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T cell regeneration after immunological injury
Following periods of haematopoietic cell stress, such as after chemotherapy, radiotherapy, infection and transplantation, patient outcomes are linked to the degree of immune reconstitution, specifically of T cells. Delayed or defective recovery of the T cell pool has significant clinical consequence...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7583557/ https://www.ncbi.nlm.nih.gov/pubmed/33097917 http://dx.doi.org/10.1038/s41577-020-00457-z |
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author | Velardi, Enrico Tsai, Jennifer J. van den Brink, Marcel R. M. |
author_facet | Velardi, Enrico Tsai, Jennifer J. van den Brink, Marcel R. M. |
author_sort | Velardi, Enrico |
collection | PubMed |
description | Following periods of haematopoietic cell stress, such as after chemotherapy, radiotherapy, infection and transplantation, patient outcomes are linked to the degree of immune reconstitution, specifically of T cells. Delayed or defective recovery of the T cell pool has significant clinical consequences, including prolonged immunosuppression, poor vaccine responses and increased risks of infections and malignancies. Thus, strategies that restore thymic function and enhance T cell reconstitution can provide considerable benefit to individuals whose immune system has been decimated in various settings. In this Review, we focus on the causes and consequences of impaired adaptive immunity and discuss therapeutic strategies that can recover immune function, with a particular emphasis on approaches that can promote a diverse repertoire of T cells through de novo T cell formation. |
format | Online Article Text |
id | pubmed-7583557 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-75835572020-10-26 T cell regeneration after immunological injury Velardi, Enrico Tsai, Jennifer J. van den Brink, Marcel R. M. Nat Rev Immunol Review Article Following periods of haematopoietic cell stress, such as after chemotherapy, radiotherapy, infection and transplantation, patient outcomes are linked to the degree of immune reconstitution, specifically of T cells. Delayed or defective recovery of the T cell pool has significant clinical consequences, including prolonged immunosuppression, poor vaccine responses and increased risks of infections and malignancies. Thus, strategies that restore thymic function and enhance T cell reconstitution can provide considerable benefit to individuals whose immune system has been decimated in various settings. In this Review, we focus on the causes and consequences of impaired adaptive immunity and discuss therapeutic strategies that can recover immune function, with a particular emphasis on approaches that can promote a diverse repertoire of T cells through de novo T cell formation. Nature Publishing Group UK 2020-10-23 2021 /pmc/articles/PMC7583557/ /pubmed/33097917 http://dx.doi.org/10.1038/s41577-020-00457-z Text en © Springer Nature Limited 2020 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Review Article Velardi, Enrico Tsai, Jennifer J. van den Brink, Marcel R. M. T cell regeneration after immunological injury |
title | T cell regeneration after immunological injury |
title_full | T cell regeneration after immunological injury |
title_fullStr | T cell regeneration after immunological injury |
title_full_unstemmed | T cell regeneration after immunological injury |
title_short | T cell regeneration after immunological injury |
title_sort | t cell regeneration after immunological injury |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7583557/ https://www.ncbi.nlm.nih.gov/pubmed/33097917 http://dx.doi.org/10.1038/s41577-020-00457-z |
work_keys_str_mv | AT velardienrico tcellregenerationafterimmunologicalinjury AT tsaijenniferj tcellregenerationafterimmunologicalinjury AT vandenbrinkmarcelrm tcellregenerationafterimmunologicalinjury |