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The most recent version of this article was published on 1 October 2008

Ann Rheum Dis. Published Online First: 24 August 2007. doi:10.1136/ard.2007.076745
Copyright © 2007 BMJ Publishing Group Ltd & European League Against Rheumatism.

Review Article

The B cell in systemic lupus erythematosus: a rational target for more effective therapy

D B Driver 1, M Ishimori 1 and M H Weisman 1*

1 Cedars-Sinai Medical Center, United States

* To whom correspondence should be addressed. E-mail: weisman{at}cshs.org.

Accepted 8 August 2007


Abstract

Current treatment options for systemic lupus erythematosus (SLE) are diverse and poorly defined, and aggressive therapy can be associated with serious toxicity and tolerability issues. There is, therefore, a need for new and improved treatments to be studied thoroughly in well-designed controlled trials. B-cell dysfunction has emerged as a key pathophysiological component of SLE and is a prime target for the development of new agents for a wide range of lupus severity, including advanced disease. Although many current drugs appear to modify B-cell function, the advent of new targeted therapies offers the hope of improved efficacy and a better long-term tolerability profile.

Keywords: B-cells, pathogenesis, systemic lupus erythematosus


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This article has been cited by other articles:

  • Ramos-Casals, M, Soto, M., Cuadrado, M., Khamashta, M. (2009). Rituximab in systemic lupus erythematosusA systematic review of off-label use in 188 cases. Lupus 18: 767-776 [Abstract]  

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