T-cell-targeted biologicals for psoriasis

    Research output: Contribution to journalArticlepeer-review

    Abstract

    Psoriasis is now accepted as a T-cell-mediated disease and that targeting of T cell function and/or trafficking is a logical approach to therapy. As a consequence of recombinant DNA technologies biologic therapies are synthesisable in sufficient quantities for clinical use. The original proof of concept for T-cell-targeted therapies in psoriasis came with the demonstration that anti-CD4 monoclonal antibodies were effective. Progress is such that two T-cell-directed biologicals - alefacept and efalizumab - have recently been approved in the U.S.A. for the treatment of psoriasis. In addition to providing new therapies the T-cell-targeted biologicals with their selective approach can be used as sophisticated tools to dissect out and help our understanding of key pathomechanisms in psoriasis; the non - efficacy of anti - E-selectin is a case in point. It is likely that the most appropriate place for T-cell-directed biologicals in the management of chronic plaque psoriasis will be for maintenance, rather than induction, of remission. This is a reflection of mode of action and relative safety for long-term administration. © 2004 Bentham Science Publishers Ltd.
    Original languageEnglish
    Pages (from-to)157-161
    Number of pages4
    JournalCurrent Drug Targets: Inflammation and Allergy
    Volume3
    Issue number2
    DOIs
    Publication statusPublished - Jun 2004

    Keywords

    • Alefacept
    • Anti-CD25
    • Anti-CD28
    • Anti-CD4
    • E-selectin
    • Efalizumab

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