Hypercytokinemia is the main immunopathological mechanism contributing to a more severe clinical course in influenza A (H1N1) virus infections. Most patients infected with the influenza A (H1N1) pdm09 virus had increased systemic levels of pro-inflammatory cytokines; including interleukin IL-6, IL-8, and tumor necrosis factor-alpha (TNF-α). We propose that single-nucleotide polymorphisms (SNPs) in the promoter regions of pro-inflammatory genes are associated with the severity of influenza A (H1N1) pdm09 virus infection.
145 patients with influenza A (H1N1) (pA/H1N1), 133 patients with influenza-like illness (ILI), and 360 asymptomatic healthy contacts (AHCs) were included. Eleven SNPs were genotyped in six genes (TNF, LT, IL1B, IL6, CCL1, and IL8) using real-time PCR; the ancestral genotype was used for comparison. Genotypes were correlated with 27 clinical severity variables. Ten cytokines (GM-CSF, TNF-α, IL-2, IL-1β, IL-6, IL-8, IFN-γ, IL-10, IL-5, and IL-4) were measured on a Luminex 100.
The IL6 rs1818879 (GA) heterozygous genotype was associated with severe influenza A (H1N1) virus infection (odds ratio [OR] = 5.94, 95% confidence interval [CI] 3.05–11.56), and two IL1B SNPs, rs16944 AG and rs3136558 TC, were associated with a decreased risk of infection (OR = 0.52 and OR = 0.51, respectively). Genetic susceptibility was determined (pA/H1N1 vs. AHC): the LTA rs909253 TC heterozygous genotype conferred greater risk (OR = 1.9), and a similar association was observed with the IL1B rs3136558 CC genotype (OR = 1.89). Additionally, severely ill patients were compared with moderately ill patients. The TNF-238 GA genotype was associated with an increased risk of disease severity (OR = 16.06, p = 0.007). Compared with ILIs, patients with severe pA/H1N1 infections exhibited increased serum IL-5 (p <0.001) and IL-6 (p = 0.007) levels.
Citation: García-Ramírez RA, Ramírez-Venegas A, Quintana-Carrillo R, Camarena ÁE, Falfán-Valencia R, Mejía-Aranguré JM (2015) TNF, IL6, and IL1B Polymorphisms Are Associated with Severe Influenza A (H1N1) Virus Infection in the Mexican Population. PLoS ONE 10(12): e0144832. https://doi.org/10.1371/journal.pone.0144832
Editor: Juan C. de la Torre, The Scripps Research Institute, UNITED STATES
Received: September 2, 2015; Accepted: October 26, 2015; Published: December 14, 2015
Copyright: © 2015 García-Ramírez et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited
Data Availability: All relevant data are within paper and its supporting information files.
Funding: This paper constitutes a partial fulfillment of the Graduate Program in Biological Sciences of the National Autonomous University of México (UNAM) for RAGR. RA García-Ramírez acknowledges the academic support provided by the National Council of Science and Technology (CONACyT) and Posgrado en Ciencias Biológicas, UNAM. The authors thank the Coordinación de Investigación en Salud of the IMSS for covering the translation and publishing costs. This study was funded by the Mexican Institute of Social Security, Grants FIS/IMSS/PROT/G13/1212 and CONACyT-FOSIS SALUD2009-C02-126699.
Competing interests: The authors have declared that no competing interests exist.
