Dynamic alterations of circulating lymphocytes during the trajectory of Hantaan virus-induced hemorrhagic fever with renal syndrome

Here, we revealed phase-specific immune patterns: CD8<sup>+</sup> T, CD8<sup>+</sup> Tems, and activated CD8<sup>+</sup> T, MAIT and NKT cells peaked during febrile/oliguric phases before declining in polyuria/recovery, while CD4<sup>+</sup> T and MAIT cells showed inverse fluctuation patterns. Higher frequencies of CD8<sup>+</sup> Tem, B, and CD56<sup>dim</sup> NK cells during the febrile phase correlated with severe disease, enabling early risk stratification. Lower CD4<sup>+</sup> Tcm levels in the oliguric phase marked progression to severe HFRS, indicating potential therapeutic strategies aimed at enhancing CD4<sup>+</sup> Tcm generation or inhibiting effector differentiation. Additionally, CD38 and CD161 expression predicted specific lymphocyte subset dynamics, offering novel biomarkers for immunomodulatory strategies. Our study thus provides the first comprehensive atlas of lymphocyte evolution in HTNV-induced HFRS, connecting immune dysregulation with clinical outcomes.

Authors

Institutions

Publication Details

Journal
Frontiers in Immunology
Published
2025-05-29
DOI
https://doi.org/10.3389/fimmu.2025.1567306
Primary Topic
Viral Infections and Vectors
Type
article
Field-Weighted Citation Impact
0.00

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Dynamic alterations of circulating lymphocytes during the trajectory of Hantaan virus-induced hemorrhagic fever with renal syndrome

Tianyan Chen, Yuan Cheng, Lei Shi, Shuangjuan Liu et al.
Frontiers in Immunology
Viral Infections and Vectors
article

Dynamic alterations of circulating lymphocytes during the trajectory of Hantaan virus-induced hemorrhagic fever with renal syndrome

Tianyan Chen, Yuan Cheng, Lei Shi, Shuangjuan Liu, Jinsong Hu, Xiaojiao Li, Yawen Wang, Juanjuan Gao, Lin Su, Ran Guo, Li’ao Zhang, Yu He
article en

Abstract

Here, we revealed phase-specific immune patterns: CD8<sup>+</sup> T, CD8<sup>+</sup> Tems, and activated CD8<sup>+</sup> T, MAIT and NKT cells peaked during febrile/oliguric phases before declining in polyuria/recovery, while CD4<sup>+</sup> T and MAIT cells showed inverse fluctuation patterns. Higher frequencies of CD8<sup>+</sup> Tem, B, and CD56<sup>dim</sup> NK cells during the febrile phase correlated with severe disease, enabling early risk stratification. Lower CD4<sup>+</sup> Tcm levels in the oliguric phase marked progression to severe HFRS, indicating potential therapeutic strategies aimed at enhancing CD4<sup>+</sup> Tcm generation or inhibiting effector differentiation. Additionally, CD38 and CD161 expression predicted specific lymphocyte subset dynamics, offering novel biomarkers for immunomodulatory strategies. Our study thus provides the first comprehensive atlas of lymphocyte evolution in HTNV-induced HFRS, connecting immune dysregulation with clinical outcomes.

Frontiers in ImmunologyVol. 16
First Affiliated Hospital of Xi'an Jiaotong University (CN), Weinan Central Hospital (CN), Xi'an Jiaotong University (CN)
Xi’an Jiaotong University
Openalex Percentile: Top 84%
Viral Infections and Vectors
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.