Yurovsky V V
University of Maryland School of Medicine, Baltimore 21201, USA.
Crit Rev Immunol. 1995;15(2):155-65. doi: 10.1615/critrevimmunol.v15.i2.30.
Certain T cell subsets are increased in systemic sclerosis patients, particularly V delta 1+ gamma delta T cells in the blood and lungs and CD8+ alpha beta T cells in the lungs. The repertoires of T cell antigen receptor (TCR) V delta 1, V alpha, and V beta gene families were examined by two methods of analysis. First, the relative abundance of V alpha and V beta gene transcripts was determined in the blood and bronchoalveolar fluid of the patients. Second, the diversity of the junctional regions in TCR V delta 1 transcripts and in different V alpha and V beta gene families was analyzed. Limited V delta 1-C delta junctional region lengths were observed in the patients compared with controls. This was confirmed by sequence analysis of V delta 1-C delta junctional regions after subcloning amplified products in a bacterial vector. Evidence for selection of the V delta 1+ T cells in the tissues of patients came from the findings that the same V delta 1-C delta junctional sequences persisted in an individual patient over time and that identical junctional sequences were isolated from multiple sites. A restricted diversity of the junctional region lengths was also detected in a number of V alpha and V beta gene families, particularly within bronchoalveolar CD8+ T cell subset. These data suggest that the oligoclonal expansion of the corresponding alpha beta and gamma delta T cells is antigen-driven and may be important in the pathogenesis of systemic sclerosis.
系统性硬化症患者的某些T细胞亚群会增加,尤其是血液和肺部中的Vδ1 + γδT细胞以及肺部中的CD8 + αβT细胞。通过两种分析方法检测了T细胞抗原受体(TCR)Vδ1、Vα和Vβ基因家族的谱系。首先,测定患者血液和支气管肺泡灌洗液中Vα和Vβ基因转录本的相对丰度。其次,分析TCR Vδ1转录本以及不同Vα和Vβ基因家族中连接区的多样性。与对照组相比,在患者中观察到Vδ1-Cδ连接区长度有限。在细菌载体中对扩增产物进行亚克隆后,通过Vδ1-Cδ连接区的序列分析证实了这一点。患者组织中Vδ1 + T细胞选择的证据来自以下发现:同一患者体内相同的Vδ1-Cδ连接序列随时间持续存在,并且从多个部位分离出相同的连接序列。在许多Vα和Vβ基因家族中也检测到连接区长度的有限多样性,特别是在支气管肺泡CD8 + T细胞亚群中。这些数据表明,相应的αβ和γδT细胞的寡克隆扩增是由抗原驱动的,可能在系统性硬化症的发病机制中起重要作用。