a process that demands substantial amounts of energy and cellular biosynthesis. This leads to an increased demand for nutrients, including glucose and glutamine as well as amino acids such as serine and arginine, to fuel both bioenergetic and biosynthetic pathways (Figs. 1 and 2)4,6,7,8. Effector T cells have high rates of glucose and glutamine uptake, which are then metabolised by aerobic glycolysis in the cytoplasm and the tricarboxylic acid (TCA) cycle in the mitochondria9,10,11. Effector T cells also have increased uptake of other amino acids including, but not limited to, leucine, serine and tryptophan6,7. This metabolic configuration supports the combined cellular needs of effector T cells for energy and biosynthesis (Fig. 1). By contrast, memory T cells return to a quiescent state and have reduced biosynthetic demands, and revert to using oxidative metabolism for more efficient energy production. Memory T cells also generate intracellular fuel reserves in the form of glycogen and triacylglycerides that provide them with metabolic security and plasticity essential to support the longevity and rapid recall responses that are central to their functions4,5. Regulatory T cells, important in exerting control over effector T cells, do not have large biosynthetic demands and so predominantly engage in OXPHOS, which is fuelled by exogenous fatty acids imported and metabolised via a pathway called fatty acid oxidation to generate energy, (Fig. 1)12. It should be noted that when regulatory T cells do engage in cellular division, they switch on glycolytic metabolism to support the biosynthetic demands for growth and proliferation13,14. Disrupting cellular metabolism in T cells results in impaired T cell function and alters the differentiation of T cells towards effector, memory or regulatory subsets3.
B lymphocytes, or B cells, are important for humoral immunity and are the cells that produce antibodies. B cells also up-regulate glucose uptake and metabolic genes upon B cell antigen receptor activation to fuel both energy production and biosynthesis; in particular, de novo lipogenesis is required during the differentiation of plasma cells, which are responsible for making large amounts of high affinity antibody15,16. Glutamine can also be used by B cells and is particularly important for B cell survival in hypoxic conditions17. Other lymphocytes, such as activated natural killer (NK) cells are fuelled primarily by glucose but not by glutamine (Fig. 2). Here glucose simultaneously supports high rates of aerobic glycolysis and mitochondrial respiration, with the latter being achieved by engaging the citrate–malate shuttle, rather than the TCA cycle, to drive OXPHOS18,19. It is not yet clear why NK cells adopt this metabolic configuration but it seems likely that it is important to support epigenetic regulation as the citrate–malate shuttle also generates acetyl-CoA, the substrate for histone acetylation.
Myeloid cells have also been reported to adopt distinct metabolic phenotypes and have differing requirements for nutrients. Inflammatory M1 macrophages adopt a glycolytic metabolism and largely shut down OXPHOS; the TCA cycle is not operating in these cells, and the TCA cycle enzymes are repurposed into two linear metabolic pathways that produce important immune regulatory molecules, meaning that this metabolic configuration is essential for the proinflammatory functions of these cells (reviewed in ref. 20). In contrast, M2 macrophages, which are longer lived than M1 macrophages, are implicated in wound healing and tissue repair, and maintain an intact TCA cycle and favour oxidative metabolism fuelling OXPHOS with glutamine and fatty acids2. In this regard, interfering with macrophage metabolism can alter the differentiation of M1 versus M2 macrophages, such that the inhibition of glycolysis promotes the differentiation of M2 macrophages over M1 macrophages3. Lastly, the amino acid arginine is important for both M1 and M2 macrophages as a substrate for the enzymes inducible nitric oxide synthase (iNOS) and arginase, respectively.
Granulocytes such as neutrophils have very low levels of OXPHOS and rely primarily on glycolysis3. Interestingly, inflammatory neutrophils contain large glycogen deposits that are intracellular fuel stores that can be used to sustain this glycolytic metabolism in the absence of glucose21. This may provide neutrophils with an advantage in inflammatory microenvironments where extracellular glucose levels are limiting. Dendritic cells (DCs) have also been shown to contain glycogen stores that are important in fuelling the immediate glycolytic response following lipopolysaccharide stimulation22. Interestingly, glycolytic restriction can both inhibit and enhance DC functions depending on its timing during DC activation. Inhibition of glycolysis during initial activation results in impaired DC function, while inhibition of glycolysis 8 h after initial activation, a time point when DCs are likely to have reached the draining lymph node, enhances DC proinflammatory function and induction of T cell responses22,23,24,25.
