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研究中的 A₃ 腺苷受体靶向药物。

Investigational A₃ adenosine receptor targeting agents.

机构信息

University of Medicine and Dentistry of New Jersey, New Jersey Medical School, Department of Surgery, 185 South Orange Avenue, Newark, NJ 07103, USA.

出版信息

Expert Opin Investig Drugs. 2011 Jun;20(6):757-68. doi: 10.1517/13543784.2011.573785. Epub 2011 Apr 2.

Abstract

INTRODUCTION

Adenosine is an endogenous nucleoside that accumulates in the extracellular space in response to metabolic stress and cell damage. Extracellular adenosine is a signaling molecule that signals by activating four GPCRs: the A(1), A(2A), A(2B) and A(3) receptors. Since the discovery of A(3) adenosine receptors, accumulating evidence has identified these receptors as potential targets for therapeutic intervention.

AREAS COVERED

A(3) adenosine receptors are expressed on the surface of most immune cell types, including neutrophils, macrophages, dendritic cells, lymphocytes and mast cells. A(3) adenosine receptor activation on immune cells governs a broad array of immune cell functions, which include cytokine production, degranulation, chemotaxis, cytotoxicity, apoptosis and proliferation. In accordance with their multitudinous immunoregulatory actions, targeting A(3) adenosine receptors has been shown to impact the course of a wide spectrum of immune-related diseases, such as asthma, rheumatoid arthritis, cancer, ischemia and inflammatory disorders.

EXPERT OPINION

Given the existence of both preclinical and early clinical data supporting the utility of A(3) adenosine receptor ligands in treating immune-related diseases, further development of A(3) adenosine receptor ligands is anticipated.

摘要

简介

腺苷是一种内源性核苷,在代谢应激和细胞损伤时会在细胞外间隙中积累。细胞外腺苷是一种信号分子,通过激活四个 GPCR 来传递信号:A(1)、A(2A)、A(2B)和 A(3)受体。自发现 A(3)腺苷受体以来,越来越多的证据表明这些受体是治疗干预的潜在靶点。

涵盖领域

A(3)腺苷受体表达于大多数免疫细胞类型的表面,包括中性粒细胞、巨噬细胞、树突状细胞、淋巴细胞和肥大细胞。免疫细胞上 A(3)腺苷受体的激活控制着广泛的免疫细胞功能,包括细胞因子产生、脱颗粒、趋化性、细胞毒性、细胞凋亡和增殖。根据其众多的免疫调节作用,靶向 A(3)腺苷受体已被证明可影响广泛的免疫相关疾病的病程,如哮喘、类风湿关节炎、癌症、缺血和炎症性疾病。

专家意见

鉴于支持 A(3)腺苷受体配体在治疗免疫相关疾病方面的临床前和早期临床数据的存在,预计将进一步开发 A(3)腺苷受体配体。

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