CCR5受体拮抗剂
趋化因子受体CCR5
马拉维洛克
趋化因子受体
化学
受体
小分子
单克隆抗体
趋化因子
CCR1
趋化因子受体
共受体
药理学
人类免疫缺陷病毒(HIV)
免疫学
抗体
生物
生物化学
作者
Baokun Qi,Qiang Fu,Shiyuan Liu,Wei Hou,Jian Li,Yung T. Huang,Jianyou Shi
标识
DOI:10.1016/j.ejmech.2020.112819
摘要
C–C chemokine receptor 5(CCR5) is a cell membrane protein from G protein-coupled receptors (GPCR) family, which is an important modulator for leukocyte activation and mobilization. In the 1980s, several reports suggest that lack of the HIV-1 co-receptor, the chemokine receptor CCR5, offers protection against HIV infection. Later, it was shown that CCR5 was confirmed to be the most common co-receptor for the HIV-1 virus R5 strain. In recent years, many studies have shown that CCR5 is closely related to the development of various cancers and inflammations to facilitate the discovery of CCR5 antagonists. There are many types of CCR5 antagonists, mainly including chemokine derivatives, non-peptide small molecule compounds, monoclonal antibodies, and peptide compounds. This review focus on the recent research processes and pharmacological effects of CCR5 antagonists such as Maraviroc, TAK-779 and PRO 140. After focusing on the therapeutic effect of CCR5 antagonists on AIDS, it also discusses the therapeutic prospect of CCR5 in other diseases such as inflammation and tumor.
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