Ferreira Cristina, Furmanski Anna, Millrain Maggie, Bartok Istvan, Guillaume Philippe, Lees Rosemary, Simpson Elizabeth, MacDonald H Robson, Dyson Julian
Transplantation Biology Group, Department of Immunology, Imperial College, Hammersmith Hospital, Du Cane Road, London, United Kingdom.
J Immunol. 2006 Aug 15;177(4):2477-85. doi: 10.4049/jimmunol.177.4.2477.
How positive selection molds the T cell repertoire has been difficult to examine. In this study, we use TCR-beta-transgenic mice in which MHC shapes TCR-alpha use. Differential AV segment use is directly related to the constraints placed on the composition of the CDR3 loops. Where these constraints are low, efficient selection of alphabeta pairs follows. This mode of selection preferentially uses favored AV-AJ rearrangements and promotes diversity. Increased constraint on the alpha CDR3 loops leads to inefficient selection associated with uncommon recombination events and limited diversity. Further, the two modes of selection favor alternate sets of AJ segments. We discuss the relevance of these findings to the imprint of self-MHC restriction and peripheral T cell activation.
阳性选择如何塑造T细胞库一直难以研究。在本研究中,我们使用TCR-β转基因小鼠,其中MHC决定TCR-α的使用。不同的AV节段使用与CDR3环组成所受的限制直接相关。当这些限制较低时,αβ对的有效选择随之而来。这种选择模式优先使用有利的AV-AJ重排并促进多样性。对α CDR3环的限制增加会导致与罕见重组事件相关的低效选择和有限的多样性。此外,这两种选择模式有利于不同的AJ节段组合。我们讨论了这些发现与自身MHC限制印记和外周T细胞活化的相关性。