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Journal of Virology, October 2003, p. 11220-11231, Vol. 77, No. 20
0022-538X/03/$08.00+0     DOI: 10.1128/JVI.77.20.11220-11231.2003
Copyright © 2003, American Society for Microbiology. All Rights Reserved.

Long-Term Specific Immune Responses Induced in Humans by a Human Immunodeficiency Virus Type 1 Lipopeptide Vaccine: Characterization of CD8+-T-Cell Epitopes Recognized

Hanne Gahéry-Ségard,1* Gilles Pialoux,2 Suzanne Figueiredo,1 Céline Igéa,1 Mathieu Surenaud,1 Jessintha Gaston,1 Helene Gras-Masse,3 Jean-Paul Lévy,4 and Jean-Gérard Guillet1

Département d'Immunologie-Membre de l'IFR 116-INSERM U567, Institut Cochin, 75014 Paris,1 Département des Maladies Infectieuses, Hôpital Tenon, 75020 Paris,2 UMR 8525 CNRS-Université Lille II, Institut Pasteur de Lille, 1, 59021 Lille,3 Institut Pasteur, 75015 Paris, France4

Received 27 March 2003/ Accepted 29 July 2003

We studied the effect of booster injections and the long-term immune response after injections of an anti-human immunodeficiency virus type 1 (HIV-1) lipopeptide vaccine. This vaccine was injected alone or with QS21 adjuvant to 28 HIV-uninfected volunteers. One month later, after a fourth injection of the vaccine, B- and T-cell anti-HIV responses were detected in >85% of the vaccinated volunteers. One year after this injection, a long-term immune response was observed in >50% of the volunteers. At this point, a positive QS21 effect was observed only in the sustained B-cell and CD4+-T-cell responses. To better characterize the CD8+-T-cell response, we used a gamma interferon enzyme-linked immunospot method and a bank of 59 HIV-1 epitopes. For the six most common HLA molecules (HLA-A2, -A3, -A11, -A24, -B7 superfamily, and -B8), an average of 10 (range, 3 to 15) HIV-1 epitopes were tested. CD8+-T-cell responses were evaluated according to the HLA class I molecules of the volunteers. Each assessment was based on 18 HIV-1 epitopes in average. We showed that 31 HIV-1 epitopes elicited specific CD8+-T-cell responses after vaccination. The most frequently recognized peptides were Nef 68-76 (-B7), Nef 71-79 (-B7), Nef 84-92 (-A11), Nef 135-143 (-B7), Nef 136-145 (-A2), Nef 137-145 (-A2), Gag 259-267 (-B8), Gag 260-268 (-A2), Gag 267-274 (-A2), Gag 267-277 (-B7), and Gag 276-283 (A24). We found that CD8+-T-cell epitopes were induced at a higher number after a fourth injection (P < 0.05 compared to three injections), which indicates an increase in the breadth of HIV CD8+-T-cell epitope recognition after the boost.

* Corresponding author. Mailing address: Département d'Immunologie-Institut Cochin, Hôpital Cochin, 27, rue du faubourg Saint-Jacques, 75014 Paris, France. Phone: 33(0)1-43-21-04-80. Fax: 33(0)1-40-48-83-52. E-mail: gahery{at}cochin.inserm.fr.

Journal of Virology, October 2003, p. 11220-11231, Vol. 77, No. 20
0022-538X/03/$08.00+0     DOI: 10.1128/JVI.77.20.11220-11231.2003
Copyright © 2003, American Society for Microbiology. All Rights Reserved.



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