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Clinical Characteristics of Peripheral Lymphocyte Subtypes in Chronic Active Epstein-Barr Virus Infection.

Authors :
Wei, Ang
Ou, Wenxin
Zhao, Yunze
Ma, Honghao
Zhang, Liping
Lian, Hongyun
Zhao, Xiaoxi
Zhang, Qing
Wang, Dong
Li, Zhigang
Wang, Tianyou
Zhang, Rui
Source :
Journal of Infectious Diseases. 7/15/2024, Vol. 230 Issue 1, p95-102. 8p.
Publication Year :
2024

Abstract

Background We aimed to analyze the clinical characteristics of peripheral Epstein-Barr virus (EBV)-infected lymphocyte subtypes in children with chronic active EBV infection (CAEBV). Methods The levels of peripheral EBV infection of CD4+ T cells, CD8+ T cells, and CD56+ natural killer (NK) cells were determined by flow cytometry and quantitative polymerase chain reaction (qPCR) in patients with CAEBV from July 2017 to July 2022. Results In total, 112 children with CAEBV were evaluated. Of these, CD4+ type, CD8+ type, and CD56+ type were defined in 44, 21, and 47 patients, respectively. Patients with CD8+ T-cell type had a significantly higher frequency of rash, while hepatomegaly was more common in patients with CD4+ T-cell type. Generally, patients with CD8+ T-cell type had the lowest overall survival rate (P =.017). Patients treated with chemotherapy and hematopoietic stem cell transplantation (HSCT) had a better prognosis (P =.001). In multivariate analysis, rash, hemophagocytic lymphohistiocytosis, CD8+ T-cell type, and no decrease of plasma EBV-DNA after treatment were independent indicators of poor prognosis (P =.002,.024,.022, and.012, respectively). Conclusions In children with CAEBV, rash was more frequent in patients with CD8+ T-cell type, whereas patients with CD4+ T-cell type were more likely to develop hepatomegaly. Patients with CD8+ T-cell type had a poor prognosis despite receiving chemotherapy or further HSCT. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00221899
Volume :
230
Issue :
1
Database :
Academic Search Index
Journal :
Journal of Infectious Diseases
Publication Type :
Academic Journal
Accession number :
178738641
Full Text :
https://doi.org/10.1093/infdis/jiad435