Plata F
J Exp Med. 1982 Apr 1;155(4):1050-62. doi: 10.1084/jem.155.4.1050.
The specificities of cloned cytolytic T lymphocytes (CTL) were studied for the analysis of CTL populations generated against murine leukemia viruses (MuLV) in H-2 congenic BALB/c (H-2d) and BALB.B (H-2b) mice. In particular, CTL generated in response to tumors induced by Gross MuLV and Friend MuLV were studied; these tumors expressed virus-induced antigens that do not cross-react and that can be distinguished from each other. The systematic study of 92 CTL clones clearly indicated that MuLV-immune CTL were highly heterogeneous with respect to both the intensities of target cell lysis that they mediated and to their specificity of recognition of MuLV-induced tumor target cells. Various categories of CTL clones were identified, ranging from CTL clones tht were tightly H-2 restricted and specific for the immunizing tumor to CTL clones that displayed no discernible patterns of specificity and that attacked a large number of different target cells. In addition, the surface markers of these cloned CTL were defined, and the best conditions for their prolonged maintenance in culture were determined. The present data indicate that future efforts in the definition of target antigens recognized by tumor-specific CTL should be performed with monoclonal lymphocytes.
为分析针对H-2同基因BALB/c(H-2d)和BALB.B(H-2b)小鼠体内鼠白血病病毒(MuLV)产生的细胞毒性T淋巴细胞(CTL)群体,对克隆CTL的特异性进行了研究。特别对因格罗斯MuLV和弗瑞德MuLV诱导的肿瘤产生的CTL进行了研究;这些肿瘤表达不发生交叉反应且可相互区分的病毒诱导抗原。对92个CTL克隆的系统研究清楚表明,MuLV免疫CTL在介导的靶细胞裂解强度及其对MuLV诱导的肿瘤靶细胞的识别特异性方面高度异质性。鉴定出了各类CTL克隆,从严格受H-2限制且对免疫肿瘤特异的CTL克隆到无明显特异性模式且攻击大量不同靶细胞的CTL克隆。此外,还确定了这些克隆CTL的表面标志物以及在培养中延长其维持时间的最佳条件。目前的数据表明,未来在确定肿瘤特异性CTL识别的靶抗原方面的工作应以单克隆淋巴细胞进行。