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iNKT-cell responses to glycolipids.

Abstract
Invariant natural killer T (iNKT) cells are an unusual group of T lymphocytes that recognize glycolipid antigens presented by the major histocompatibility complex class I-related protein CD1d. Because iNKT cells play a regulatory role in the immune system, they are attractive targets for immunotherapy. The marine-sponge-derived glycolipid alpha-galactosylceramide (alpha-GalCer) potently activates iNKT cells. In vivo administration of alpha-GalCer to mice or humans results in rapid and robust cytokine secretion by iNKT cells, followed by the activation of a variety of cell types of the innate and adaptive immune systems. These potent immunomodulatory activities of alpha-GalCer are being exploited for therapeutic purposes. Preclinical studies in mice have demonstrated that alpha-GalCer and related glycolipids can protect mice against a variety of diseases, including cancer, infections, and several autoimmune and inflammatory conditions. Although alpha-GalCer treatment of mice is associated with unwanted side-effects, it has been proven safe in clinical trials with cancer patients. These studies have raised significant enthusiasm for the development of effective and safe iNKT-cell-based immunotherapies for a variety of human diseases.
AuthorsVrajesh V Parekh, Michael T Wilson, Luc Van Kaer
JournalCritical reviews in immunology (Crit Rev Immunol) Vol. 25 Issue 3 Pg. 183-213 ( 2005) ISSN: 1040-8401 [Print] United States
PMID16048435 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, U.S. Gov't, P.H.S., Review)
Chemical References
  • Antigens, CD1
  • Galactosylceramides
  • Glycolipids
  • alpha-galactosylceramide
Topics
  • Animals
  • Antigens, CD1 (analysis)
  • Autoimmune Diseases (drug therapy)
  • Carbohydrate Sequence
  • Galactosylceramides (immunology)
  • Glycolipids (immunology)
  • Humans
  • Infections (drug therapy)
  • Inflammation (drug therapy)
  • Killer Cells, Natural (immunology)
  • Mice
  • Molecular Sequence Data
  • Molecular Structure
  • Neoplasms (drug therapy)
  • T-Lymphocyte Subsets (immunology)

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