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Harnessing regulatory T cells for therapeutic purposes.

Abstract
Lai and colleagues demonstrate that pretreatment with N,N-dimethylsphingosine (DMS), a naturally occurring sphingosine derivative, provides renoprotection in ischemia/reperfusion injury. This DMS-induced renoprotection was abolished by the administration of agents that suppress regulatory T cells (Tregs) or by anti-CTLA-4 or anti-CD45 monoclonal antibodies, suggesting that Tregs played a critical role. The finding that Tregs are recruited to the kidney via DMS points to the exciting potential of new approaches to harnessing Tregs for therapeutic purposes.
AuthorsLaurence Chan
JournalKidney international (Kidney Int) Vol. 81 Issue 10 Pg. 935-936 (May 2012) ISSN: 1523-1755 [Electronic] United States
PMID22543901 (Publication Type: Journal Article, Comment)
Chemical References
  • Immunologic Factors
  • N,N-dimethylsphingosine
  • Sphingosine
Topics
  • Acute Kidney Injury (prevention & control)
  • Animals
  • Chemotaxis, Leukocyte (drug effects)
  • Immunologic Factors (pharmacology)
  • Ischemia (drug therapy)
  • Kidney (drug effects)
  • Male
  • Reperfusion Injury (prevention & control)
  • Sphingosine (analogs & derivatives, pharmacology)
  • T-Lymphocytes, Regulatory (drug effects)

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