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Early Alterations of Lymphocyte Subsets in Acute Respiratory Distress Syndrome Caused by Acinetobacter baumannii Pneumonia: A Prospective Observational Study

Background: To prospectively observe the early alterations of lymphocyte subsets in ARDS caused by Acinetobacter baumannii. Methods: ARDS patients admitted to our ICU between January 1, 2017 and May 30, 2020 were selected. We enrolled all the pulmonary ARDS caused by Acinetobacter baumannii pneumoni...

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Autores principales: Cheng, Wei, Zhang, Jiahui, Li, Dongkai, Bai, Guangxu, Han, Wen, Chen, Jianwei, Wang, Hao, Cui, Na
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8542783/
https://www.ncbi.nlm.nih.gov/pubmed/34708062
http://dx.doi.org/10.3389/fmed.2021.762724
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author Cheng, Wei
Zhang, Jiahui
Li, Dongkai
Bai, Guangxu
Han, Wen
Chen, Jianwei
Wang, Hao
Cui, Na
author_facet Cheng, Wei
Zhang, Jiahui
Li, Dongkai
Bai, Guangxu
Han, Wen
Chen, Jianwei
Wang, Hao
Cui, Na
author_sort Cheng, Wei
collection PubMed
description Background: To prospectively observe the early alterations of lymphocyte subsets in ARDS caused by Acinetobacter baumannii. Methods: ARDS patients admitted to our ICU between January 1, 2017 and May 30, 2020 were selected. We enrolled all the pulmonary ARDS caused by Acinetobacter baumannii pneumonia who required mechanical ventilation or vasopressors. All the available clinical data, follow up information and lymphocyte subsets were recorded. Results: Eighty-seven of all the 576 ARDS patients were enrolled. The 28-day mortality of the enrolled patients was 20.7% (18/87). The T lymphocyte count (452 vs. 729 cells/ul, P = 0.004), especially the CD8(+) T lymphocyte count (104 vs. 253 cells/ul, P = 0.002) was significantly lower in non-survivors, as were counts of the activated T cell subsets (CD8(+)CD28(+) and CD8(+)CD38(+)). The CD8(+) T cell count was an independent risk factor for 28-day mortality, and a cutoff value of 123 cells/ul was a good indicator to predict the prognosis of ARDS caused by Acinetobacter baumannii pneumonia, with sensitivity of 74.6% and specificity of 83.3% (AUC 0.812, P < 0.0001). Conclusions: Lower CD8(+) T cell count was associated with higher severity and early mortality in ARDS patients caused by Acinetobacter baumannii pneumonia, which could be valuable for outcome prediction.
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spelling pubmed-85427832021-10-26 Early Alterations of Lymphocyte Subsets in Acute Respiratory Distress Syndrome Caused by Acinetobacter baumannii Pneumonia: A Prospective Observational Study Cheng, Wei Zhang, Jiahui Li, Dongkai Bai, Guangxu Han, Wen Chen, Jianwei Wang, Hao Cui, Na Front Med (Lausanne) Medicine Background: To prospectively observe the early alterations of lymphocyte subsets in ARDS caused by Acinetobacter baumannii. Methods: ARDS patients admitted to our ICU between January 1, 2017 and May 30, 2020 were selected. We enrolled all the pulmonary ARDS caused by Acinetobacter baumannii pneumonia who required mechanical ventilation or vasopressors. All the available clinical data, follow up information and lymphocyte subsets were recorded. Results: Eighty-seven of all the 576 ARDS patients were enrolled. The 28-day mortality of the enrolled patients was 20.7% (18/87). The T lymphocyte count (452 vs. 729 cells/ul, P = 0.004), especially the CD8(+) T lymphocyte count (104 vs. 253 cells/ul, P = 0.002) was significantly lower in non-survivors, as were counts of the activated T cell subsets (CD8(+)CD28(+) and CD8(+)CD38(+)). The CD8(+) T cell count was an independent risk factor for 28-day mortality, and a cutoff value of 123 cells/ul was a good indicator to predict the prognosis of ARDS caused by Acinetobacter baumannii pneumonia, with sensitivity of 74.6% and specificity of 83.3% (AUC 0.812, P < 0.0001). Conclusions: Lower CD8(+) T cell count was associated with higher severity and early mortality in ARDS patients caused by Acinetobacter baumannii pneumonia, which could be valuable for outcome prediction. Frontiers Media S.A. 2021-10-11 /pmc/articles/PMC8542783/ /pubmed/34708062 http://dx.doi.org/10.3389/fmed.2021.762724 Text en Copyright © 2021 Cheng, Zhang, Li, Bai, Han, Chen, Wang and Cui. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Medicine
Cheng, Wei
Zhang, Jiahui
Li, Dongkai
Bai, Guangxu
Han, Wen
Chen, Jianwei
Wang, Hao
Cui, Na
Early Alterations of Lymphocyte Subsets in Acute Respiratory Distress Syndrome Caused by Acinetobacter baumannii Pneumonia: A Prospective Observational Study
title Early Alterations of Lymphocyte Subsets in Acute Respiratory Distress Syndrome Caused by Acinetobacter baumannii Pneumonia: A Prospective Observational Study
title_full Early Alterations of Lymphocyte Subsets in Acute Respiratory Distress Syndrome Caused by Acinetobacter baumannii Pneumonia: A Prospective Observational Study
title_fullStr Early Alterations of Lymphocyte Subsets in Acute Respiratory Distress Syndrome Caused by Acinetobacter baumannii Pneumonia: A Prospective Observational Study
title_full_unstemmed Early Alterations of Lymphocyte Subsets in Acute Respiratory Distress Syndrome Caused by Acinetobacter baumannii Pneumonia: A Prospective Observational Study
title_short Early Alterations of Lymphocyte Subsets in Acute Respiratory Distress Syndrome Caused by Acinetobacter baumannii Pneumonia: A Prospective Observational Study
title_sort early alterations of lymphocyte subsets in acute respiratory distress syndrome caused by acinetobacter baumannii pneumonia: a prospective observational study
topic Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8542783/
https://www.ncbi.nlm.nih.gov/pubmed/34708062
http://dx.doi.org/10.3389/fmed.2021.762724
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