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2000
Volume 2, Issue 1
  • ISSN: 1573-3955
  • E-ISSN: 1875-631X

Abstract

Recent advances in our understanding of the mechanisms through which T cells are activated have led to new therapeutic approaches in the treatment of immunological disorders. An emerging target for selective immune intervention has been the manipulation of T cell costimulatory pathways. Impressive results in animal models have shown that the tumor-necrosis-factor receptor (TNFR) family member, OX40 (CD134), and its binding partner OX40L, are key costimulatory molecules involved in the regulation of many T cell mediated immune disorders. In this review we will highlight these new findings with a particular emphasis on their potential implications for immunotherapy of human disease.

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/content/journals/cir/10.2174/157339506775471884
2006-02-01
2025-09-05
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/content/journals/cir/10.2174/157339506775471884
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  • Article Type:
    Research Article
Keyword(s): allergy; autoimmunity; cancer; immunotherapy; OX40; OX40L; T cells; transplantation; viruses
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