Literature DB >> 22236448

Treatment of systemic lupus erythematosus: new advances in targeted therapy.

Mindy S Lo1, George C Tsokos.   

Abstract

Treatment for systemic lupus erythematosus (SLE) has traditionally been restricted to broad-based immunosuppression, with glucocorticoids being central to care. Recent insights into lupus pathogenesis promise new, selective therapies with more favorable side effect profiles. The best example of this is belimumab, which targets the B cell cytokine BLyS and has now received Food and Drug Administration (FDA) approval for its use in SLE. Strategies targeting other cytokines, such as interleukin 6 (IL-6) and interferon (IFN)-α, are also on the horizon. Blockade of costimulatory interactions between immune cells offers another opportunity for therapeutic intervention, as do small molecule inhibitors that interfere with cell signaling pathways. We review here the current strategies for SLE treatment, with particular focus on therapies now in active pharmaceutical development. We will also discuss new understandings in lupus pathogenesis that may lead to future advances in therapy.
© 2012 New York Academy of Sciences.

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Year:  2012        PMID: 22236448     DOI: 10.1111/j.1749-6632.2011.06263.x

Source DB:  PubMed          Journal:  Ann N Y Acad Sci        ISSN: 0077-8923            Impact factor:   5.691


  13 in total

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4.  Retinoic acid-producing, ex-vivo-generated human tolerogenic dendritic cells induce the proliferation of immunosuppressive B lymphocytes.

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Authors:  Guo-Min Deng; George C Tsokos
Journal:  Nat Rev Rheumatol       Date:  2015-08-04       Impact factor: 20.543

Review 8.  The pathogenesis of systemic lupus erythematosus-an update.

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Journal:  Curr Opin Immunol       Date:  2012-11-03       Impact factor: 7.486

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Journal:  Arthritis Res Ther       Date:  2012-11-08       Impact factor: 5.156

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Journal:  Arthritis Res Ther       Date:  2013-02-27       Impact factor: 5.156

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