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利用CDR3谱型分析法检测T细胞群的克隆性扩增
ANALYSIS OF CLONAL PREDOMINANCE OF T CELL RECEPTORS BY CDR 3 SIZE SPECTRATYPING
【摘要】 介绍一种快速、简便检测T细胞群克隆性扩增的方法。T细胞抗原受体(TCR)α和β链与抗原/MHC复合物相互反应是由CDR1、CDR2和CDR3环完成的;其中CDR3环是由V-(D)-J片断所组成直接与抗原相结合,因此长度及序列在不同的T细胞克隆之间均有变化,而单一T细胞克隆则长度、序列是一致的。应用PCR技术分析TCRVβ家族中CDR3的长度谱型可检测样品中T细胞克隆特异性。为研究感染性疾病及自身免疫病末梢血及病灶组织T细胞克隆性扩增提供快速、经济、可行的方法。
【Abstract】 Structural models for the TCR α/β predict that CDR 1,CDR 2 and CDR 3 loops of both the α and β chains contribute to specific interactions with the Ag/MHC complex. The CDR 3 loops are constructed by joining events invo ving the V (D) J segments,and thus may vary in both sequence and length. We developed a polymerase chain reaction assay to assess the lenngth variation of the CDR 3 loop in TCR derived from Vβ segments families in peripheral blood T cells,T cell clone and brain samples. The result showed that spectrotype analysis is applicable to the studies of specific repertoire skewing such as may be associated with inflammatory and autoimune disorders.
- 【文献出处】 免疫学杂志 ,IMMUNOLOGICAL JOURNAL , 编辑部邮箱 ,1997年01期
- 【分类号】R392
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