Increased levels of interferon-γ (IFN-γ) are routinely observed in the respiratory tract following influenza virus infection, yet its potential role remains unclear. We now demonstrate that influenza-induced IFN-γ restricts protective innate lymphoid cell group II (ILC2) function in the lung following challenge with the pandemic H1N1 A/CA/04/2009 (CA04) influenza virus. Specifically, IFN-γ deficiency resulted in enhanced ILC2 activity, characterized by increased production of interleukin (IL)-5 and amphiregulin, and improved tissue integrity, yet no change in ILC2 numbers, viral load or clearance. We further found that IFN-γ-deficient mice, as well as wild-type animals treated with neutralizing anti-IFN-γ antibody, exhibited decreased susceptibility to lethal infection with H1N1 CA04 influenza virus, and moreover that survival was dependent on the presence of IL-5. The beneficial effects of IFN-γ neutralization were not observed in ILC2-deficient animals. These data support the novel concept that IFN-γ can have a detrimental role in the pathogenesis of influenza through a restriction in ILC2 activity. Thus, regulation of ILC2 activity is a potential target for post-infection therapy of influenza.
Interferon-γ (IFN-γ) is a cytokine that is critical for regulating both the innate and adaptive immune response.1 Increased production of IFN-γ in the respiratory tract is observed during influenza infection, yet its physiological importance remains unclear.2 Most studies have indicated that IFN-γ is dispensable for survival following influenza infection.3, 4, 5 However, some reports suggested that IFN-γ deficiency can result in increased viral burden or mortality.6, 7, 8 These discrepancies are likely to be due to differences in experimental design, i.e., viral strain, gene deficiency versus anti-cytokine monoclonal antibody (mAb), and/or immunization routes. Despite this, the general consensus in the field is that deficiency in IFN-γ or its receptor does not significantly have an impact on susceptibility in a mouse model of influenza.
Group II innate lymphoid cells (ILC2s) are essential mediators of mucosal immunity, particularly in the lung.9, 10 ILC2s respond to epithelial cell-derived cytokines, such as interleukin (IL)-33 and IL-25, with rapid production of IL-5 and IL-13, which in turn leads to eosinophil recruitment, mucus secretion, goblet cell hyperplasia, and airway hyperreactivity.11, 12, 13 Furthermore, lung ILC2s secrete the epidermal growth factor amphiregulin, which promotes epithelial cell proliferation and tissue regeneration following virus-induced tissue damage.10 The biological effects of these ILC2-mediated activities can vary, including enhanced development of allergies and asthma, induction of protective immunity against parasitic worms, and regulation of adipocyte development and metabolic homeostasis.14, 15, 16 During influenza infection, ILC2s are similarly thought to have diverse roles.9, 10 Considering that large amounts of IFN-γ are produced during influenza and that IFN-γ can inhibit IL-33-dependent activation of ILC2s,17, 18, 19 we have now examined the specific role of IFN-γ in ILC2 regulation during influenza infection. Our results demonstrate that lethal challenge with the pandemic H1N1 A/CA/04/2009 influenza (CA04) virus caused IFN-γ-mediated suppression of ILC2 function in the lung. IFN-γ deficiency resulted in enhanced ILC2 activity, characterized by increased production of IL-5 and amphiregulin. Unexpectedly, IFN-γ-deficient mice, as well as wild-type (WT) animals treated with neutralizing anti-IFN-γ antibody, were protected against lethal CA04 infection and increased resistance was dependent on the presence of ILC2s and IL-5. We therefore reveal an unanticipated role for IFN-γ in the pathogenesis of CA04 influenza virus infection, specifically in promoting increased susceptibility through the suppression of ILC2 protective responses. We further provide evidence that induced IL-5 and, possibly, increased eosinophilia support survival following lethal viral challenge. These results indicate that specific regulation of ILC2-mediated immune responses could be a promising therapeutic approach for enhancing recovery following influenza infection.
