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A role for human leucocyte antigens in the susceptibility to SARS‐Cov‐2 infection observed in transplant patients
We analysed data from 80 patients who tested positive for SARS‐CoV‐2 RNA who had previously been HLA typed to support transplantation. Data were combined from two adjacent centres in Manchester and Leeds to achieve a sufficient number for early analysis. HLA frequencies observed were compared agains...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7361549/ https://www.ncbi.nlm.nih.gov/pubmed/32623831 http://dx.doi.org/10.1111/iji.12505 |
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author | Poulton, Kay Wright, Paul Hughes, Pamela Savic, Sinisa Welberry Smith, Matthew Guiver, Malcolm Morton, Muir van Dellen, David Tholouli, Eleni Wynn, Robert Clark, Brendan |
author_facet | Poulton, Kay Wright, Paul Hughes, Pamela Savic, Sinisa Welberry Smith, Matthew Guiver, Malcolm Morton, Muir van Dellen, David Tholouli, Eleni Wynn, Robert Clark, Brendan |
author_sort | Poulton, Kay |
collection | PubMed |
description | We analysed data from 80 patients who tested positive for SARS‐CoV‐2 RNA who had previously been HLA typed to support transplantation. Data were combined from two adjacent centres in Manchester and Leeds to achieve a sufficient number for early analysis. HLA frequencies observed were compared against two control populations: first, against published frequencies in a UK deceased donor population (n = 10,000) representing the target population of the virus, and second, using a cohort of individuals from the combined transplant waiting lists of both centres (n = 308), representing a comparator group of unaffected individuals of the same demographic. We report a significant HLA association with HLA‐ DQB1*06 (53% vs. 36%; p < .012; OR 1.96; 95% CI 1.94–3.22) and infection. A bias towards an increased representation of HLA‐A*26, HLA‐DRB1*15, HLA‐DRB1*10 and DRB1*11 was also noted but these were either only significant using the UK donor controls, or did not remain significant after correction for multiple tests. Likewise, HLA‐A*02, HLA‐B*44 and HLA‐C*05 may exert a protective effect, but these associations did not remain significant after correction for multiple tests. This is relevant information for the clinical management of patients in the setting of the current SARS‐CoV‐2 pandemic and potentially in risk‐assessing staff interactions with infected patients. |
format | Online Article Text |
id | pubmed-7361549 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-73615492020-07-15 A role for human leucocyte antigens in the susceptibility to SARS‐Cov‐2 infection observed in transplant patients Poulton, Kay Wright, Paul Hughes, Pamela Savic, Sinisa Welberry Smith, Matthew Guiver, Malcolm Morton, Muir van Dellen, David Tholouli, Eleni Wynn, Robert Clark, Brendan Int J Immunogenet Hla & Disease We analysed data from 80 patients who tested positive for SARS‐CoV‐2 RNA who had previously been HLA typed to support transplantation. Data were combined from two adjacent centres in Manchester and Leeds to achieve a sufficient number for early analysis. HLA frequencies observed were compared against two control populations: first, against published frequencies in a UK deceased donor population (n = 10,000) representing the target population of the virus, and second, using a cohort of individuals from the combined transplant waiting lists of both centres (n = 308), representing a comparator group of unaffected individuals of the same demographic. We report a significant HLA association with HLA‐ DQB1*06 (53% vs. 36%; p < .012; OR 1.96; 95% CI 1.94–3.22) and infection. A bias towards an increased representation of HLA‐A*26, HLA‐DRB1*15, HLA‐DRB1*10 and DRB1*11 was also noted but these were either only significant using the UK donor controls, or did not remain significant after correction for multiple tests. Likewise, HLA‐A*02, HLA‐B*44 and HLA‐C*05 may exert a protective effect, but these associations did not remain significant after correction for multiple tests. This is relevant information for the clinical management of patients in the setting of the current SARS‐CoV‐2 pandemic and potentially in risk‐assessing staff interactions with infected patients. John Wiley and Sons Inc. 2020-07-05 2020-08 /pmc/articles/PMC7361549/ /pubmed/32623831 http://dx.doi.org/10.1111/iji.12505 Text en © 2020 The Authors. International Journal of Immunogenetics published by John Wiley & Sons Ltd https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Hla & Disease Poulton, Kay Wright, Paul Hughes, Pamela Savic, Sinisa Welberry Smith, Matthew Guiver, Malcolm Morton, Muir van Dellen, David Tholouli, Eleni Wynn, Robert Clark, Brendan A role for human leucocyte antigens in the susceptibility to SARS‐Cov‐2 infection observed in transplant patients |
title | A role for human leucocyte antigens in the susceptibility to SARS‐Cov‐2 infection observed in transplant patients |
title_full | A role for human leucocyte antigens in the susceptibility to SARS‐Cov‐2 infection observed in transplant patients |
title_fullStr | A role for human leucocyte antigens in the susceptibility to SARS‐Cov‐2 infection observed in transplant patients |
title_full_unstemmed | A role for human leucocyte antigens in the susceptibility to SARS‐Cov‐2 infection observed in transplant patients |
title_short | A role for human leucocyte antigens in the susceptibility to SARS‐Cov‐2 infection observed in transplant patients |
title_sort | role for human leucocyte antigens in the susceptibility to sars‐cov‐2 infection observed in transplant patients |
topic | Hla & Disease |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7361549/ https://www.ncbi.nlm.nih.gov/pubmed/32623831 http://dx.doi.org/10.1111/iji.12505 |
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