The role of CD40 ligand in systemic lupus erythematosus

Author:

Yazdany J1,Davis J2

Affiliation:

1. Division of Rheumatology, University of California San Francisco, San Francisco, USA

2. Division of Rheumatology, University of California San Francisco, San Francisco, USA,

Abstract

CD40 ligand (CD40L, also known as CD154 or gp39) is a member of the tumor necrosis superfamily of transmembrane proteins. The interaction of CD40L on activated T cells with its receptor, CD40 on B cells, is necessary for normal immune function, including B cell differentiation, germinal center formation, and antibody isotype switching. Abnormal expressionof CD40L in patients with systemic lupus erythematosus (SLE) may contribute to autoantibody production and disease pathogenesis. Although murine models of monoclonal antibodies directed against CD40L initially showed promise, human trials either have failed to demonstrate efficacy or have been associated with adverse events. This review will summarize in vitro and murine model data and human clinical trials involving anti-CD40L monoclonal antibody.

Publisher

SAGE Publications

Subject

Rheumatology

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