Chien Yueh-hsiu, Konigshofer Yves
Department of Microbiology and Immunology, Program in Immunology, Stanford University, Stanford, CA, USA.
Immunol Rev. 2007 Feb;215:46-58. doi: 10.1111/j.1600-065X.2006.00470.x.
gammadelta T cells contribute to host immune competence uniquely. This is most likely because they have distinctive antigen-recognition properties. While the basic organization of gammadelta T-cell receptor (TCR) loci is similar to that of alphabeta TCR loci, there is a striking difference in how the diversity of gammadelta TCRs is generated. gammadelta and alphabeta T cells have different antigen-recognition requirements and almost certainly recognize a different set of antigens. While it is unclear what most gammadelta T cells recognize, the non-classical major histocompatibility complex class I molecules T10 and T22 were found to be the natural ligands for a sizable population (0.2-2%) of murine gammadelta T cells. The recognition of T10/T22 may be a way by which gammadelta T cells regulate cells of the immune system, and this system has been used to determine the antigen-recognition determinants of gammadelta T cells. T10/T22-specific gammadelta T cells have TCRs that are diverse in both V gene usage and CDR3 sequences. Their Vgamma usage reflects their tissue origin, and their antigen specificity is conferred by a motif in the TCR delta chain that is encoded by V and D segments and by P-nucleotide addition. Sequence variations around this motif modulate affinities between TCRs and T10/T22. That this CDR3 motif is important in antigen recognition is confirmed by the crystal structure of a gammadelta TCR bound to its ligand. The significance of these observations is discussed in the context of gammadelta T-cell biology.
γδ T细胞对宿主免疫能力有独特贡献。这很可能是因为它们具有独特的抗原识别特性。虽然γδ T细胞受体(TCR)基因座的基本组织与αβ TCR基因座相似,但γδ TCR多样性的产生方式存在显著差异。γδ T细胞和αβ T细胞有不同的抗原识别要求,几乎可以肯定识别的是不同的抗原组。虽然尚不清楚大多数γδ T细胞识别什么,但发现非经典的主要组织相容性复合体I类分子T10和T22是相当一部分(0.2 - 2%)小鼠γδ T细胞的天然配体。对T10/T22的识别可能是γδ T细胞调节免疫系统细胞的一种方式,并且这个系统已被用于确定γδ T细胞的抗原识别决定因素。T10/T22特异性γδ T细胞的TCR在V基因使用和CDR3序列方面都具有多样性。它们的Vγ使用情况反映了它们的组织来源,其抗原特异性由TCR δ链中的一个基序赋予,该基序由V和D区段以及P核苷酸添加编码。围绕这个基序的序列变异调节TCR与T10/T22之间的亲和力。与配体结合的γδ TCR的晶体结构证实了这个CDR3基序在抗原识别中很重要。在γδ T细胞生物学的背景下讨论了这些观察结果的意义。