S100A4-neutralizing monoclonal antibody 6B12 counteracts the established experimental skin fibrosis induced by bleomycin
Jazyk angličtina Země Anglie, Velká Británie Médium print
Typ dokumentu časopisecké články
Grantová podpora
023728
Ministry of Health of the Czech Republic
Ministry of Education Youth and Sports
SVV 260638
Czech Republic
German Research Foundation
2013.056.1
German Research Foundation
PubMed
37314987
PubMed Central
PMC10907816
DOI
10.1093/rheumatology/kead295
PII: 7197827
Knihovny.cz E-zdroje
- Klíčová slova
- 6B12, S100A4, SSc, established dermal fibrosis, monoclonal antibody, treatment,
- MeSH
- alarminy * MeSH
- bleomycin toxicita MeSH
- fibróza MeSH
- kůže * patologie MeSH
- lidé MeSH
- modely nemocí na zvířatech MeSH
- monoklonální protilátky farmakologie MeSH
- myši MeSH
- S100 kalcium vázající protein A4 genetika MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- myši MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- alarminy * MeSH
- bleomycin MeSH
- monoklonální protilátky MeSH
- S100 kalcium vázající protein A4 MeSH
- S100A4 protein, human MeSH Prohlížeč
OBJECTIVES: Our previous studies have demonstrated that the Damage Associated Molecular Pattern (DAMP) protein, S100A4, is overexpressed in the involved skin and peripheral blood of patients with SSc. It is associated with skin and lung involvement, and disease activity. By contrast, lack of S100A4 prevented the development of experimental dermal fibrosis. Herein we aimed to evaluate the effect of murine anti-S100A4 mAb 6B12 in the treatment of preestablished experimental dermal fibrosis. METHODS: The effects of 6B12 were assessed at therapeutic dosages in a modified bleomycin-induced dermal fibrosis mouse model by evaluating fibrotic (dermal thickness, proliferation of myofibroblasts, hydroxyproline content, phosphorylated Smad3-positive cell count) and inflammatory (leukocytes infiltrating the lesional skin, systemic levels of selected cytokines and chemokines) outcomes, and transcriptional profiling (RNA sequencing). RESULTS: Treatment with 7.5 mg/kg 6B12 attenuated and might even reduce pre-existing dermal fibrosis induced by bleomycin as evidenced by reduction in dermal thickness, myofibroblast count and collagen content. These antifibrotic effects were mediated by the downregulation of TGF-β/Smad signalling and partially by reducing the number of leukocytes infiltrating the lesional skin and decrease in the systemic levels of IL-1α, eotaxin, CCL2 and CCL5. Moreover, transcriptional profiling demonstrated that 7.5 mg/kg 6B12 also modulated several profibrotic and proinflammatory processes relevant to the pathogenesis of SSc. CONCLUSION: Targeting S100A4 by the 6B12 mAb demonstrated potent antifibrotic and anti-inflammatory effects on bleomycin-induced dermal fibrosis and provided further evidence for the vital role of S100A4 in the pathophysiology of SSc.
1st Faculty of Medicine Charles University Prague Czech Republic
Agiana Pharmaceuticals Oslo Norway
Department of Rheumatology 1st Faculty of Medicine Charles University Prague Czech Republic
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