Born Willi K, O'Brien Rebecca L
Integrated Department of Immunology, National Jewish Health, 1400 Jackson Street, Denver, CO 80206, USA.
Arch Immunol Ther Exp (Warsz). 2009 Mar-Apr;57(2):129-35. doi: 10.1007/s00005-009-0017-x. Epub 2009 Mar 31.
After more than two decades of investigation, the biological role of the gammadelta T-cell receptors (TCRs) remains elusive. In fact, a theory of ligand recognition is still lacking that accounts for their adaptable structure, their peripheral selection, and the observed responses of gammadelta T cells, which do not require immunization but only include cells sharing germline-encoded components of the TCR. Assuming that all gammadelta T cells recognize ligands by a common mechanism, we now propose that germline-encoded components of the gammadelta TCRs provide for the specific recognition of a select set of antigenic determinants (Ags) which appear on the cell surface in various molecular associations. Furthermore, we hypothesize that the adaptivity of the gammadelta TCRs serves to increase affinity for the molecules with which these Ags associate rather than for the Ags themselves. Here we outline this hypothetical mechanism and discuss its possible implications for thymic selection and potential for complementing known innate and adaptive mechanisms of immune defense.
经过二十多年的研究,γδ T细胞受体(TCR)的生物学作用仍然难以捉摸。事实上,目前仍缺乏一种配体识别理论来解释其适应性结构、外周选择以及γδ T细胞的观察到的反应,γδ T细胞的反应不需要免疫,仅包括共享TCR种系编码成分的细胞。假设所有γδ T细胞通过共同机制识别配体,我们现在提出,γδ TCR的种系编码成分可特异性识别一组特定的抗原决定簇(Ag),这些抗原决定簇以各种分子组合形式出现在细胞表面。此外,我们假设γδ TCR的适应性有助于增加对与这些Ag相关联的分子的亲和力,而不是对Ag本身的亲和力。在此,我们概述这一假说机制,并讨论其对胸腺选择的可能影响以及补充已知的先天性和适应性免疫防御机制的潜力。