Maryanski J L, Jongeneel C V, Bucher P, Casanova J L, Walker P R
Ludwig Institute for Cancer Research, Swiss Institute for Experimental Cancer Research, Epalinges, Switzerland.
Immunity. 1996 Jan;4(1):47-55. doi: 10.1016/s1074-7613(00)80297-6.
Taking advantage of a potent MHC class I-restricted response that allows the identification of antigen-selected CD8 T cells directly ex vivo, we characterized the antigen-specific T cell repertoires that develop in individual mice by single-cell PCR analysis. Each of the immune mice displayed distinct yet structurally similar TCR repertoires. The overall repertoire size was estimated to be in the range of 15-20 for most mice. No major differences were observed between primary and secondary responses. Moreover, for a hyperimmunized mouse the antigen-specific TCR repertoire expressed 8 months after the initial immunization was very similar to that found at the peak of the primary response. Our results demonstrate that a high magnitude immune response may be composed of very few clones, and that at least in the system analyzed, the memory response largely reflects the repertoire selected by the peak of the primary response.
利用一种强大的主要组织相容性复合体I类限制性反应,该反应能够直接在体外鉴定抗原选择的CD8 T细胞,我们通过单细胞PCR分析对单个小鼠体内发育的抗原特异性T细胞库进行了表征。每只免疫小鼠都表现出独特但结构相似的TCR库。大多数小鼠的总体库大小估计在15 - 20个范围内。在初次和二次反应之间未观察到主要差异。此外,对于一只超免疫小鼠,初次免疫8个月后表达的抗原特异性TCR库与初次反应高峰期发现的库非常相似。我们的结果表明,高强度免疫反应可能由极少数克隆组成,并且至少在所分析的系统中,记忆反应在很大程度上反映了初次反应高峰期选择的库。