IFN-γ increases susceptibility to CA04 influenza virus challenge
The role of IFN-γ during primary infection with influenza virus remains unresolved. We therefore investigated the response of BALB/c IFN-γ−/− mice to lethal challenge with the 2009 pandemic strain A/California/04/2009 (CA04) H1N1 virus. BALB/c IFN-γ+/+ mice produced large amounts of IFN-γ in the bronchoalveolar lavage fluid (BALF) starting at Day 3 post infection and continuing through Day 9 (Figure 1a). Similar to previous reports,3, 20 the absence of IFN-γ did not have an impact on viral burden (Figure 1a,b); however, BALB/c IFN-γ−/− mice surprisingly exhibited increased resistance to lethal infection (Figure 1c), an observation that has never been reported in the literature.3, 20 This increased resistance was not restricted to a particular mouse strain, as both BALB/c and C57Bl/6 IFN-γ−/− mice exhibited the same phenotype (Figure 1c,d). The data show that the presence IFN-γ caused decreased survival of CA04 virus-infected mice, but this was not due to altered viral clearance.
IFN-γ−/− mice exhibit decreased immunopathology
IFN-γ is a pleiotropic cytokine that regulates both the adaptive and innate immune response. We therefore determined whether the increased resistance of BALB/c IFN-γ−/− mice was due to an altered immune response. Analysis of influenza virus-specific antibody titers revealed that the levels of IgM, IgG, or IgA anti-CA04 antibodies were comparable between BALB/c IFN-γ+/+ and IFN-γ−/− mice (Supplementary Figure S1a online). We further measured titers of IgG antibody subclasses IgG1, IgG2a, IgG2b, and IgG3 (Supplementary Figure S1b). Antibody titers of the IgG2a and IgG3 isotypes, which are normally stimulated during Th1-type immune responses,21 were reduced, whereas titers of the Th2-associated IgG1 isotype were modestly increased in BALB/c IFN-γ−/− mice (Supplementary Figure S1c), suggesting a predominately type-2 immune response in BALB/c IFN-γ−/− mice. This was not surprising, as IFN-γ is known to be a key switch factor for IgG2a and IgG3 production. Consistent with the antibody titers, hemagglutination inhibition assays also demonstrated that there were no significant differences in functional antibody responses in BALB/c IFN-γ+/+ and IFN-γ−/− mice (Supplementary Figure S1c). We observed a transient increase in CD4+ and CD8+ T-cell numbers in BALB/c IFN-γ−/− mice at day 6 post infection (Supplementary Figure S2a); however, granzyme B levels in the BALF were diminished (Supplementary Figure S2b). In addition, levels of inflammatory cytokines in the BALF were comparable in both BALB/c IFN-γ+/+ and IFN-γ−/− mice (Supplementary Figure S2c). Thus, in agreement with the similar viral burdens observed in BALB/c IFN-γ+/+ and IFN-γ−/− mice, there were no significant differences in antibody or T- cell responses that could account for the enhanced survival of BALB/c IFN-γ−/− mice.
Viral respiratory infection can cause massive destruction of the epithelial lung tissue as a result of viral replication, production of inflammatory cytokines by innate and adaptive immune cells, and apoptosis of infected epithelial cells. Recovery from infection therefore not only requires viral clearance but also the regeneration of the lung tissue, which is crucial for normal respiratory function. Taking into account that both BALB/c IFN-γ+/+ and IFN-γ−/− mice exhibited similar levels of viral lung titers (Figure 1b) and comparable effector immune responses, we postulated that survival differences might be attributed to influenza-induced lung injury. We initially examined lung histopathology but the differences between WT and IFN-γ−/− mice were inconclusive. We therefore used quantitative methods of detecting tissue integrity and lung permeability, as these would be suitable for revealing subtle differences. One measure of respiratory distress is pulmonary edema, a correlate of tissue permeability. Pulmonary edema was markedly increased in BALB/c IFN-γ+/+ mice by day 9 following infection. However, BALB/c IFN-γ−/− mice presented with a significant reduction in pulmonary edema following infection compared with BALB/c IFN-γ+/+ mice (Figure 2a). Similarly, albumin and total protein levels in the BALF of BALB/c IFN-γ−/− mice were significantly reduced when compared with WT mice (Figure 2b,c), further indicating improved tissue integrity in the absence of IFN-γ. Of note, before day 9 post infection, signs of tissue permeability were equivalent in both BALB/c IFN-γ+/+ and IFN-γ−/− animals, suggesting that IFN-γ-deficient mice exhibit enhanced lung repair following infection (Figure 2a–c). Nitrite levels in the BALF of BALB/c IFN-γ−/− mice were likewise reduced, indicating that BALB/c IFN-γ−/− mice exhibited decreased inflammation following infection with CA04 virus (Figure 2d). In addition, the levels of IL-10 were increased in the absence of IFN-γ (Supplementary Figure S2c). Taken together, these data demonstrate that BALB/c IFN-γ−/− mice exhibit diminished immunopathology and respiratory damage following influenza infection compared with WT animals. These results suggest that the increased resistance of BALB/c IFN-γ−/− mice is due not to enhanced viral clearance, but rather to suppressed immunopathology.
