Suppr超能文献

PI3Kδ 在人类免疫系统中的稳态和致病作用。

Homeostatic and pathogenic roles of PI3Kδ in the human immune system.

机构信息

Division of Clinical Immunology and Rheumatology, Hannover Medical University, Hannover, Germany.

Division of Clinical Immunology and Rheumatology, Hannover Medical University, Hannover, Germany.

出版信息

Adv Immunol. 2020;146:109-137. doi: 10.1016/bs.ai.2020.02.001. Epub 2020 Mar 19.

Abstract

Phosphoinositide 3-kinase delta (PI3Kδ) mediates signaling transduction downstream of diverse immune receptors, including the T cell receptor (TCR), the B cell receptor (BCR), costimulatory molecules and cytokine receptors. Our understanding of the role of PI3Kδ in the immune system comes primarily from mice, and especially from the consequences of pharmacological inhibition of PI3Kδ in mouse models of human disease as well as the consequences of genetic manipulation, resulting in hyperactivation or loss of PI3Kδ function. In case of humans, in vitro studies with PI3Kδ-specific inhibitors, the consequences of treatment of hematologic malignancies with the PI3Kδ-specific inhibitor idelalisib and primary immunodeficiency disorders due to germline variants hyper- or underactivating PI3Kδ provide most of our knowledge on the role of PI3Kδ in immunity and immune regulation. In this review, we summarize the physiological and pathophysiological roles of PI3Kδ in the human immune system, focusing on immunodeficiency due to defects in PI3Kδ signaling and especially on the recently reported cases with mutations resulting in loss of PI3Kδ activity.

摘要

磷酸肌醇 3-激酶 δ(PI3Kδ)介导多种免疫受体下游的信号转导,包括 T 细胞受体(TCR)、B 细胞受体(BCR)、共刺激分子和细胞因子受体。我们对 PI3Kδ 在免疫系统中的作用的理解主要来自于小鼠,特别是来自于在人类疾病的小鼠模型中对 PI3Kδ 的药理学抑制的后果以及遗传操作的后果,导致 PI3Kδ 功能的过度激活或丧失。就人类而言,使用 PI3Kδ 特异性抑制剂的体外研究、用 PI3Kδ 特异性抑制剂idelalisib 治疗血液恶性肿瘤的后果以及由于种系变异导致 PI3Kδ 过度或激活不足的原发性免疫缺陷疾病,为我们提供了关于 PI3Kδ 在免疫和免疫调节中的作用的大部分知识。在这篇综述中,我们总结了 PI3Kδ 在人类免疫系统中的生理和病理生理作用,重点关注由于 PI3Kδ 信号传导缺陷引起的免疫缺陷,特别是最近报道的由于导致 PI3Kδ 活性丧失的突变引起的病例。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验