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免疫蛋白酶体:在同种异体免疫中具有新颖和新兴作用的老牌选手。

The immunoproteasome: An old player with a novel and emerging role in alloimmunity.

机构信息

Transplantation Research Center, Renal Division, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.

Department of Internal Medicine, Division of Nephrology, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.

出版信息

Am J Transplant. 2017 Dec;17(12):3033-3039. doi: 10.1111/ajt.14435. Epub 2017 Aug 30.

Abstract

Modern treatment strategies for the maintenance of allograft acceptance frequently target ubiquitously-expressed pathways, leading to significant side-effects and poor long-term allograft outcomes. Constitutive proteasome inhibitors, which have recently been introduced for the treatment of antibody-mediated rejection, target the ubiquitously-expressed proteasome. To limit off-target effects and serious mechanism-based toxicity, however, these inhibitors are administered intermittently and suboptimally. Immunoproteasomes, which are an inducible subset of proteasomes enriched in immune cells, replace constitutive proteasomes after cell exposure to proinflammatory cytokines such as interferon-γ. While immunoproteasomes were first described as processors of antigen for presentation by major histocompatibility complex molecules, recent findings point to its broader biological roles. These vary from activating different subsets of the immune system, by controlling transcriptional activators and downstream cytokines, to affecting their differentiation and survival. These emerging roles of the immunoproteasome in activated immune cells have made it a rational candidate for the targeted treatment of immune-mediated diseases. Preclinical studies have established its role in maintaining allograft acceptance without significant short- or long-term toxicity. This review provides a brief background of the immunoproteasome and outlines its role in immunological pathways and its potential in alloimmunity.

摘要

现代维持同种异体移植物接受的治疗策略经常针对广泛表达的途径,导致严重的副作用和较差的长期同种异体移植物结局。最近被引入用于治疗抗体介导的排斥反应的组成型蛋白酶体抑制剂,靶向广泛表达的蛋白酶体。然而,为了限制脱靶效应和严重的基于机制的毒性,这些抑制剂需要间歇性和次优地给药。免疫蛋白酶体是蛋白酶体的一种诱导亚群,在细胞暴露于干扰素-γ等促炎细胞因子后替代组成型蛋白酶体。虽然免疫蛋白酶体最初被描述为主要组织相容性复合物分子呈递抗原的处理器,但最近的发现表明其具有更广泛的生物学作用。这些作用包括通过控制转录激活因子和下游细胞因子来激活免疫系统的不同亚群,以及影响其分化和存活。免疫蛋白酶体在激活的免疫细胞中的这些新兴作用使其成为免疫介导疾病靶向治疗的合理候选物。临床前研究已经确立了其在维持同种异体移植物接受而没有明显的短期或长期毒性中的作用。本综述简要介绍了免疫蛋白酶体的背景,并概述了其在免疫途径中的作用及其在同种异体免疫中的潜力。

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