ILC2 activity is modulated by IFN-γ
The above results indicated that IFN-γ−/− mice have both improved tissue integrity and reduced inflammation following influenza infection. However, BALB/c IFN-γ−/− mice also exhibited increased airway hyperreactivity (Supplementary Figure S2d). ILC2s have been implicated in both maintaining tissue homeostasis and promoting airway hyperreactivity following influenza infection.9, 10 We therefore evaluated the ILC2 response after CA04 virus infection. Flow cytometry analysis of intracellular cytokine expression revealed that the lungs and BALF of BALB/c IFN-γ−/− mice contained significantly greater numbers and percentages of IL-5+ ILC2s compared with BALB/c IFN-γ+/+ mice (Figure 3a–c and Supplementary Figure S3a). However, the number and percentage of IL-13+ILC2s or IL-5+IL-13+ILC2s remained unchanged in the absence of IFN-γ (Figure 3a–c and Supplementary Figure S4c-b,e-f). Interestingly, ILC2 production of IL-5 and IL-5 levels in the BALF were not increased in BALB/c IFN-γ−/− mice before day 9 post infection (Supplementary Figure S4a,d), which correlates with improved tissue integrity in these mice (Figure 2a–c). The total numbers of ILC2s were equivalent in BALB/c IFN-γ+/+ and IFN-γ−/− mice in both the lung or BALF (Figure 3d, e), suggesting that IFN-γ did not have an impact on generation of ILC2s following CA04 virus infection. We further observed major increases in levels of amphiregulin and IL-5, but not IL-13, in the BALF of BALB/c IFN-γ−/− mice following CA04 virus infection (Figure 3f–h). Increased IL-5 production in BALB/c IFN-γ−/− mice consequently contributed to enhanced eosinophil recruitment (Figure 3i and Supplementary Figure S3b). Of note, depletion of CD4+ T cells using neutralizing antibodies did not have an impact on the levels of amphiregulin, IL-5, or IL-13 in the BALF (Supplementary Figure S5), indicating that Th2 cells were dispensable for the production of these cytokines. Thus, expression of IFN-γ strongly correlated with suppression of ILC2 function, specifically IL-5 and amphiregulin expression, and increased lung permeability during CA04 virus infection.
ILC2s express the IFN-γ receptor on their surface
ILC2s become activated in response to alarmin expression by damaged epithelial cells. We therefore evaluated the epithelial cytokines IL-25 and IL-33, which stimulate ILC2 function.11, 13 Infection with CA04 virus did not trigger IL-25 responses in either BALB/c IFN-γ+/+ or IFN-γ−/− mice (Figure 4a), an observation consistent with the literature.22 In contrast, IL-33 was highly upregulated following CA04 virus infection but IFN-γ deficiency had no impact on IL-33 production (Figure 4b) or the expression of ST2 (IL-33R) on the surface of ILC2s (Figure 4c). These data suggest that IFN-γ does not suppress ILC2 function through inhibition of IL-33 production or the expression of the IL-33 receptor. To determine whether IFN-γ might regulate ILC2 function directly, we evaluated ILC2s for surface expression of IFN-γR1 by flow cytometry. ILC2s from both BALB/c IFN-γ+/+ and IFN-γ−/− mice expressed similar levels of IFN-γR1 (Figure 4d). These results, together with previous studies reporting the impact of IFN-γ on ILC2 activity,17, 19 suggest that IFN-γ produced during influenza infection modulates ILC2 functions by directly binding to receptors found on the surface of ILC2s.
