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BTLA as a biomarker and mediator of sepsis-induced immunosuppression

Recent research indicates that T-lymphocyte dysfunction may contribute to sepsis-associated morbidity and mortality. B and T lymphocyte attenuator (BTLA) is a co-inhibitory receptor expressed by T lymphocytes and B lymphocytes that is important in regulating lymphocyte activation during inflammation...

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Detalles Bibliográficos
Autores principales: Sherwood, Edward R, Hotchkiss, Richard S
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4059397/
https://www.ncbi.nlm.nih.gov/pubmed/24321139
http://dx.doi.org/10.1186/cc13143
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author Sherwood, Edward R
Hotchkiss, Richard S
author_facet Sherwood, Edward R
Hotchkiss, Richard S
author_sort Sherwood, Edward R
collection PubMed
description Recent research indicates that T-lymphocyte dysfunction may contribute to sepsis-associated morbidity and mortality. B and T lymphocyte attenuator (BTLA) is a co-inhibitory receptor expressed by T lymphocytes and B lymphocytes that is important in regulating lymphocyte activation during inflammation and infection. Shubin and colleagues report that higher mean BTLA expression in critically ill patients may have value in identifying patients with infection. Further studies provide evidence that BTLA activation contributes to T-lymphocyte apoptosis during sepsis. Although this study will require follow-up and further investigation, the results advance current knowledge regarding potential mechanisms underlying sepsis-induced immunosuppression and identify BTLA as a candidate biomarker and mediator of T-cell dysfunction during sepsis.
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spelling pubmed-40593972014-12-09 BTLA as a biomarker and mediator of sepsis-induced immunosuppression Sherwood, Edward R Hotchkiss, Richard S Crit Care Commentary Recent research indicates that T-lymphocyte dysfunction may contribute to sepsis-associated morbidity and mortality. B and T lymphocyte attenuator (BTLA) is a co-inhibitory receptor expressed by T lymphocytes and B lymphocytes that is important in regulating lymphocyte activation during inflammation and infection. Shubin and colleagues report that higher mean BTLA expression in critically ill patients may have value in identifying patients with infection. Further studies provide evidence that BTLA activation contributes to T-lymphocyte apoptosis during sepsis. Although this study will require follow-up and further investigation, the results advance current knowledge regarding potential mechanisms underlying sepsis-induced immunosuppression and identify BTLA as a candidate biomarker and mediator of T-cell dysfunction during sepsis. BioMed Central 2013 2013-12-09 /pmc/articles/PMC4059397/ /pubmed/24321139 http://dx.doi.org/10.1186/cc13143 Text en Copyright © 2013 BioMed Central Ltd.
spellingShingle Commentary
Sherwood, Edward R
Hotchkiss, Richard S
BTLA as a biomarker and mediator of sepsis-induced immunosuppression
title BTLA as a biomarker and mediator of sepsis-induced immunosuppression
title_full BTLA as a biomarker and mediator of sepsis-induced immunosuppression
title_fullStr BTLA as a biomarker and mediator of sepsis-induced immunosuppression
title_full_unstemmed BTLA as a biomarker and mediator of sepsis-induced immunosuppression
title_short BTLA as a biomarker and mediator of sepsis-induced immunosuppression
title_sort btla as a biomarker and mediator of sepsis-induced immunosuppression
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4059397/
https://www.ncbi.nlm.nih.gov/pubmed/24321139
http://dx.doi.org/10.1186/cc13143
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