Literature DB >> 32544428

CXCR4 antagonist AMD3100 (plerixafor): From an impurity to a therapeutic agent.

Jingzhe Wang1, Bakhos A Tannous2, Mark C Poznansky3, Huabiao Chen4.   

Abstract

AMD3100 (plerixafor), a CXCR4 antagonist, has opened a variety of avenues for potential therapeutic approaches in different refractory diseases. The CXCL12/CXCR4 axis and its signaling pathways are involved in diverse disorders including HIV-1 infection, tumor development, non-Hodgkin lymphoma, multiple myeloma, WHIM Syndrome, and so on. The mechanisms of action of AMD3100 may relate to mobilizing hematopoietic stem cells, blocking infection of X4 HIV-1, increasing circulating neutrophils, lymphocytes and monocytes, reducing myeloid-derived suppressor cells, and enhancing cytotoxic T-cell infiltration in tumors. Here, we first revisit the pharmacological discovery of AMD3100. We then review monotherapy of AMD3100 and combination use of AMD3100 with other agents in various diseases. Among those, we highlight the perspective of AMD3100 as an immunomodulator to regulate immune responses particularly in the tumor microenvironment and synergize with other therapeutics. All the pre-clinical studies support the clinical testing of the monotherapy and combination therapies with AMD3100 and further development for use in humans.
Copyright © 2020 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  AMD3100; CXCR4; Combination therapy; Monotherapy

Mesh:

Substances:

Year:  2020        PMID: 32544428     DOI: 10.1016/j.phrs.2020.105010

Source DB:  PubMed          Journal:  Pharmacol Res        ISSN: 1043-6618            Impact factor:   7.658


  20 in total

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