Overall, it is clear that different immune cell subsets have distinct demands for nutrients, so they will be differentially affected by nutrient-restrictive microenvironments such as tumours or sites of infection. This argues that nutrient availability could play an important role in shaping immune responses.
Availability of nutrients within immune microenvironments
Tumours have long been known to be highly glycolytic and to have a prodigious appetite for glucose, which is used to support unrestrained tumour growth and proliferation. This elevated glucose utilisation by tumour cells rapidly consumes the glucose delivered to the tumour from the blood resulting in low extracellular levels of glucose within solid tumours26,27,28. Some tumours also rely on glutamine to support their energy and biosynthetic demands29,30, and there is some evidence to suggest that glutamine levels may become limiting in some tumour microenvironments31. These features make the tumour microenvironment a metabolically restrictive setting for infiltrating immune cells, and this has been reported to have an effect on the efficacy of cancer immunotherapies; in the case of human melanoma, tumour cells with high glycolytic rates have been found to be resistant to adoptive T cell therapy showing poor T cell infiltration and cytotoxicity32.
Do similar mechanisms to those observed in the tumour microenvironment affect immune cells at other immunological sites? There is certainly evidence that competition for nutrients is also relevant at sites of pathogen infection. Many viruses reprogramme the cells that they infect for increased glycolysis33,34,35,36,37,38,39, and some have been reported to increase glutamine metabolism in the cells that they infect40,41. Increased glycolysis and/or glutaminolysis are advantageous for the virus, as they provide the biosynthetic material to construct new viral particles and complete the viral life cycle. Similarly, intracellular bacteria, such as Mycobacterium tuberculosis, also reprogramme the host cell for increased glucose metabolism and glycolysis42,43,44,45. Increased fuel consumption in these infected cells is likely to lead to decreased concentrations of extracellular glucose and glutamine in the local microenvironment. Additionally, many extracellular bacteria, such as Staphylococcus aureus, use glucose as their primary fuel source, and large numbers of bacteria can accumulate at a given site during infection46. Therefore, it is likely that glucose levels will become depleted at such sites of bacterial infection. Indeed, reduced glucose levels are reported in patients with bacterial meningitis47. Therefore, it is likely that at sites of infection, the increased utilisation of glucose and glutamine by bacteria or virally infected cells will affect responding immune cells through decreased nutrient availability in the local immune microenvironment.
Beyond the competitive utilisation of glucose and glutamine, the levels of other nutrients can be manipulated within immune microenvironments. Tumours can deplete amino acids, such as arginine and tryptophan, from the tumour microenvironment by expressing catabolic enzymes or by recruiting cells that express such enzymes. In this regard, arginine can be consumed by the enzymes iNOS, often expressed in tumour cells48,49, and by arginase, expressed by tumour-associated fibroblasts and macrophages (TAMs)50. Arginine is important for T and NK cell responses and arginine depletion in the tumour microenvironment has been shown to inhibit anti-tumour T cells responses8,51,52,53,54. Additionally, tryptophan can be depleted by the enzyme Indoleamine 2,3-dioxygenase (IDO), which is often highly expressed in tumour cells or in tumour-associated cells such as tolerogenic DCs50,55. IDO-mediated inhibition of T and NK cells is due to a combination of tryptophan depletion and the production of the metabolite kynurenine, which impacts the function of NK and T cells, at least in part, through acting upon the aryl hydrocarbon receptor (AhR)56. Originally, IDO was described as an innate mechanism of host defence against infection57. The effects of IDO activity on the local distribution of tryptophan and kynurenine is implicated in growth inhibition of certain bacteria, parasites and viruses58,59. The activity of IDO at these sites of infection will, therefore, also have implications for immune cells including T cells and NK cells.
