Kourilsky P, Fazilleau N
Laboratory of Molecular Biology of the Gene, U.277 INSERM, Institute Pasteur, Paris, France.
Int Rev Immunol. 2001 Oct;20(5):575-91. doi: 10.3109/08830180109045579.
Twenty years ago, antigenic and self peptides presented by MHC molecules were absent from the immunological scene. While foreign peptides could be assayed by immune reactions, self peptides, as elusive and invisible as they were at the time, were bound to have an immunological role. How self peptides are selected and presented by MHC molecules, and how self MHC-peptide complexes are seen or not seen by T cells raised multiple questions particularly related to MHC restriction, alloreactivity, positive and negative selection, the nature of tumor antigens and tolerance. These issues were addressed in the "peptiditic self model" (1986) and subsequent hypothesis. They are retrospectively and critically reviewed here in the context of our current understanding of these major immunological phenomena.
二十年前,主要组织相容性复合体(MHC)分子所呈递的抗原肽和自身肽在免疫学领域尚不为人知。虽然外来肽可通过免疫反应进行检测,但自身肽在当时既难以捉摸又不可见,不过它们必然具有免疫学作用。MHC分子如何选择和呈递自身肽,以及T细胞如何识别或不识别自身MHC-肽复合物,引发了多个与MHC限制、同种异体反应性、阳性和阴性选择、肿瘤抗原的性质以及耐受性等特别相关的问题。这些问题在“肽性自身模型”(1986年)及后续假说中得到了探讨。在此,我们结合当前对这些主要免疫学现象的理解,对它们进行回顾性和批判性的审视。