Abstract

Background The treatment of systemic sclerosis (SSc) is a clinical challenge because of its complex pathogenesis. The rationale for the use of rituximab (RTX), able to downregulate the B-cell over expression, is demonstrated in different autoimmune diseases, some reports have suggested its key role in regulating both vascular, fibrotic, and immune T- and B-lymphocyte-mediated alterations that characterize several SSc manifestations. According to our previous experience with RTX [1], we suggested a possible therapeutical role of RTX in SSc, along with its good safety profile. Objectives To investigate the role and efficacy of RTX in our SSc patients’ series. Methods A series of 24 SSc patients (M/F 7/17, mean age 55.2±14.7SD years, mean disease duration 11.7± 7.3SD years, L/D cutaneous subsets 11/13) were treated with one or more cycles of RTX (4 weekly infusions of 375 mg/m2) and evaluated during a mean follow-up period of 12.3 ± 6.6SD years, range 2-26 years. The indications to RTX were interstitial lung disease, cutaneous, articular manifestations, evaluating its effects after 6 months of the first cycle and at the end of follow-up. Results After the first 6 months the extent of skin sclerosis measured with modified Rodnan skin score (mRSS) significantly improved (from 16.3±9.8 to 12.3±7.1; p Conclusion The present study reinforces the previous trials and our preliminary researches on this topic, showing the efficacy of RTX in the management of SSc with good safety profile. The specific therapeutical role of RTX on B-cell-driven autoimmunity, might explain its beneficial effects on some SSc clinical alterations. The improvement of skin sclerosis, articular symptoms and the stabilization of lung involvement were identified as the main results. Further exploration of the potential clinical efficacy of RTX in SSc with multicentre, double blind, controlled study is needed. Reference [1] Giuggioli D, et al. Rituximab in the treatment of patients with systemic sclerosis. Our experience and review of the literature. Autoimmun Rev. 2015;14(11):1072-8 Disclosure of Interests None declared

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