Safety and immunogenicity evaluation of recombinant BCG vaccine against respiratory syncytial virus in a randomized, double-blind, placebo-controlled phase I clinical trial. (October 2020)

• Record Type: Journal Article
• Authors: Abarca, Katia; Rey-Jurado, Emma; Muñoz-Durango, Natalia; Vázquez, Yaneisi; Soto, Jorge A.; Gálvez, Nicolás M.S.; Valdés-Ferrada, Javier; Iturriaga, Carolina; Urzúa, Marcela; Borzutzky, Arturo; Cerda, Jaime; Villarroel, Luis; Madrid, Victoria; González, Pablo A.; González-Aramundiz, José V.; Bueno, Susan M.; Kalergis, Alexis M.
• Is Part Of: EClinicalMedicine. Volume 27(2020)
• Publication Date: 2020-10
• Subjects: Human respiratory syncytial virus -- BCG vaccine -- Phase I clinical trial -- Safety -- Transmissibility -- Immunogenicity; Medicine -- Research -- Periodicals; Medical policy -- Periodicals; Clinical Medicine; Health Policy; Public Health; Medical policy; Medicine -- Research; Periodical; Electronic journals; Periodicals; 613
• DOI: 10.1016/j.eclinm.2020.100517
• Languages: English
• ISSNs: 2589-5370

Abstract

Abstract: Background: Respiratory syncytial virus (RSV) is responsible for most respiratory tract infections and hospitalizations in infants and represents a significant economic burden for public health. The development of a safe, effective, and affordable vaccine is a priority for the WHO. Methods: We conducted a double-blinded, escalating-dose phase 1 clinical trial in healthy males aged 18-50 years to evaluate safety, tolerability, and immunogenicity of a recombinant Mycobacterium bovis BCG vaccine expressing the nucleoprotein of RSV (rBCG-N-hRSV). Once inclusion criteria were met, volunteers were enrolled in three cohorts in an open and successive design. Each cohort included six volunteers vaccinated with 5 × 10 3, 5 × 10 4, or 1 × 10 5 CFU, as well as two volunteers vaccinated with the full dose of the standard BCG vaccine. This clinical trial (clinicaltrials.gov NCT03213405) was conducted in Santiago, Chile. Findings: The rBCG-N-RSV vaccine was safe, well-tolerated, and no serious adverse events related to the vaccine were recorded. Serum IgG-antibodies directed against Mycobacterium and the N-protein of RSV increased after vaccination, which were capable of neutralizing RSV in vitro . Additionally, all volunteers displayed increased cellular response consisting of IFN-γ and IL-2 production against PPD and the N-protein, starting at day 14 and 30 post-vaccination respectively. Interpretation: The rBCG-N-hRSV vaccine had a good safety profile and induced specific cellular and humoral responses. Funding: This work was supported by Millennium Institute on Immunology and Immunotherapy from Chile (P09/016), FONDECYT 1190830, and FONDEF D11E1098.