Safety and efficacy of the peptide-based therapeutic vaccine for HIV-1, Vacc-4x

A phase 2 randomised, double-blind, placebo-controlled trial

Richard B. Pollard, Jürgen K. Rockstroh, Giuseppe Pantaleo, David M. Asmuth, Barry Peters, Adriano Lazzarin, Felipe Garcia, Kim Ellefsen, Daniel Podzamczer, Jan Van Lunzen, Keikawus Arastéh, Dirk Schürmann, Bonaventura Clotet, W. David Hardy, Ronald Mitsuyasu, Graeme Moyle, Andreas Plettenberg, Martin Fisher, Gerd Fätkenheuer, Margaret A Fischl & 9 others Babafemi Taiwo, Ingebjørg Baksaas, Darren Jolliffe, Stefan Persson, Øyvind Jelmert, Arnt Ove Hovden, Maja A. Sommerfelt, Vidar Wendel-Hansen, Birger Sørensen

Research output: Contribution to journalArticle

51 Citations (Scopus)

Abstract

Background: Present combination antiretroviral therapy (cART) alone does not cure HIV infection and requires lifelong drug treatment. The potential role of HIV therapeutic vaccines as part of an HIV cure is under consideration. Our aim was to assess the efficacy, safety, and immunogenicity of Vacc-4x, a peptide-based HIV-1 therapeutic vaccine targeting conserved domains on p24Gag, in adults infected with HIV-1. Methods: Between July, 2008, and June, 2010, we did a multinational double-blind, randomised, phase 2 study comparing Vacc-4x with placebo. Participants were adults infected with HIV-1 who were aged 18-55 years and virologically suppressed on cART (viral load <50 copies per mL) with CD4 cell counts of 400 × 106 cells per L or greater. The trial was done at 18 sites in Germany, Italy, Spain, the UK, and the USA. Participants were randomly assigned (2:1) to Vacc-4x or placebo. Group allocation was masked from participants and investigators. Four primary immunisations, weekly for 4 weeks, containing Vacc-4x (or placebo) were given intradermally after administration of adjuvant. Booster immunisations were given at weeks 16 and 18. At week 28, cART was interrupted for up to 24 weeks. The coprimary endpoints were cART resumption and changes in CD4 counts during treatment interruption. Analyses were by modified intention to treat: all participants who received one intervention. Furthermore, safety, viral load, and immunogenicity (as measured by ELISPOT and proliferation assays) were assessed. The 52 week follow-up period was completed in June, 2011. For the coprimary endpoints the proportion of participants who met the criteria for cART resumption was analysed with a logistic regression model with the treatment effect being assessed in a model including country as a covariate. This study is registered with ClinicalTrials.gov, number NCT00659789. Findings: 174 individuals were screened; because of slow recruitment, enrolment stopped with 136 of a planned 345 participants and 93 were randomly assigned to receive Vacc-4x and 43 to receive placebo. There were no differences between the two groups for the primary efficacy endpoints in those participants who stopped cART at week 28. Of the participants who resumed cART, 30 (34%) were in the Vacc-4x group and 11 (29%) in the placebo group, and percentage changes in CD4 counts were not significant (mean treatment difference -5·71, 95% CI -13·01 to 1·59). However, a significant difference in viral load was noted for the Vacc-4x group both at week 48 (median 23 100 copies per mL Vacc-4x vs 71 800 copies per mL placebo; p=0·025) and week 52 (median 19 550 copies per mL vs 51 000 copies per mL; p=0·041). One serious adverse event, exacerbation of multiple sclerosis, was reported as possibly related to study treatment. Vacc-4x was immunogenic, inducing proliferative responses in both CD4 and CD8 T-cell populations. Interpretation: The proportion of participants resuming cART before end of study and change in CD4 counts during the treatment interruption showed no benefit of vaccination. Vacc-4x was safe, well tolerated, immunogenic, seemed to contribute to a viral-load setpoint reduction after cART interruption, and might be worth consideration in future HIV-cure investigative strategies. Funding: Norwegian Research Council GLOBVAC Program and Bionor Pharma ASA.