Abbreviations: AHC, Asymptomatic healthy contacts; AMV, Assisted mechanical ventilation; ARDS, Acute respiratory distress syndrome; BMI, Body mass index; BUN, Blood urea nitrogen; CCL1, Chemokine (C-C motif) ligand 1; CDC, U.S. Centers for Disease Control and Prevention; CI, 95% confidence interval; CPK, Creatine phosphokinase; CRP, C-reactive protein; GLR, Global lethal rate; HLA, Human leukocyte antigen; ICU, Intensive care unit; IFN, Interferon; IL, Interleukin; ILI, Influenza-like illness; LDH, Lactate dehydrogenase; LTA, Lymphotoxin α; OR, Odds ratio; PaO2, Partial pressure of oxygen in arterial blood; SNP, Single nucleotide polymorphism; RT-PCR, Real-time PCR; TNF, Tumor necrosis factor; WHO, World Health Organization
In mid-April 2009, the influenza A (H1N1) pdm09 virus emerged in Mexico and rapidly expanded across the globe. Worldwide, the mortality rate was approximately 0.2–1.23%; in Mexico, mortality was close to 0.4% . The greatest number of deaths from influenza A (H1N1) pdm09 occurred in the central region of the country where healthcare systems are better than in the rest of the country and where access to healthcare services is greater because of better transportation routes and the presence of hospitals that provide care to patients with severe illnesses. However, the numbers of cases were similar in the northern and southern regions of the country . The most affected groups were individuals aged 30–46 years , and a high percentage had no comorbidities that could explain the most severe forms of the disease.
Hypercytokinemia ("cytokine storm") is the main immunopathological mechanism underlying a more severe clinical course in cases of seasonal influenza and is the ultimate cause of death . Most patients infected with the influenza A (H1N1) pdm09 virus have increased serum levels of pro-inflammatory cytokines, such as interleukin IL-6, IL-8, IL-1β and tumor necrosis factor-alpha (TNF-α) [4–7]. In particular, elevated IL-1β and IL-6 serum levels have been identified as markers of severity in acute lung injury during infection by the influenza A (H1N1) pdm09 virus, specifically among patients who do not respond to conventional antiviral treatments [8, 9]. Multiple cytokines are associated with the pathophysiology of inflammation and lung remodeling. Several reports from around the world have shown the presence of an imbalance of pro-inflammatory cytokine responses in severe H1N1 pneumonia [10, 11]; however, little is known about why these differences occur.
Cytokine production varies among individuals due in part to genetic factors and, particularly, the presence of polymorphisms in important regulatory regions such as promoters [12, 13]. In this study, the differential expression of cytokines among individuals with influenza pA/H1N1, those who developed a clinical picture similar to influenza but were not positive for the pandemic virus, and AHCs was examined.
In a previous study performed by our team, several single-nucleotide polymorphisms (SNPs) associated with the risk of influenza infection, including CCL1 rs2282692, LTA rs909253, and TNF 1800750, were identified in a population in Mexico City.  Other groups have reported associations between SNPs in pro-inflammatory cytokines and disease severity [14–16].
According to Borja et al. 2012, the fourth-wave pattern of influenza A (H1N1) observed in Mexico during the 2011–2012 season was not reported in other countries. These differences may be explained by vaccination coverage or genetic susceptibility in the Mexican population . In this study, we included a greater number of patients from the fourth wave of virus infection and aimed to establish the association between polymorphisms in inflammation-related genes (TNF, IL6, IL8, IL1B, LTA, CCL1) and disease development, severity and death from influenza A (H1N1) virus infection in patients from the central region of Mexico.
Materials and Methods
This case-control, ambispective study was performed from April 2009 to March 2012 using nasopharyngeal swab samples from 278 patients hospitalized with clinical symptoms of influenza-like illness.
This study was reviewed and approved by both the Bioethics Committee and Science Committee in Research, with protocol number B05-10 at INER (National Institute of Respiratory Diseases Ismael Cosio Villegas) and Institutional Review Board No. 13CI 09015 213 at IMSS (Mexican Institute of Social Security) authorized by COFEPRIS/SSA.
A trained and responsible physician informed the patient about a possible diagnosis of influenza-like illness (ILI). All participants were invited to participate voluntarily by a trained researcher and gave signed informed consent prior their enrollment. All patients received medical care even if they chose not to participate in the research protocol. The signed consent forms and ethics committee approval letters are documented at HLA Laboratory INER. Data were obtained using clinical records according to the Mexican Official Standard NOM-168-SSA1-1998. A clinical investigation was conducted according to the principles expressed in the Declaration of Helsinki. The ethics committees described above approved our data recording procedures.
