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各种皮肤病和自身免疫性疾病中的免疫组库

Immune Repertoires in Various Dermatologic and Autoimmune Diseases.

作者信息

Terhaar Hanna, Jiminez Victoria, Grant Emily, Collins Camden, Khass Mohamed, Yusuf Nabiha

机构信息

Heersink School of Medicine, University of Alabama at Birmingham, Birmingham, AL 35294, USA.

Department of Endodontics, University of Alabama at Birmingham, Birmingham, AL 35294, USA.

出版信息

Genes (Basel). 2024 Dec 11;15(12):1591. doi: 10.3390/genes15121591.

Abstract

The immune repertoire (IR) is a term that defines the combined unique genetic rearrangements of antigen receptors expressed by B and T lymphocytes. The IR determines the ability of the immune system to identify and respond to foreign antigens while preserving tolerance to host antigens. When immune tolerance is disrupted, development of autoimmune diseases can occur due to the attack of self-antigens. Recent technical advances in immune profiling allowed identification of common patterns and shared antigen-binding sequences unique to diverse array of diseases. However, there is no current literature to date evaluates IR findings in autoimmune and skin inflammatory conditions. In this review, we provide an overview of the past and current research findings of IR in various autoimmune and dermatologic conditions. Enriching our understanding of IRs in these conditions is critical for understanding the pathophysiology behind autoimmune skin disease onset and progression. Furthermore, understanding B-cell and T-cell IR will help devise therapeutic treatments in the hopes of restoring immune tolerance and preventing disease onset and progression.

摘要

免疫组库(IR)是一个定义B淋巴细胞和T淋巴细胞表达的抗原受体独特基因重排组合的术语。免疫组库决定了免疫系统识别和应对外来抗原的能力,同时维持对自身抗原的耐受性。当免疫耐受被破坏时,由于自身抗原的攻击,自身免疫性疾病可能会发生。免疫谱分析技术的最新进展使得能够识别各种疾病所共有的模式和独特的抗原结合序列。然而,目前尚无文献评估自身免疫性和皮肤炎症性疾病中的免疫组库研究结果。在本综述中,我们概述了免疫组库在各种自身免疫性和皮肤病学疾病中的既往和当前研究结果。深入了解这些疾病中的免疫组库对于理解自身免疫性皮肤病发病和进展背后的病理生理学至关重要。此外,了解B细胞和T细胞免疫组库将有助于设计治疗方法,以期恢复免疫耐受并预防疾病的发生和进展。

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本文引用的文献

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B cell receptor repertoire abnormalities in autoimmune disease.自身免疫性疾病中的 B 细胞受体库异常。
Front Immunol. 2024 Jan 31;15:1326823. doi: 10.3389/fimmu.2024.1326823. eCollection 2024.

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