B细胞受体(BCR)抗原特异性研究进展综述

Qingqun Li, Zhuoxuan Yang, Bin Shi
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引用次数: 0

摘要

B细胞受体(BCR)是参与B细胞特异性识别和抗原结合产生适应性体液免疫反应的关键分子。B细胞分化过程中的基因重排和高频突变是BCR分化的主要机制。BCR的巨大多样性和独特的分子结构决定了抗原识别的多样性和特异性,形成了具有广泛抗原特异性集合的复杂B细胞库。因此,BCR抗原特异性信息对于了解不同疾病的适应性免疫特性至关重要。随着B细胞相关研究技术的发展,如单细胞分选技术、高通量测序(HTS)、通过测序(LIBRA-seq)将B细胞受体与抗原特异性联系起来,我们将BCR库与抗原特异性联系起来的能力得到了增强。它可以帮助研究人员更好地了解体液免疫反应,确定疾病发病机制,监测疾病进展,设计疫苗,开发治疗性抗体和药物。本文综述了近年来在感染、疫苗接种、自身免疫性疾病和癌症中抗原特异性BCR的研究进展。通过分析SLE的自身抗体序列,由于这种特性,自身抗原的鉴定成为可能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[A review of progress in B cell receptor (BCR) antigen specificity].

B cell receptor (BCR) is a key molecule involved in B cell specific recognition and the binding of antigens to produce adaptive humoral immune response. Gene rearrangement and high frequency mutation during B cell differentiation are the main mechanisms of BCR diversification. The enormous diversity and unique molecular structure of BCR determine the diversity and specificity of antigen recognition, shaping complex B cell repertoire with extensive collections of antigen specificities. Therefore, BCR antigen-specific information is vital to understanding the adaptive immune characteristics of different diseases. Our ability to connect BCR repertoire and antigen specificity has been enhanced with the development of B cell related research technologies, such as single cell sorting techniques, high-throughput sequencing (HTS), linking B cell receptor to antigen specificity through sequencing (LIBRA-seq). It could help researchers to better understand humoral immune responses, identify disease pathogenesis, monitor disease progression, design vaccines, and develop therapeutic antibodies and drugs. We summarizes recent studies on antigen-specific BCR of infections, vaccinations, autoimmune diseases and cancer. By analyzing autoantibody sequences of SLE as a case, the identification of autoantigens has become potentially possible due to this characterization.

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