Schmitt-Verhulst A M, Garbarino C A, Shearer G M
J Immunol. 1977 Apr;118(4):1420-7.
Secondary cell-mediated lympholysis (CML) and mixed lymphocyte reactions (MLR) were generated in a tissue culture system against trinitrophenyl (TNP)-modified murine syngeneic spleen cells. H-2 homology between primary and secondary TNP-modified stimulating cells was required in order to restimulate in the secondary CML. Strong proliferative responses (MLR) were detected only in the secondary cultures, for which H-2 homology was also required between TNP-modified primary and secondary immunogens. Intra-H-2 mapping for the secondary MLR indicated that the relevant regions of homology were I, D, and K and/or I-A. Homology throughout the entire major histocompatibility complex or at K plus I-A gave stronger MLR than did cultures in which there was homology between the primary and secondary phases at I or D only.
在组织培养系统中,针对三硝基苯(TNP)修饰的同基因小鼠脾细胞产生了继发性细胞介导的淋巴细胞溶解(CML)和混合淋巴细胞反应(MLR)。为了在继发性CML中进行再刺激,原发性和继发性TNP修饰的刺激细胞之间需要H-2同源性。仅在继发性培养物中检测到强烈的增殖反应(MLR),对于继发性培养物,TNP修饰的原发性和继发性免疫原之间也需要H-2同源性。继发性MLR的H-2内部图谱表明,相关的同源区域是I、D和K以及/或者I-A。整个主要组织相容性复合体的同源性或者K加I-A处的同源性比仅在I或D处原发性和继发性阶段存在同源性的培养物产生更强的MLR。