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Vaccine strategies against Epstein-Barr virus-associated diseases: lessons from studies on cytotoxic T-cell-mediated immune regulation.

Abstract
Development of a vaccine against Epstein-Barr virus (EBV) is constrained by the latency phenotypes adopted by different EBV-associated diseases. Over the last few years an immense body of information on the pattern of viral gene expression in EBV-associated diseases and the role of cytotoxic T cells in the control of these diseases has accumulated. It would seem reasonable to suggest that emerging technologies are at a level where vaccine trials aimed at controlling infectious mononucleosis, post-transplant lymphoproliferative disease, nasopharyngeal carcinoma and Hodgkin's disease are justified. On the other hand, a more cautious approach may be required for the development of vaccines or immunotherapeutic strategies against Burkitt's lymphoma.
AuthorsR Khanna, D J Moss, S R Burrows
JournalImmunological reviews (Immunol Rev) Vol. 170 Pg. 49-64 (Aug 1999) ISSN: 0105-2896 [Print] England
PMID10566141 (Publication Type: Journal Article, Review)
Chemical References
  • Antigens, Viral
  • Viral Vaccines
Topics
  • Animals
  • Antigens, Viral
  • Burkitt Lymphoma (immunology, therapy)
  • Disease Models, Animal
  • Epstein-Barr Virus Infections (immunology, prevention & control, virology)
  • Herpesvirus 4, Human (genetics, immunology, pathogenicity)
  • Humans
  • Immunotherapy
  • Infant, Newborn
  • Infectious Mononucleosis (immunology, prevention & control)
  • Mice
  • Phenotype
  • Primates
  • T-Lymphocytes, Cytotoxic (immunology)
  • Viral Vaccines (pharmacology)

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