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Protection against Plasmodium falciparum malaria by PfSPZ Vaccine

Authors :
Peter F. Billingsley
Mary Carrington
Judith E. Epstein
Donna Tosh
Martha Sedegah
Amy Tillman
Natasha Kc
Minglin Li
Shon Remich
B. Kim Lee Sim
Elizabeth Saverino
Jun Huang
Arnel Belmonte
Richard C. Ruck
Kevin Hauns
Tao Li
Abraham G. Eappen
Debbie Padilla
Alexandra Singer
Anita Manoj
Robin Nielsen
Adam Ruben
Maria Belmonte
Lindsey S. Garver
Kara A. Moser
Silas A. Davidson
Sumana Chakravarty
Eric R. James
Harini Ganeshan
Jessica Case
Eileen Villasante
Thomas L. Richie
Tooba Murshedkar
Sharina Reyes
Stephen L. Hoffman
Joana C. Silva
April Stafford
James E. Moon
Patrick S. Twomey
Yonas Abebe
Esteban Abot
Susan Cicatelli
Jason A. Regules
Carlos S. Vasquez
Bradley Hickey
Kristopher M. Paolino
Anusha Gunasekera
Source :
JCI Insight. 2
Publication Year :
2017
Publisher :
American Society for Clinical Investigation, 2017.

Abstract

BACKGROUND: A radiation-attenuated Plasmodium falciparum (Pf) sporozoite (SPZ) malaria vaccine, PfSPZ Vaccine, protected 6 of 6 subjects (100%) against homologous Pf (same strain as in the vaccine) controlled human malaria infection (CHMI) 3 weeks after 5 doses administered intravenously. The next step was to assess protective efficacy against heterologous Pf (different from Pf in the vaccine), after fewer doses, and at 24 weeks. METHODS: The trial assessed tolerability, safety, immunogenicity, and protective efficacy of direct venous inoculation (DVI) of 3 or 5 doses of PfSPZ Vaccine in non-immune subjects. RESULTS: Three weeks after final immunization, 5 doses of 2.7 × 105 PfSPZ protected 12 of 13 recipients (92.3% [95% CI: 48.0, 99.8]) against homologous CHMI and 4 of 5 (80.0% [10.4, 99.5]) against heterologous CHMI; 3 doses of 4.5 × 105 PfSPZ protected 13 of 15 (86.7% [35.9, 98.3]) against homologous CHMI. Twenty-four weeks after final immunization, the 5-dose regimen protected 7 of 10 (70.0% [17.3, 93.3]) against homologous and 1 of 10 (10.0% [-35.8, 45.6]) against heterologous CHMI; the 3-dose regimen protected 8 of 14 (57.1% [21.5, 76.6]) against homologous CHMI. All 22 controls developed Pf parasitemia. PfSPZ Vaccine was well tolerated, safe, and easy to administer. No antibody or T cell responses correlated with protection. CONCLUSIONS: We have demonstrated for the first time to our knowledge that PfSPZ Vaccine can protect against a 3-week heterologous CHMI in a limited group of malaria-naive adult subjects. A 3-dose regimen protected against both 3-week and 24-week homologous CHMI (87% and 57%, respectively) in this population. These results provide a foundation for developing an optimized immunization regimen for preventing malaria. TRIAL REGISTRATION: ClinicalTrials.gov NCT02215707. FUNDING: Support was provided through the US Army Medical Research and Development Command, Military Infectious Diseases Research Program, and the Naval Medical Research Center's Advanced Medical Development Program.

Details

ISSN :
23793708
Volume :
2
Database :
OpenAIRE
Journal :
JCI Insight
Accession number :
edsair.doi...........9976e88d3f77ada6d92b19159efdf7e3