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doi: 10.1097/QAD.0000000000000343
Clinical Science

Safety and immunogenicity of the M72/AS01 candidate tuberculosis vaccine in HIV-infected adults on combination antiretroviral therapy: a phase I/II, randomized trial

Thacher, Eleonora G.a,*; Cavassini, Matthiasb,*; Audran, Réginea; Thierry, Anne-Christinea; Bollaerts, Annec; Cohen, Joec; Demoitié, Marie-Angec; Ejigu, Dawitc; Mettens, Pascalc; Moris, Philippec; Ofori-Anyinam, Opokuac,†; Spertini, Françoisa,†

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In this paper by Eleonora et al. [1], there is an error in the legend of the Y-axis of Fig 4a: M72-specific CD4+ T-cell responses following vaccination with M72/A S01.

The legend of Y-axis in Fig 4a incorrectly refers to ‘M72-specific CD4+ T cells expressing at least 3 markers (%)’. The correct Y-axis legend should read ‘M72-specific CD4+ T cells expressing at least 2 markers (%)’.

Please see the corrected Fig 4a here.

AIDS. 29(7):865, April 24, 2015.

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Objective: Tuberculosis (TB) is highly prevalent among HIV-infected people, including those receiving combination antiretroviral therapy (cART), necessitating a well tolerated and efficacious TB vaccine for these populations. We evaluated the safety and immunogenicity of the candidate TB vaccine M72/AS01 in adults with well controlled HIV infection on cART.

Design: A randomized, observer-blind, controlled trial (NCT00707967).

Methods: HIV-infected adults on cART in Switzerland were randomized 3 : 1 : 1 to receive two doses, 1 month apart, of M72/AS01, AS01 or 0.9% physiological saline (N = 22, N = 8 and N = 7, respectively) and were followed up to 6 months postdose 2 (D210). Individuals with CD4+ cell counts below 200 cells/μl were excluded. Adverse events (AEs) including HIV-specific and laboratory safety parameters were recorded. Cell-mediated (ICS) and humoral (ELISA) responses were evaluated before vaccination, 1 month after each dose (D30, D60) and D210.

Results: Thirty-seven individuals [interquartile range (IQR) CD4+ cell counts at screening: 438–872 cells/μl; undetectable HIV-1 viremia] were enrolled; 73% of individuals reported previous BCG vaccination, 97.3% tested negative for the QuantiFERON-TB assay. For M72/AS01 recipients, no vaccine-related serious AEs or cART-regimen adjustments were recorded, and there were no clinically relevant effects on laboratory safety parameters, HIV-1 viral loads or CD4+ cell counts. M72/AS01 was immunogenic, inducing persistent and polyfunctional M72-specific CD4+ T-cell responses [medians 0.70% (IQR 0.37–1.07) at D60] and 0.42% (0.24–0.61) at D210, predominantly CD40L+IL-2+TNF-α+, CD40L+IL-2+ and CD40L+IL-2+TNF-α+IFN-γ+]. All M72/AS01 vaccines were seropositive for anti-M72 IgG after second vaccination until study end.

Conclusion: M72/AS01 was clinically well tolerated and immunogenic in this population, supporting further clinical evaluation in HIV-infected individuals in TB-endemic settings.

© 2014 Lippincott Williams & Wilkins, Inc.


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