Ro52/TRIM21-从宿主防御到自身免疫。

IF 3.7 4区 医学 Q2 CELL BIOLOGY Cellular immunology Pub Date : 2023-10-15 DOI:10.1016/j.cellimm.2023.104776
Emilia Holwek , Aleksandra Opinc-Rosiak , Joanna Sarnik , Joanna Makowska
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引用次数: 0

摘要

Ro52(TRIM21)属于泛素连接酶家族。这种蛋白质在许多免疫过程中发挥着至关重要的作用,包括抗体依赖性细胞内中和、与补体系统的协同作用、抗病毒反应、死亡介导、氧化应激反应和蛋白质泛素化。TRIM21的异常表达可以破坏免疫耐受并导致产生针对TRIM21自身抗体。在各种自身免疫性疾病中检测到针对TRIM21的抗体,包括干燥综合征(SS)、系统性红斑狼疮(SLE)或肌炎。然而,抗TRIM21的存在并不局限于自身免疫性结缔组织疾病。它在恶性肿瘤、各种癌过程、传染病和特发性间质性肺炎患者中观察到。TRIM21自身抗体的发生也与临床特征有关,如间质性肺病的患病率以及结缔组织疾病中的心脏或血液学受累。这篇综述的目的是总结目前对TRIM21免疫功能的了解,并分析抗TRIM21抗体在病程中的临床意义。
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Ro52/TRIM21 – From host defense to autoimmunity

Ro52 (TRIM21) belongs to the ubiquitin ligase family. This protein plays a crucial role in many immunological processes, including antibody-dependent intracellular neutralization, synergy with the complement system, antiviral response, death mediation, oxidative stress response, and protein ubiquitination. Abnormal expression of TRIM21 can break immunological tolerance and lead to the production of autoantibodies against TRIM21. Antibodies against TRIM21 are detected in various autoimmune diseases, including Sjögren's syndrome (SS), systemic lupus erythematosus (SLE), or myositis. However, anti-TRIM21 presence is not limited to autoimmune connective tissue disorders. It was observed in patients with malignancies, various cancerous processes, infectious diseases, and idiopathic interstitial pneumonia. The occurrence of TRIM21 autoantibodies is also associated with clinical features, such as the prevalence of interstitial lung diseases and cardiac or haematological involvement in connective tissue disorders. The purpose of this review was to summarize current knowledge of the immunological functions of TRIM21 and analyze the clinical implications of anti-TRIM21 antibodies in the disease course.

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来源期刊
Cellular immunology
Cellular immunology 生物-免疫学
CiteScore
8.20
自引率
2.30%
发文量
102
审稿时长
30 days
期刊介绍: Cellular Immunology publishes original investigations concerned with the immunological activities of cells in experimental or clinical situations. The scope of the journal encompasses the broad area of in vitro and in vivo studies of cellular immune responses. Purely clinical descriptive studies are not considered. Research Areas include: • Antigen receptor sites • Autoimmunity • Delayed-type hypersensitivity or cellular immunity • Immunologic deficiency states and their reconstitution • Immunologic surveillance and tumor immunity • Immunomodulation • Immunotherapy • Lymphokines and cytokines • Nonantibody immunity • Parasite immunology • Resistance to intracellular microbial and viral infection • Thymus and lymphocyte immunobiology • Transplantation immunology • Tumor immunity.
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