Fractional Third and Fourth Dose of RTS,S/AS01 Malaria Candidate Vaccine: A Phase 2a Controlled Human Malaria Parasite Infection and Immunogenicity Study.

نویسندگان

  • Jason A Regules
  • Susan B Cicatelli
  • Jason W Bennett
  • Kristopher M Paolino
  • Patrick S Twomey
  • James E Moon
  • April K Kathcart
  • Kevin D Hauns
  • Jack L Komisar
  • Aziz N Qabar
  • Silas A Davidson
  • Sheetij Dutta
  • Matthew E Griffith
  • Charles D Magee
  • Mariusz Wojnarski
  • Jeffrey R Livezey
  • Adrian T Kress
  • Paige E Waterman
  • Erik Jongert
  • Ulrike Wille-Reece
  • Wayne Volkmuth
  • Daniel Emerling
  • William H Robinson
  • Marc Lievens
  • Danielle Morelle
  • Cynthia K Lee
  • Bebi Yassin-Rajkumar
  • Richard Weltzin
  • Joe Cohen
  • Robert M Paris
  • Norman C Waters
  • Ashley J Birkett
  • David C Kaslow
  • W Ripley Ballou
  • Christian F Ockenhouse
  • Johan Vekemans
چکیده

BACKGROUND Three full doses of RTS,S/AS01 malaria vaccine provides partial protection against controlled human malaria parasite infection (CHMI) and natural exposure. Immunization regimens, including a delayed fractional third dose, were assessed for potential increased protection against malaria and immunologic responses. METHODS In a phase 2a, controlled, open-label, study of healthy malaria-naive adults, 16 subjects vaccinated with a 0-, 1-, and 2-month full-dose regimen (012M) and 30 subjects who received a 0-, 1-, and 7-month regimen, including a fractional third dose (Fx017M), underwent CHMI 3 weeks after the last dose. Plasmablast heavy and light chain immunoglobulin messenger RNA sequencing and antibody avidity were evaluated. Protection against repeat CHMI was evaluated after 8 months. RESULTS A total of 26 of 30 subjects in the Fx017M group (vaccine efficacy [VE], 86.7% [95% confidence interval [CI], 66.8%-94.6%]; P < .0001) and 10 of 16 in the 012M group (VE, 62.5% [95% CI, 29.4%-80.1%]; P = .0009) were protected against infection, and protection differed between schedules (P = .040, by the log rank test). The fractional dose boosting increased antibody somatic hypermutation and avidity and sustained high protection upon rechallenge. DISCUSSIONS A delayed third fractional vaccine dose improved immunogenicity and protection against infection. Optimization of the RTS,S/AS01 immunization regimen may lead to improved approaches against malaria. CLINICAL TRIALS REGISTRATION NCT01857869.

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عنوان ژورنال:
  • The Journal of infectious diseases

دوره 214 5  شماره 

صفحات  -

تاریخ انتشار 2016