Kristensen T, Grunnet N, Jorgensen F, Lamm L U, Kissmeyer-Nielsen F
Tissue Antigens. 1976 Nov;8(5):299-316. doi: 10.1111/j.1399-0039.1976.tb00582.x.
From approximately 3,000 CML combinations, originally established in order to evaluate the qualitative and quantitative influence of the serologically defined HLA-A, B, and C antigens on cellular, complement independent cytolysis, 12 combinations were selected yielding reproducible positive cytolysis on allogenic target cells, although no HLA-antigenic sharing could be demonstrated between stimulator and target lymphocytes. These 12 CytoToxic Lymphocytes (CTL's) have been tested in parallell as "CML typing combinations" against lymphocytes from a random population sample of 100 unrelated Danes. Based on a pairwise analysis 11 of these CTL's could be classified into two groups of significantly correlated CTL's. These two groups do not define monospecific traits of allelic genetic origin as judged by a mutually positive correlation and a poor fit to Hardy-Weinberg equilibrium. The traits defined by these groups may be either partially identical or governed by closely linked loci. The same groups were identified and the same conclusions reached after exclusion of those individuals in the population sample where HLA-A, B, C, or D antigens may be targets for destruction. Thus, this study gives direct evidence that known HLA antigens are not sole target determinants in CML or that cytotoxic lymphocytes recognize HLA molecules in a different way than lymphocytotoxic antibodies. The studies underline the immunogenetic complexity of CML although this reaction is most probably governed by genes in the HLA region. It is suggested that cytotoxic lymphocytes may recognize "backbone structures" of the HLA molecules.
最初建立了大约3000种慢性粒细胞白血病(CML)组合,目的是评估血清学定义的HLA - A、B和C抗原对细胞性、补体非依赖性细胞溶解的定性和定量影响。从中选择了12种组合,这些组合在同种异体靶细胞上产生了可重复的阳性细胞溶解,尽管在刺激细胞和靶淋巴细胞之间未证明有HLA抗原共享。这12种细胞毒性淋巴细胞(CTL)已作为“CML分型组合”与来自100名不相关丹麦人的随机人群样本的淋巴细胞进行了平行测试。基于成对分析,其中11种CTL可分为两组显著相关的CTL。根据相互正相关和与哈迪 - 温伯格平衡的拟合不佳判断,这两组并未定义等位基因遗传起源的单特异性特征。这些组所定义的特征可能部分相同或由紧密连锁的基因座控制。在排除人群样本中HLA - A、B、C或D抗原可能成为破坏靶点的个体后,鉴定出了相同的组并得出了相同的结论。因此,本研究提供了直接证据,表明已知的HLA抗原不是CML中的唯一靶标决定因素,或者细胞毒性淋巴细胞识别HLA分子的方式与淋巴细胞毒性抗体不同。这些研究强调了CML的免疫遗传复杂性,尽管这种反应很可能受HLA区域中的基因控制。有人提出细胞毒性淋巴细胞可能识别HLA分子的“主干结构”。