Similarly to tumours, pathogens also utilise mechanisms to deprive immune cells of arginine as part of their immune evasion strategies. For example, Helicobacter pylori bacteria express arginase to deplete the local microenvironment of arginine and in doing so prevent iNOS-expressing macrophages from producing anti-microbial nitric oxide (NO)60. Low levels of systemic arginine and reduced NO production are also a feature of severe malarial infection61.
Therefore, there are multiple mechanisms that can result in the depletion of glucose and various amino acids in pathological immune microenvironments, and this can result in altered immune function and response to tumours or infection.
It is clear that tumours and pathogens compete with immune cells for nutrients as part of their immune evasion strategies, but equally there can be competition for nutrients between different immune cells, which may also be a normal physiological mechanism for regulating immune responses. Certainly, there are immunological situations where immune cells with elevated metabolism and nutrient demands compete with each other for the available fuels, such as within inflammatory lymph nodes where there is a rapid increase in the number of activated immune cells, or within the germinal centres where there is a concentration of metabolically active B cells and T follicular helper cells. Perhaps the best example where competition for nutrients between immune cells can play a role in shaping immune responses comes from studying DC–T cell interactions. There is evidence that an antigen-presenting DC can become starved of nutrients, such as glucose, due to competitive nutrient uptake by neighbouring cells, in particular activating CD8 T cells25. Interestingly, glucose deprivation of DC can result in increased DC proinflammatory outputs, including the expression of interleukin-12 and costimulatory molecules, which leads to enhanced CD8 T cell responses25.
It is well established that T lymphocytes greatly increase nutrient uptake in response to antigen stimulation through up-regulating the expression of nutrient transporters. This is critically important in the generation of effector cells; indeed T cells lacking certain glucose or amino acid transporters fail to differentiate into effector cells. During activation, CD8 T cells cluster around antigen-presenting DCs within the lymph node62,63,64. These clustering T cells can potentially deplete the nutrients from the microenvironment surrounding the DCs (Fig. 3). In support of this, co-cultures of clustering CD8 T cells can inactivate the nutrient-sensitive mammalian Target of Rapamycin Complex 1 (mTORC1) signalling pathways in the interacting DCs25 (Fig. 3). In fact, antigen-presenting DCs can be found at the centre of cell clusters consisting of numerous different types of activated immune cells with elevated nutrient uptake rates in addition to CD8 T cells, including NK cells, CD4 T cells and pDC65,66,67,68. Therefore, it is tempting to speculate that starvation of DCs, and the resultant increase in DC outputs, is a physiological mechanism for the regulation of DC-induced T cells responses, a scenario where nutrients are acting as an immunological signal (Fig. 3). This is an interesting concept that remains to be formally tested.
Competition for nutrients between T cells has also been proposed as a mechanism for the selection of T cells that recognise antigen with high affinity69. Compared with those from low-affinity TCR, high-affinity TCR-antigen interactions induce a more robust and sustained metabolic response, with increased expression of glucose transporters and glycolytic genes70. Therefore, it is suggested that high-affinity T cell clones could outcompete their low-affinity counterparts for nutrients leading to nutrient starvation and apoptosis of these low-affinity T cell clones69. It is easy to imagine other situations where neighbouring immune cells would compete for nutrients in similar ways. For example, during B cell germinal centre responses, a solitary follicular helper T cell is surrounded by a large number of activating B cells with elevated nutrients demands. However, the inability to visualise nutrient abundance at the single-cell level represents a technical barrier that currently limits further exploration of nutrients as important immunological signals.
