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γδ T细胞受体:功能相关性

gammadelta T-cell receptors: functional correlations.

作者信息

O'Brien Rebecca L, Roark Christina L, Jin Niyun, Aydintug M Kemal, French Jena D, Chain Jennifer L, Wands J M, Johnston Molly, Born Willi K

机构信息

Integrated Deaprtment of Immunology, National Jewish Medical and Research Center, Denver, CO 80206, USA.

出版信息

Immunol Rev. 2007 Feb;215:77-88. doi: 10.1111/j.1600-065X.2006.00477.x.

Abstract

The gammadelta T-cell receptors (TCRs) are limited in their diversity, suggesting that their natural ligands may be few in number. Ligands for gammadeltaTCRs that have thus far been determined are predominantly of host rather than foreign origin. Correlations have been noted between the Vgamma and/or Vdelta genes a gammadelta T cell expresses and its functional role. The reason for these correlations is not yet known, but several different mechanisms are conceivable. One possibility is that interactions between particular TCR-V domains and ligands determine function or functional development. However, a recent study showed that at least for one ligand, receptor specificity is determined by the complementarity-determining region 3 (CDR3) component of the TCR-delta chain, regardless of the Vgamma and/or Vdelta. To determine what is required in the TCR for other specificities and to test whether recognition of certain ligands is connected to cell function, more gammadeltaTCR ligands must be defined. The use of recombinant soluble versions of gammadeltaTCRs appears to be a promising approach to finding new ligands, and recent results using this method are reviewed.

摘要

γδ T细胞受体(TCR)的多样性有限,这表明它们的天然配体数量可能很少。迄今为止已确定的γδ TCR配体主要来源于宿主而非外源。已观察到γδ T细胞表达的Vγ和/或Vδ基因与其功能作用之间存在相关性。这些相关性的原因尚不清楚,但有几种不同的机制是可以想象的。一种可能性是特定TCR-V结构域与配体之间的相互作用决定了功能或功能发育。然而,最近的一项研究表明,至少对于一种配体而言,受体特异性是由TCR-δ链的互补决定区3(CDR3)成分决定的,而与Vγ和/或Vδ无关。为了确定TCR对其他特异性的要求,并测试某些配体的识别是否与细胞功能相关,必须定义更多的γδ TCR配体。使用重组可溶性形式的γδ TCR似乎是寻找新配体的一种有前途的方法,本文将对使用该方法的最新结果进行综述。

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