Safety and immunogenicity of investigational tuberculosis vaccine M72/AS01 in people living with HIV in South Africa: an observer-blinded, randomised, controlled, phase 2 trial.

BACKGROUND

M72/AS01 is a recombinant fusion protein vaccine candidate derived from two Mycobacterium tuberculosis antigens (Mtb32A and Mtb39A) and AS01 adjuvant. We evaluated safety and immunogenicity of M72/AS01 in people living with HIV in South Africa.

METHODS

In this observer-blinded, randomised, controlled, phase 2 trial, participants aged 16-35 years with well controlled HIV were enrolled from urban, semi-urban, and semi-rural settings in South Africa, including sites with high tuberculosis and HIV prevalence, as well as agricultural and mining communities. Participants were randomly assigned (1:1), stratified by site and interferon-gamma release assay (IGRA) status, to receive two intramuscular doses of M72/AS01 or placebo. Eligibility criteria included antiretroviral therapy for at least 3 months, HIV viral load of less than 200 copies per mL, CD4 counts of 200 cells per μL or higher, and previous completion of tuberculosis preventive therapy and no tuberculosis history. The sponsor and its delegates, the laboratory team, investigators, site staff, and participants were blinded to randomisation, whereas an unblinded pharmacist who was not involved in trial procedures prepared placebo and reconstituted M72/AS01 in unit-dose syringes covered with a blinding label. All participants who received at least one dose of either M72/AS01 or placebo were included in the safety population for safety analyses. Immunogenicity analyses were conducted using the per-protocol population, which included participants who received the intervention as planned and did not substantially deviate from the protocol procedures. Safety assessments included solicited adverse events in the first 7 days after each dose, unsolicited adverse events in the first 28 days after each dose, and serious adverse events. Humoral responses were measured with ELISA and cellular responses were assessed using multiparameter flow cytometry, in the per-protocol population. This study is complete and is registered with ClinicalTrials.gov, NCT04556981.

FINDINGS

Between Nov 17, 2020, and Aug 12, 2022, 402 eligible participants were assigned treatment, of whom 401 participants received at least one dose of M72/AS01 (n=201; 175 [87%] were female and 26 [13%] were male; 196 [98%] were Black) or placebo (n=200; [176 [88%] were female and 24 [12%] were male; 196 [98%] were Black) and followed for a median duration of 372 days (IQR 364-389). Among M72/AS01 recipients, solicited adverse events were more frequent, ranging from 17% (33 of 199) for gastrointestinal symptoms to 77% (140 of 183) for injection-site pain. Most events were mild to moderate, with severe events ranging from 0% (0 of 197) for swelling and (0 of 198) redness to 13% (24 of 183) for injection-site pain, resolving within 3 days. Unsolicited adverse events related to vaccine were mainly injection-site reactions in the M72/AS01 group (8% [15 of 201] vs 1% [two of 200] in the placebo group), including erythema, pruritis, swelling, bruising, induration, and pain. No vaccine-related serious adverse events were reported. Among M72/AS01 recipients at day 57 (1 month after dose two), M72-specific antibody geometric mean concentration (GMC) was 479·70 EU/mL (95% CI 421·79-545·56) with median magnitude of CD4 cells of 0·383% (IQR 0·177%-0·663). Among M72/AS01 recipients, at day 57 GMCs were 559·49 EU/mL (95% CI 461·75-677·93) in with baseline IGRA positivity and 424·95 EU/mL (357·74-504·80) in those without; median magnitudes of CD4 cells were 0·447% (IQR 0·287-0·819) and 0·321% (0·147-0·581).

INTERPRETATION

The two-dose regimen of the M72/AS01 tuberculosis vaccine was immunogenic, with an acceptable safety profile. These outcomes led to the inclusion of people living with HIV in the ongoing global registration phase 3 trial.

FUNDING

Gates Foundation and the Wellcome Trust.