Consequences of altered nutrient availability: signalling and immune outputs
Nutrient-restrictive microenvironments will directly impinge upon metabolic pathways in immune cells, but will also impact upon nutrient-sensitive signalling pathways important in immune regulation. Glucose and glutamine can impact multiple signalling pathways that are integral to the control of immune responses (Fig. 4). AMP-activated protein kinase (AMPK) is an indirect glucose sensor that becomes activated when ATP, or glycolytic intermediate fructose-1,6-bisphosphate, levels are decreased due to glucose restriction71. In effector T cells, AMPK can be activated within an hour of being placed in low concentrations of glucose72,73. Glutamine is also important for ATP production in effector T cells and AMPK can be activated by glutamine restriction in these cells73. AMPK negatively regulates the mTORC1, an important metabolic regulator with widespread roles in controlling immune cell functions72,73,74 (Fig. 4). Roles for mTORC1 include shaping T cell differentiation, controlling NK cells differentiation and effector function, and regulating the function of antigen-presenting DCs74 (Fig. 5). Therefore, the consequences of altered AMPK/mTORC1 signalling due to glucose restriction will include the inhibition inflammatory T cell and NK cell responses while promoting TReg differentiation (Fig. 5).
Interestingly, fructose-1,6-bisphosphate is not the only glycolytic intermediate that impacts important immune signalling pathways. Phosphenolpyruvate (PEP), another glucose metabolite, can affect Ca2+ signalling and the activation of the nuclear factor of activated T cells (NFAT) transcription factor in antigen-stimulated T cells (Fig. 4). PEP represses sarco/ER Ca2+-ATPase (SERCA) activity, which is responsible for Ca2+ reuptake into the ER; therefore, PEP prolongs cytosolic Ca2+ signalling and NFAT nuclear activity. T cells stimulated through the T cell antigen receptor in low glucose conditions, such as tumour microenvironments, have reduced PEP levels, reduced cytosolic Ca2+ signalling and less nuclear NFAT, leading to defective T cell activation27.
In addition to fueling glycolysis and OXPHOS, glucose and glutamine are also used for generation of uridine diphosphate N-acetylglucosamine (UDP-GlcNAc); this is the substrate for O-GlcNAcylation, which is the reversible addition of N-acetylglucosamine (GlcNAc) to proteins on serine or threonine residues by O-linked N-acetylglucosaminyltransferase (OGT). O-GlcNAcylation is dependent on the supply of both glucose and glutamine in T cells, suggesting that OGT and O-GlcNAcylation are important nutrient-sensing mechanisms in these cells9. Indeed, OGT is reported to be essential for normal T cell development, activation and clonal expansion9,75. Mechanistically, a number of signalling molecules that are important for T cell function are found to be O-GlcNAcylated, including c-Myc, NFAT and nuclear factor-κB9,75,76. This protein modification has not yet been studied in depth in other immune cell subsets.
Apart from glutamine, other amino acids also control numerous signalling pathways that are important for immune function. For example, the activity of mTORC1 is acutely sensitive to the levels of a number of amino acids including leucine, arginine and glutamine77. In addition, the transcription factor c-Myc is also regulated by amino acid availability. cMyc protein has a very short half-life in lymphocytes and sustained expression of cMyc is only possible in cells that have high rates of amino acid uptake and protein synthesis6,9,19,78. cMyc plays a crucial role during the activation and differentiation of T cell subsets and also of other lymphocytes including B cells and NK cells (Fig. 5)11,19,78,79. Moreover, the serine/threonine protein kinase General control nonderepressible 2 (GCN2) is a direct sensor of low cellular amino acid levels, and is activated through binding to uncharged transfer RNA (tRNA) (Fig. 4)80. GCN2 activity has been linked to the functions of various immune cells. In DCs, GCN2 activation results in enhanced antigen presentation to CD8 cells81. Conversely, GCN2 activity in gut antigen-presenting cells restrains excessive Th17 responses, with mice deficient of GCN2 developing stronger Th17 responses and more severe colitis in an induced colitis model82. IDO suppresses T cell responses, at least in part, by depleting tryptophan levels, leading to the activation of GCN2 within the T cell (Fig. 4). Activation of GCN2 in CD8 T cells results in proliferative arrest and anergy, while activation of GCN2 in CD4 T cells can lead to the generation of regulatory T cells (Fig. 5)83,84.
