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Journal of Virology, March 2002, p. 2676-2682, Vol. 76, No. 6
0022-538X/02/$04.00+0 DOI: 10.1128/JVI.76.6.2676-2682.2002
Copyright © 2002, American Society for Microbiology. All Rights Reserved.
Improving DNA Vaccine Potency by Linking Marek's Disease Virus Type 1 VP22 to an Antigen
Chien-Fu Hung,1 Liangmei He,1 Jeremy Juang,1 Tzyy-Jye Lin,1 Morris Ling,1 and T.-C. Wu1,2,3,4*
Pathology,1
Oncology,2
Obstetrics and Gynecology,3
Molecular Microbiology and Immunology, The Johns Hopkins Medical Institutions, Baltimore, Maryland 212054
Received 17 September 2001/
Accepted 13 December 2001
We have previously employed an intercellular spreading strategy using herpes simplex virus type 1 (HSV-1) VP22 protein to enhance DNA vaccine potency because DNA vaccines lack the intrinsic ability to amplify in cells. Recently, studies have demonstrated that the protein encoded by UL49 of Marek's disease virus type 1 (MDV-1) exhibits some degree of homology to the HSV-1 VP22 protein and features the property of intercellular transport. We therefore generated a DNA vaccine encoding MDV-1 VP22 linked to a model antigen, human papillomavirus type 16 E7. We demonstrated that compared with mice vaccinated with DNA encoding wild-type E7, mice vaccinated with MDV-1 VP22/E7 DNA exhibited a significant increase in number of gamma-interferon-secreting, E7-specific CD8+-T-cell precursors as well as stronger tumor prevention and treatment effects. Furthermore, our data indicated that the antitumor effect was CD8 dependent. These results suggested that the development of vaccines encoding VP22 fused to a target antigen might be a promising strategy for improving DNA vaccine potency.
* Corresponding author. Mailing address: Department of Pathology, The Johns Hopkins University School of Medicine, Ross Research Building, Room 659, 720 Rutland Ave., Baltimore, MD 21205. Phone: (410) 614-3899. Fax: (410) 614-3548. E-mail:
wutc{at}jhmi.edu.
Journal of Virology, March 2002, p. 2676-2682, Vol. 76, No. 6
0022-538X/02/$04.00+0 DOI: 10.1128/JVI.76.6.2676-2682.2002
Copyright © 2002, American Society for Microbiology. All Rights Reserved.
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