Becoming aware of γδ T cells.

3区 医学 Q2 Medicine Advances in Immunology Pub Date : 2022-01-01 DOI:10.1016/bs.ai.2021.12.002
Willi K Born, Rebecca L O'Brien
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引用次数: 0

Abstract

The discovery that B cells and αβ T cells exist was predictable: These cells gave themselves away through their products and biological effects. In contrast, there was no reason to anticipate the existence of γδ T cells. Even the accidental discovery of a novel TCR-like gene (later named γ) that did not encode TCR α or β proteins did not immediately change this. TCR-like γ had no obvious function, and its early expression in the thymus encouraged speculation about a possible role in αβ T cell development. However, the identification of human PBL-derived cell-lines which expressed CD3 in complex with the TCR-like γ protein, but not the αβ TCR, first indicated that a second T cell-type might exist, and the TCR-like γ chain was observed to co-precipitate with another protein. Amid speculation about a possible second TCR, this potential dimeric partner was named δ. To determine if the δ protein was indeed TCR-like, we undertook to sequence it. Meanwhile, a fourth TCR-like gene was discovered and provisionally named x. TCR-like x had revealed itself through genomic rearrangements early in T cell development, and was an attractive candidate for the gene encoding δ. The observation that δ protein sequences matched the predicted amino acid sequences encoded by the x gene, as well as serological cross-reactivity, confirmed that the TCR-like x gene indeed encoded the δ protein. Thus, the γδ heterodimer was established as a second TCR, and the cells that express it (the γδ T cells) consequently represented a third lymphocyte-population with the potential of recognizing diverse antigens. Soon, it became clear that γδ T cells are widely distributed and conserved among the vertebrate species, implying biological importance. Consistently, early functional studies revealed their roles in host resistance to pathogens, tissue repair, immune regulation, metabolism, organ physiology and more. Albeit discovered late, γδ T cells have repeatedly proven to play a distinct and often critical immunological role, and now generate much interest.

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开始意识到γδ T细胞。
B细胞和αβ T细胞存在的发现是可以预见的:这些细胞通过它们的产物和生物效应出卖了自己。相比之下,没有理由预测γδ T细胞的存在。即使偶然发现了一种不编码TCR α或β蛋白的新型TCR样基因(后来被命名为γ),也没有立即改变这一点。TCR-like γ没有明显的功能,其在胸腺中的早期表达促使人们猜测其可能在αβ T细胞发育中起作用。然而,鉴定人类pbl衍生的细胞系表达CD3与TCR样γ蛋白复合物,而不表达αβ TCR,首次表明可能存在第二种T细胞类型,并且观察到TCR样γ链与另一种蛋白共沉淀。在对可能的第二个TCR的猜测中,这个潜在的二聚体伙伴被命名为δ。为了确定δ蛋白是否确实是tcr样蛋白,我们对其进行了测序。同时,第四个tcr样基因被发现,暂时命名为x。tcr样x在T细胞发育早期通过基因组重排发现,是编码δ基因的有吸引力的候选者。观察到δ蛋白序列与预测的x基因编码的氨基酸序列相匹配,以及血清学交叉反应性,证实了tcr样x基因确实编码了δ蛋白。因此,γδ异源二聚体被确定为第二种TCR,表达它的细胞(γδ T细胞)因此代表了具有识别多种抗原潜力的第三种淋巴细胞群。很快,人们发现γδ T细胞在脊椎动物物种中广泛分布并保守,这意味着其生物学重要性。与此一致,早期的功能研究揭示了它们在宿主抵抗病原体、组织修复、免疫调节、代谢、器官生理等方面的作用。尽管发现较晚,但γδ T细胞已多次被证明发挥着独特且通常至关重要的免疫作用,现在引起了广泛的兴趣。
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来源期刊
Advances in Immunology
Advances in Immunology 医学-免疫学
CiteScore
9.90
自引率
0.00%
发文量
13
期刊介绍: Advances in Immunology has provided students and researchers with the latest information in Immunology for over 50 years. You can continue to rely on Advances in Immunology to provide you with critical reviews that examine subjects of vital importance to the field through summary and evaluation of current knowledge and research. The articles stress fundamental concepts, but also evaluate the experimental approaches.
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