The challenge of in vivo metabolic analysis
In vitro or ex vivo metabolic analyses have helped bring forth advances in our understanding of the metabolic phenotypes adopted by immune cells. While these studies have been extremely informative, the reported metabolic phenotypes may not be recapitulated in vivo. The metabolic phenotypes of immune cells are dependent on the supply of the relevant fuels such as glucose and glutamine, which are certainly less abundant in vivo than in culture conditions used in the laboratory. The consequence of a limiting supply of these fuels in vivo, within discrete immune microenvironments will be the restriction of metabolic pathways and the alteration of nutrient-sensitive signalling pathways that affect immune cell fate and function. However, our understanding of when and where nutrients are available in vivo is severely hampered by the lack of research tools to measure nutrient distribution at the single-cell level. Therefore, elucidating how nutrient supply affects the metabolism, signalling and thus function of immune cells in diverse and complex immune microenvironments remains a significant challenge for the immunometabolism field.
O’Neill, L. A., Kishton, R. J. & Rathmell, J. A guide to immunometabolism for immunologists. Nat. Rev. Immunol. 16, 553–565 (2016).
Murray, P. J., Rathmell, J. & Pearce, E. SnapShot: immunometabolism. Cell Metab. 22, 190–190 e1 (2015).
Loftus, R. M. & Finlay, D. K. Immunometabolism: cellular metabolism turns immune regulator. J. Biol. Chem. 291, 1–10 (2016).
Buck, M. D., O’Sullivan, D. & Pearce, E. L. T cell metabolism drives immunity. J. Exp. Med. 212, 1345–1360 (2015).
Ma, R. et al. A Pck1-directed glycogen metabolic program regulates formation and maintenance of memory CD8+ T cells. Nat. Cell Biol. 20, 21–27 (2018).
Sinclair, L. V. et al. Control of amino-acid transport by antigen receptors coordinates the metabolic reprogramming essential for T cell differentiation. Nat. Immunol. 14, 500–508 (2013).
Ma, E. H. et al. Serine is an essential metabolite for effector T cell expansion. Cell Metab. 25, 345–357 (2017).
Geiger, R. et al. L-arginine modulates T cell metabolism and enhances survival and anti-tumor activity. Cell 167, 829–842 e13 (2016).
Swamy, M. et al. Glucose and glutamine fuel protein O-GlcNAcylation to control T cell self-renewal and malignancy. Nat. Immunol. 17, 712–720 (2016).
Finlay, D. K. et al. PDK1 regulation of mTOR and hypoxia-inducible factor 1 integrate metabolism and migration of CD8+ T cells. J. Exp. Med. 209, 2441–2453 (2012).
Wang, R. et al. The transcription factor Myc controls metabolic reprogramming upon T lymphocyte activation. Immunity 35, 871–882 (2011).
Zeng, H. & Chi, H. Metabolic control of regulatory T cell development and function. Trends Immunol. 36, 3–12 (2015).
Gerriets, V. A. et al. Foxp3 and Toll-like receptor signaling balance Treg cell anabolic metabolism for suppression. Nat. Immunol. 17, 1459–1466 (2016).
Zeng, H. et al. mTORC1 couples immune signals and metabolic programming to establish T(reg)-cell function. Nature 499, 485–490 (2013).
Doughty, C. A. et al. Antigen receptor-mediated changes in glucose metabolism in B lymphocytes: role of phosphatidylinositol 3-kinase signaling in the glycolytic control of growth. Blood 107, 4458–4465 (2006).
Dufort, F. J. et al. Glucose-dependent de novo lipogenesis in B lymphocytes: a requirement for atp-citrate lyase in lipopolysaccharide-induced differentiation. J. Biol. Chem. 289, 7011–7024 (2014).
Le, A. et al. Glucose-independent glutamine metabolism via TCA cycling for proliferation and survival in B cells. Cell Metab. 15, 110–121 (2012).
Assmann, N. et al. Srebp-controlled glucose metabolism is essential for NK cell functional responses. Nat. Immunol. 18, 1197–1206 (2017).
Loftus, R. M. et al. Amino acid-dependent cMyc expression is essential for NK cell metabolic and functional responses in mice. Nat. Commun. 9, 2341 (2018).
O’Neill, L. A. & Pearce, E. J. Immunometabolism governs dendritic cell and macrophage function. J. Exp. Med. 213, 15–23 (2016).
