抗cenp - b自身抗体的临床和分子特征

Rahul M. Prasad, A. Bellacosa, T. Yen
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引用次数: 4

摘要

着丝粒蛋白是装配着丝点的基础,着丝点是有丝分裂过程中染色体精确分离所必需的大分子复合物。抗着丝粒抗体(ACAs)是针对着丝粒蛋白(CENP-A, CENP-B, CENP-C)的多克隆自身抗体,主要是CENP-B,并且与风湿病(lcSSc/CREST综合征)高度相关。在没有风湿病症状的癌症患者中也发现了CENP-B自身抗体。肿瘤免疫治疗的兴起激发了人们对抗cenp - b自身抗体形成的方式和原因的研究。在这篇综述中,我们描述了抗cenp - b自身抗体、风湿病和癌症之间的临床相关性;CENP-B的分子特征;自体抗原性的可能解释;最后是诱导自身抗体形成的可能机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Clinical and Molecular Features of Anti-CENP-B Autoantibodies
Centromeric proteins are the foundation for assembling the kinetochore, a macromolecular complex that is essential for accurate chromosome segregation during mitosis. Anti-centromere antibodies (ACAs) are polyclonal autoantibodies targeting centromeric proteins (CENP-A, CENP-B, CENP-C), predominantly CENP-B, and are highly associated with rheumatologic disease (lcSSc/CREST syndrome). CENP-B autoantibodies have also been reported in cancer patients without symptoms of rheumatologic disease. The rise of oncoimmunotherapy stimulates inquiry into how and why anti-CENP-B autoantibodies are formed. In this review, we describe the clinical correlations between anti-CENP-B autoantibodies, rheumatologic disease, and cancer; the molecular features of CENP-B; possible explanations for autoantigenicity; and, finally, a possible mechanism for induction of autoantibody formation.
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