Clinical significance of chemokine receptor antagonists
Miao Miao1, Erik De Clercq2, Guangdi Li1
1Department of Epidemiology and Health Statistics, Xiangya School of Public Health, Central South University, Hunan, China.
Abstract:
Introduction: Chemokine receptors are important therapeutic targets for the treatment of many human diseases. This study will provide an overview of approved chemokine receptor antagonists and promising candidates in advanced clinical trials.Areas covered: We will describe clinical aspects of chemokine receptor antagonists regarding their clinical efficacy, mechanisms of action, and re-purposed applications.Expert opinion: Three chemokine antagonists have been approved: (i) plerixafor is a small-molecule CXCR4 antagonist that mobilizes hematopoietic stem cells; (ii) maraviroc is a small-molecule CCR5 antagonist for anti-HIV treatment; and (iii) mogamulizumab is a monoclonal-antibody CCR4 antagonist for the treatment of mycosis fungoides or Sézary syndrome. Moreover, phase 3 trials are ongoing to evaluate many potent candidates, including CCR5 antagonists (e.g. leronlimab), dual CCR2/CCR5 antagonists (e.g. cenicriviroc), and CXCR4 antagonists (e.g. balixafortide, mavorixafor, motixafortide). The success of chemokine receptor antagonists depends on the selective blockage of disease-relevant chemokine receptors which are indispensable for disease progression. Although clinical translation has been slow, antagonists targeting chemokine receptors with multifaced functions offer the potential to treat a broad spectrum of human diseases.
Insights
Approved chemokine receptor antagonists like plerixafor and maraviroc show therapeutic promise. Ongoing trials for novel CXCR4 and CCR5 antagonists highlight their potential for treating diverse human diseases.
Area of Science:
- Immunology
- Pharmacology
- Oncology
Background:
- Chemokine receptors are crucial targets in numerous human diseases.
- Understanding their antagonists is key for developing new therapies.
Purpose of the Study:
- To review approved chemokine receptor antagonists and candidates in clinical trials.
- To discuss their clinical efficacy, mechanisms, and potential re-purposed applications.
Main Methods:
- Literature review of approved drugs and ongoing clinical trials.
- Analysis of clinical efficacy and mechanisms of action.
Main Results:
- Three antagonists are approved: plerixafor (CXCR4), maraviroc (CCR5), and mogamulizumab (CCR4).
- Numerous CXCR4, CCR5, and dual CCR2/CCR5 antagonists are in Phase 3 trials.
Conclusions:
- Selective blockage of disease-relevant chemokine receptors is vital for therapeutic success.
- Chemokine receptor antagonists offer broad potential for treating various human diseases.
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