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人类CD20 T细胞的起源:身份被盗用?

The origin of human CD20 T cells: a stolen identity?

作者信息

von Essen Marina Rode, Stolpe Lisbeth Egelykke, Bach Søndergaard Helle, Sellebjerg Finn

机构信息

The Danish Multiple Sclerosis Center, Department of Neurology, Rigshospitalet, University of Copenhagen, Glostrup, Denmark.

出版信息

Front Immunol. 2024 Nov 22;15:1487530. doi: 10.3389/fimmu.2024.1487530. eCollection 2024.

Abstract

Human T cells expressing CD20 play an important role in the defense against virus and cancer and are central in the pathogenesis of both malignancies and various autoimmune disorders. Therapeutic modulation of CD20 T cells and the CD20 expression level is therefore of significant interest. In rodents, CD20 on T cells is likely the product of an active transfer of CD20 from a donor B cell interacting with a recipient T cell in a process termed trogocytosis. Whether the same applies to human CD20 T cells is highly debated. Investigating this dispute showed that human CD20 T cells could achieve CD20 along with a series of other B-cell markers from B cells through trogocytosis. However, none of these B-cell markers were co-expressed with CD20 on human CD20 T cells in blood or inflamed CSF, implying that additional mechanisms may be involved in the development of human CD20 T cells. In support of this, we identified true naïve CD20 T cells, measured endogenous production of CD20, and observed that CD20 could be inherited to daughter cells, contradicting that all human CD20 T cells are a product of trogocytosis.

摘要

表达CD20的人类T细胞在抵御病毒和癌症方面发挥着重要作用,并且在恶性肿瘤和各种自身免疫性疾病的发病机制中都起着核心作用。因此,对CD20 T细胞和CD20表达水平进行治疗性调节具有重大意义。在啮齿动物中,T细胞上的CD20可能是在一个称为“胞啃作用”的过程中,由与受体T细胞相互作用的供体B细胞主动转移CD20的产物。这一情况是否同样适用于人类CD20 T细胞,目前存在激烈争论。对这一争议的研究表明,人类CD20 T细胞可以通过胞啃作用从B细胞获得CD20以及一系列其他B细胞标志物。然而,在血液或发炎的脑脊液中的人类CD20 T细胞上,这些B细胞标志物均未与CD20共表达,这意味着人类CD20 T细胞的发育可能涉及其他机制。支持这一观点的是,我们鉴定出了真正的初始CD20 T细胞,测量了CD20的内源性产生,并观察到CD20可以遗传给子代细胞,这与所有人类CD20 T细胞都是胞啃作用产物的观点相矛盾。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff91/11621209/02855c160396/fimmu-15-1487530-g001.jpg

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