Krensky A M, Clayberger C
Department of Pediatrics, Stanford University Medical Center, CA 94305-5119.
Curr Opin Nephrol Hypertens. 1993 Nov;2(6):898-903. doi: 10.1097/00041552-199311000-00007.
Understanding the nature of allorecognition is fundamental to the design of antigen-specific therapies for transplantation. As recently as 10 years ago it was generally believed that recognition of major histocompatibility complex (MHC) molecules by T lymphocytes was direct and represented the "simplest" kind of T-lymphocyte interaction. It is now clear that the nature of allorecognition is complex, involving a variety of different forms of MHC antigens with or without peptides contained in their antigen-binding groove. In addition, there is renewed interest in alternative forms of allorecognition, including so-called indirect allorecognition, in which donor alloantigens are recognized as peptides in the context of recipient self. Lastly, it appears that cells other than T lymphocytes, eg, natural killer cells, are capable of antigen-specific recognition and may be responsible for heretofore underappreciated mechanisms of transplant rejection.
了解同种异体识别的本质是设计移植抗原特异性疗法的基础。就在10年前,人们普遍认为T淋巴细胞对主要组织相容性复合体(MHC)分子的识别是直接的,代表了T淋巴细胞相互作用的“最简单”形式。现在很清楚,同种异体识别的本质是复杂的,涉及多种不同形式的MHC抗原,其抗原结合槽中含有或不含有肽段。此外,人们对同种异体识别的替代形式重新产生了兴趣,包括所谓的间接同种异体识别,即供体同种异体抗原在受体自身背景下被识别为肽段。最后,似乎除了T淋巴细胞之外的细胞,例如自然杀伤细胞,也能够进行抗原特异性识别,并且可能是迄今为止未被充分认识的移植排斥机制的原因。