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Journal of Virology, July 2001, p. 5939-5948, Vol. 75, No. 13
0022-538X/01/$04.00+0   DOI: 10.1128/JVI.75.13.5939-5948.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.

Immunogenicity and Protective Efficacy of Recombinant Human T-Cell Leukemia/Lymphoma Virus Type 1 NYVAC and Naked DNA Vaccine Candidates in Squirrel Monkeys (Saimiri sciureus)

Mirdad Kazanji,1,2,* James Tartaglia,3,4 Genoveffa Franchini,5 Benoit de Thoisy,6 Antoine Talarmin,1 Hugues Contamin,6 Antoine Gessain,2 and Guy de Thé2

Laboratoire de Rétrovirologie1 and Centre de Primatologie,6 Institut Pasteur de la Guyane, Cayenne, French Guiana; Unité d'Oncologie Virale, Institut Pasteur, Paris, France2; Aventis-Pasteur, Toronto, Ontario, Canada3; Virogenetics Corporation, Troy, New York4; and Division of Basic Sciences, National Cancer Institute, National Institutes of Health, Bethesda, Maryland5

Received 12 June 2000/Accepted 30 March 2001

We assessed the immunogenicities and efficacies of two highly attenuated vaccinia virus-derived NYVAC vaccine candidates encoding the human T-cell leukemia/lymphoma virus type 1 (HTLV-1) env gene or both the env and gag genes in prime-boost pilot regimens in combination with naked DNA expressing the HTLV-1 envelope. Three inoculations of NYVAC HTLV-1 env at 0, 1, and 3 months followed by a single inoculation of DNA env at 9 months protected against intravenous challenge with HTLV-1-infected cells in one of three immunized squirrel monkeys. Furthermore, humoral and cell-mediated immune responses against HTLV-1 Env could be detected in this protected animal. However, priming the animal with a single dose of env DNA, followed by immunization with the NYVAC HTLV-1 gag and env vaccine at 6, 7, and 8 months, protected all three animals against challenge with HTLV-1-infected cells. With this protocol, antibodies against HTLV-1 Env and cell-mediated responses against Env and Gag could also be detected in the protected animals. Although the relative superiority of a DNA prime-NYVAC boost regimen over addition of the Gag component as an immunogen cannot be assessed directly, our findings nevertheless show that an HTLV-1 vaccine approach is feasible and deserves further study.


* Corresponding author. Mailing address: Laboratoire de Rétrovirologie, Institut Pasteur de la Guyane, B.P. 6010, 23 Av. Pasteur, 97306 Cayenne, French Guiana. Phone: 0594 29 68 44. Fax: 0594 30 94 16. E-mail: mkazanji{at}pasteur-cayenne.fr.


Journal of Virology, July 2001, p. 5939-5948, Vol. 75, No. 13
0022-538X/01/$04.00+0   DOI: 10.1128/JVI.75.13.5939-5948.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.



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