The objective of this project is to develop a safe, efficacious single dose live attenuated vaccine for prevention of disease in humans caused by dengue virus. A chimeric YF/dengue2 virus (YF/Den2) was constructed using a recombinant cDNA infectious clone of the yellow fever (YF17D) vaccine strain as a backbone into which the premembrane (prM) and envelope (E) genes of a human isolate (PUO218) of dengue-2 virus were inserted. Viruses were recovered upon transfection of Vero cells with mRNA and amplified twice in these cells to yield a titer of 6.3 log(10p)fu/ml. This strategy has been successfully applied for construction of an attenuated chimeric YF-Japanese encephalitis vaccine which is currently in manufacturing. The YF/Den2 virus grows to high titers in acceptable cell lines for human use. In this research project the YF/Den2 chimeric virus will be evaluated in vitro and in vivo. At the completion of this study it will be determined if the chimeric YF/Den2 virus is sufficiently attenuated/immunogenic to be considered as a vaccine candidate for human use. In addition, information obtained from this work will be used to select proper starins (attentuated or wild type) for other 3 dengue serotypes (1,3 and 4) to produce a tetravalent vaccine against all 4 serotypes.

Proposed Commercial Applications

Dengue virus is a world-wide public health problem. Over 2 billion persons are at risk of dengue infection and 100 million cases of primary dangue fever and over 450,000 cases of dengue haemorrhagic fever occurs annually. Currently no vaccine available. The vaccine made through this project has a large market potential (> $300 mm/year) and can e used for traveler and military in the US, Europe, Japan, Australia as well as for routine childhood immunization in dengue epidemic/endemic countries.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Small Business Innovation Research Grants (SBIR) - Phase I (R43)
Project #
1R43AI044565-01
Application #
2792872
Study Section
Special Emphasis Panel (ZRG2-SSS-4 (02))
Program Officer
Meegan, James M
Project Start
1999-09-30
Project End
2000-03-31
Budget Start
1999-09-30
Budget End
2000-03-31
Support Year
1
Fiscal Year
1999
Total Cost
Indirect Cost
Name
Acambis, Inc.
Department
Type
DUNS #
City
Cambridge
State
MA
Country
United States
Zip Code
02139
Guirakhoo, F; Weltzin, R; Chambers, T J et al. (2000) Recombinant chimeric yellow fever-dengue type 2 virus is immunogenic and protective in nonhuman primates. J Virol 74:5477-85
Foo, S Y; Nolan, G P (1999) NF-kappaB to the rescue: RELs, apoptosis and cellular transformation. Trends Genet 15:229-35
Nolan, G P; Shatzman, A R (1998) Expression vectors and delivery systems. Curr Opin Biotechnol 9:447-50