All patients underwent the QuickVue Influenza A + B test (Quidel, San Diego, CA, USA). Additionally, peripheral blood from patients and asymptomatic healthy contacts (AHC) was collected; these interventions adhered to the guidelines and recommendations of the Centers for Disease Control and Prevention of the United States (CDC) and the World Health Organization (WHO). Subsequently, the RespiFinder assay was administered, and the presence of influenza A (H1N1) virus was confirmed.
All subjects included in our study were evaluated according to a clinical questionnaire, which contained questions regarding influenza vaccination. The inclusion period was from May 2009 to March 2012, so the subjects examined during the study belonged to three different waves of influenza in Mexico.
A total of 278 subjects with clinical symptoms and signs of influenza were enrolled, of which 145 were positive and 133 were negative for influenza A (H1N1) infection; the influenza-negative patients were deemed to have ILI. On admission to the hospital, all patients with suspected influenza were treated with oseltamivir.
In this study, most patients sought medical attention 3–4 days after the onset of symptoms. All clinical data were collected retrospectively; nonetheless, blood samples and nasopharyngeal swabs were collected at the hospital during the first 24 hours after admission. In the group of AHCs, 360 biologically unrelated, intra-household contacts were enrolled who were asymptomatic and in close, continuous contact with ILI or H1N1 patients before and during admission to the hospital (Fig 1). None of the AHCs developed symptoms or was hospitalized for influenza virus infection. Peripheral blood from these individuals was tested for anti-A (H1N1) antibody titers by hemagglutination inhibition assay according to the method described by Julkunen I, 1985  to determine exposure to the virus. All subjects included in this group had HI titers greater than 1:16, indicating direct contact with the virus. All pA/H1N1 subjects were less than 60 years of age, precluding any cases of cross-reactive antibodies, which are prevalent in older age groups due to H1N1/1918-1919 infection . Because this cohort was not progressively monitored for the dynamics of anti-A H1N1/09 antibody titers over time, these results are not shown.
Data Collection and Variables
The study protocol was explained to all participants, and authorization was obtained with an informed consent form. The information collected included demographic data as well as laboratory data, medical histories, and drug treatment records.
Genotyping of Allelic Variants (SNPs)
DNA samples were genotyped for TNF rs361525, rs1800629, and rs1800750; LTA rs909253; IL1B rs16944, rs3136558, and rs2227307; IL6 rs1818879, rs2069840, and rs2066992; and CCL1 rs2282691 polymorphisms using commercial TaqMan assays (Applied Biosystems, CA, USA). The genetic data for the SNPs are described in S1 Table. The polymorphisms were characterized by real-time PCR allelic discrimination on a 7300 Real-Time PCR System using 15 ng of DNA. The amplification conditions were as follows: 50°C for 2 min and 95°C for 10 min followed by 40 cycles of 95°C for 15 s and 60°C for 1 min.
Haploview version 4.2 was used to determine the presence of haplotypes in IL6, IL1B and TNF genes associated with the risk of both H1N1 viral infection and greater clinical severity.
Serum samples were taken from patients with ILI or a suspected ILI diagnosis upon hospital admission. The enrolled patients and the healthy volunteers gave whole blood, which was allowed to clot for 30 minutes at 37°C and was stored thereafter at -70°C until use. The resulting serum was used for cytokine measurement. Ten cytokines (GM-CSF, TNF-α, IL-2, IL-1β, IL-6, IL-8, IFN-γ, IL-10, IL-5, and IL-4) were measured on a Luminex 100 (Luminex Corporation, Austin, TX, USA) using a multiplex cytokine kit as well as the Cytokine Human 10-Plex Panel (Novex, Life Technologies, CA, USA) in accordance with the manufacturer's instructions.
Differences between the group proportions were analyzed using the chi-square test. Differences between clinical parameters, continuous variables, and each polymorphism were analyzed using the Mann-Whitney U test. The ancestral genotype was used as a reference for each polymorphism. Odds ratios (ORs) were calculated with 95% confidence intervals (CIs). The ORs were adjusted for age and disease severity in the logistic regression model. SPSS 21 (Chicago, IL, USA) and Epi-Info 7.0 (CDC, GA, USA) were used for these analyses.