Diverse groups of ILC2s, such as inflammatory ILC2s, which express IL-17rb and possess the potential to transdifferentiate into ILC3-like cells, have been described.23 We therefore evaluated ILCs in lungs for production of ILC1 and ILC3 cytokines. Consistent with the lack of IL-25 production (Figure 4a), we did not observe an increase in inflammatory ILC2s in the lung (data not shown). We further demonstrated comparable numbers of IL-22+ILCs, IL-22+IL-17+ILCs, and IL-17+ILCs in the lungs and BALF of IFN-γ+/+ and IFN-γ−/− mice (Supplementary Figure S6a,b). Similar results were found when we evaluated cytokine levels in the BALF (Supplementary Figure S6c,d). These results indicate that no detectable differences in inflammatory ILC2s or ILC3-like cells were found in BALB/c IFN-γ+/+ and IFN-γ−/− mice during CA04 virus infection.
Anti-IFN-γ treatment promotes resistance to CA04 infection in WT mice
To further examine the role of IFN-γ as a suppressor of ILC2 activity, we treated BALB/c IFN-γ+/+ mice with neutralizing anti-IFN-γ antibodies following CA04 infection (Figure 5a,b). IFN-γ neutralization caused significant increases in IL-5 and amphiregulin levels in the BALF of infected mice, but IL-13 levels were unaffected (Figure 5c–e). Consistent with elevated production of IL-5, the numbers of eosinophils in the lung were also increased (Figure 5f). Moreover, anti-IFN-γ-treated mice exhibited an increase in the number of IL-5+ ILC2s in the lung (Figure 5g). However, neutralization of IFN-γ did not impact the numbers of lung IL-13+ILC2s or IL-5+IL-13+ILC2s (Figure 5h,i). Similar to BALB/c IFN-γ−/− mice, mice treated therapeutically with neutralizing anti-IFN-γ antibody did not exhibit changes in viral burden compared to mice treated with IgG isotype control (Figure 5j). Nevertheless, neutralization of IFN-γ in CA04 virus-infected mice resulted in resistance to infection, as evidenced by diminished levels of BALF albumin and total protein, and increased survival rates, compared to IgG-treated mice (Figure 5k–m). These data, together with results obtained from BALB/c IFN-γ−/− animals, demonstrate that IFN-γ is detrimental during CA04 infection, causing increased morbidity and mortality due to a reduction in tissue integrity.
The beneficial effects of IFN-γ neutralization in CA04 virus-infected mice requires ILC2s
To confirm the protective role of ILC2s in the absence of IFN-γ during CA04 virus infection, we evaluated the impact of anti-IFN-γ on Roraflox/flox IL7rcre mice, which are deficient in ILC2s.24 Similar to BALB/c IFN-γ+/+ mice, control littermates (Rora+/f IL7rcre) were protected against CA04 virus infection following treatment with anti-IFN-γ (Figure 6a,b). However, this protection was lost in ILC2-deficient mice (Roraf/f IL7rcre) (Figure 6a,b). Importantly, ILC2-deficient animals showed increased susceptibility to infection compared to WT mice, regardless of the presence of IFN-γ (Figure 6a,b). Of note, the survival of IgG isotype-treated control littermates was marginally, but not significantly improved when compared to IgG isotype-treated ILC2-deficient mice (Figure 6a,b), most likely due to the fact that the presence of IFN-γ blocks the protective activity of ILC2s. These results indicate that the beneficial effect of IFN-γ deficiency is mediated by ILC2s.
IL-5 neutralization restores susceptibility to CA04 virus infection
To determine whether increased survival from CA04 infection in BALB/c IFN-γ−/− mice was dependent on IL-5, we treated animals post virus infection with either neutralizing anti-IL-5 antibody or IgG isotype control (Figure 7a). BALB/c IFN-γ−/− mice treated with anti-IL-5 succumbed to infection around day 9 and had a significantly diminished survival rate when compared with IgG control-treated BALB/c IFN-γ−/− mice (Figure 7b). Neutralization of IL-5 in BALB/c IFN-γ−/− mice resulted in a major reduction in IL5+ ILC2 and eosinophil numbers compared to BALB/c IFN-γ−/− mice treated with IgG isotype control (Figure 7c,d). However, numbers of IL13+ ILC2s and IL5+13+ ILC2s remained consistent in all mouse groups (Supplementary Figure S7a,b online). In addition, numbers of alveolar macrophages, recruited macrophages, and neutrophils were similar between IgG- and anti-IL-5-treated mice (Supplementary Figure S7c–e online). Furthermore, amphiregulin and IL-13 levels, as well as viral burdens, remained unaffected by anti-IL-5 treatment (Figure 7f–h). Inflammation, as measured by the amount of nitrite in the BALF, was slightly increased in the absence of IL-5 (Figure 7i); however, IL-10 levels remained unchanged following anti-IL-5 administration (Supplementary Figure S7f). Indicative of diminished tissue integrity, total protein and albumin levels were also increased in IL-5-neutralized BALB/c IFN-γ−/− mice (Figure 7j,k). The observed trends are consistent with the involvement of IL-5 in protective lung tissue regeneration. These data support the novel finding that IFN-γ production contributes to increased susceptibility to influenza virus infection.
