Tyrosine hydroxylase-based DNA-vaccination is effective against murine neuroblastoma

Med Pediatr Oncol. 2000 Dec;35(6):641-6. doi: 10.1002/1096-911x(20001201)35:6<641::aid-mpo34>3.0.co;2-r.

Abstract

Background: The disruption of self-tolerance against neuroblastoma is the ultimate goal of an effective DNA-vaccine.

Procedure: Here we demonstrate the induction of a protective immunity against syngeneic murine NXS2 neuroblastoma in A/J mice, following vaccination with tyrosine hydroxylase (TH) derived antigens. Oral gene delivery was accomplished using an attenuated strain of Salmonella typhimurium as a carrier harboring vectors encoding for mTH antigens.

Results: Vaccination was effective in protecting animals from a lethal challenge with wild-type NXS2 tumor cells.

Conclusions: These results provide the first evidence of the TH self antigen being recognized by T-cells and demonstrate that a TH-based DNA vaccine is a potentially useful immunotherapeutic strategy for neuroblastoma.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Gene Transfer Techniques
  • Mice
  • Neuroblastoma / immunology
  • Neuroblastoma / prevention & control*
  • Plasmids
  • Tyrosine 3-Monooxygenase* / genetics
  • Vaccines, DNA*

Substances

  • Vaccines, DNA
  • Tyrosine 3-Monooxygenase