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HLA Sensitization in the Era of COVID-19: Single-Center Experience

It is well known that several viral infections are capable of triggering the formation of HLA antibodies; however, an association between SARS-CoV-2 and the development of anti-HLA antibodies is not yet confirmed. In this study, we compared the prevalence of HLA antibody before and after COVID-19 in...

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Autores principales: Awaji, Mohammad, Alajlan, Kenana, Shaikh, Alaa, Alkebasi, Shaima, Kutty, Clara, Alshami, Alanoud, Attas, Rabab Ali Al
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9537251/
https://www.ncbi.nlm.nih.gov/pubmed/36372565
http://dx.doi.org/10.1016/j.transproceed.2022.10.024
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author Awaji, Mohammad
Alajlan, Kenana
Shaikh, Alaa
Alkebasi, Shaima
Kutty, Clara
Alshami, Alanoud
Attas, Rabab Ali Al
author_facet Awaji, Mohammad
Alajlan, Kenana
Shaikh, Alaa
Alkebasi, Shaima
Kutty, Clara
Alshami, Alanoud
Attas, Rabab Ali Al
author_sort Awaji, Mohammad
collection PubMed
description It is well known that several viral infections are capable of triggering the formation of HLA antibodies; however, an association between SARS-CoV-2 and the development of anti-HLA antibodies is not yet confirmed. In this study, we compared the prevalence of HLA antibody before and after COVID-19 infection in a cohort of 3 groups included 58 healthy nonsensitized employees (HNEs), 130 kidney transplant recipients (KTRs), and 62 kidney transplant candidates. There were no significant changes observed in HLA class I antibodies in any of the groups, but evaluation of antibodies to HLA class II revealed a significant change in the KTR group (P = .0184) after acquiring COVID-19 infection and in the HNE group (P = .0043) when compared to the reported prevalence in a similar population. Although we observed the emergence of convalescent de novo donor-specific antibodies in 2 patients, we did not encounter any rejection episodes in the KTR group. Finally, the results of flow cytometry crossmatch in the HNE group were not consistent with the state of antibodies. In conclusion, COVID-19 infection has the potential to produce class II antibodies but with little effect on preexisting sensitization. These antibodies are likely to be transient and not necessarily causing positive crossmatch with the corresponding antigens at the proper mean fluorescent intensity and therefore should not affect access to transplantation. There is a need for further evaluation to ascertain the genuineness of these antibodies and their exact effect on transplant readiness and outcomes.
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spelling pubmed-95372512022-10-11 HLA Sensitization in the Era of COVID-19: Single-Center Experience Awaji, Mohammad Alajlan, Kenana Shaikh, Alaa Alkebasi, Shaima Kutty, Clara Alshami, Alanoud Attas, Rabab Ali Al Transplant Proc Article It is well known that several viral infections are capable of triggering the formation of HLA antibodies; however, an association between SARS-CoV-2 and the development of anti-HLA antibodies is not yet confirmed. In this study, we compared the prevalence of HLA antibody before and after COVID-19 infection in a cohort of 3 groups included 58 healthy nonsensitized employees (HNEs), 130 kidney transplant recipients (KTRs), and 62 kidney transplant candidates. There were no significant changes observed in HLA class I antibodies in any of the groups, but evaluation of antibodies to HLA class II revealed a significant change in the KTR group (P = .0184) after acquiring COVID-19 infection and in the HNE group (P = .0043) when compared to the reported prevalence in a similar population. Although we observed the emergence of convalescent de novo donor-specific antibodies in 2 patients, we did not encounter any rejection episodes in the KTR group. Finally, the results of flow cytometry crossmatch in the HNE group were not consistent with the state of antibodies. In conclusion, COVID-19 infection has the potential to produce class II antibodies but with little effect on preexisting sensitization. These antibodies are likely to be transient and not necessarily causing positive crossmatch with the corresponding antigens at the proper mean fluorescent intensity and therefore should not affect access to transplantation. There is a need for further evaluation to ascertain the genuineness of these antibodies and their exact effect on transplant readiness and outcomes. Elsevier Inc. 2022-12 2022-10-07 /pmc/articles/PMC9537251/ /pubmed/36372565 http://dx.doi.org/10.1016/j.transproceed.2022.10.024 Text en © 2022 Elsevier Inc. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Awaji, Mohammad
Alajlan, Kenana
Shaikh, Alaa
Alkebasi, Shaima
Kutty, Clara
Alshami, Alanoud
Attas, Rabab Ali Al
HLA Sensitization in the Era of COVID-19: Single-Center Experience
title HLA Sensitization in the Era of COVID-19: Single-Center Experience
title_full HLA Sensitization in the Era of COVID-19: Single-Center Experience
title_fullStr HLA Sensitization in the Era of COVID-19: Single-Center Experience
title_full_unstemmed HLA Sensitization in the Era of COVID-19: Single-Center Experience
title_short HLA Sensitization in the Era of COVID-19: Single-Center Experience
title_sort hla sensitization in the era of covid-19: single-center experience
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9537251/
https://www.ncbi.nlm.nih.gov/pubmed/36372565
http://dx.doi.org/10.1016/j.transproceed.2022.10.024
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