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Immune Response in Neurological Pathology: Emerging Role of Central and Peripheral Immune Crosstalk

期刊

FRONTIERS IN IMMUNOLOGY
卷 12, 期 -, 页码 -

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fimmu.2021.676621

关键词

inflammation; neuroinflammation; neurological disorders; neurodegenerative diseases; immune crosstalk; stroke; Alzheimer's disease; ALS

资金

  1. National Science and Technology Center for Emergent Behaviors of Integrated Cellular Systems [0939511]

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Neuroinflammation plays a crucial role in neurological disorders, with recent recognition of the importance of interactions between central and peripheral immune cells. Traditional approaches often separate these systems, but there is significant crosstalk between central and peripheral immune cells in the context of neurological disorders. Targeting these interactions may offer a potential improved therapeutic strategy for addressing failures in clinical translation.
Neuroinflammation is a key component of neurological disorders and is an important therapeutic target; however, immunotherapies have been largely unsuccessful. In cases where these therapies have succeeded, particularly multiple sclerosis, they have primarily focused on one aspect of the disease and leave room for improvement. More recently, the impact of the peripheral immune system is being recognized, since it has become evident that the central nervous system is not immune-privileged, as once thought. In this review, we highlight key interactions between central and peripheral immune cells in neurological disorders. While traditional approaches have examined these systems separately, the immune responses and processes in neurological disorders consist of substantial crosstalk between cells of the central and peripheral immune systems. Here, we provide an overview of major immune effector cells and the role of the blood-brain barrier in regard to neurological disorders and provide examples of this crosstalk in various disorders, including stroke and traumatic brain injury, multiple sclerosis, neurodegenerative diseases, and brain cancer. Finally, we propose targeting central-peripheral immune interactions as a potential improved therapeutic strategy to overcome failures in clinical translation.

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