Juretić A, Nagy Z A, Klein J
Immunogenetics. 1981;14(1-2):73-83. doi: 10.1007/BF00344301.
Primary CML was generated in strain combinations 4R anti-2R, R107 anti-3R, 7R anti-9R, and GD anti-R101-combinations differing only in the chromosomal interval between the I-A subregion and the Ss locus. No CML could be obtained in any of the reciprocal combinations of these strains. This unidirectionality of the CML reaction correlates with the expression or nonexpression of the E molecules encoded by this interval: the reaction occurred in combinations in which the responder strain lacked and the stimulator strain expressed the E molecules in the cell membrane. The CML reaction was positive when tested on LPS-stimulated blast cells but weak on Con A-stimulated blasts and negative on Ia-negative tumor cells. The reaction could partially be inhibited by monoclonal antibodies to the Ia.m7 determinant presumably carried gy the E alpha chain; it was not inhibited by monoclonal antibodies specific for Ia determinants carried by the A molecule. Cytotoxic lymphocytes specific for a particular combination of E beta and E alpha chains reacted with all cells expressing the particular E beta chain, no matter what the origin of the E alpha chain associated with the E beta chain was. Attempts to generate cytotoxic lymphocytes specifically reactive with allotypic determinants on E alpha chains failed. In F1 hybrids expressing one type of E alpha chain and two types of E beta chain, the single E alpha chain was found to associate with both beta chains, producing two types of E molecule. We conclude from these experiments that the CML determinants detected in the strain combinations used are encoded by the same loci as those coding for the serologically detectable Ia determinants. The CML determinants are carried by the E beta chains; the E alpha chain does not contribute in any way to the specificity of determinant recognition by the cytotoxic lymphocytes. No evidence for allotypic variation of the E alpha chain as detected by the CML assay could be found in this study.
原发性慢性移植物抗宿主病(CML)产生于4R抗2R、R107抗3R、7R抗9R以及GD抗R101等品系组合中,这些组合仅在I-A亚区和Ss位点之间的染色体区间存在差异。在这些品系的任何反向组合中均未获得CML。CML反应的这种单向性与该区间编码的E分子的表达或不表达相关:反应发生在应答品系缺乏而刺激品系在细胞膜上表达E分子的组合中。当在脂多糖(LPS)刺激的母细胞上进行测试时,CML反应呈阳性,但在刀豆蛋白A(Con A)刺激的母细胞上反应较弱,而在Ia阴性肿瘤细胞上反应为阴性。该反应可被针对Ia.m7决定簇的单克隆抗体部分抑制,推测该决定簇由Eα链携带;它不受针对A分子携带的Ia决定簇的特异性单克隆抗体的抑制。针对特定Eβ链和Eα链组合的细胞毒性淋巴细胞与所有表达特定Eβ链的细胞发生反应,无论与Eβ链相关的Eα链的来源如何。试图产生与Eα链上的同种异型决定簇特异性反应的细胞毒性淋巴细胞的尝试失败了。在表达一种类型的Eα链和两种类型的Eβ链的F1杂种中,发现单一的Eα链与两种β链都相关联,产生两种类型的E分子。我们从这些实验得出结论,在所使用的品系组合中检测到的CML决定簇与编码血清学可检测的Ia决定簇的基因座相同。CML决定簇由Eβ链携带;Eα链对细胞毒性淋巴细胞识别决定簇的特异性没有任何贡献。在本研究中未发现通过CML检测法检测到的Eα链存在同种异型变异的证据。