| Literature DB >> 30874446 |
Tomohiro Koga1,2, Kunihiro Ichinose1, Atsushi Kawakami1, George C Tsokos3.
Abstract
INTRODUCTION: Systemic lupus erythematosus (SLE) is an autoimmune disease characterized by autoantibodies production and immune complex deposition with systemic clinical manifestations. Interleukin (IL)-17-producing cells play a crucial role in disease pathogenesis and represent an attractive therapeutic target. Areas covered: This review provides an update on the possibility of targeting IL-17 in SLE. The rational for this approach as well as currently available and future targets are discussed. Expert opinion: Although human expression studies and animal models indicate that IL-17 blocking may be a promising therapeutic strategy for SLE, direct evidence for IL-17 inhibition in SLE patients is unavailable. Biologic therapies and small-molecule drugs that target IL-17 production are required for the achievement of a favorable clinical effect in SLE patients.Entities:
Keywords: T cells; immune responses; interleukin (IL)-17; lupus nephritis; systemic lupus erythematosus (SLE)
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Year: 2019 PMID: 30874446 DOI: 10.1080/1744666X.2019.1593141
Source DB: PubMed Journal: Expert Rev Clin Immunol ISSN: 1744-666X Impact factor: 4.473