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ESAT-6-gpi DNA vaccine augmented the specific antitumour efficacy induced by the tumour vaccine B16F10-ESAT-6-gpi/IL-21 in a mouse model.

Abstract
In this study, we hypothesized that the mice immunized with the glycosylphosphatidylinositol (GPI) anchored 6-kDa early-secreted antigenic target (ESAT-6) DNA vaccine (ESAT-6-gpi) and the tumour vaccine B16F10-ESAT-6-gpi/IL-21 might significantly enhance immune responses and antimelanoma efficacy. Our experimental results indicated that the anti-ESAT-6 antibody induced by the DNA vaccine ESAT-6-gpi bound ESAT-6 to the surface of tumour vaccine to activate a complement classical pathway and resulted in the B16F10 tumour cell lysis and apoptosis, which served as a potential trigger for breaking melanomatous immune tolerance to elicit an initiation of natural antimelanoma immunity. Our innovative approach of using the DNA vaccine ESAT-6-gpi priming and the tumour vaccine B16F10-ESAT-6-gpi/IL-21 boosting induced strong antimelanoma immunity that inhibited melanomatous growth. These findings highlighted the DNA vaccine ESAT-6-gpi as an immune enhancer to augment the immune efficacy of the tumour vaccine B16F10-ESAT -6-gpi/IL-21 against melanoma in a mouse model.
AuthorsX He, J Wang, F Zhao, D Chen, J Chen, H Zhang, C Yang, Y Liu, J Dou
JournalScandinavian journal of immunology (Scand J Immunol) Vol. 78 Issue 1 Pg. 69-78 (Jul 2013) ISSN: 1365-3083 [Electronic] England
PMID23679337 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Copyright© 2013 John Wiley & Sons Ltd.
Chemical References
  • Antigens, Bacterial
  • Bacterial Proteins
  • Cancer Vaccines
  • ESAT-6 protein, Mycobacterium tuberculosis
  • Glycosylphosphatidylinositols
  • Interleukins
  • Vaccines, DNA
  • plasmanylinositol glycan
  • interleukin-21
Topics
  • Animals
  • Antigens, Bacterial (immunology)
  • Bacterial Proteins (immunology)
  • Cancer Vaccines (immunology)
  • Cell Line, Tumor
  • Glycosylphosphatidylinositols (administration & dosage)
  • Immunization
  • Interleukins (immunology)
  • Melanoma, Experimental (therapy)
  • Mice
  • Mice, Inbred C57BL
  • Vaccines, DNA (immunology)

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