The dual CCR2/CCR5 chemokine receptor antagonist Cenicriviroc reduces macrophage infiltration and disease severity in Duchenne muscular dystrophy (Dmdmdx-4Cv) mice

• Published in: PloS one 2018-03, Vol.13 (3), p.e0194421-e0194421
• Main Authors: Liang, Feng, Giordano, Christian, Shang, Dong, Li, Qian, Petrof, Basil J
• Format: Article
• Language: English
• Subjects: Biology and Life Sciences; Care and treatment; CC chemokine receptors; CCR2 protein; CCR5 protein; CD4 antigen; CD8 antigen; Chemokine receptors; Chemokines; Cytometry; Development and progression; Diaphragm; Diaphragms; Disease; Duchenne muscular dystrophy; Duchenne's muscular dystrophy; Dystrophy; Fibers; Fibrosis; Flow cytometry; Gangrene; Genetic aspects; Health aspects; HIV; Homology; Human immunodeficiency virus; Immune response; Infiltration; Inflammation; Laboratories; Leukocytes (neutrophilic); Ligands; Lymphocytes; Lymphocytes T; Macrophages; Medicine and Health Sciences; Mice; Monocyte chemoattractant protein 1; Muscle contraction; Muscles; Muscular dystrophy; Musculoskeletal system; Necrosis; Nitric-oxide synthase; Reduction; Regeneration; Respiratory diseases; Rodents; Therapy
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0194421

Duchenne muscular dystrophy (DMD) is characterized by progressive muscle weakness which is ultimately fatal, most often due to involvement of the diaphragm. Macrophage infiltration of dystrophic muscles has been strongly linked to muscle damage and fibrosis in DMD. We hypothesized that cenicriviroc (CVC), a dual chemokine receptor (CCR2/CCR5) antagonist currently under clinical evaluation for other diseases, could prevent macrophage accumulation and blunt disease progression in the diaphragms of mdx mice (genetic homologue of DMD). Treatment with CVC (20 mg/kg/day intraperitoneally) or vehicle was initiated in mdx mice at 2 weeks of age (prior to the onset of muscle necrosis) and continued for 4 weeks. Flow cytometry to assess inflammatory cell subsets as well as histological and force generation parameters were determined in mdx diaphragms at the conclusion of the treatment. CVC therapy induced a major (3.9-fold) reduction in total infiltrating macrophages, whereas total numbers of neutrophils and T lymphocytes (CD4+ and CD8+) were unaffected. No changes in macrophage polarization status (inflammatory versus anti-inflammatory skewing based on iNOS and CD206 expression) were observed. Muscle fiber size and fibrosis were not altered by CVC, whereas a significant reduction in centrally nucleated fibers was found suggesting a decrease in prior necrosis-regeneration cycles. In addition, maximal isometric force production by the diaphragm was increased by CVC therapy. These results suggest that CVC or other chemokine receptor antagonists which reduce pathological macrophage infiltration may have the potential to slow disease progression in DMD.