Fc受体作为治疗过敏、自身免疫性疾病和癌症的潜在靶点。

Toshiyuki Takai, Akira Nakamura, Kenichi Akiyama
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引用次数: 10

摘要

免疫系统中各种细胞的激活阈值是由免疫抑制受体调节的。抑制性Fc受体FcgammaRIIB是保持免疫细胞沉默的关键因素之一。过敏反应和自身免疫性疾病的小鼠模型说明了FcgammaRIIB在抑制这些免疫疾病中不可或缺的作用。相反,激活型Fc受体对此类疾病的发病和恶化至关重要。此外,最近的报道揭示了Fc受体在增强树突状细胞抗原呈递中的关键作用,从而导致有效的主要组织相容性复合体I类和ii类限制性T细胞活化。在这种情况下,可以通过将肿瘤抗原靶向树突状细胞上的Fc受体来增强抗癌免疫增强。本文综述了近年来Fc受体的生物医学研究进展,以期将其作为过敏、自身免疫性疾病和癌症的潜在治疗靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Fc receptors as potential targets for the treatment of allergy, autoimmune disease and cancer.

The activation threshold of various cells in the immune system is tuned by immune inhibitory receptors. The inhibitory Fc receptor, FcgammaRIIB, is one of the critical elements for keeping immune cells silent. Murine models for allergic responses and autoimmune diseases illustrate the indispensable roles of FcgammaRIIB in the suppression of these immune disorders. On the contrary, activating-type Fc receptors are crucial for the onset and exacerbation of such diseases. In addition, recent reports have revealed the pivotal roles of Fc receptors in enhancing antigen presentation by dendritic cells, which leads to efficient major histocompatibility complex class I- and class II-restricted T cell activation. In this context, anti-cancer immunopotentiation could be augmented by targeting the tumor antigens to Fc receptors on dendritic cells. This review summarizes recent advances in Fc receptor biomedicine in light of exploiting them as potential therapeutic targets for allergy, autoimmune disease and cancer.

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