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ABSTRACT: Objectives
SLE is a severe autoimmune disease characterized by autoreactive B cells and IC formation, which causes systemic inflammation. B cell-targeted therapy could be a promising treatment strategy in SLE patients; nevertheless, randomized clinical trials have not always been successful. However, some groups have demonstrated beneficial effects in severe SLE patients with off-label rituximab (RTX) with belimumab (BLM), or bortezomib (BTZ), which targeted different B cells subsets. This study assembled sera from SLE cohorts treated with RTX+BLM (n = 15), BTZ (n = 11) and RTX (n = 16) to get an in-depth insight into the immunological effects of these therapies on autoantibodies and IC formation.Methods
Autoantibodies relevant for IC formation and the avidity of anti-dsDNA
SUBMITTER: van Dam LS
PROVIDER: S-EPMC7516125 | biostudies-literature | 2020 Oct
REPOSITORIES: biostudies-literature