HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Multiple roles for CD4+ T cells in anti-tumor immune responses.

Abstract
Our understanding of the importance of CD4+ T cells in orchestrating immune responses has grown dramatically over the past decade. This lymphocyte family consists of diverse subsets ranging from interferon-gamma (IFN-gamma)-producing T-helper 1 (Th1) cells to transforming growth factor-beta (TGF-beta)-secreting T-regulatory cells, which have opposite roles in modulating immune responses to pathogens, tumor cells, and self-antigens. This review briefly addresses the various T-cell subsets within the CD4+ T-cell family and discusses recent research efforts aimed at elucidating the nature of the 'T-cell help' that has been shown to be essential for optimal immune function. Particular attention is paid to the role of Th cells in tumor immunotherapy. We review some of our own work in the field describing how CD4+ Th cells can enhance anti-tumor cytotoxic T-lymphocyte (CTL) responses by enhancing clonal expansion at the tumor site, preventing activation-induced cell death and functioning as antigen-presenting cells for CTLs to preferentially generate immune memory cells. These unconventional roles for Th lymphocytes, which require direct cell-to-cell communication with CTLs, are clear examples of how versatile these immunoregulatory cells are.
AuthorsRichard Kennedy, Esteban Celis
JournalImmunological reviews (Immunol Rev) Vol. 222 Pg. 129-44 (Apr 2008) ISSN: 1600-065X [Electronic] England
PMID18363998 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Review)
Chemical References
  • Cancer Vaccines
  • Epitopes, T-Lymphocyte
Topics
  • Animals
  • CD4-Positive T-Lymphocytes (immunology)
  • Cancer Vaccines
  • Cytotoxicity, Immunologic
  • Epitopes, T-Lymphocyte (immunology)
  • Humans
  • Immunity, Cellular
  • Immunity, Innate
  • Immunologic Memory
  • Immunotherapy
  • Killer Cells, Natural (immunology)
  • Mice
  • Models, Immunological
  • Neoplasms (immunology, pathology, therapy)
  • T-Lymphocyte Subsets (immunology)
  • T-Lymphocytes, Regulatory (immunology)
  • Th1 Cells (immunology)
  • Th2 Cells (immunology)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: