Role of CXCR4 in HIV infection and its potential as a therapeutic target

被引:15
作者
Murakami, Tsutomu [2 ]
Yamamoto, Naoki [1 ]
机构
[1] Natl Univ Singapore, Dept Microbiol, Yong Loo Lin Sch Med, Singapore 117597, Singapore
[2] Natl Inst Infect Dis, AIDS Res Ctr, Shinjuku Ku, Tokyo 1628640, Japan
关键词
anti-HIV therapy; cancer metastasis; CCR5; chemokine receptor; CXCR4; antagonist; hematopoietic stem cell mobilizer; HIV infection; rheumatoid arthritis; HUMAN-IMMUNODEFICIENCY-VIRUS; CHEMOKINE RECEPTOR CXCR4; T-CELL-LINE; SYNCYTIUM-INDUCING PHENOTYPE; SMALL-MOLECULE ANTAGONIST; CANCER METASTASIS; CCR5; ANTAGONIST; HIGHLY POTENT; V3; DOMAIN; IN-VIVO;
D O I
10.2217/FMB.10.67
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The chemokine receptors CCR5 and CXCR4 are the two major coreceptors for HIV entry. Numerous efforts have been made to develop a new class of anti-HIV agents that target these coreceptors as an additional or alternative therapy to standard HAART. Among the CCR5 inhibitors developed so far, maraviroc is the first drug that has been approved by the US FDA for treating patients with R5 HIV-1. Although many CXCR4 inhibitors, some of which are highly active and orally bioavailable, have also been studied, they are still at preclinical stages or have been suspended during development. Importantly, the interaction between CXCR4 and its ligand SDF-1 is involved in various disease conditions, such as cancer cell metastasis, leukemia cell proliferation, rheumatoid arthritis and pulmonary fibrosis. Therefore, CXCR4 inhibitors have potential as novel therapeutics for the treatment of these diseases as well as HIV infection.
引用
收藏
页码:1025 / 1039
页数:15
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