Papadopoulou Maria, Sanchez Sanchez Guillem, Vermijlen David
Department of Pharmacotherapy and Pharmaceutics, Université Libre de Bruxelles (ULB), Brussels, Belgium.
Institute for Medical Immunology (IMI), Université Libre de Bruxelles (ULB), Gosselies, Belgium.
Immunol Rev. 2020 Nov;298(1):99-116. doi: 10.1111/imr.12926. Epub 2020 Nov 4.
γδ T cells comprise the third cell lineage of lymphocytes that use, like αβ T cells and B cells, V(D)J gene rearrangement with the potential to generate a highly diverse T cell receptor (TCR) repertoire. There is no obvious conservation of γδ T cell subsets (based on TCR repertoire and/or function) between mice and human, leading to the notion that human and mouse γδ T cells are highly different. In this review, we focus on human γδ T cells, building on recent studies using high-throughput sequencing to analyze the TCR repertoire in various settings. We make then the comparison with mouse γδ T cell subsets highlighting the similarities and differences and describe the remarkable changes during lifespan of innate and adaptive γδ T cells. Finally, we propose mechanisms contributing to the generation of innate versus adaptive γδ T cells. We conclude that key elements related to the generation of the γδ TCR repertoire and γδ T cell activation/development are conserved between human and mice, highlighting the similarities between these two species.
γδ T细胞是淋巴细胞的第三个细胞谱系,与αβ T细胞和B细胞一样,利用V(D)J基因重排,有可能产生高度多样化的T细胞受体(TCR)库。小鼠和人类之间的γδ T细胞亚群(基于TCR库和/或功能)没有明显的保守性,这导致了人类和小鼠γδ T细胞高度不同的观点。在这篇综述中,我们基于最近使用高通量测序分析各种情况下TCR库的研究,重点关注人类γδ T细胞。然后,我们将其与小鼠γδ T细胞亚群进行比较,突出异同,并描述先天和适应性γδ T细胞生命周期中的显著变化。最后,我们提出了有助于先天和适应性γδ T细胞产生的机制。我们得出结论,人类和小鼠之间与γδ TCR库的产生以及γδ T细胞激活/发育相关的关键要素是保守的,突出了这两个物种之间的相似性。