Geczy A F, Coulits N
Immunology. 1983 Apr;48(4):755-62.
The genetic basis of guinea-pig leucocyte antigen (GPLA)-B.2-associated unresponsiveness in the guinea-pig mixed leucocyte culture (MLC) was investigated using fibroblasts as stimulating cells. Guinea-pig foetal fibroblasts bearing the B.2 specificity can stimulate allogeneic but not syngeneic lymph node lymphocytes, whereas B.2-bearing peritoneal exudate cells (PEC) induce specific unresponsiveness. The inhibition of the mixed leucocyte-fibroblast reaction is seen only when the alloantisera are directed against the stimulatory fibroblast rather than the responding lymph node lymphocytes. Furthermore, B.2-bearing fibroblasts, in contrast to B.2-bearing PEC, fail to elaborate MLC-suppressor factor. It appears therefore, that in guinea-pig fibroblasts there is an apparent dissociation between major histocompatibility complex (MHC; in the region of the B locus) genes and the gene(s) coding for B.2-associated MLC suppressor cells and factor(s).
利用成纤维细胞作为刺激细胞,研究了豚鼠白细胞抗原(GPLA)-B.2相关的豚鼠混合淋巴细胞培养(MLC)无反应性的遗传基础。携带B.2特异性的豚鼠胎儿成纤维细胞可刺激同种异体而非同基因淋巴结淋巴细胞,而携带B.2的腹腔渗出细胞(PEC)则诱导特异性无反应性。仅当同种抗血清针对刺激成纤维细胞而非反应性淋巴结淋巴细胞时,才会出现混合淋巴细胞-成纤维细胞反应的抑制。此外,与携带B.2的PEC不同,携带B.2的成纤维细胞不能产生MLC抑制因子。因此,在豚鼠成纤维细胞中,主要组织相容性复合体(MHC;在B位点区域)基因与编码B.2相关MLC抑制细胞和因子的基因之间似乎存在明显的分离。