For cytokine analysis, the subjects were stratified into three groups: 18 patients with A (H1N1) influenza, 15 patients with ILI, and 21 AHCs. Descriptive statistics included means and standard deviations or medians and interquartile ranges for continuous variables with normal and non-normal distributions, respectively. The Fisher exact test and the chi-square test were used for categorical variables. The Mann-Whitney U test was used for nonparametric variables. The nonparametric Wilcoxon test was used to compare two paired groups. The association between nonparametric variables was determined using the Spearman correlation coefficient (r). Any value of p<0.05 was considered statistically significant. GraphPad Prism version 5.03 for Windows (GraphPad Software, La Jolla, CA, USA) was used for these analyses.
This study compared three groups: patients with confirmed influenza A (H1N1) (pA/H1N1), subjects with influenza-like illness (ILI), and AHCs. Gender distributions were similar in the three groups of patients, and differences between the groups were not significant. Patients in the pA/H1N1 group were slightly younger (42±14 years) than those in the ILI group (45±15 years, p = 0.068). In addition, the presence of comorbidities was assessed, including diabetes, hypertension, asthma, and chronic obstructive pulmonary disease (COPD); interestingly, in the pA/H1N1 group, there was a higher rate of diabetes than in the ILI group (12.5% vs. 5.21%, respectively; p = 0.03). There were no statistically significant differences for the other comorbidities studied (Table 1).
Patients with confirmed influenza A (H1N1) consistently showed a greater disruption of clinical parameters influencing evolution toward greater disease severity (Table 2).
Risk of Severe Influenza A (H1N1) Infection
To determine the risk of severe influenza A (H1N1) virus infection, the genotypes of individual SNPs were compared in both groups of patients (pA/H1N1 and ILI).
Genotypes associated with influenza A (H1N1) virus infection were identified. The IL6 rs1818879 (GA) heterozygous genotype showed a risk association with viral infection (p<0.001; OR = 5.94, 95% CI: 3.05–11.56). Two IL1B SNPs were associated with a decreased risk of infection: rs16944 AG (OR = 0.52, 95% CI: 0.28–0.97) and rs3136558 TC (OR = 0.50, 95% CI: 0.29–0.88) (Table 3).
When the pA/H1N1 group was compared with the AHC group, we observed that the LTA rs909253 TC heterozygous genotype showed a risk association with disease susceptibility (p = 0.003; OR = 1.9, 95% CI: 1.25–2.87); a similar association occurred with the IL1B rs3136558 CC genotype (p = 0.041; OR = 1.89, 95% CI: 1.02–3.51). In contrast, the IL6 rs2066992 GT genotype was protective (p = 0.002; OR = 0.53, 95% CI: 0.35–0.80) for individuals carrying the homozygous genotype for the ancestral allele (Table 3).
Susceptibility to Greater Severity of A (H1N1) Infection
To determine the susceptibility to greater disease severity in relation to the SNPs present in pro-inflammatory genes, two subgroups were compared: patients admitted to the ICU and those who did not enter the unit and therefore did not require AMV; including both pAH1N1 patients and ILI patients (53%vs. 17%). Of the 11 SNPs studied, the TNF rs361525 SNP was associated with greater disease severity (p = 0.007; OR = 16.06) (S3 Table).
With respect to LTA rs909253, allele A is a risk factor for disease development (pA/H1N1 vs. AHC: p = 0.049; OR 1.34, 95% CI: 1.01–1.80), whereas the IL6 rs2066992 T allele is a protective factor (pA/H1N1 vs. AHC: p = 0.007; OR = 0.62, 95% CI: 0.43–0.98). In addition, the IL1B rs16944 G allele is protective against the development of severe influenza A (H1N1) virus infection (pA/H1N1 vs. ILI: p = 0.048; OR = 0.70, 95% CI: 0.50–0.98) (S2 Table).
Thirty-one patients positive for influenza A (H1N1) virus died, whereas four patients with ILI died. None of the polymorphisms/genotypes were directly associated with mortality. We also aimed to demonstrate whether there was any additional risk besides mortality associated with the presence of comorbidities; only the IL6 rs2069869 GG genotype was associated with mortality risk in patients with diabetes in the pA/H1N1 group (p = 0.011; OR = 40.8, 95% CI: 2.31–720.24). Only statistically significant data are shown.
