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High-Dose Recombinant Canarypox Vaccine Expressing HIV-1 Protein, in Seronegative Human Subjects.

Authors :
Goepfert, Paul A.
Horton, Helen
McElrath, M. Juliana
Gurunathan, Sanjay
Ferrari, Guido
Tomaras, Georgia D.
Montefiori, David C.
Allen, Mary
Ya-Lin Chiu
Spearman, Paul
Fuchs, Jonathan D.
Koblin, Beryl A.
Blattner, William A.
Frey, Sharon
Keefer, Michael C.
Baden, Lindsey R.
Corey, Lawrence
Source :
Journal of Infectious Diseases; 10/1/2005, Vol. 192 Issue 7, p1249-1259, 11p
Publication Year :
2005

Abstract

Background. In clinical trials, canarypox ALVAC-human immunodeficiency virus (HIV) vaccines have been shown to elicit human HIV-specific cytotoxic T lymphocyte (CTL) responses in some but not all healthy uninfected adults. Methods. A clinical trial was conducted to examine whether the vaccine vCP1452 would elicit a greater HIVspecific CTL response when given at a dose of 10<superscript>8.0</superscript> TCID<subscript>50</subscript> (60 participants) than when given at the regular dose, 10<superscript>7.26</superscript> TCID<subscript>50</subscript> (40 participants); as a control, a placebo vaccine preparation also was administered (10 participants). Results. Two weeks after the last vaccination in a series, HIV-specific CTL responses were not significantly different when measured by either chromium-release assay (8% and 16% in the high- and regular-dose recipients, respectively) or interferon-γ ELISpot assay (8% and 15% in the high- and regular-dose recipients, respectively); moreover, recipients of the higher dose had greater local and systemic reactions (P < .001 ). Conclusions. High reactogenicity associated with an increased dose of vCP1452 negates the need for further evaluation of this strategy to boost the frequency of HIV-specific CTL response in seronegative human subjects. Development of highly immunogenic canarypox vectors requires further work to optimize vector and insert design, as well as novel ways to increase dosage and to reduce reactogenicity. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00221899
Volume :
192
Issue :
7
Database :
Complementary Index
Journal :
Journal of Infectious Diseases
Publication Type :
Academic Journal
Accession number :
18331147