Construction and Characterization of Recombinant Poliovirus that Delivers T-cell epitope

T-cell Epitope을 운반할 수 있는 재조합소아마비바이러스 벡터의 제조 및 특성연구

  • Cho, Seong-Pil (Eukaryotic Gene Expression Lab, Mogam Biotechnology Research Institute) ;
  • Lee, Bum-Young (Eukaryotic Gene Expression Lab, Mogam Biotechnology Research Institute) ;
  • Chung, Soo-Il (Eukaryotic Gene Expression Lab, Mogam Biotechnology Research Institute) ;
  • Min, Mi-Kyung (Eukaryotic Gene Expression Lab, Mogam Biotechnology Research Institute)
  • 조성필 (목암 생명공학 연구소 고등생물유전자발현실) ;
  • 이범용 (목암 생명공학 연구소 고등생물유전자발현실) ;
  • 정수일 (목암 생명공학 연구소 고등생물유전자발현실) ;
  • 민미경 (목암 생명공학 연구소 고등생물유전자발현실)
  • Published : 1998.06.30

Abstract

Recombinant polioviruses have been developed by many research groups for use as vaccine vector because poliovirus induces mucosal immunity as well as humoral immunity through oral uptake. We assessed the potential use of poliovirus as a T-cell epitope carrier. Recombinant poliovirus V129 5L was constructed to have a substituted T-helper epitope from the core protein of Hepatitis B virus at neutralization antigenic site 1 on its VP1 capsid protein. The recombinant virus replicated less efficiently than type 1 poliovirus Mahoney strain. The V129 5L formed a little smaller plaques than the Mahoney strain and showed some 1.25 log unit lower titer at the peak in the one-step growth kinetics though it had similar growth profile to that of the Mahoney strain. Since V129 5L recombinant virus was genetically stable even after 24 successive passages in HeLa cells, the antigenic site 1 on VP1 capsid protein was confirmed for its ability of carrying T cell epitope. The genetic stability of V129 5L also indicated that recombinant poliovirus can be successfully utilized for the development of the multivalent vaccines.

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