| Literature DB >> 26466969 |
Lazaro E Aira1, Patricia Hernández1, Dinorah Prada2, Araceli Chico3, Jorge A Gómez2, Zuyén González1, Karla Fuentes1, Carmen Viada1, Zaima Mazorra1.
Abstract
Rheumatoid arthritis is an autoimmune disease characterized by joint inflammation that affects approximately 1% of the general population. Itolizumab, a monoclonal antibody specific for the human CD6 molecule mainly expressed on T lymphocytes, has been shown to inhibit proliferation of T cells and proinflammatory cytokine production in psoriasis patients. We have now assessed the immunological effect of itolizumab in combination with methotrexate in rheumatoid arthritis by analyzing clinical samples taken from 30 patients enrolled in a clinical trial. T and B cell subpopulations were measured at different time points of the study. Plasma cytokine levels and anti-idiotypic antibody response to itolizumab were also evaluated. The combined treatment of itolizumab and methotrexate led to a reduction in the frequency of T cell subpopulations, and plasma levels of proinflammatory cytokines showed a significant decrease up to at least 12 weeks after treatment ended. No anti-idiotypic antibody response was detected. These results support the relevance of the CD6 molecule as a therapeutic target for the treatment of this disease.Entities:
Keywords: anti-idiotypic antibody response; itolizumab; peripheral lymphocytic counts; proinflammatory cytokines; rheumatoid arthritis
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Year: 2015 PMID: 26466969 PMCID: PMC4966522 DOI: 10.1080/19420862.2015.1105416
Source DB: PubMed Journal: MAbs ISSN: 1942-0862 Impact factor: 5.857