The results presented here establish an unanticipated role for ILC2s in promoting survival during influenza susceptibility and a crucial role for IFN-γ as a suppressor of ILC2-mediated protection. Our data further showed that resistance to CA04 virus infection was dependent on the production of IL-5, which appeared to be required to maintain tissue repair post-infection. Gorski et al.22 have previously demonstrated that ILC2s produce IL-5 in response to influenza virus infection in WT mice. Interestingly, in Rag2−/− mice, which lack T and B cells, and thus exhibit significantly reduced IFN-γ production,25 levels of IL-5 production are dramatically increased.22 Recent data further suggest that IFN-γ diminishes ILC2 activity to limit excessive inflammation following helminth infection or asthma exacerbation by fungal infection.18, 19 However, these reports described a role of IFN-γ in terminating ILC2-mediated inflammation and did not characterize/elucidate the regulation of ILC2-mediated functions during an immune response dominated by IFN-γ, e.g., influenza virus infection. In these previous studies, IFN-γ was reported to inhibit production of both IL-5 and IL-13 by ILC2s;18, 19 however, our results demonstrated that IL-13 production by ILC2s was not enhanced following viral infection. Furthermore, analysis of BALF samples indicated that IL-13 levels were nearly undetectable in either BALB/c IFN-γ+/+ or IFN-γ−/− mice, suggesting that CA04 virus infection did not elicit a strong IL-13 response. Most evidence presented in the literature suggests that ILC2 expression of IL-5 and IL-13 is regulated concurrently by transcription factors including Gata-3, TCF-1, and Bcl11b.26, 27, 28, 29 As such, the loss of one or more of these transcription factors results in reduced production of both IL-5 and IL-13. However, the Gfi-1 transcription factor is known to only regulate IL-5 production as evidenced by the fact that genetic ablation of Gfi-1 causes the specific downregulation of IL-5 production but not IL-13,30 further suggesting that IL-5 and IL-13 are regulated by independent mechanisms.
Monticelli et al.10 discovered that ILC2s mediated enhanced lung function and repair following H1N1 (PR8) virus infection through production of amphiregulin. Furthermore, although ILC2s were important for regeneration of lung tissue, they were dispensable for survival following PR8 infection.10 Alternatively, our results suggest that in the absence of IFN-γ, ILC2s are required for improved survival following CA04 virus infection. These findings suggest the concept of a strain-specific contribution of ILC2s to protection against influenza virus infection. Although both PR8 and CA04 are H1N1 influenza viruses, they have distinct origins.31 CA04 virus is derived from the 2009 pandemic strain and is the result of a recombination event involving a Eurasian avian-like swine virus and a triple assortment composed of bird, swine, and human flu viruses.31 In addition to its unique origin, the CA04 viral strain possesses a truncated form of the PB1-F2 protein, which is thought to contribute to its reduced pathogenicity.31, 32, 33 Full-length PB1-F2, which is expressed in PR8 as well as in isolates derived from the 1918 influenza virus, promotes apoptosis of immune cells, contributes to increased immunopathology, and negatively impacts viral clearance.31, 32, 33, 34 As a result, the PR8 virus exhibits significantly increased virulence compared with the 2009 pandemic strain, which may overcome ILC2-mediated protection.
