Tourne S, Miyazaki T, Oxenius A, Klein L, Fehr T, Kyewski B, Benoist C, Mathis D
Institut de Génétique et de Biologie Moléculaire et Cellulaire, Centre National de la Recherche Scientifique/Institut National de la Santé et de la Recherche Médicale, Strasbourg, France.
Immunity. 1997 Aug;7(2):187-95. doi: 10.1016/s1074-7613(00)80522-1.
According to past reports, H-2Ma0/0 mice express a single major histocompatiblity complex class II molecule, A(b), heavily loaded with a single peptide derived from the invariant chain, CLIP. Despite the highly restricted diversity of the class II:peptide complexes expressed on thymic stromal cells in the mutant animals, a large and diverse population of CD4+ T cells is positively selected. However, two important issues remained unresolved and are addressed here: Just how preponderant is CLIP occupancy of the class II molecules from H-2M0/0 mice? How extensive and functionally competent is the CD4+ population selected in the mutant animals? Our results argue that a single class II:peptide complex can select a very broad, though not complete, repertoire of CD4+ T cells.
根据以往的报道,H-2Mα0/0小鼠表达一种单一的主要组织相容性复合体II类分子A(b),该分子大量负载了一种源自恒定链CLIP的单一肽段。尽管突变动物胸腺基质细胞上表达的II类:肽复合物的多样性受到高度限制,但仍有大量多样的CD4+ T细胞群体被阳性选择。然而,有两个重要问题仍未解决,本文将予以探讨:H-2M0/0小鼠II类分子中CLIP占据的优势程度究竟如何?在突变动物中选择的CD4+群体有多广泛且功能健全?我们的结果表明,单一的II类:肽复合物可以选择一个非常广泛(尽管不完整)的CD4+ T细胞库。