Efficacy and safety of Ramucirumab and methotrexate co-therapy in rheumatoid arthritis experimental model: Involvement of angiogenic and immunomodulatory signaling

Abdel-Maged, Amany E; Gad, Amany M; Wahdan, Sara; Azab, Samar S;

Abstract


Rheumatoid arthritis (RA) is a chronic and progressive autoimmune inflammatory disease associated with irreversible joint destruction that leads to permanent motor disability and compromised quality of life. However, the main cause of RA is still unknown though stimulation of immune system and cells plays pivotal role in disease development and progression. Ramucirumab (RAM) is the monoclonal antibody against VEGF- receptor. This study aimed to investigate and evaluate the therapeutic effect of RAM with or without Methotrexate (MTX) against adjuvant-induced arthritis in rats. Complete Freund's adjuvant (CFA)-induced arthritic rats were treated for three consecutive weeks with MTX or RAM alone and MTX-RAM co-therapy. Arthritic score, gait score, ankle diameter, paw thickness, angiogenic, inflammatory cytokines, bone erosion markers, and apoptotic markers were assessed to evaluate the anti-arthritic effect. RAM monotherapy exhibited anti-inflammatory, anti-angiogenic and anti-apoptotic effects similar to MTX alone to treat RA in the current study. Furthermore, RAM alone had a protective effect on bone and cartilage health better than standard anti-rheumatic agent MTX. Interestingly, combined therapy of MTX and RAM produced significant differences in comparison with MTX or RAM monotherapy in all tested parameters. Moreover, the current study proved that MTX-RAM co-therapy has a synergistic effect.


Other data

Title Efficacy and safety of Ramucirumab and methotrexate co-therapy in rheumatoid arthritis experimental model: Involvement of angiogenic and immunomodulatory signaling
Authors Abdel-Maged, Amany E; Gad, Amany M; Wahdan, Sara ; Azab, Samar S
Keywords Adjuvant Induced Arthritis;Immune Response;Ramucirumab;Rats
Issue Date 2019
Publisher ACADEMIC PRESS INC ELSEVIER SCIENCE
Journal Toxicology and applied pharmacology 
Volume 380
ISSN 0041-008X
DOI 10.1016/j.taap.2019.114702
PubMed ID 31398424
Scopus ID 2-s2.0-85070860320
Web of science ID WOS:000484646100015

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Citations 5 in pubmed
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