Long-term CD4⁺ and CD8⁺ T-cell responses induced in HIV-uninfected volunteers following intradermal or intramuscular administration of an HIV-lipopeptide vaccine (ANRS VAC16)

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• 作者：Odile Launay ; Mathieu Surenaud ; Corinne Desaint ; Nadine Ben Hamouda ; Gilles Pialoux ; B¨¦n¨¦dicte Bonnet ; Isabelle Poizot-Martin ; Gustavo Gonzales ; Lise Cuzin ; Isabelle Bourgault-Villada ; Yves L¨¦vy ; Jeannine Choppin ; Christine Durier
• 关键词：HIV-1 vaccine ; Randomised trial ; Intradermal injection ; Lipopeptides
• 刊名：Vaccine
• 出版年：2013
• 出版时间：13 September, 2013
• 年：2013
• 卷：31
• 期：40
• 页码：4406-4415
• 全文大小：1692 K

文摘

Background

We have shown that the intradermal (ID) administration of an HIV-1 lipopeptide candidate vaccine (LIPO-4) is well tolerated in healthy volunteers, with one fifth the IM dose delivered by this route inducing HIV-1-specific CD8⁺ T-cell responses of a magnitude and quality similar to those achieved by IM administration. In this long-term follow-up, we aimed to investigate the sustainability and epitopic breadth of the immune responses induced.

Methods

In a prospective multicentre trial, 68 healthy volunteers were randomised to receive, at weeks 0, 4 and 12, either a 0.5 ml IM (500 ¦Ìg of each lipopeptide; 35 volunteers) dose or a 0.1 ml ID (100 ¦Ìg of each lipopeptide; 33 volunteers) dose of the LIPO-4 vaccine, in the deltoid region of the non-dominant arm. All 68 volunteers received the first two vaccinations, and 44 volunteers in the ID group and 22 in the IM group received the third. We describe here the long-term CD8⁺ and CD4⁺ T-cell immune responses, up to 48 weeks after the first immunisation.

Results

Response frequency was highest at week 14 for CD4⁺ T cells, at 85 % (28/33) for the IM group and 61 % (20/33) for the ID group (p = 0.027), and at week 48 for CD8⁺ T cells, at 36 % (12/33) for the ID group and 31 % (11/35) for the IM group (p = 0.67). Response rates tended to be lower for volunteers receiving the third vaccination boost, whether IM or ID. Finally, we also observed a striking change in the specificity of the CD8⁺ T-cell responses induced shortly (2 weeks) or several months (48 weeks) after LIPO-4 vaccination.

Conclusion

Lipopeptide vaccines elicited sustainable CD4⁺ and CD8⁺ T-cell responses, following IM or ID administration. CD8⁺ T-cell responses had shifted and expanded to different epitopes after one year of follow-up. These results should facilitate the design of the next generation of prime-boost trials with repeated doses of lipopeptide vaccines.