CD19+ B cell depletion: a novel strategy to alleviate ischemic stroke damage

Temporary inhibition of B-cell activity via aCD19 antibody injection alleviated ischemic brain injury in a mouse model of stroke by suppressing systemic immune reactions. Changes in immune cells within the meninges may play a role, and further investigation is needed to understand the mechanisms involved. These findings suggest that cerebral and systemic immune responses contribute to the pathogenesis of ischemic stroke, and temporary B cell depletion may represent a potential therapeutic target for stroke therapy.

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Publication Details

Journal
Frontiers in Immunology
Published
2025-04-17
DOI
https://doi.org/10.3389/fimmu.2025.1528471
Primary Topic
Neuroinflammation and Neurodegeneration Mechanisms
Type
article
Field-Weighted Citation Impact
0.00

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article

CD19+ B cell depletion: a novel strategy to alleviate ischemic stroke damage

Min Gao, Lamei Cheng, Yizhong Yan, Jing Peng et al.
Frontiers in Immunology
Neuroinflammation and Neurodegeneration Mechanisms
article

CD19+ B cell depletion: a novel strategy to alleviate ischemic stroke damage

Min Gao, Lamei Cheng, Yizhong Yan, Jing Peng, Hongjing Zang, Yu Xu, Yu Zhou
article en

Abstract

Temporary inhibition of B-cell activity via aCD19 antibody injection alleviated ischemic brain injury in a mouse model of stroke by suppressing systemic immune reactions. Changes in immune cells within the meninges may play a role, and further investigation is needed to understand the mechanisms involved. These findings suggest that cerebral and systemic immune responses contribute to the pathogenesis of ischemic stroke, and temporary B cell depletion may represent a potential therapeutic target for stroke therapy.

Frontiers in ImmunologyVol. 16
Central South University (CN), National Engineering Research Center of Human Stem Cells (CN), Second Xiangya Hospital of Central South University (CN)
National Natural Science Foundation of China, Natural Science Foundation of Hunan Province
Openalex Percentile: Top 89%
Neuroinflammation and Neurodegeneration Mechanisms
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