Immune‐mediated disruption of the blood–brain barrier after intracerebral hemorrhage: Insights and potential therapeutic targets

Author:

Jia Peijun123,Peng Qinfeng2,Fan Xiaochong1,Zhang Yumeng2,Xu Hanxiao2,Li Jiaxin2,Sonita Houn2,Liu Simon4ORCID,Le Anh5,Hu Qiongqiong6,Zhao Ting7,Zhang Shijie3,Wang Junmin2,Zille Marietta8ORCID,Jiang Chao7,Chen Xuemei2ORCID,Wang Jian12ORCID

Affiliation:

1. Department of Pain Medicine The First Affiliated Hospital of Zhengzhou University Zhengzhou China

2. Department of Human Anatomy School of Basic Medical Sciences of Zhengzhou University Zhengzhou China

3. School of Life Sciences Zhengzhou University Zhengzhou China

4. David Geffen School of Medicine University of California Los Angeles Los Angeles California USA

5. George Washington School of Medicine and Health Sciences Washington DC USA

6. Department of Neurology Zhengzhou Central Hospital Affiliated to Zhengzhou University Zhengzhou Henan China

7. Department of Neurology People's Hospital of Zhengzhou University Zhengzhou China

8. Division of Pharmacology and Toxicology, Department of Pharmaceutical Sciences University of Vienna Vienna Austria

Abstract

AbstractAimsIntracerebral hemorrhage (ICH) is a condition that arises due to the rupture of cerebral blood vessels, leading to the flow of blood into the brain tissue. One of the pathological alterations that occurs during an acute ICH is an impairment of the blood–brain barrier (BBB), which leads to severe perihematomal edema and an immune response.DiscussionA complex interplay between the cells of the BBB, for example, pericytes, astrocytes, and brain endothelial cells, with resident and infiltrating immune cells, such as microglia, monocytes, neutrophils, T lymphocytes, and others accounts for both damaging and protective mechanisms at the BBB following ICH. However, the precise immunological influence of BBB disruption has yet to be richly ascertained, especially at various stages of ICH.ConclusionThis review summarizes the changes in different cell types and molecular components of the BBB associated with immune‐inflammatory responses during ICH. Furthermore, it highlights promising immunoregulatory therapies to protect the integrity of the BBB after ICH. By offering a comprehensive understanding of the mechanisms behind BBB damage linked to cellular and molecular immunoinflammatory responses after ICH, this article aimed to accelerate the identification of potential therapeutic targets and expedite further translational research.

Funder

National Natural Science Foundation of China

Publisher

Wiley

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