Original languageEnglish
Pages (from-to)291-300
Number of pages10
JournalThe Lancet Infectious Diseases
Volume14
Issue number4
DOIs
StatePublished - Jan 1 2014

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HIV-1
Vaccines
Placebos
Safety
Peptides
Therapeutics
CD4 Lymphocyte Count
Viral Load
Vacc-4x
Logistic Models
HIV
Enzyme-Linked Immunospot Assay
Secondary Immunization
AIDS Vaccines
Spain
Italy
Multiple Sclerosis
HIV Infections
Germany
Immunization

ASJC Scopus subject areas

  • Infectious Diseases

Cite this

Safety and efficacy of the peptide-based therapeutic vaccine for HIV-1, Vacc-4x : A phase 2 randomised, double-blind, placebo-controlled trial. / Pollard, Richard B.; Rockstroh, Jürgen K.; Pantaleo, Giuseppe; Asmuth, David M.; Peters, Barry; Lazzarin, Adriano; Garcia, Felipe; Ellefsen, Kim; Podzamczer, Daniel; Van Lunzen, Jan; Arastéh, Keikawus; Schürmann, Dirk; Clotet, Bonaventura; Hardy, W. David; Mitsuyasu, Ronald; Moyle, Graeme; Plettenberg, Andreas; Fisher, Martin; Fätkenheuer, Gerd; Fischl, Margaret A; Taiwo, Babafemi; Baksaas, Ingebjørg; Jolliffe, Darren; Persson, Stefan; Jelmert, Øyvind; Hovden, Arnt Ove; Sommerfelt, Maja A.; Wendel-Hansen, Vidar; Sørensen, Birger.

In: The Lancet Infectious Diseases, Vol. 14, No. 4, 01.01.2014, p. 291-300.

Research output: Contribution to journalArticle

Pollard, RB, Rockstroh, JK, Pantaleo, G, Asmuth, DM, Peters, B, Lazzarin, A, Garcia, F, Ellefsen, K, Podzamczer, D, Van Lunzen, J, Arastéh, K, Schürmann, D, Clotet, B, Hardy, WD, Mitsuyasu, R, Moyle, G, Plettenberg, A, Fisher, M, Fätkenheuer, G, Fischl, MA, Taiwo, B, Baksaas, I, Jolliffe, D, Persson, S, Jelmert, Ø, Hovden, AO, Sommerfelt, MA, Wendel-Hansen, V & Sørensen, B 2014, 'Safety and efficacy of the peptide-based therapeutic vaccine for HIV-1, Vacc-4x: A phase 2 randomised, double-blind, placebo-controlled trial', The Lancet Infectious Diseases, vol. 14, no. 4, pp. 291-300. https://doi.org/10.1016/S1473-3099(13)70343-8
Pollard, Richard B. ; Rockstroh, Jürgen K. ; Pantaleo, Giuseppe ; Asmuth, David M. ; Peters, Barry ; Lazzarin, Adriano ; Garcia, Felipe ; Ellefsen, Kim ; Podzamczer, Daniel ; Van Lunzen, Jan ; Arastéh, Keikawus ; Schürmann, Dirk ; Clotet, Bonaventura ; Hardy, W. David ; Mitsuyasu, Ronald ; Moyle, Graeme ; Plettenberg, Andreas ; Fisher, Martin ; Fätkenheuer, Gerd ; Fischl, Margaret A ; Taiwo, Babafemi ; Baksaas, Ingebjørg ; Jolliffe, Darren ; Persson, Stefan ; Jelmert, Øyvind ; Hovden, Arnt Ove ; Sommerfelt, Maja A. ; Wendel-Hansen, Vidar ; Sørensen, Birger. / Safety and efficacy of the peptide-based therapeutic vaccine for HIV-1, Vacc-4x : A phase 2 randomised, double-blind, placebo-controlled trial. In: The Lancet Infectious Diseases. 2014 ; Vol. 14, No. 4. pp. 291-300.
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T1 - Safety and efficacy of the peptide-based therapeutic vaccine for HIV-1, Vacc-4x

T2 - A phase 2 randomised, double-blind, placebo-controlled trial

AU - Pollard, Richard B.

