Division of Rheumatology, Department of Internal Medicine, Interdisciplinary Graduate Program in Immunology, University of Iowa College of Medicine, Iowa City, IA 52242, USA.
J Immunol. 2010 Jun 1;184(11):6209-22. doi: 10.4049/jimmunol.1000231. Epub 2010 May 5.
gammadelta T cells differ from alphabeta T cells in the Ags they recognize and their functions in immunity. Although most alphabeta TCRs recognize peptides presented by MHC class I or II, human gammadelta T cells expressing Vgamma2Vdelta2 TCRs recognize nonpeptide prenyl pyrophosphates. To define the molecular basis for this recognition, the effect of mutations in the TCR CDR was assessed. Mutations in all CDR loops altered recognition and cover a large footprint. Unlike murine gammadelta TCR recognition of the MHC class Ib T22 protein, there was no CDR3delta motif required for recognition because only one residue is required. Instead, the length and sequence of CDR3gamma was key. Although a prenyl pyrophosphate-binding site was defined by Lys109 in Jgamma1.2 and Arg51 in CDR2delta, the area outlined by critical mutations is much larger. These results show that prenyl pyrophosphate recognition is primarily by germline-encoded regions of the gammadelta TCR, allowing a high proportion of Vgamma2Vdelta2 TCRs to respond. This underscores its parallels to innate immune receptors. Our results also provide strong evidence for the existence of an Ag-presenting molecule for prenyl pyrophosphates.
γδ T 细胞在识别抗原和在免疫中的功能上与 αβ T 细胞不同。虽然大多数 αβ TCR 识别 MHC Ⅰ类或Ⅱ类呈递的肽,但表达 Vγ2Vδ2 TCR 的人 γδ T 细胞识别非肽类异戊烯焦磷酸。为了定义这种识别的分子基础,评估了 TCR CDR 突变的影响。所有 CDR 环的突变都改变了识别,覆盖了一个大的足迹。与鼠 γδ TCR 识别 MHC 类 Ib T22 蛋白不同,不需要 CDR3δ 基序来识别,因为只需要一个残基。相反,CDR3γ 的长度和序列是关键。尽管 Jγ1.2 中的 Lys109 和 CDR2δ 中的 Arg51 定义了异戊烯焦磷酸结合位点,但关键突变所界定的区域要大得多。这些结果表明,异戊烯焦磷酸的识别主要是通过 γδ TCR 的胚系编码区域,允许大量的 Vγ2Vδ2 TCR 做出反应。这突显出它与先天免疫受体的平行关系。我们的结果也为异戊烯焦磷酸的抗原呈递分子的存在提供了有力证据。