The haplotype study was conducted to determine their associations with disease severity. The analysis included the IL6, TNF, and IL1B genes with their respective SNPs and considered both the pA/H1N1 group vs. the ILI group and each group individually. When comparing the two groups of patients, haplotypes were not formed, only independent alleles, in groups of patients (ILI or pA/H1N1). Fig 2 shows the haplotypes consisting of the TNF SNPs located on chromosome 6 in the patients with ILI; these haplotypes are not in high linkage disequilibrium (r2 = 0.75), although the value was close to the minimum required (0.80). Polymorphisms evaluated in the TNF and IL6 genes met Hardy-Weinberg equilibrium (Fig 2).
Five parameters of infection severity were considered: mechanical ventilation, admission to ICU, presence of Acute Respiratory Distress Syndrome, development of pneumonia, and fatal outcome.
The analysis of severity variables confirmed that these variables per se are significantly associated with disease severity (Table 3). Interestingly, associations were identified between the values for lymphocytes <1,000 and glucose >119 mg/dL with the rs16944 and rs1818879 GG genotypes in IL1B and IL6, respectively. Additionally, the rs16944 GG genotype was associated with thrombocytopenia and the rs1818879 GG genotype with the use of AMV (Table 4).
Serum Cytokine Expression
We determined the levels of ten diverse pro-inflammatory cytokines in serum samples. Because the cytokine concentrations showed significant inter-individual variation, we represented the quantification in a box plot in Fig 3. The concentrations of cytokines were in the range of 5–80 pg/mL. In the case of pA/H1N1 patients, the concentrations of all cytokine were higher than in the other study groups. In particular, IL5 showed increased concentrations in pA/H1N1 patients vs. ILI patients or AHCs. The three groups were compared using one-way ANOVA for multiple comparisons. All comparisons were considered statically significant at p<0.01 and p<0.05; for Tukey corrections, p<0.03 was considered significant. For IL6, the multiple comparisons ANOVA model produced a marginal p = 0.03.
Box and whisker plots of cytokine levels in sera from the AHC, ILI, and pA/H1N1 groups. Boxes represents the 25–75 quartile, the whiskers represent the range of values, the middle line inside the box is the median, and the outlier values are represented as circles outside the boxes. The p-values (** and * representing <0.001 and <0.05, respectively) were calculated by one-way ANOVA and are presented above the graphs.
Compared with ILI patients, severe pA/H1N1 patients exhibited markedly increased levels of serum IL-5 (p <0.001) and IL-6 (p = 0.007) and similar levels of GM-CSF (p = 0.967). We found no statistically significant differences for the remaining seven analytes evaluated. These results show that severe pA/H1N1 patients secrete higher levels of serum IL-6 and IL-5 than do ILI patients, suggesting a particular mechanism of pathophysiology in pA/H1N1 infection.
Although the levels of serum IL-6 in pA/H1N1 patients were higher than those of healthy controls, no statistically significant differences were observed (Fig 3).
Finally, we examined the correlation between cytokine levels and severe clinical parameters, including obesity and leukocyte counts. The median IL-5 concentrations for obese ILI patients and for obese pA/H1N1 patients were 3.08 and 3.07, respectively. In contrast, compared with non-obese ILI patients, non-obese pA/H1N1 patients showed a 9-fold increase: median of 3.03 vs. median of 29.93 (p<0.01), respectively. Concentrations of IL-6 in obese ILI patients and in obese pA/H1N1 patients were 10.58 and 32.30, respectively. Compared with non-obese ILI patients, non-obese pA/H1N1 patients showed an increase: 19.41 vs. 49.17; however there was no significant difference (p = 0.28).
Pearson’s analysis showed no significant difference between BMI and IL-5 and IL-6 concentrations or leukocyte counts and IL-5 and IL-6 in the pA/H1N1 group.