AU - Rockstroh, Jürgen K.

AU - Pantaleo, Giuseppe

AU - Asmuth, David M.

AU - Peters, Barry

AU - Lazzarin, Adriano

AU - Garcia, Felipe

AU - Ellefsen, Kim

AU - Podzamczer, Daniel

AU - Van Lunzen, Jan

AU - Arastéh, Keikawus

AU - Schürmann, Dirk

AU - Clotet, Bonaventura

AU - Hardy, W. David

AU - Mitsuyasu, Ronald

AU - Moyle, Graeme

AU - Plettenberg, Andreas

AU - Fisher, Martin

AU - Fätkenheuer, Gerd

AU - Fischl, Margaret A

AU - Taiwo, Babafemi

AU - Baksaas, Ingebjørg

AU - Jolliffe, Darren

AU - Persson, Stefan

AU - Jelmert, Øyvind

AU - Hovden, Arnt Ove

AU - Sommerfelt, Maja A.

AU - Wendel-Hansen, Vidar

AU - Sørensen, Birger

PY - 2014/1/1

Y1 - 2014/1/1

N2 - Background: Present combination antiretroviral therapy (cART) alone does not cure HIV infection and requires lifelong drug treatment. The potential role of HIV therapeutic vaccines as part of an HIV cure is under consideration. Our aim was to assess the efficacy, safety, and immunogenicity of Vacc-4x, a peptide-based HIV-1 therapeutic vaccine targeting conserved domains on p24Gag, in adults infected with HIV-1. Methods: Between July, 2008, and June, 2010, we did a multinational double-blind, randomised, phase 2 study comparing Vacc-4x with placebo. Participants were adults infected with HIV-1 who were aged 18-55 years and virologically suppressed on cART (viral load <50 copies per mL) with CD4 cell counts of 400 × 106 cells per L or greater. The trial was done at 18 sites in Germany, Italy, Spain, the UK, and the USA. Participants were randomly assigned (2:1) to Vacc-4x or placebo. Group allocation was masked from participants and investigators. Four primary immunisations, weekly for 4 weeks, containing Vacc-4x (or placebo) were given intradermally after administration of adjuvant. Booster immunisations were given at weeks 16 and 18. At week 28, cART was interrupted for up to 24 weeks. The coprimary endpoints were cART resumption and changes in CD4 counts during treatment interruption. Analyses were by modified intention to treat: all participants who received one intervention. Furthermore, safety, viral load, and immunogenicity (as measured by ELISPOT and proliferation assays) were assessed. The 52 week follow-up period was completed in June, 2011. For the coprimary endpoints the proportion of participants who met the criteria for cART resumption was analysed with a logistic regression model with the treatment effect being assessed in a model including country as a covariate. This study is registered with ClinicalTrials.gov, number NCT00659789. Findings: 174 individuals were screened; because of slow recruitment, enrolment stopped with 136 of a planned 345 participants and 93 were randomly assigned to receive Vacc-4x and 43 to receive placebo. There were no differences between the two groups for the primary efficacy endpoints in those participants who stopped cART at week 28. Of the participants who resumed cART, 30 (34%) were in the Vacc-4x group and 11 (29%) in the placebo group, and percentage changes in CD4 counts were not significant (mean treatment difference -5·71, 95% CI -13·01 to 1·59). However, a significant difference in viral load was noted for the Vacc-4x group both at week 48 (median 23 100 copies per mL Vacc-4x vs 71 800 copies per mL placebo; p=0·025) and week 52 (median 19 550 copies per mL vs 51 000 copies per mL; p=0·041). One serious adverse event, exacerbation of multiple sclerosis, was reported as possibly related to study treatment. Vacc-4x was immunogenic, inducing proliferative responses in both CD4 and CD8 T-cell populations. Interpretation: The proportion of participants resuming cART before end of study and change in CD4 counts during the treatment interruption showed no benefit of vaccination. Vacc-4x was safe, well tolerated, immunogenic, seemed to contribute to a viral-load setpoint reduction after cART interruption, and might be worth consideration in future HIV-cure investigative strategies. Funding: Norwegian Research Council GLOBVAC Program and Bionor Pharma ASA.

