tetano
Editor, Senior Moderator
Virol J. 2019 Jun 13;16(1):79. doi: 10.1186/s12985-019-1187-8.
[h=1]Association of polymorphisms in inflammatory cytokines encoding genes with severe cases of influenza A/H1N1 and B in an Iranian population.[/h] Keshavarz M[SUP]1,[/SUP][SUP]2[/SUP], Namdari H[SUP]3[/SUP], Farahmand M[SUP]4[/SUP], Mehrbod P[SUP]5[/SUP], Mokhtari-Azad T[SUP]4[/SUP], Rezaei F[SUP]6[/SUP].
[h=3]Author information[/h]
[h=3]Abstract[/h] [h=4]BACKGROUND:[/h] The increased levels of blood cytokines is the main immunopathological process that were attributed to severe clinical outcomes in cases of influenza A, influenza B and people with influenza-like illness (ILI). Functional genetic polymorphisms caused by single nucleotide polymorphisms (SNPs) in inflammatory cytokines genes can influence their functions either qualitatively or quantitatively, which is associated with the possibility of severe influenza infections. The aim of the present case-control study was to investigate the association of polymorphisms in inflammatory cytokines genes with influenza patients and ILI group in an Iranian population.
[h=4]METHODS:[/h] Total number of 30 influenza B, 50 influenza A (H1N1) and 96 ILI inpatient individuals were confirmed by Real-time RT-PCR and HI assays. The genotype determination was assessed for defined SNPs in IL-1β, IL-17, IL-10 and IL-28 genes.
[h=4]RESULTS:[/h] The frequencies of the IL-1β rs16944 (P = 0.007) and IL-17 rs2275913 (P = 0.006) genotypes were associated with severe influenza disease, while the frequencies of IL-10 rs1800872 and IL-28 rs8099917 were not associated with the disease (P > 0.05). Also, the absence of A allele in IL-17 rs2275913 SNP increased the risk of influenza A (H1N1) infection (P = 0.008).
[h=4]CONCLUSIONS:[/h] This study demonstrated that influenza A- (H1N1) and B-infected patients and also ILI controls have different profiles of immune parameters, and individuals carrying the specific cytokine-derived polymorphisms may show different immune responses towards severe outcome.
[h=4]KEYWORDS:[/h] Cytokine; Inflammatory response; Influenza; Influenza-like illness; Single nucleotide polymorphism
PMID: 31196204 PMCID: PMC6567579 DOI: 10.1186/s12985-019-1187-8
Free PMC Article
[h=1]Association of polymorphisms in inflammatory cytokines encoding genes with severe cases of influenza A/H1N1 and B in an Iranian population.[/h] Keshavarz M[SUP]1,[/SUP][SUP]2[/SUP], Namdari H[SUP]3[/SUP], Farahmand M[SUP]4[/SUP], Mehrbod P[SUP]5[/SUP], Mokhtari-Azad T[SUP]4[/SUP], Rezaei F[SUP]6[/SUP].
[h=3]Author information[/h]
[h=3]Abstract[/h] [h=4]BACKGROUND:[/h] The increased levels of blood cytokines is the main immunopathological process that were attributed to severe clinical outcomes in cases of influenza A, influenza B and people with influenza-like illness (ILI). Functional genetic polymorphisms caused by single nucleotide polymorphisms (SNPs) in inflammatory cytokines genes can influence their functions either qualitatively or quantitatively, which is associated with the possibility of severe influenza infections. The aim of the present case-control study was to investigate the association of polymorphisms in inflammatory cytokines genes with influenza patients and ILI group in an Iranian population.
[h=4]METHODS:[/h] Total number of 30 influenza B, 50 influenza A (H1N1) and 96 ILI inpatient individuals were confirmed by Real-time RT-PCR and HI assays. The genotype determination was assessed for defined SNPs in IL-1β, IL-17, IL-10 and IL-28 genes.
[h=4]RESULTS:[/h] The frequencies of the IL-1β rs16944 (P = 0.007) and IL-17 rs2275913 (P = 0.006) genotypes were associated with severe influenza disease, while the frequencies of IL-10 rs1800872 and IL-28 rs8099917 were not associated with the disease (P > 0.05). Also, the absence of A allele in IL-17 rs2275913 SNP increased the risk of influenza A (H1N1) infection (P = 0.008).
[h=4]CONCLUSIONS:[/h] This study demonstrated that influenza A- (H1N1) and B-infected patients and also ILI controls have different profiles of immune parameters, and individuals carrying the specific cytokine-derived polymorphisms may show different immune responses towards severe outcome.
[h=4]KEYWORDS:[/h] Cytokine; Inflammatory response; Influenza; Influenza-like illness; Single nucleotide polymorphism
PMID: 31196204 PMCID: PMC6567579 DOI: 10.1186/s12985-019-1187-8
Free PMC Article