IFN-γ−/− mice were protected against lethal challenge with CA04 virus, without substantial differences in viral burden when compared with WT animals. BALB/c IFN-γ−/− mice also exhibited lower levels of total protein content and albumin in the BALF, indicating decreased epithelial and/or endothelial barrier permeability. This suggests that enhanced survival was most likely to be dependent upon improved tissue integrity and not increased viral clearance. ILC2 production of amphiregulin is known to support lung repair and tissue homeostasis following viral infection,35, 10 and although we demonstrated that mice lacking IFN-γ exhibited elevated levels of amphiregulin in the BALF following viral infection, our data suggested that increased production of IL-5 in the absence of IFN-γ was most crucial to improved survival following CA04 virus infection. In support of this, antibody-mediated neutralization of IL-5 resulted in increased susceptibility accompanied by a mild reduction in tissue integrity. These findings reveal a possible unexpected role for IL-5 in airway epithelial cell regeneration and tissue maintenance following lung injury, resulting in enhanced survival following influenza infection. However, neutralization of IL-5 in BALB/c IFN-γ−/− mice did not significantly alter lung permeability or inflammation. As previously described,10 the presence of amphiregulin probably contributed to the maintenance of tissue regeneration, but was not sufficient by itself to promote survival. Further studies will be required to elucidate the precise mechanisms of IL-5-mediated protection.
In addition to IL-5, survival may be dependent on the presence of pulmonary eosinophils. Eosinophils promote allergic inflammation and asthma in the lung, but published evidence suggests that they may also enhance anti-viral resistance during respiratory syncytial virus36 and parainfluenza virus37 infections. Although eosinophils are primarily known for their destructive impact on tissue epithelium, previous studies have shown that increased eosinophilia may actually limit airway hypersensitivity during viral infection.36 Moreover, eosinophils have been reported to reduce inflammation and promote tissue homeostasis.38 Furthermore, recent evidence suggests that eosinophils have an important role in restricting ILC2 plasticity during Th1 immune responses.39 Thus, it is possible that recruitment of eosinophils can contribute to ILC2 stability during influenza infection. Whether eosinophils participate in protection against CA04 virus infection requires further exploration.
Based on our results and the work of others,17, 18, 19 we postulate that IFN-γ acts directly on ILC2s, signaling through the IFN-γ receptor to alter their function. Nevertheless, it is also possible that IFN-γ blocks ILC2 function through a bystander mechanism, possibly through interference with the IL-33 signaling pathway. As evidenced by our data, IL-33 secretion is stimulated after influenza infection both in the presence and absence of IFN-γ; therefore, one possibility is that IFN-γ limits the influence of IL-33 on ILC2 activity. The IL-33 receptor, a member of the Toll-like/IL-1 receptor super family, is composed of IL-1 receptor accessory protein and ST2L, an isoform of ST2 that contains an extracellular domain, a transmembrane region and a cytoplasmic domain.40, 41, 42, 43 It has been reported that soluble ST2, a secreted isoform of ST2, which lacks the transmembrane and cytoplasmic regions, sequesters IL-33 to suppress signaling and activation of ILC2s.44 Mast cells produce soluble ST2 following FcɛRI activation45 and moreover IFN-γ regulates FcɛRI-dependent mast cell activities during allergic airway inflammation,46 indicating a possible role for IFN-γ in the expression of soluble ST2 by mast cells. The potential indirect impact of IFN-γ on ILC2 activity is an area for further investigation.
In summary, we report the novel finding that IFN-γ production contributes to increased susceptibility to influenza virus infection. IFN-γ appears to have a major role as a suppressor of ILC2-mediated protection, namely in restricting the production of IL-5. Inhibition of IL-5 with neutralizing antibodies resulted in reduced survival in IFN-γ-deficient mice, indicating that protection was dependent on the production of IL-5 and possibly increased eosinophilia. These results establish an unanticipated role for ILC2s in promoting resistance against influenza infection. Therefore, specific regulation of ILC2 activity during infection could ultimately prove to be a potent avenue for the development of more effective influenza treatments, as well as enhanced vaccination procedures.
Mouse strains and viruses
BALB/c and C57Bl/6 IFN-γ+/+ and IFN-γ−/− mice were originally obtained from Jackson Laboratories (Bar Harbor, ME). Rora+/floxIl7rCre mice were generated in the lab of Dr. Andrew N.J. McKenzie (MRC Laboratory of Molecular Biology).24 All mice were maintained under specific pathogen-free conditions in the Animal Research Facility at Albany Medical College. Mice were anesthetized by intraperitoneal injection with 100 μl xylazine (20 mg ml−1) and ketamine (1 mg ml−1) in phosphate-buffered saline. For influenza infections, anesthetized IFN-γ+/+ and IFN-γ−/− mice were intranasally inoculated with a lethal dose (2,000 plaque-forming units) H1N1 A/California/04/2009 (CA04). ILC2-deficient animals and their littermate controls (Rora+/floxIl7rCre) were given the median lethal dose of 500 plaque-forming units. Survival and weight loss were monitored daily for 20 days. The virus was propagated in 10-day-old embryonated chicken eggs (Charles River, Wilmington, MA). The stock titer was measured by standard plaque assay. All experimental procedures were approved by the Institutional Animal Care and Use Committee at Albany Medical College (Protocol Number 11-04004).