AB - Background: Present combination antiretroviral therapy (cART) alone does not cure HIV infection and requires lifelong drug treatment. The potential role of HIV therapeutic vaccines as part of an HIV cure is under consideration. Our aim was to assess the efficacy, safety, and immunogenicity of Vacc-4x, a peptide-based HIV-1 therapeutic vaccine targeting conserved domains on p24Gag, in adults infected with HIV-1. Methods: Between July, 2008, and June, 2010, we did a multinational double-blind, randomised, phase 2 study comparing Vacc-4x with placebo. Participants were adults infected with HIV-1 who were aged 18-55 years and virologically suppressed on cART (viral load <50 copies per mL) with CD4 cell counts of 400 × 106 cells per L or greater. The trial was done at 18 sites in Germany, Italy, Spain, the UK, and the USA. Participants were randomly assigned (2:1) to Vacc-4x or placebo. Group allocation was masked from participants and investigators. Four primary immunisations, weekly for 4 weeks, containing Vacc-4x (or placebo) were given intradermally after administration of adjuvant. Booster immunisations were given at weeks 16 and 18. At week 28, cART was interrupted for up to 24 weeks. The coprimary endpoints were cART resumption and changes in CD4 counts during treatment interruption. Analyses were by modified intention to treat: all participants who received one intervention. Furthermore, safety, viral load, and immunogenicity (as measured by ELISPOT and proliferation assays) were assessed. The 52 week follow-up period was completed in June, 2011. For the coprimary endpoints the proportion of participants who met the criteria for cART resumption was analysed with a logistic regression model with the treatment effect being assessed in a model including country as a covariate. This study is registered with ClinicalTrials.gov, number NCT00659789. Findings: 174 individuals were screened; because of slow recruitment, enrolment stopped with 136 of a planned 345 participants and 93 were randomly assigned to receive Vacc-4x and 43 to receive placebo. There were no differences between the two groups for the primary efficacy endpoints in those participants who stopped cART at week 28. Of the participants who resumed cART, 30 (34%) were in the Vacc-4x group and 11 (29%) in the placebo group, and percentage changes in CD4 counts were not significant (mean treatment difference -5·71, 95% CI -13·01 to 1·59). However, a significant difference in viral load was noted for the Vacc-4x group both at week 48 (median 23 100 copies per mL Vacc-4x vs 71 800 copies per mL placebo; p=0·025) and week 52 (median 19 550 copies per mL vs 51 000 copies per mL; p=0·041). One serious adverse event, exacerbation of multiple sclerosis, was reported as possibly related to study treatment. Vacc-4x was immunogenic, inducing proliferative responses in both CD4 and CD8 T-cell populations. Interpretation: The proportion of participants resuming cART before end of study and change in CD4 counts during the treatment interruption showed no benefit of vaccination. Vacc-4x was safe, well tolerated, immunogenic, seemed to contribute to a viral-load setpoint reduction after cART interruption, and might be worth consideration in future HIV-cure investigative strategies. Funding: Norwegian Research Council GLOBVAC Program and Bionor Pharma ASA.

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