共抑制分子:控制效应器还是控制控制器?

Self/nonself Pub Date : 2010-04-01 Epub Date: 2010-02-16 DOI:10.4161/self.1.2.11548
Govindarajan Thangavelu, Christa Smolarchuk, Colin C Anderson
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引用次数: 21

摘要

大约40年前,有人提出淋巴细胞受到现在所谓的共抑制信号的负调控。然而,直到最近才发现了许多共抑制剂及其关键功能,才将共抑制带到了免疫学研究的前沿。虽然共抑制信号被认为直接调节常规T细胞,但最近的数据表明,共抑制信号与其他主要的外周负调控机制之间存在收敛,这是由调节性T细胞介导的。此外,现在很清楚,淋巴细胞不是共抑制信号的唯一领域,因为先天免疫系统的细胞本身是免疫的控制者,它们表达的共抑制剂对其进行调节。因此,为了更好地理解外周细胞的负调控,并将这些知识应用于疾病的治疗,未来的一个主要焦点应该是定义共抑制控制效应细胞的内在与外在条件(通过调节细胞或先天细胞)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Co-inhibitory molecules: Controlling the effectors or controlling the controllers?

Co-inhibitory molecules: Controlling the effectors or controlling the controllers?

Co-inhibitory molecules: Controlling the effectors or controlling the controllers?

Co-inhibitory molecules: Controlling the effectors or controlling the controllers?

Nearly forty years ago the concept was proposed that lymphocytes are negatively regulated by what are now called co-inhibitory signals. Nevertheless, it is only the more recent identification of numerous co-inhibitors and their critical functions that has brought co-inhibition to the forefront of immunologic research. Although co-inhibitory signals have been considered to directly regulate conventional T cells, more recent data has indicated a convergence between co-inhibitory signals and the other major negative control mechanism in the periphery that is mediated by regulatory T cells. Furthermore, it is now clear that lymphocytes are not the sole domain of co-inhibitory signals, as cells of the innate immune system, themselves controllers of immunity, are regulated by co-inhibitors they express. Thus, in order to better understand negative regulation in the periphery and apply this knowledge to the treatment of disease, a major focus for the future should be the definition of the conditions where co-inhibition controls effector cells intrinsically versus extrinsically (via regulatory or innate cells).

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