Correia-Neves M, Waltzinger C, Wurtz J M, Benoist C, Mathis D
Institut de Génétique et de Biologie Moléculaire et Cellulaire, Illkirch, Strasbourg, France.
J Immunol. 1999 Nov 15;163(10):5471-7.
Some TCR variable regions are preferentially expressed in CD4+ or CD8+ T cells, reflecting a predilection for interacting with MHC class II or class I molecules. The molecular basis for MHC class bias has been studied previously, in particular for V alpha 3 family members, pointing to a dominant role for two amino acid positions in complementary-determining regions (CDRs) 1 and 2. We have evaluated the generality of these findings by examining the MHC class bias of V alpha 2 family members, an attractive system because it shows more variability within the CDR1 and -2, exhibits variation in the framework regions, and includes a member for which the crystal structure has been determined. We find that preferential recognition of MHC class I or II molecules does not always depend on residues at the same positions of CDR1 and -2; rules for one family may be reversed in another. Instead, there are multiple influences exerted by various CDR1/2 positions as well as the CDR3s of both the TCR alpha- and TCR beta-chains.
一些TCR可变区在CD4⁺或CD8⁺T细胞中优先表达,这反映出它们倾向于与MHCⅡ类或Ⅰ类分子相互作用。先前已对MHC类偏好的分子基础进行了研究,特别是针对Vα3家族成员,结果表明互补决定区(CDR)1和2中的两个氨基酸位置起主导作用。我们通过检查Vα2家族成员的MHC类偏好来评估这些发现的普遍性,这是一个很有吸引力的系统,因为它在CDR1和 -2内表现出更多变异性,在构架区也有变异,并且包括一个其晶体结构已确定的成员。我们发现,对MHCⅠ类或Ⅱ类分子的优先识别并不总是取决于CDR1和 -2相同位置的残基;一个家族的规则在另一个家族中可能会相反。相反,TCRα链和TCRβ链的各种CDR1/2位置以及CDR3会产生多种影响。