In vivo electroporation enhances the immunogenicity of an HIV-1 DNA vaccine candidate in healthy volunteers.
2011
Journal Article
Authors:
Vasan, S.;
Hurley, A.;
Schlesinger, S.J.;
Hannaman, D.;
Gardiner, D.F.;
Dugin, D.P.;
Boente-Carrera, M.;
Vittorino, R.;
Caskey, M.;
Andersen, J.;
Huang, Y.;
Cox, J.H.;
Tarragona-Fiol, T.;
Gill, D.K.;
Cheeseman, H.;
Clark, L.;
Dally, L.;
Smith, C.;
Schmidt, C.;
Park, H.H.;
Kopycinski, J.T.;
Gilmour, J.;
Fast, P.;
Bernard, R.;
Ho, D.D.
Secondary:
PLoS One
Volume:
6
Pagination:
e19252
Issue:
5
PMID:
21603651
DOI:
10.1371/journal.pone.0019252
Keywords:
Adolescent; Adult; AIDS Vaccines; Cytokines; Double-Blind Method; Electroporation; Female; HIV-1; Humans; Immunity, Cellular; Injections, Intramuscular; Male; Middle Aged; T-Lymphocytes; Vaccines, DNA; Young Adult
Abstract:
BACKGROUND: DNA-based vaccines have been safe but weakly immunogenic in humans to date.METHODS AND FINDINGS: We sought to determine the safety, tolerability, and immunogenicity of ADVAX, a multigenic HIV-1 DNA vaccine candidate, injected intramuscularly by in vivo electroporation (EP) in a Phase-1, double-blind, randomized placebo-controlled trial in healthy volunteers. Eight volunteers each received 0.2 mg, 1 mg, or 4 mg ADVAX or saline placebo via EP, or 4 mg ADVAX via standard intramuscular injection at weeks 0 and 8. A third vaccination was administered to eleven volunteers at week 36. EP was safe, well-tolerated and considered acceptable for a prophylactic vaccine. EP delivery of ADVAX increased the magnitude of HIV-1-specific cell mediated immunity by up to 70-fold over IM injection, as measured by gamma interferon ELISpot. The number of antigens to which the response was detected improved with EP and increasing dosage. Intracellular cytokine staining analysis of ELISpot responders revealed both CD4+ and CD8+ T cell responses, with co-secretion of multiple cytokines.CONCLUSIONS: This is the first demonstration in healthy volunteers that EP is safe, tolerable, and effective in improving the magnitude, breadth and durability of cellular immune responses to a DNA vaccine candidate.TRIAL REGISTRATION: ClinicalTrials.gov NCT00545987.
