Cargando…

Cross-Reactive Anti-Viral T Cells Increase Prior to an Episode of Viral Reactivation Post Human Lung Transplantation

Human Cytomegalovirus (CMV) reactivation continues to influence lung transplant outcomes. Cross-reactivity of anti-viral memory T cells against donor human leukocyte antigens (HLA) may be a contributing factor. We identified cross-reactive HLA-A*02:01-restricted CMV-specific cytotoxic T lymphocytes...

Descripción completa

Detalles Bibliográficos
Autores principales: Nguyen, Thi H. O., Westall, Glen P., Bull, Tara E., Meehan, Aislin C., Mifsud, Nicole A., Kotsimbos, Tom C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3566045/
https://www.ncbi.nlm.nih.gov/pubmed/23405250
http://dx.doi.org/10.1371/journal.pone.0056042
_version_ 1782258518322053120
author Nguyen, Thi H. O.
Westall, Glen P.
Bull, Tara E.
Meehan, Aislin C.
Mifsud, Nicole A.
Kotsimbos, Tom C.
author_facet Nguyen, Thi H. O.
Westall, Glen P.
Bull, Tara E.
Meehan, Aislin C.
Mifsud, Nicole A.
Kotsimbos, Tom C.
author_sort Nguyen, Thi H. O.
collection PubMed
description Human Cytomegalovirus (CMV) reactivation continues to influence lung transplant outcomes. Cross-reactivity of anti-viral memory T cells against donor human leukocyte antigens (HLA) may be a contributing factor. We identified cross-reactive HLA-A*02:01-restricted CMV-specific cytotoxic T lymphocytes (CTL) co-recognizing the NLVPMVATV (NLV) epitope and HLA-B27. NLV-specific CD8+ T cells were expanded for 13 days from 14 HLA-A*02:01/CMV seropositive healthy donors and 11 lung transplant recipients (LTR) then assessed for the production of IFN-γ and CD107a expression in response to 19 cell lines expressing either single HLA-A or -B class I molecules. In one healthy individual, we observed functional and proliferative cross-reactivity in response to B*27:05 alloantigen, representing approximately 5% of the NLV-specific CTL population. Similar patterns were also observed in one LTR receiving a B27 allograft, revealing that the cross-reactive NLV-specific CTL gradually increased (days 13–193 post-transplant) before a CMV reactivation event (day 270) and reduced to basal levels following viral clearance (day 909). Lung function remained stable with no acute rejection episodes being reported up to 3 years post-transplant. Individualized immunological monitoring of cross-reactive anti-viral T cells will provide further insights into their effects on the allograft and an opportunity to predict sub-clinical CMV reactivation events and immunopathological complications.
format Online
Article
Text
id pubmed-3566045
institution National Center for Biotechnology Information
language English
publishDate 2013
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-35660452013-02-12 Cross-Reactive Anti-Viral T Cells Increase Prior to an Episode of Viral Reactivation Post Human Lung Transplantation Nguyen, Thi H. O. Westall, Glen P. Bull, Tara E. Meehan, Aislin C. Mifsud, Nicole A. Kotsimbos, Tom C. PLoS One Research Article Human Cytomegalovirus (CMV) reactivation continues to influence lung transplant outcomes. Cross-reactivity of anti-viral memory T cells against donor human leukocyte antigens (HLA) may be a contributing factor. We identified cross-reactive HLA-A*02:01-restricted CMV-specific cytotoxic T lymphocytes (CTL) co-recognizing the NLVPMVATV (NLV) epitope and HLA-B27. NLV-specific CD8+ T cells were expanded for 13 days from 14 HLA-A*02:01/CMV seropositive healthy donors and 11 lung transplant recipients (LTR) then assessed for the production of IFN-γ and CD107a expression in response to 19 cell lines expressing either single HLA-A or -B class I molecules. In one healthy individual, we observed functional and proliferative cross-reactivity in response to B*27:05 alloantigen, representing approximately 5% of the NLV-specific CTL population. Similar patterns were also observed in one LTR receiving a B27 allograft, revealing that the cross-reactive NLV-specific CTL gradually increased (days 13–193 post-transplant) before a CMV reactivation event (day 270) and reduced to basal levels following viral clearance (day 909). Lung function remained stable with no acute rejection episodes being reported up to 3 years post-transplant. Individualized immunological monitoring of cross-reactive anti-viral T cells will provide further insights into their effects on the allograft and an opportunity to predict sub-clinical CMV reactivation events and immunopathological complications. Public Library of Science 2013-02-06 /pmc/articles/PMC3566045/ /pubmed/23405250 http://dx.doi.org/10.1371/journal.pone.0056042 Text en © 2013 Nguyen et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Nguyen, Thi H. O.
Westall, Glen P.
Bull, Tara E.
Meehan, Aislin C.
Mifsud, Nicole A.
Kotsimbos, Tom C.
Cross-Reactive Anti-Viral T Cells Increase Prior to an Episode of Viral Reactivation Post Human Lung Transplantation
title Cross-Reactive Anti-Viral T Cells Increase Prior to an Episode of Viral Reactivation Post Human Lung Transplantation
title_full Cross-Reactive Anti-Viral T Cells Increase Prior to an Episode of Viral Reactivation Post Human Lung Transplantation
title_fullStr Cross-Reactive Anti-Viral T Cells Increase Prior to an Episode of Viral Reactivation Post Human Lung Transplantation
title_full_unstemmed Cross-Reactive Anti-Viral T Cells Increase Prior to an Episode of Viral Reactivation Post Human Lung Transplantation
title_short Cross-Reactive Anti-Viral T Cells Increase Prior to an Episode of Viral Reactivation Post Human Lung Transplantation
title_sort cross-reactive anti-viral t cells increase prior to an episode of viral reactivation post human lung transplantation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3566045/
https://www.ncbi.nlm.nih.gov/pubmed/23405250
http://dx.doi.org/10.1371/journal.pone.0056042
work_keys_str_mv AT nguyenthiho crossreactiveantiviraltcellsincreasepriortoanepisodeofviralreactivationposthumanlungtransplantation
AT westallglenp crossreactiveantiviraltcellsincreasepriortoanepisodeofviralreactivationposthumanlungtransplantation
AT bulltarae crossreactiveantiviraltcellsincreasepriortoanepisodeofviralreactivationposthumanlungtransplantation
AT meehanaislinc crossreactiveantiviraltcellsincreasepriortoanepisodeofviralreactivationposthumanlungtransplantation
AT mifsudnicolea crossreactiveantiviraltcellsincreasepriortoanepisodeofviralreactivationposthumanlungtransplantation
AT kotsimbostomc crossreactiveantiviraltcellsincreasepriortoanepisodeofviralreactivationposthumanlungtransplantation