Chimeric hepatitis A vaccine

Drug – bio-affecting and body treating compositions – Antigen – epitope – or other immunospecific immunoeffector – Virus or component thereof

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4242041, 4242051, 4242251, 4352351, 4352361, 435237, 435320, 536 231, A61K 3929, A61K 3912, C12N 700, C12N 704

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active

058372601

ABSTRACT:
A full-length cDNA copy of an attenuated, cell culture-adapted hepatitis-A virus genome has been constructed. The HAV cDNA when inserted, without the oligo (dG) oligo (dC) tails, into an RNA transcription vector yielded a plasmid designated pHAV/7. Transfection of monkey kidney cells with pHAV/7 DNA yielded HAV. Transfection with RNA transcripts produced in vitro from pHAV/7 yielded about 10-fold more HAV than transfection with pHAV/7 DNA. HAV thus produced are useful as a vaccine.

REFERENCES:
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Ticehurst, et al., (1983) Proc. Natl. Acad. Sci. USA 80:5885-5889.
Cohen, et al., (1987) Journal of Virology 61:50-59.
Cohen, et al., (1987) Proc. Natl. Acad. Sci. USA, 84:2497-2501.
Provost et al. (A) Proc. Soc. Exp. Bio. Med., 170:8-14, 1982.
Provost et al. (B) Proc. Soc. Exp. Bio. Med., 172:357-363, 1983.
Fienstone et al., Develop. Biol. Stano., 54:429-432, 1983.
Ticehurst et al., PNAS USA, 80:5885-5889, Oct. 1983.
Provost et al. (D) Proc. Soc. Exp. Bio. Med., 159:201-203, 1978.

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