Robinson, J. M., Karnovsky, M. L. & Karnovsky, M. J. Glycogen accumulation in polymorphonuclear leukocytes, and other intracellular alterations that occur during inflammation. J. Cell Biol. 95, 933–942 (1982).
Thwe, P. M. et al. Cell-intrinsic glycogen metabolism supports early glycolytic reprogramming required for dendritic cell immune responses. Cell Metab. 26, 558–567 e5 (2017).
Everts, B. et al. TLR-driven early glycolytic reprogramming via the kinases TBK1-IKKvarepsilon supports the anabolic demands of dendritic cell activation. Nat. Immunol. 15, 323–332 (2014).
Krawczyk, C. M. et al. Toll-like receptor-induced changes in glycolytic metabolism regulate dendritic cell activation. Blood 115, 4742–4749 (2010).
Lawless, S. et al. Glucose represses dendritic cell-induced T cell responses. Nat. Commun. 8, 15620 (2017).
Hirayama, A. et al. Quantitative metabolome profiling of colon and stomach cancer microenvironment by capillary electrophoresis time-of-flight mass spectrometry. Cancer Res. 69, 4918–4925 (2009).
Ho, P. C. et al. Phosphoenolpyruvate is a metabolic checkpoint of anti-tumor T cell responses. Cell 162, 1217–1218 (2015).
Chang, C. H. et al. Metabolic competition in the tumor microenvironment is a driver of cancer progression. Cell 162 1229–1241 (2015).
Still, E. R. & Yuneva, M. O. Hopefully devoted to Q: targeting glutamine addiction in cancer. Br. J. Cancer 116, 1375–1381 (2017).
Zhu, L. et al. Metabolic imaging of glutamine in cancer. J. Nucl. Med. 58, 533–537 (2017).
Zhou, R. et al. [(18)F](2S,4R)4-Fluoroglutamine PET detects glutamine pool size changes in triple-negative breast cancer in response to glutaminase inhibition. Cancer Res. 77, 1476–1484 (2017).
Cascone, T. et al. Increased tumor glycolysis characterizes immune resistance to adoptive T cell therapy. Cell Metab. 27, 977–987 e4 (2018).
Thai, M. et al. Adenovirus E4ORF1-induced MYC activation promotes host cell anabolic glucose metabolism and virus replication. Cell Metab. 19, 694–701 (2014).
Piccoli, C. et al. HCV infection induces mitochondrial bioenergetic unbalance: causes and effects. Biochim. Biophys. Acta 1787, 539–546 (2009).
Ripoli, M. et al. Hepatitis C virus-linked mitochondrial dysfunction promotes hypoxia-inducible factor 1 alpha-mediated glycolytic adaptation. J. Virol. 84, 647–660 (2010).
Yu, Y., Maguire, T. G. & Alwine, J. C. Human cytomegalovirus activates glucose transporter 4 expression to increase glucose uptake during infection. J. Virol. 85, 1573–1580 (2011).
Gualdoni, G. A. et al. Rhinovirus induces an anabolic reprogramming in host cell metabolism essential for viral replication. Proc. Natl Acad. Sci. USA 115, E7158–E7165 (2018).
Palmer, C. S. et al. Increased glucose metabolic activity is associated with CD4+ T-cell activation and depletion during chronic HIV infection. AIDS 28, 297–309 (2014).
Smallwood, H. S. et al. Targeting metabolic reprogramming by influenza infection for therapeutic intervention. Cell Rep. 19, 1640–1653 (2017).
Chi, P. I. et al. Avian reovirus sigmaA-modulated suppression of lactate dehydrogenase and upregulation of glutaminolysis and the mTOC1/eIF4E/HIF-1alpha pathway to enhance glycolysis and the TCA cycle for virus replication. Cell Microbiol. 20, e12946 (2018).
Thai, M. et al. MYC-induced reprogramming of glutamine catabolism supports optimal virus replication. Nat. Commun. 6, 8873 (2015).
