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T‐lymphocyte subtyping: an early warning and a potential prognostic indicator of active cytomegalovirus infection in patients with sepsis

Cytomegalovirus (CMV) infection is very common in patients suffering from sepsis and may cause poor prognosis. To explore the relationship between immune status of patients with sepsis and CMV infection, we assessed T lymphocyte subtyping and other commonly used clinical parameters in patients with...

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Autores principales: Bai, Guangxu, Cui, Na, Wang, Hao, Cheng, Wei, Han, Wen, Chen, Jianwei, Guo, Ye, Wang, Fei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9828035/
https://www.ncbi.nlm.nih.gov/pubmed/36106958
http://dx.doi.org/10.1111/imcb.12586
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author Bai, Guangxu
Cui, Na
Wang, Hao
Cheng, Wei
Han, Wen
Chen, Jianwei
Guo, Ye
Wang, Fei
author_facet Bai, Guangxu
Cui, Na
Wang, Hao
Cheng, Wei
Han, Wen
Chen, Jianwei
Guo, Ye
Wang, Fei
author_sort Bai, Guangxu
collection PubMed
description Cytomegalovirus (CMV) infection is very common in patients suffering from sepsis and may cause poor prognosis. To explore the relationship between immune status of patients with sepsis and CMV infection, we assessed T lymphocyte subtyping and other commonly used clinical parameters in patients with sepsis upon admission to the intensive care unit (ICU) and evaluated their potential impact on diagnosis and outcomes of active CMV infection. In our study, 82 of 599 patients with sepsis were diagnosed with active CMV infection. The 28‐day mortality was higher in active CMV–infected than nonactive CMV–infected patients (20.7% versus 9.9%); 51of 82 active CMV–infected patients with sepsis were assessed to have CMV‐DNA–negative conversion, while 31 were persistently positive for CMV DNA. Higher CD8(+)CD28(+) T‐cell counts at presentation were associated with CMV‐DNA–negative conversion and lower 28‐day mortality. The CMV‐DNA–negative conversion and 28‐day mortality of active CMV–infected patients with sepsis could be predicted using cutoff values of 151 (74.5% sensitivity and 87.1% specificity) and 64.5 (52.9% sensitivity and 92.3% specificity) CD8(+)CD28(+) T cells mL(−1) at ICU admission, respectively. Higher CD8(+)CD28(+) T‐cell count was significantly associated with active CMV infection, higher CMV‐DNA–negative conversion and lower 28‐day mortality, which may be a potential marker for early warning of active CMV infection and outcome prediction.
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spelling pubmed-98280352023-01-10 T‐lymphocyte subtyping: an early warning and a potential prognostic indicator of active cytomegalovirus infection in patients with sepsis Bai, Guangxu Cui, Na Wang, Hao Cheng, Wei Han, Wen Chen, Jianwei Guo, Ye Wang, Fei Immunol Cell Biol Original Articles Cytomegalovirus (CMV) infection is very common in patients suffering from sepsis and may cause poor prognosis. To explore the relationship between immune status of patients with sepsis and CMV infection, we assessed T lymphocyte subtyping and other commonly used clinical parameters in patients with sepsis upon admission to the intensive care unit (ICU) and evaluated their potential impact on diagnosis and outcomes of active CMV infection. In our study, 82 of 599 patients with sepsis were diagnosed with active CMV infection. The 28‐day mortality was higher in active CMV–infected than nonactive CMV–infected patients (20.7% versus 9.9%); 51of 82 active CMV–infected patients with sepsis were assessed to have CMV‐DNA–negative conversion, while 31 were persistently positive for CMV DNA. Higher CD8(+)CD28(+) T‐cell counts at presentation were associated with CMV‐DNA–negative conversion and lower 28‐day mortality. The CMV‐DNA–negative conversion and 28‐day mortality of active CMV–infected patients with sepsis could be predicted using cutoff values of 151 (74.5% sensitivity and 87.1% specificity) and 64.5 (52.9% sensitivity and 92.3% specificity) CD8(+)CD28(+) T cells mL(−1) at ICU admission, respectively. Higher CD8(+)CD28(+) T‐cell count was significantly associated with active CMV infection, higher CMV‐DNA–negative conversion and lower 28‐day mortality, which may be a potential marker for early warning of active CMV infection and outcome prediction. John Wiley and Sons Inc. 2022-10-12 2022 /pmc/articles/PMC9828035/ /pubmed/36106958 http://dx.doi.org/10.1111/imcb.12586 Text en © 2022 The Authors. Immunology & Cell Biology published by John Wiley & Sons Australia, Ltd on behalf of Australian and New Zealand Society for Immunology, Inc. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Bai, Guangxu
Cui, Na
Wang, Hao
Cheng, Wei
Han, Wen
Chen, Jianwei
Guo, Ye
Wang, Fei
T‐lymphocyte subtyping: an early warning and a potential prognostic indicator of active cytomegalovirus infection in patients with sepsis
title T‐lymphocyte subtyping: an early warning and a potential prognostic indicator of active cytomegalovirus infection in patients with sepsis
title_full T‐lymphocyte subtyping: an early warning and a potential prognostic indicator of active cytomegalovirus infection in patients with sepsis
title_fullStr T‐lymphocyte subtyping: an early warning and a potential prognostic indicator of active cytomegalovirus infection in patients with sepsis
title_full_unstemmed T‐lymphocyte subtyping: an early warning and a potential prognostic indicator of active cytomegalovirus infection in patients with sepsis
title_short T‐lymphocyte subtyping: an early warning and a potential prognostic indicator of active cytomegalovirus infection in patients with sepsis
title_sort t‐lymphocyte subtyping: an early warning and a potential prognostic indicator of active cytomegalovirus infection in patients with sepsis
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9828035/
https://www.ncbi.nlm.nih.gov/pubmed/36106958
http://dx.doi.org/10.1111/imcb.12586
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