4.5 Article

PKC inhibitors: potential in T cell-dependent immune diseases

期刊

CURRENT OPINION IN CELL BIOLOGY
卷 21, 期 2, 页码 262-267

出版社

CURRENT BIOLOGY LTD
DOI: 10.1016/j.ceb.2008.12.008

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资金

  1. FWF Austrian Science Fund [SFB-021, P1119.50.5-1305]
  2. Tyrolian Science Fund [TWF-2008-1-563]
  3. OeNB Austrian National Bank [12196]
  4. European Community [HEALTH-F4-2008-201106]

向作者/读者索取更多资源

The basic mechanisms of serine/threonine protein kinase signaling networks have been elucidated in the past decade. Members of the protein kinase C (PKC) family are crucial in T cell signaling pathways. Particularly, PIKC alpha, PKC beta, and PKC theta isotypes determine the nature of lymphocyte-specific in vivo effector responses. Therefore, PKC isotypes are validated drug targets in adaptive immunity. Selective PKC kinase inhibitors have been discovered and are currently in clinical development, where they may provide new therapeutic options for different immune disorders. Here we review the topic of PKC pathway activity in the regulation of T lymphocytes both in the cytokine response and adhesive capacity, and review recent results with PKC inhibitors in vitro and in vivo.

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