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2000
Volume 17, Issue 26
  • ISSN: 0929-8673
  • E-ISSN: 1875-533X

Abstract

Recent results using animal models of inflammatory skin conditions have shown that blockers of the voltage-gated potassium channel, Kv1.3 hold great promise for clinical utility. Kv1.3 blockers act as immunosuppressants by modulating the various subsets of inflammatory T and B cells involved in autoimmune disorders. While peptidic inhibitors based on naturally occurring venoms demonstrate potent and selective Kv1.3 blockade, these require parenteral administration and may face potential immunogenicity problems. Small molecule blockers show considerable diversity, however selectivity over other Kv1-family channels has been difficult to achieve. More recent advances have added to the evidence that Kv1.3 channels are a suitable therapeutic target and that the development of novel and selective agents will herald new drugs for inflammatory skin disorders.

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/content/journals/cmc/10.2174/092986710792065072
2010-09-01
2025-12-06
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/content/journals/cmc/10.2174/092986710792065072
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  • Article Type:
    Research Article
Keyword(s): autoimmune disorder; drug design; inflammation; Kv1.3 channel; Psoriasis
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