tetano
Editor, Senior Moderator
Viruses
. 2021 Feb 22;13(2):344.
doi: 10.3390/v13020344.
Role of the Host Genetic Susceptibility to 2009 Pandemic Influenza A H1N1
Gloria P?rez-Rubio[SUP] 1 [/SUP], Marco Antonio Ponce-Gallegos[SUP] 1 [/SUP], Bruno Andr? Dom?nguez-Mazzocco[SUP] 1 [/SUP], Jaime Ponce-Gallegos[SUP] 2 [/SUP], Rom?n Alejandro Garc?a-Ram?rez[SUP] 1 [/SUP], Ramc?s Falf?n-Valencia[SUP] 1 [/SUP]
Affiliations
Abstract
Influenza A virus (IAV) is the most common infectious agent in humans, and infects approximately 10-20% of the world's population, resulting in 3-5 million hospitalizations per year. A scientific literature search was performed using the PubMed database and the Medical Subject Headings (MeSH) "Influenza A H1N1" and "Genetic susceptibility". Due to the amount of information and evidence about genetic susceptibility generated from the studies carried out in the last influenza A H1N1 pandemic, studies published between January 2009 to May 2020 were considered; 119 papers were found. Several pathways are involved in the host defense against IAV infection (innate immune response, pro-inflammatory cytokines, chemokines, complement activation, and HLA molecules participating in viral antigen presentation). On the other hand, single nucleotide polymorphisms (SNPs) are a type of variation involving the change of a single base pair that can mean that encoded proteins do not carry out their functions properly, allowing higher viral replication and abnormal host response to infection, such as a cytokine storm. Some of the most studied SNPs associated with IAV infection genetic susceptibility are located in the FCGR2A, C1QBP, CD55, and RPAIN genes, affecting host immune responses through abnormal complement activation. Also, SNPs in IFITM3 (which participates in endosomes and lysosomes fusion) represent some of the most critical polymorphisms associated with IAV infection, suggesting an ineffective virus clearance. Regarding inflammatory response genes, single nucleotide variants in IL1B, TNF, LTA IL17A, IL8, IL6, IRAK2, PIK3CG, and HLA complex are associated with altered phenotype in pro-inflammatory molecules, participating in IAV infection and the severest form of the disease.
Keywords: cytokine storm; genetic susceptibility; inflammation; influenza; polymorphisms.
. 2021 Feb 22;13(2):344.
doi: 10.3390/v13020344.
Role of the Host Genetic Susceptibility to 2009 Pandemic Influenza A H1N1
Gloria P?rez-Rubio[SUP] 1 [/SUP], Marco Antonio Ponce-Gallegos[SUP] 1 [/SUP], Bruno Andr? Dom?nguez-Mazzocco[SUP] 1 [/SUP], Jaime Ponce-Gallegos[SUP] 2 [/SUP], Rom?n Alejandro Garc?a-Ram?rez[SUP] 1 [/SUP], Ramc?s Falf?n-Valencia[SUP] 1 [/SUP]
Affiliations
- PMID: 33671828
- PMCID: PMC7926867
- DOI: 10.3390/v13020344
Abstract
Influenza A virus (IAV) is the most common infectious agent in humans, and infects approximately 10-20% of the world's population, resulting in 3-5 million hospitalizations per year. A scientific literature search was performed using the PubMed database and the Medical Subject Headings (MeSH) "Influenza A H1N1" and "Genetic susceptibility". Due to the amount of information and evidence about genetic susceptibility generated from the studies carried out in the last influenza A H1N1 pandemic, studies published between January 2009 to May 2020 were considered; 119 papers were found. Several pathways are involved in the host defense against IAV infection (innate immune response, pro-inflammatory cytokines, chemokines, complement activation, and HLA molecules participating in viral antigen presentation). On the other hand, single nucleotide polymorphisms (SNPs) are a type of variation involving the change of a single base pair that can mean that encoded proteins do not carry out their functions properly, allowing higher viral replication and abnormal host response to infection, such as a cytokine storm. Some of the most studied SNPs associated with IAV infection genetic susceptibility are located in the FCGR2A, C1QBP, CD55, and RPAIN genes, affecting host immune responses through abnormal complement activation. Also, SNPs in IFITM3 (which participates in endosomes and lysosomes fusion) represent some of the most critical polymorphisms associated with IAV infection, suggesting an ineffective virus clearance. Regarding inflammatory response genes, single nucleotide variants in IL1B, TNF, LTA IL17A, IL8, IL6, IRAK2, PIK3CG, and HLA complex are associated with altered phenotype in pro-inflammatory molecules, participating in IAV infection and the severest form of the disease.
Keywords: cytokine storm; genetic susceptibility; inflammation; influenza; polymorphisms.