Pulmonary viral burdens
Influenza viral loads were measured in BALF samples by plaque assay on Madin–Darby canine kidney cells.
Analysis of lung lavage samples
To collect BALF samples, a small incision was made in the trachea and an 18-gauge cannula was inserted. Lungs were lavaged with 1 ml of phosphate-buffered saline and samples were centrifuged to remove cells. Cells were used for flow cytometry analysis. Cell-free supernatants were analyzed for protein levels of IL-2, IL-4, IL-5, IL-10, IL-12, tumor necrosis factor, and IFN-γ using Bio-Plex mouse cytokine assays (Bio-Rad, Hercules, CA). TGFβ1, amphiregulin, IL-25, IL-33, and IFN-γ levels were also measured using commercially available kits from BD Biosciences (San Jose, CA), eBioscience (San Diego, CA), and R&D Systems (Minneapolis, MN). Total protein concentrations in the cell free fractions of BALF were determined using a Pierce BCA protein assay kit (Thermo Scientific, Rockford, IL). Nitrite levels were quantified using a colorimetric Griess reagent kit (Life Technologies, Carlsbad, CA). Levels of albumin in BALF were determined with the BCG albumin assay kit (Sigma-Aldrich, St. Louis, MO).
Measurement of pulmonary edema
Whole mouse lungs were harvested on day 9 post infection. Lung weight (wet) was measured using an AX105 Delta Range analytical balance (Mettler Toledo, Columbus, OH) followed by 72 h incubation at 60 °C. Dried lungs were weighed and edema was expressed as a ratio of lung wet/dry weight.47
Hemagglutination inhibition assay
Heat-inactivated BALF samples from CA04 infected mice were serially diluted and incubated with 50 μl of CA04 (4 HAU) in a 96-well plate at room temperature for 30 min. Chicken red blood cells (Hemostat Laboratories, Dixon, CA) was added to each well and incubated at room temperature for an additional hour. Hemagglutination inhibition titers were determined as the last reciprocal sample dilutions that fully inhibited influenza virus hemagglutination.
Characterization of lung ILC2s
Lungs were perfused by injecting 10 ml phosphate-buffered saline through the right ventricle, followed by digestion of the lung tissue in phosphate-buffered saline buffer containing DNAse I (150 μg ml−1; Roche) and collagenase D (1 mg g ml−1; Roche) for 45 min at 37 °C. Following digestion, lung tissue was passed through a 40 μm filter and blood cells were subsequently removed by incubation in ACK buffer. ILC2s were identified using flow cytometry as cells which expressed CD90.2 (Thy1.2), CD127 (IL-7R), ST2 (IL-33R), and KLRG1, while excluding any cells that expressed lineage-specific markers for T cells (CD3), B cells (CD45R), myeloid cells (TER-119, CD11b, and Gr-1), and dendritic cells (CD11c).
Flow cytometric analysis
BALF cells or lung single cell suspensions were first incubated with α-mouse FcγIII/II receptor (2.4G2 mAb) for 15 min. Fc receptor-blocked cells were then stained with mixtures of anti-mouse mAbs. Cells were further stained with Fixable Viability Dye (eFluor 780; eBioscience) to label dead cells. For intracellular cytokine staining, cells were stimulated ex vivo for five hrs with 50 ng ml−1 phorbol 12-myristate 13-acetate and 500 ng ml−1 ionomycin at 37 °C, in the presence of 10 μg ml−1 Brefeldin A. Cells were stained for surface markers, followed by fixation and permeabilization in 4% paraformaldehyde and 0.05% saponin buffer, respectively, followed by intracellular cytokine staining. Stained cells were analyzed on a BD FACSCanto or LSR II (BD Biosciences, San Jose, CA). Data were analyzed using FlowJo software (Tree Star Inc., Ashland, OR).