In addition to the findings previously described, in this second study of polymorphisms in pro-inflammatory cytokine genes, our group identified genetic factors associated with susceptibility to influenza A (H1N1). In late 2012, we reported that some genotypes in TNF and LTA are associated with susceptibility to infection with the influenza A (H1N1) pdm09 virus. Interestingly, two SNPs, one in IL1B (rs16944) and one in IL6 (rs1818879), were associated with clinical severity when comparing influenza A (H1N1) patients with ILI patients.
This study confirms our previous finding that the LTA rs909253 GA genotype is a risk factor for susceptibility to developing secondary disease after contact with the influenza A (H1N1) pdm09 virus; interestingly, the minor allele (A) was associated with risk in this same comparison group (pA/H1N1 vs. AHC).
To complement these observations, an association analysis was conducted regarding the risk of severe influenza A (H1N1) infection; both IL1B and IL6 SNPs showed significant associations, particularly rs16944, which is located in the promoter region of the gene. In agreement with what has been reported previously, the GA genotype in the TNF-238 (rs361525) promoter presented a risk for greater disease severity in patients who were admitted to the ICU compared with those who only required hospitalization [2, 15, 20]. Despite having no association with the minor allele homozygous genotype for TNF-238, we may observe that the presence of allele A in the heterozygous genotype in severe influenza A (H1N1) patients increased the risk of severity.
Associations have recently been reported for the IL1A, IL1B  and IL10  genes, whereas increases in the allelic frequencies of TNF-238A (rs361525) and TNF-308G (rs1800629), IL10-592C, and IL10-1082A have been associated with increased disease severity [14–16].
Both LTA and TNF are considered biologically relevant inflammatory cytokines with various functions in the immune response. Several authors have shown that SNPs present in these genes are associated with increased susceptibility for developing infectious diseases [22–24]. The polyadenylation region in LTA and the TNF transcription start sites are in close proximity in the TNF cluster of the HLA class III region; therefore, it is difficult to obtain associations of SNPs in this region . Currently, priority is given to studies of haplotypes for candidate immune response genes, especially for multigenic control in response to infectious diseases such as influenza. Therefore, we conducted a study of haplotypes in influenza A (H1N1) and ILI patients; however, a haplotype between LTA and TNF was only identified in the latter group, and high linkage disequilibrium was not observed (r2 = 0.75). We believe that expanding the n or considering other candidate genes could improve this approach. Because cytokine production is influenced by SNPs in the promoter regions of these genes , we propose that individuals carrying associated alleles may exhibit increased cytokine production and may thus develop more severe disease.
Previous studies have reported a correlation between IL-1β and IL-6 overexpression and some clinical, radiological and immunological findings, such as pneumonia and ARDS, in both children with seasonal influenza and murine models [27–29]. TNF, IL-1β and IL-6 pro-inflammatory cytokines play crucial roles in inflammation, infection, and responses to stress caused by different types of infections. Many of the systemic effects of the acute phase are due to the combined actions of these cytokines . In particular, IL-1β and IL-6 have been identified as markers of severity in acute lung injury during influenza A (H1N1) virus infection ; IL-1β in particular has been proposed as a good early marker of the severity and progression of lung inflammation in mechanically ventilated patients . In a 2013 study by Chiaretti et al., influenza A (H1N1) virus infection was shown to induce the early and significant up-regulation of IL-1β and IL-6 in plasma, suggesting that these cytokines are responsible for different molecular reactions that lead to inflammation of the airway and increased disease severity . In turn, IL-6 plays a critical role in the acute phase response during infectious processes and is usually induced with other pro-inflammatory cytokines, such as TNF-α and IL-1β, during immune system alarms . Similarly, these cytokines are overexpressed at higher serum levels in severe patients compared with patients with moderate disease [4–7]. Strikingly, in our study, compared with obese pA/H1N1 patients, non-obese patients showed significantly higher IL-5 and IL-6 levels; furthermore, pA/H1N1 patients exhibited lower leukocyte counts. Several groups worldwide have reported that increased levels of pro-inflammatory cytokines are associated with clinical severity parameters, including obesity [34,35]. We found that IL-6 levels were higher in pAHN1 obese patients than in ILI obese patients (32.3 vs. 10.5 pg/mL), with no significant differences. In contrast, non-obese patients in the pA/H1N1 group showed a 9-fold increase in IL-5 levels. Despite the increase observed in both obese patient groups, it is important to note that compared with ILI patients and AHCs, non-obese patients with severe clinical pictures of H1N1 influenza have increased IL-5 levels. There were no significant differences for leukocyte counts and cytokine levels in pA/H1N1 and ILI patients.
