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The candidate tuberculosis vaccine Mtb72F/AS02 in PPD positive adults: a randomized controlled phase I/II study. | LitMetric

AI Article Synopsis

  • Vaccination with the candidate TB vaccine Mtb72F/AS02 showed promise in reducing the global TB burden and was well tolerated in adults previously vaccinated with BCG or infected with Mycobacterium tuberculosis.
  • In a controlled trial involving 38 adults, the vaccine induced immune responses, particularly persistent CD4(+) T-cell responses, although it was more reactive in those already infected with TB.
  • No serious adverse events were reported, and further investigation into the vaccine’s effectiveness is suggested.

Article Abstract

Unlabelled: Prevention of tuberculosis (TB) through vaccination would substantially reduce the global TB burden. Mtb72F/AS02 is a candidate TB vaccine shown to be immunogenic and well tolerated in PPD-negative adults. We evaluated the safety and immunogenicity of Mtb72F/AS02 in Mycobacterium-primed adults (BCG-vaccinated, or infected adults who had received post-exposure chemoprophylaxis or treatment for pulmonary TB disease). In this observer-blind controlled trial, 20 BCG-vaccinated adults and 18 adults previously infected with Mycobacterium tuberculosis (Mtb), were randomized 3:1 to receive three doses of Mtb72F/AS02 or AS02 at one-month intervals, and followed for 6 months post third vaccination. Mtb72F/AS02 was well tolerated in BCG-vaccinated adults, and tended to be more reactogenic in Mtb-infected adults. Adverse events were mainly self-limiting, resolving without sequelae. No serious adverse events were reported. The adverse events in Mtb72F/AS02 vaccinees were not clearly associated with vaccine-induced responses (as assessed by proinflammatory cytokines, total IgE and C-reactive protein levels). No Th2 T-cell responses, or vaccine-induced T-cell responses to Mtb antigens (CFP-10/PPD/ESAT-6) were detected by ICS. In both cohorts, Mtb72F/AS02 induced persistent polyfunctional Mtb72F-specific CD4(+) T-cell responses and anti-Mtb72F humoral responses. IFN-γ was detectable in serum one day post each vaccination. Further evaluation of the candidate vaccine, Mtb72F/AS02, is warranted.

Trial Registration: ClinicalTrials.gov identifier: NCT00146744.

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Source
http://dx.doi.org/10.1016/j.tube.2012.10.011DOI Listing

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