T-Cell Receptor Clustering Methods Used for Single Cell Analysis: Potential Application in Oncology

J. Buttigieg, K. Helmerson, B. Coventry
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Abstract

We know that T-cell activation and effector function is integral for cancer cell destruction in immunotherapeutic treatment in oncology. The fundamental behaviour of T-cells at the time of activation is poorly understood but is likely to be central to this action. Cellular clustering occurs on at least two levels: gathering of multiple mobile cells of similar type, and aggregation between different cell types. Receptors are implicated in both of these processes. Analysis of receptor clustering is a different process whereby receptors form clusters on the cell membrane surface and can be studied to determine their relationship to immune activation. Receptor clustering has been shown to occur in some (perhaps all) cell types, but little is known about this phenomenon, particularly in T-lymphocytes. T-Cell Receptors (TCRs) which are important for the activation of T-lymphocytes. T-cell receptors, also known as cluster of differentiation 3 (CD3) molecules, bind specific antigen to create intracellular signaling in the process of T-cell activation as part of the immune response. The detail of how TCRs physically behave on the T-lymphocyte surface and specifically how they cluster remains unclear, including during the early phases of initiation of immune activation in the T-cell response. The aim of this review is to investigate how receptor clustering that has been studied, can be more effectively studied in the future and what the current evidence suggests about TCR clustering/T-cell activity relationships.
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用于单细胞分析的t细胞受体聚类方法:在肿瘤中的潜在应用
我们知道t细胞的激活和效应功能是肿瘤免疫治疗中癌细胞破坏的组成部分。t细胞在激活时的基本行为尚不清楚,但很可能是这一作用的核心。细胞聚集至少发生在两个层面上:相似类型的多个可移动细胞的聚集,以及不同类型细胞之间的聚集。受体参与了这两个过程。受体聚类分析是一个不同的过程,即受体在细胞膜表面形成簇,可以研究确定它们与免疫激活的关系。受体聚集已被证明发生在某些(也许是所有)细胞类型中,但对这种现象知之甚少,特别是在t淋巴细胞中。t细胞受体(TCRs)对t淋巴细胞的激活起着重要的作用。t细胞受体,也被称为CD3分子簇,在t细胞激活过程中结合特异性抗原产生细胞内信号,作为免疫反应的一部分。tcr在t淋巴细胞表面的物理行为,特别是它们如何聚集的细节仍不清楚,包括在t细胞反应中免疫激活的早期阶段。这篇综述的目的是探讨如何在未来更有效地研究受体聚类,以及目前的证据表明TCR聚类与t细胞活性的关系。
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