In vivo cytokine neutralization
For IL-5 neutralization, BALB/c IFNγ+/+ and IFNγ−/− mice were intraperitoneally treated with 150 μg of α-IL-5 mAb (clone TRFK5; BioXcell, West Lebanon, NH) or IgG isotype control on days 2, 4, 6, 8, and 10 post infection. The efficacy of eosinophil depletion and IL-5 neutralization in the BALF was confirmed on day 9 post infection by flow cytometry and MILLIPLEX MAP mouse cytokine multiplex assay, respectively. For IFN-γ neutralization, mice were intraperitoneally injected with 600 μg α-IFN-γ mAb (clone XMG1.2; BioXcell) or IgG isotype control on days 2, 4, 6, 7, 8, 10, 11, and 12 post infection. The efficiency of IFN-γ neutralization in the BALF was determined 9 days after infection by enzyme-linked immunosorbent assay. For CD4 depletion, mice were intraperitoneally injected with 500 μg α-CD4 mAb (clone GK1.5; BioXcell) or IgG isotype control on days 2, 4, 6, and 8 post infection. The efficiency of CD4 depletion was confirmed by fluorescence-activated cell sorting analysis.
Airway responsiveness to increasing doses of methacholine was measured on day 10 post infection, as previously described.48 Infected mice were anesthetized, tracheostomized, paralyzed with pancuronium bromide, and then connected to a computer-controlled small-animal ventilator (flexiVent; SCIREQ, Montreal, Canada).
Cells were analyzed using the following antibodies: α-CD4 (clone GK1.5) (allophycocyanin; BD Pharmingen, San Jose, CA), α-CD8 (clone 53-6.7) (phycoerythrin (PE); BD Pharmingen), α-CD19 (clone 6D5) (PerCP-Cy5.5; Biolegend, San Diego, CA), α-CD11b (clone M1/70) (fluorescein isothiocyanate; eBioscience), α-Siglec F (clone E50-2440) (PE; BD Pharmingen), α-Ly6G (clone 1A8) (PE-Cy7; Biolegend), α-CD11c (clone HLC) (allophycocyanin; BD Pharmingen), α-CD3ɛ (clone 145-2C11) (Biotin; eBioscience), α-TER-119 (clone TER-119) (Biotin; eBioscience), α-Gr1 (clone RB6-8C5) (Biotin; eBioscience), α-CD45R (clone RA3-6B2) (Biotin; eBioscience), α-CD11b (clone M1/70) (Biotin; eBioscience), α-CD11c (clone N418) (Biotin; eBioscience), α-CD90.2 (clone 53-2.1) (PE-Cy7; eBioscience), α-CD127 (clone A7R34) (allophycocyanin-eFluor 780; eBioscience), α-ST2 (clone DJ8) (fluorescein isothiocyanate; MDBioproducts, Zurich, Switzerland), α-IL-5 (clone TRFK5) (PE; eBioscience), α-IL-13 (clone eBio13A) (eFluor 660; eBioscience), anti-IL17 (clone ebio17B7) (fluorescein isothiocyanate; eBioscience), anti-IL22 (clone IL22JOP) (allophycocyanin; eBioscience), and Streptavidin (PerCP-Cy5.5; eBioscience).
All statistical calculations were performed using GraphPad Prism (La Jolla, CA). Tests between two groups used a two-tailed Mann–Whitney U-test. Tests between multiple groups used two-way analysis of variance with Bonferroni’s multiple comparisons. Survival curves were evaluated by log-rank Mantel–Cox test and weight loss data were analyzed by using a two-tailed Mann–Whitney U-test.
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We thank Dr Katherine C. MacNamara for providing IFN-γR1−/− mice. We also thank the Department of Immunology and Microbial Disease Immunology Core Laboratory for their technical assistance. This work was supported by NIH grant RO1 AI75312 to D.W.M., NIH grant R01 A1067846 to D.A. and by American Lung Association Biomedical Research Grant RG-341974 to Y.F.
The authors declared no conflict of interest.
D.C., Y.F., and S.R. conducted the experiments and analyzed the data. D.A. advised on the experimental procedures. D.C., Y.F., and D.W.M. conceived and designed the experiments. A.N.J.M. provided ILC2-deficient mice. D.C., Y.F., S.R., D.A., and D.W.M. wrote the paper.
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Califano, D., Furuya, Y., Roberts, S. et al. IFN-γ increases susceptibility to influenza A infection through suppression of group II innate lymphoid cells. Mucosal Immunol 11, 209–219 (2018). https://doi.org/10.1038/mi.2017.41
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