Publication: HLA-A*11:01 and HLA-C*04:01 are associated with severe COVID-19
| dc.contributor.author | Castro-Santos, Patricia | |
| dc.contributor.author | Rojas-Martinez, Augusto | |
| dc.contributor.author | Riancho, José A. | |
| dc.contributor.author | Lapunzina, Pablo | |
| dc.contributor.author | Flores, Carlos | |
| dc.contributor.author | Carracedo, Angel | |
| dc.contributor.author | Díaz-Peña, Roberto | |
| dc.contributor.author | García-Vázquez, Elisa | |
| dc.contributor.author | Scourge Cohort Group | |
| dc.contributor.department | Medicina | |
| dc.date.accessioned | 2024-07-08T10:51:19Z | |
| dc.date.available | 2024-07-08T10:51:19Z | |
| dc.date.issued | 2023-08-01 | |
| dc.description | © 2023 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd. This document is the Published, version of a Published Work that appeared in final form in HLA: Immune Response Genetics. To access the final edited and published work see https://doi.org/10.1111/tan.15160 | es |
| dc.description.abstract | We analyzed the association between HLA polymorphisms and susceptibility to SARS-CoV-2 infection and disease severity. Genotyping data from a total of 9373 COVID-19-positive cases from the Spanish Coalition to Unlock Research on Host Genetics on COVID-19 (SCOURGE) consortium and 5943 population controls were included in the study. We found an association of the alleles HLA-B*14:02 and HLA-C*08:02 with a lower risk to COVID-19 infection (p = 0.006, OR = 0.84, 95% CI = [0.75–0.95], p = 0.024, OR = 0.86, 95% CI = [0.78–0.95], respectively). We also found the alleles HLA-A*11:01 and HLA- C*04:01 associated with disease severity (p = 0.033, OR = 1.16, 95% CI = [1.04–1.31], p = 0.045, OR = 1.14, 95% CI = [1.05–1.25], respectively). These results suggest that an effective presentation of viral peptides by HLA class I alleles involve a faster infection clearance, decreasing the susceptibility and severity of COVID-19. | es |
| dc.format | application/pdf | es |
| dc.format.extent | 9 | es |
| dc.identifier.citation | HLA: Immune Response Genetics. 2023 102(6): 731-739 | |
| dc.identifier.doi | https://doi.org/10.1111/tan.15160 | |
| dc.identifier.issn | Print: 2059-2302 | |
| dc.identifier.issn | Electronic: 2059-2310 | |
| dc.identifier.uri | http://hdl.handle.net/10201/142903 | |
| dc.language | eng | es |
| dc.publisher | John Wiley & Sons | es |
| dc.relation | Instituto de Salud Carlos III, Grant/Award. Numbers: COV20_00622, CP21/00003; European Union (ERDF) | es |
| dc.relation.publisherversion | https://onlinelibrary.wiley.com/doi/10.1111/tan.15160 | es |
| dc.rights.accessRights | info:eu-repo/semantics/restrictedAccess | |
| dc.subject | COVID-19 | es |
| dc.subject | HLA evolutionary divergence | es |
| dc.subject | HLA-A*11:01 | es |
| dc.subject | HLA-C*04:01 | es |
| dc.subject | Immunogenetics | es |
| dc.subject | SARS-CoV-2 | es |
| dc.title | HLA-A*11:01 and HLA-C*04:01 are associated with severe COVID-19 | es |
| dc.type | info:eu-repo/semantics/article | es |
| dspace.entity.type | Publication | es |
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