| Literature DB >> 27449502 |
Roberta Fenoglio1, Carla Naretto1, Bruno Basolo1, Giacomo Quattrocchio1, Michela Ferro1, Paola Mesiano1, Giulietta Beltrame1, Dario Roccatello2.
Abstract
Henoch-Schonlein purpura, also called IgA-vasculitis, is a systemic small vessels vasculitis with immunoglobulin A1-dominant immune deposits. The optimal treatment remains controversial. Because IgA-vasculitis is characterized by leukocyte infiltration of the blood vessel walls along with immunoglobulin A deposition, and because glucocorticosteroids inhibit inflammatory processes, early administration of glucocorticosteroids has been postulated to be effective, but this indication remains controversial. Immunosuppressive agents (azathioprine, cyclophosphamide, cyclosporine, mycophenolate) have been used in combination with glucocorticosteroids without definitive evidence of effectiveness. The efficacy of rituximab in adult IgA-vasculitis has been reported in few cases. We described a monocentric experience on the use of rituximab in adult IgA-vasculitis with biopsy-proven nephritis. The patients achieved a complete remission of nephritis and syndromic manifestations, and no patients experienced adverse reactions. These data have been compared with the limited literature nowadays available.Entities:
Keywords: ANCA-associated vasculitis; B cell depletion therapy; Henoch–Schonlein purpura nephritis; Henoch–Schonlein treatment; IgA-vasculitis; Rituximab
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Year: 2017 PMID: 27449502 DOI: 10.1007/s12026-016-8827-5
Source DB: PubMed Journal: Immunol Res ISSN: 0257-277X Impact factor: 2.829