Escoll, P. & Buchrieser, C. Metabolic reprogramming of host cells upon bacterial infection: why shift to a Warburg-like metabolism? FEBS J. 285, 2146–2160 (2018).
Gleeson, L. E. et al. Cutting edge: Mycobacterium tuberculosis induces aerobic glycolysis in human alveolar macrophages that is required for control of intracellular bacillary replication. J. Immunol. 196, 2444–2449 (2016).
Shi, L. et al. Infection with Mycobacterium tuberculosis induces the Warburg effect in mouse lungs. Sci. Rep. 5, 18176 (2015).
Bowden, S. D. et al. Glucose and glycolysis are required for the successful infection of macrophages and mice by Salmonella enterica serovar typhimurium. Infect. Immun. 77, 3117–26 (2009).
Vitko, N. P., Spahich, N. A. & Richardson, A. R. Glycolytic dependency of high-level nitric oxide resistance and virulence in Staphylococcus aureus. MBio 6, https://doi.org/10.1128/mBio.00045-15 (2015).
Tamune, H. et al. Cerebrospinal fluid/blood glucose ratio as an indicator for bacterial meningitis. Am. J. Emerg. Med 32, 263–266 (2014).
Cheng, H. et al. Nitric oxide in cancer metastasis. Cancer Lett. 353, 1–7 (2014).
Kostourou, V. et al. The role of tumour-derived iNOS in tumour progression and angiogenesis. Br. J. Cancer 104, 83–90 (2011).
Mondanelli, G. et al. The immune regulation in cancer by the amino acid metabolizing enzymes ARG and IDO. Curr. Opin. Pharm. 35, 30–39 (2017).
Fletcher, M. et al. l-Arginine depletion blunts antitumor T-cell responses by inducing myeloid-derived suppressor cells. Cancer Res. 75, 275–283 (2015).
Lamas, B. et al. Altered functions of natural killer cells in response to L-Arginine availability. Cell Immunol. 280, 182–190 (2012).
Goh, C. C. et al. Hepatitis C virus-induced myeloid-derived suppressor cells suppress NK cell IFN-gamma production by altering cellular metabolism via Arginase-1. J. Immunol. 196, 2283–2292 (2016).
Norian, L. A. et al. Tumor-infiltrating regulatory dendritic cells inhibit CD8+ T cell function via L-arginine metabolism. Cancer Res. 69, 3086–3094 (2009).
Munn, D. H. & Mellor, A. L. IDO in the tumor mcroenvironment: inflammation, counter-regulation, and tolerance. Trends Immunol. 37, 193–207 (2016).
Prendergast, G. C. et al. Indoleamine 2,3-dioxygenase pathways of pathogenic inflammation and immune escape in cancer. Cancer Immunol. Immunother. 63, 721–735 (2014).
Taylor, M. W. & Feng, G. S. Relationship between interferon-gamma, indoleamine 2,3-dioxygenase, and tryptophan catabolism. FASEB J. 5, 2516–2522 (1991).
Schmidt, S. V. & Schultze, J. L. New insights into IDO biology in bacterial and viral infections. Front. Immunol. 5, 384 (2014).
Daubener, W. et al. Restriction of Toxoplasma gondii growth in human brain microvascular endothelial cells by activation of indoleamine 2,3-dioxygenase. Infect. Immun. 69, 6527–6531 (2001).
Gobert, A. P. et al. Helicobacter pylori arginase inhibits nitric oxide production by eukaryotic cells: a strategy for bacterial survival. Proc. Natl Acad. Sci. USA 98, 13844–13849 (2001).
Weinberg, J. B. et al. Arginine, nitric oxide, carbon monoxide, and endothelial function in severe malaria. Curr. Opin. Infect. Dis. 21, 468–475 (2008).
Gerard, A. et al. Secondary T cell-T cell synaptic interactions drive the differentiation of protective CD8+ T cells. Nat. Immunol. 14, 356–363 (2013).
Bousso, P. & Robey, E. Dynamics of CD8+ T cell priming by dendritic cells in intact lymph nodes. Nat. Immunol. 4, 579–585 (2003).