According to published reports, cytokine levels are affected over time [10, 36]. Nevertheless, our study only examined associations between SNPs and susceptibility to infection and disease severity; we did not investigate how oseltamivir affects cytokine levels over time. Oseltamivir treatment may modify the expression of cytokines, but that does not affect the association between certain SNPs and disease severity among patients and AHCs. The median number of days from the onset of symptoms to oseltamivir administration was 5.0, although 92% of study patients were administered oseltamivir within 1 day after admission . Therefore, associations were analyzed by the severe clinical picture regardless of immune regulation by the antiviral, which was reinforced by the fact that the patients were subjected to the same doses and began treatment similarly. One major limitation of this study was that samples were only collected in the central region of the country where mortality was higher; therefore, we believe that expanding the sampling area to other geographical regions would enable us to clearly identify areas with greater "genetic vulnerability" to be able to overcome future challenges of potentially lethal subtypes of influenza.
Concerning age at presentation, our results indicate that many patients who are not in the age groups at greatest risk of death or who have no comorbidities associated with an increased risk of death from influenza may have genetic characteristics that make them more susceptible to developing influenza and presenting with greater disease severity. With respect to the population of 2010 and 2012 and in accordance with what has been reported by other authors [38–40], approximately 95% of our study population had not previously received an influenza vaccine due to the vaccination guidelines suggested by the Ministry of Health prior to 2013. In addition to this intricate scenario, many patients are reluctant to receive vaccines due to mistrust of the vaccine or infection with H1N1 . In this way and based on our exclusion criteria, >90% of our study population was excluded from the risk group. We reasoned that associations with the severity of influenza A (H1N1) virus infections would be determined more by genetic variables than an immune response to the influenza vaccine. This view is supported by the fact that the group of AHCs is in the same age group and therefore has the same vaccination characteristics. Therefore, it is unlikely that our results would be modified by vaccination status.
Our observations highlight the need to take into account that any patient may progress to severe disease because of the influence of their genetic background. Therefore, influenza mortality prevention strategies should consider universal vaccination. The TNF rs361525 GA genotype is associated with greater disease severity. SNPs in IL6 are associated with susceptibility to developing influenza A (H1N1) infection. In addition, the IL6 rs2069869 GG is associated with mortality from influenza A (H1N1) infection in the presence of diabetes. IL-6 levels are increased in both obese pA/H1N1 and ILI patients compared with AHCs, but greater than an obese patient alone. Strikingly, non-obese pA/H1N1 patients presented much higher IL-6 levels than did obese patients. Influenza A (H1N1) virus infection and its severity are determined by the genetic characteristics of the individual, especially among genes that regulate inflammation.
S1 Table. Genetic information to identify each of the SNPs studied.
S2 Table. Allele frequencies and associations with susceptibility and risk of severe influenza A (H1N1) infection.
This paper constitutes a partial fulfillment of the Graduate Program in Biological Sciences of the National Autonomous University of México (UNAM) for RAGR. RA García-Ramírez acknowledges the academic support provided by the National Council of Science and Technology (CONACyT) and Posgrado en Ciencias Biológicas, UNAM. The authors thank the Coordinación de Investigación en Salud of the IMSS for covering the translation and publishing costs. This study was funded by the Mexican Institute of Social Security, Grants FIS/IMSS/PROT/G13/1212 and CONACyT-FOSIS SALUD2009-C02-126699.
Conceived and designed the experiments: RAGR JMMA RFV. Performed the experiments: RAGR RFV. Analyzed the data: RQC ARV JMMA. Contributed reagents/materials/analysis tools: ARV AEC. Wrote the paper: RAGR RFV.
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