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Another tool against cytomegalovirus after allogeneic hematopoietic cell transplantation

Cytomegalovirus (CMV) viremia from reactivation of latent infection is a common complication after allogeneic hematopoietic cell transplantation (HCT). Untreated, CMV viremia can progress to affect other organs, resulting in organ dysfunction with high morbidity and mortality. In this issue of the J...

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Autores principales: Chen, George L., Shpall, Elizabeth J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Clinical Investigation 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10178833/
https://www.ncbi.nlm.nih.gov/pubmed/37183817
http://dx.doi.org/10.1172/JCI170282
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author Chen, George L.
Shpall, Elizabeth J.
author_facet Chen, George L.
Shpall, Elizabeth J.
author_sort Chen, George L.
collection PubMed
description Cytomegalovirus (CMV) viremia from reactivation of latent infection is a common complication after allogeneic hematopoietic cell transplantation (HCT). Untreated, CMV viremia can progress to affect other organs, resulting in organ dysfunction with high morbidity and mortality. In this issue of the JCI, Prockop and authors demonstrate that third-party donor T cells sensitized ex vivo to CMV pp65-derived overlapping pentadecapeptides are safe and effective for the treatment of CMV reactivation or CMV disease refractory to first-line pharmacotherapies occurring after HCT. They also provide insight into the biological differences between responders and nonresponders. This work confirms the utility of third-party CMV pp65 VSTs and suggests strategies for further improving the efficacy of this cell-therapy approach.
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spelling pubmed-101788332023-05-15 Another tool against cytomegalovirus after allogeneic hematopoietic cell transplantation Chen, George L. Shpall, Elizabeth J. J Clin Invest Commentary Cytomegalovirus (CMV) viremia from reactivation of latent infection is a common complication after allogeneic hematopoietic cell transplantation (HCT). Untreated, CMV viremia can progress to affect other organs, resulting in organ dysfunction with high morbidity and mortality. In this issue of the JCI, Prockop and authors demonstrate that third-party donor T cells sensitized ex vivo to CMV pp65-derived overlapping pentadecapeptides are safe and effective for the treatment of CMV reactivation or CMV disease refractory to first-line pharmacotherapies occurring after HCT. They also provide insight into the biological differences between responders and nonresponders. This work confirms the utility of third-party CMV pp65 VSTs and suggests strategies for further improving the efficacy of this cell-therapy approach. American Society for Clinical Investigation 2023-05-15 /pmc/articles/PMC10178833/ /pubmed/37183817 http://dx.doi.org/10.1172/JCI170282 Text en © 2023 Chen et al. https://creativecommons.org/licenses/by/4.0/This work is licensed under the Creative Commons Attribution 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Commentary
Chen, George L.
Shpall, Elizabeth J.
Another tool against cytomegalovirus after allogeneic hematopoietic cell transplantation
title Another tool against cytomegalovirus after allogeneic hematopoietic cell transplantation
title_full Another tool against cytomegalovirus after allogeneic hematopoietic cell transplantation
title_fullStr Another tool against cytomegalovirus after allogeneic hematopoietic cell transplantation
title_full_unstemmed Another tool against cytomegalovirus after allogeneic hematopoietic cell transplantation
title_short Another tool against cytomegalovirus after allogeneic hematopoietic cell transplantation
title_sort another tool against cytomegalovirus after allogeneic hematopoietic cell transplantation
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10178833/
https://www.ncbi.nlm.nih.gov/pubmed/37183817
http://dx.doi.org/10.1172/JCI170282
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