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Expert Rev Clin Immunol ; 13(10): 925-938, 2017 10.
Artigo em Inglês | MEDLINE | ID: mdl-28847197

RESUMO

INTRODUCTION: Loss of B cell tolerance is a hallmark feature of the pathogenesis of Systemic Lupus Erythematosus (SLE). Recent advances in B cell therapy have focused on targeted therapy aimed at inhibiting B cell activation and reducing B cell survival. Belimumab, a human monoclonal antibody against B cell activating factor (BAFF) was licensed in 2011 for the treatment of SLE. Areas covered: We review the data on the intravenous and subcutaneous formulations of belimumab in the management of patients with SLE. BLISS-52 and BLISS-76 demonstrated the efficacy of intravenous belimumab (10mg/kg) as an add-on therapy in SLE patients with active disease. A recent phase III trial of intravenous belimumab reported similar results in North East Asian patients. Subcutaneous belimumab (200mg/weekly) has demonstrated similar efficacy, safety and tolerability and was approved by the FDA in 2017 for the treatment of active autoantibody positive SLE patients receiving standard therapy. Expert commentary: Belimumab is generally safe and well tolerated. The most common clinical manifestations of SLE in the clinical trials were arthritis, mucocutaneous disease and serositis. Patients with severe lupus nephritis and central nervous system disease were excluded from these clinical trials.


Assuntos
Anticorpos Monoclonais Humanizados/uso terapêutico , Imunoterapia/métodos , Lúpus Eritematoso Sistêmico/tratamento farmacológico , Administração Intravenosa , Artrite , Fator Ativador de Células B/antagonistas & inibidores , Fator Ativador de Células B/imunologia , Ensaios Clínicos como Assunto , Dermatite , Aprovação de Drogas , Prova Pericial , Humanos , Injeções Subcutâneas , Terapia de Alvo Molecular , Serosite
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