Your browser doesn't support javascript.
loading
GMMA Technology for the Development of Safe Vaccines: Meta-Analysis of Individual Patient Data to Assess the Safety Profile of Shigella sonnei 1790GAHB Vaccine in Healthy Adults, with Special Focus on Neutropenia.
De Ryck, Iris; Sarakinou, Eleanna; Nakakana, Usman; Cilio, Giulia Luna; Ndiaye, Augustin; Vella, Venanzio; Auerbach, Joachim; Granada, Juan-Paolo; Conti, Valentino; Podda, Audino.
Afiliación
  • De Ryck I; GSK, Siena, Italy. iris.x.de-ryck@gsk.com.
  • Sarakinou E; GSK Vaccines Institute for Global Health, Via Fiorentina 1, 53100, Siena, Italy.
  • Nakakana U; GSK Vaccines Institute for Global Health, Via Fiorentina 1, 53100, Siena, Italy.
  • Cilio GL; GSK, Siena, Italy.
  • Ndiaye A; Takeda Pharmaceutical International AG, Zurich, Switzerland.
  • Vella V; GSK, Siena, Italy.
  • Auerbach J; GSK Vaccines Institute for Global Health, Via Fiorentina 1, 53100, Siena, Italy.
  • Granada JP; Coalition for Epidemic Preparedness Innovations, London, UK.
  • Conti V; Ferring Pharmaceuticals, Copenhagen, Denmark.
  • Podda A; GSK Vaccines Institute for Global Health, Via Fiorentina 1, 53100, Siena, Italy.
Infect Dis Ther ; 11(2): 757-770, 2022 Apr.
Article en En | MEDLINE | ID: mdl-35118580
INTRODUCTION: Shigellosis is a major health concern among children < 5 years of age from developing countries, and there are no widely available vaccines to prevent it. The GMMA-based 1790GAHB investigational vaccine against Shigella sonnei was well tolerated and immunogenic in phase 1 and 2 studies conducted in healthy adults from Shigella endemic and non-endemic populations. Based on pooled data of five individual trials, we assessed the association between vaccine administration and the risk of neutropenia as well as the overall safety profile of 1790GAHB. METHODS: The risk ratio (RR) of neutropenia was evaluated between participants receiving 1790GAHB (vaccinees) and active comparator/placebo (controls) using different ethnicity-specific absolute neutrophil count (ANC) thresholds established to define neutropenia. Safety was assessed in terms of solicited, unsolicited, and serious adverse events (AEs). RESULTS: Of the 279 participants, 11 (5.5%) vaccinees and 4 (5.0%) controls had ANC below the appropriate threshold within 7 days post-vaccination. RR was 0.96 [95% confidence interval (CI) 0.54-1.70]. When neutrophil counts of participants of African descent were measured against an ethnicity non-specific threshold, they resulted in neutropenia episodes in 30 (37.0%) vaccinees and 16 (30.2%) controls, while only 2 (2.5%) vaccinees and 1 (1.9%) control had neutropenia when the ethnicity-specific threshold was applied. RRs were 0.98 (95% CI 0.75-1.28) and 1.30 (95% CI 0.1-17.6), respectively. Solicited and unsolicited AEs were slightly more frequent among vaccinees than controls. No serious AEs, other than neutropenia cases, were recorded in the vaccine group. CONCLUSION: By applying the appropriate threshold, no increased risk of neutropenia was identified in vaccinees compared with the controls. The frequency of neutropenia events varied drastically when ethnicity-appropriate thresholds were applied. This observation highlights the importance of selecting appropriate cut-off values according to the correct population reference. Overall, the 1790GAHB vaccine demonstrated an acceptable safety profile.
Palabras clave

Texto completo: 1 Bases de datos: MEDLINE Tipo de estudio: Clinical_trials / Systematic_reviews Idioma: En Revista: Infect Dis Ther Año: 2022 Tipo del documento: Article País de afiliación: Italia

Texto completo: 1 Bases de datos: MEDLINE Tipo de estudio: Clinical_trials / Systematic_reviews Idioma: En Revista: Infect Dis Ther Año: 2022 Tipo del documento: Article País de afiliación: Italia