Gallagher P F, Ashman R B, Blanden R V
Department of Microbiology, John Curtin School of Medical Research, Australian National University, Canberra.
Exp Clin Immunogenet. 1986;3(3):145-61.
As an approach to analyzing the factors that contribute to determining H-2 restriction specificities of cytotoxic T cells, thymectomized semiallogeneic radiation chimeras were given transplants of fetal thymus from parental strain or F1 hybrid donors. A pronounced preference for lysis of infected targets of the same H-2 haplotype as the thymus was observed, the bias ranging from an undetectable preference through to absolute restriction to the thymic H-2. Virus-immune Tc cells could also be restricted to H-2 antigenic determinants of haplotypes expressed only by donated stem cell progeny lymphomyeloid cells. T cells from chimeras that had received thymuses of both parental strains were less effective than normal syngeneic F1 hybrid T cells in lysing allogeneic cells and both infected and uninfected parental targets. Variation in H-2 restriction bias from one chimera to another was not reflected in modulations to the class I H-2 phenotypes of the chimeric spleen cells.
作为一种分析促成细胞毒性T细胞H-2限制特异性决定因素的方法,对胸腺切除的半同种异体辐射嵌合体移植来自亲本品系或F1杂交供体的胎儿胸腺。观察到对与胸腺具有相同H-2单倍型的感染靶标的裂解有明显偏好,这种偏向范围从不可检测的偏好到对胸腺H-2的绝对限制。病毒免疫的Tc细胞也可被限制于仅由捐赠的干细胞后代淋巴骨髓细胞表达的单倍型的H-2抗原决定簇。接受双亲胸腺的嵌合体的T细胞在裂解同种异体细胞以及感染和未感染的亲代靶标方面比正常同基因F1杂交T细胞效率更低。从一个嵌合体到另一个嵌合体的H-2限制偏向的变化并未反映在嵌合脾细胞I类H-2表型的调节中。