Shinohara N, Bluestone J A, Sachs D H
J Exp Med. 1986 Apr 1;163(4):972-80. doi: 10.1084/jem.163.4.972.
Cloned CTLs QM3 and QM7 isolated from a bulk CTL line B10.QBR anti-B10.MBR recognized a combination of the H-2Kb molecule and an I-Ak subregion gene product. Such a combinatorial specificity was revealed by complementation of the target antigen in F1 animals between two negative parental strains carrying H-2Kb and I-Ak, respectively. We confirmed the involvement of the H-2Kb molecule by blocking killing with anti-Kb mAb and failure of certain mutant H-2Kb genes to complement with I-Ak to generate the determinant in F1 animals. Although the nature of the I-Ak subregion gene product is not definitive, there was a correlation between the expression of Ia antigens on the cell surface and susceptibility of the cells to lysis by these CTLs, suggesting that it is the classical I-Ak class II antigen.
从大量细胞毒性T淋巴细胞(CTL)系B10.QBR抗B10.MBR中分离出的克隆CTL QM3和QM7识别H-2Kb分子和I-Ak亚区基因产物的组合。这种组合特异性通过分别携带H-2Kb和I-Ak的两个阴性亲本品系之间F1动物中靶抗原的互补得以揭示。我们通过用抗Kb单克隆抗体阻断杀伤以及某些突变的H-2Kb基因无法与I-Ak互补以在F1动物中产生决定簇,证实了H-2Kb分子的参与。尽管I-Ak亚区基因产物的性质尚不明确,但细胞表面Ia抗原的表达与这些CTL对细胞裂解的敏感性之间存在相关性,这表明它是经典的I-Ak II类抗原。