Mempel, T. R., Henrickson, S. E. & Andrian, U. H. Von T-cell priming by dendritic cells in lymph nodes occurs in three distinct phases. Nature 427, 154–159 (2004).
Mingozzi, F. et al. Prolonged contact with dendritic cells turns lymph node-resident NK cells into anti-tumor effectors. EMBO Mol. Med 8, 1039–1051 (2016).
Hor, J. L. et al. Spatiotemporally distinct interactions with dendritic cell subsets facilitates CD4+ and CD8+ T cell activation to localized viral infection. Immunity 43, 554–565 (2015).
Castellino, F. et al. Chemokines enhance immunity by guiding naive CD8+ T cells to sites of CD4+ T cell-dendritic cell interaction. Nature 440, 890–895 (2006).
Brewitz, A. et al. CD8(+) T cells orchestrate pDC-XCR1(+) dendritic cell spatial and functional cooperativity to optimize priming. Immunity 46, 205–219 (2017).
Wensveen, F. M., van Gisbergen, K. P. & Eldering, E. The fourth dimension in immunological space: how the struggle for nutrients selects high-affinity lymphocytes. Immunol. Rev. 249, 84–103 (2012).
Man, K. et al. The transcription factor IRF4 is essential for TCR affinity-mediated metabolic programming and clonal expansion of T cells. Nat. Immunol. 14, 1155–1165 (2013).
Lin, S. C. & Hardie, D. G. AMPK: sensing glucose as well as cellular energy status. Cell Metab. 27, 299–313 (2018).
Rolf, J. et al. AMPKalpha1: a glucose sensor that controls CD8 T-cell memory. Eur. J. Immunol. 43, 889–896 (2013).
Blagih, J. et al. The energy sensor AMPK regulates T cell metabolic adaptation and effector responses in vivo. Immunity 42, 41–54 (2015).
Powell, J. D. et al. Regulation of immune responses by mTOR. Annu. Rev. Immunol. 30, 39–68 (2011).
Golks, A. et al. Requirement for O-linked N-acetylglucosaminyltransferase in lymphocytes activation. EMBO J. 26, 4368–4379 (2007).
Ramakrishnan, P. et al.Activation of the transcriptional function of the NF-kappaB protein c-Rel by O-GlcNAc glycosylation. Sci. Signal. 6, ra75 (2013).
Walls, J., Sinclair, L. & Finlay, D. Nutrient sensing, signal transduction and immune responses. Semin. Immunol. 28, 396–407 (2016).
Preston, G. C. et al. Single cell tuning of Myc expression by antigen receptor signal strength and interleukin-2 in T lymphocytes. EMBO J. 34, 2008–2024 (2015).
Chou, C. et al. c-Myc-induced transcription factor AP4 is required for host protection mediated by CD8+ T cells. Nat. Immunol. 15, 884–893 (2014).
Grallert, B. & Boye, E. GCN2, an old dog with new tricks. Biochem. Soc. Trans. 41, 1687–1691 (2013).
Ravindran, R. et al. Vaccine activation of the nutrient sensor GCN2 in dendritic cells enhances antigen presentation. Science 343, 313–317 (2014).
Ravindran, R. et al. The amino acid sensor GCN2 controls gut inflammation by inhibiting inflammasome activation. Nature 531, 523–527 (2016).
Munn, D. H. et al. GCN2 kinase in T cells mediates proliferative arrest and anergy induction in response to indoleamine 2,3-dioxygenase. Immunity 22, 633–642 (2005).
Fallarino, F. et al. The combined effects of tryptophan starvation and tryptophan catabolites down-regulate T cell receptor zeta-chain and induce a regulatory phenotype in naive T cells. J. Immunol. 176, 6752–6761 (2006).
We apologize to those whose work is not cited due to space limitations. This work is supported by the Science Foundation Ireland (13/CDA/2161) and the European Research Council (ERC-CoG-770769).
The authors declare no competing interests.
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Kedia-Mehta, N., Finlay, D.K. Competition for nutrients and its role in controlling immune responses. Nat Commun 10, 2123 (2019). https://doi.org/10.1038/s41467-019-10015-4
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