VP22 enhances antibody responses from DNA vaccines but not by intercellular spread


Perkins, Stuart D., Hartley, M. Gill, Lukaszewski, Roman A., Phillpotts, Robert J., Stevenson, Freda. K. and Bennett, Alice M. (2005) VP22 enhances antibody responses from DNA vaccines but not by intercellular spread. Vaccine, 23, (16), 1931-1940. (doi:10.1016/j.vaccine.2004.10.033).

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Description/Abstract

In some species DNA vaccines elicit potent humoral and cellular immune responses. However, their performance in humans and non-human primates is less impressive. There are suggestions in the literature that an increase in the intercellular distribution of protein expressed from a DNA vaccine may enhance immunogenicity. We incorporated the Herpes Simplex Virus type 1 (HSV) VP22 gene, which encodes a protein that has been described as promoting intercellular spread, into a DNA vector in which it was fused to enhanced green fluorescent protein (EGFP). Following transfection of the plasmid DNA into mammalian cells, distribution of the fusion protein VP22-EGFP was not increased compared to EGFP alone. Furthermore, we found no evidence to suggest that VP22 was capable of mediating intercellular spread. However, when these constructs were used as DNA vaccines to immunise mice, antibody levels specific to EGFP were significantly enhanced when EGFP was fused to VP22. These data suggest that amplification of the immune response may occur via mechanisms other than VP22-mediated intercellular spread of antigen.

Item Type: Article
ISSNs: 0264-410X (print)
Related URLs:
Keywords: DNA vaccine, VP22, intercellular spread, protein transduction domain, GFP
Subjects: R Medicine > RA Public aspects of medicine > RA0421 Public health. Hygiene. Preventive Medicine
Divisions: University Structure - Pre August 2011 > School of Medicine > Cancer Sciences
ePrint ID: 26520
Date Deposited: 10 Apr 2006
Last Modified: 27 Mar 2014 18:15
Contact Email Address: sdperkins@dstl.gov.uk
URI: http://eprints.soton.ac.uk/id/eprint/26520

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