CD4 T cell loss and Th2 and Th17 bias are associated with the severity of severe fever with thrombocytopenia syndrome (SFTS)

Copyright © 2018. Published by Elsevier Inc.

Bibliographische Detailangaben
Veröffentlicht in:Clinical immunology (Orlando, Fla.). - 1999. - 195(2018) vom: 01. Okt., Seite 8-17
1. Verfasser: Li, Meng-Meng (VerfasserIn)
Weitere Verfasser: Zhang, Wen-Jing, Weng, Xiu-Fang, Li, Ming-Yue, Liu, Jia, Xiong, Yan, Xiong, Shu-E, Zou, Cong-Cong, Wang, Hua, Lu, Meng-Ji, Yang, Dong-Liang, Peng, Cheng, Zheng, Xin
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2018
Zugriff auf das übergeordnete Werk:Clinical immunology (Orlando, Fla.)
Schlagworte:Journal Article Research Support, Non-U.S. Gov't Disease severity Effector TH cell subsets Regulatory T cells Severe fever with thrombocytopenia syndrome T lymphocytes CD4 Antigens
Beschreibung
Zusammenfassung:Copyright © 2018. Published by Elsevier Inc.
Severe fever with thrombocytopenia syndrome (SFTS) is a newly emerging infectious disease caused by a novel bunyavirus with high mortality. Immune suppression is thought to be crucial in disease progression. However, data on immune responses during SFTS are scarce. This study aimed to evaluate the changes in CD4 T-cell subsets throughout the entirety of infection and analyse their relationships with disease severity in SFTS patients. In parallel with CD4 T-cell depletion, decreased Th1, Th2 and Treg numbers, but comparable Th17-cell numbers, were observed in deceased patients compared with those in surviving patients. Additionally, increased Th2 and Th17-cell percentages in the residual CD4 T-cell population led to aberrant Th2/Th1 and Th17/Treg ratios, which were positively correlated with disease severity. Collectively, our data indicated that CD4 T-cell deficiency, Th2 and Th17 bias were closely correlated with the severity of SFTS, indicating therapeutic potential of early immune interventions to ameliorate disease severity
Beschreibung:Date Completed 27.08.2019
Date Revised 04.12.2021
published: Print-Electronic
Citation Status MEDLINE
ISSN:1521-7035
DOI:10.1016/j.clim.2018.07.009