Integrated Department of Immunology, National Jewish Health, Denver, CO 80206, USA.
Cell Mol Immunol. 2013 Jan;10(1):13-20. doi: 10.1038/cmi.2012.45. Epub 2012 Oct 22.
In the last two decades, it has become clear that γδ T cells recognize a diverse array of antigens including self and foreign, large and small, and peptidic and non-peptidic molecules. In this respect, γδ antigens as a whole resemble more the antigens recognized by antibodies than those recognized by αβ T cells. Because of this antigenic diversity, no single mechanism-such as the major histocompatibility complex (MHC) restriction of αβ T cells-is likely to provide a basis for all observed T-cell antigen receptor (TCR)-dependent γδ T-cell responses. Furthermore, available evidence suggests that many individual γδ T cells are poly-specific, probably using different modes of ligand recognition in their responses to unrelated antigens. While posing a unique challenge in the maintenance of self-tolerance, this broad reactivity pattern might enable multiple overlapping uses of γδ T-cell populations, and thus generate a more efficient immune response.
在过去的二十年中,人们已经清楚地认识到,γδ T 细胞能够识别多种抗原,包括自身和外来的、大的和小的、肽类和非肽类分子。在这方面,γδ 抗原整体上更类似于抗体识别的抗原,而不是 αβ T 细胞识别的抗原。由于这种抗原的多样性,没有单一的机制(如 MHC 对 αβ T 细胞的限制)可能为所有观察到的 TCR 依赖性 γδ T 细胞反应提供基础。此外,现有证据表明,许多个体 γδ T 细胞具有多特异性,可能在对无关抗原的反应中使用不同的配体识别模式。虽然这对自身耐受的维持构成了独特的挑战,但这种广泛的反应模式可能使 γδ T 细胞群体能够多次重叠使用,从而产生更有效的免疫反应。