Geginat G, Günther E
Division of Immunogenetics, University of Göttingen, Germany.
Transplantation. 1993 Aug;56(2):448-52. doi: 10.1097/00007890-199308000-00038.
The immune response against the male-specific H-Y antigen has been studied in RT1 congenic rat strains by assaying the cytotoxic and proliferative response in vitro after in vivo priming. The capacity to respond is associated with the RT1a and RT1n major histocompatibility haplotypes, and nonresponsiveness with the RT1u haplotype. Both, genes of the RT1.A region, which encodes class I antigens, and of the RT1.B/D region, which includes class II and transporter genes, are involved in the genetic control. In F1 hybrids haplotype preference of H-Y restriction occurs in favor of RT1a. Cross-priming can be induced in F1 hybrids by parental cells for RT1a-restricted cytotoxic and proliferative T cells. Allopriming is successful only in the RT1a-carrying strain, whereas xenopriming with mouse cells could not be elicited. The results are discussed in the context of current views on processing and presentation of antigens, and their relevance for transplantation is pointed out.
通过在体内引发后体外测定细胞毒性和增殖反应,在RT1同源大鼠品系中研究了针对雄性特异性H-Y抗原的免疫反应。反应能力与RT1a和RT1n主要组织相容性单倍型相关,无反应性与RT1u单倍型相关。编码I类抗原的RT1.A区域的基因以及包括II类和转运蛋白基因的RT1.B/D区域的基因均参与遗传控制。在F1杂种中,H-Y限制的单倍型偏好有利于RT1a。亲本细胞可以在F1杂种中诱导交叉引发,以产生针对RT1a限制的细胞毒性和增殖性T细胞。同种引发仅在携带RT1a的品系中成功,而用小鼠细胞进行异种引发则无法诱导。本文根据当前关于抗原加工和呈递的观点对结果进行了讨论,并指出了其与移植的相关性。