Gallico G G, Butcher G W, Howard J C
J Exp Med. 1979 Jan 1;149(1):244-53. doi: 10.1084/jem.149.1.244.
The laboratory recombinant haplotype H-1acl of the Norway rat has been used in studies of the rejection and passive enhancement of kidney allografts. While the full H-1a haplotype provoked acute rejection, neither of the isolated subregions, H-1Aa and H-1Ba, did so. It was also found that alloantisera raised against either the H-1Aa or the H-1Ba antigens would enhance the grafts. It is suggested that both MHC subregions contain a histocompatibility locus (i) for kidney (as they do for skin) and that in the genetic combinations studied only incompatibility for both provokes a response sufficient for rejection. In other combinations, however, single region incompatibilities may be sufficient.
挪威大鼠的实验室重组单倍型H-1acl已用于肾移植排斥反应和被动增强的研究。完整的H-1a单倍型可引发急性排斥反应,而分离出的亚区域H-1Aa和H-1Ba均不会引发这种反应。还发现,针对H-1Aa或H-1Ba抗原产生的同种抗血清可增强移植效果。有人提出,两个主要组织相容性复合体(MHC)亚区域都含有一个肾脏组织相容性位点(就像它们对皮肤一样),并且在所研究的基因组合中,只有两个区域都不相容才会引发足以导致排斥反应的应答。然而,在其他组合中,单个区域不相容可能就足够了。