Back to Search Start Over

Multi-Dose Priming Regimens of PfSPZ Vaccine: Safety and Efficacy against Controlled Human Malaria Infection in Equatoguinean Adults

Authors :
Said Abdallah Jongo
L. W. Preston Church
Vicente Urbano Nsue Ndong Nchama
Ali Hamad
Raul Chuquiyauri
Kamaka Ramadhani Kassim
Thabit Athuman
Anna Deal
KC Natasha
Ali Mtoro
Maxmillian Mpina
Elizabeth Nyakarungu
Gertrudis Owono Bidjimi
Marta Alene Owono
Escolástica Raquel Mansogo Mayé
Martín Eká Ondó Mangue
Genaro Nsué Nguema Okomo
Beltrán Ekuá Ntutumu Pasialo
Dolores Mbang Ondó Mandumbi
María-Silvia A. López Mikue
Fortunata Lobede Mochomuemue
Mariano Obiang Obono
Juan Carlos Momo Besahá
José Raso Bijeri
Gabriel Mbá Abegue
Yolanda Rimoy Veri
Ines Toichoa Bela
Federico Comsil Chochi
José Enrique Lima Sánchez
Vanessa Pencelli
Griselda Gayozo
José Antonio Esono Mbá Nlang
Tobias Schindler
Eric R. James
Yonas Abebe
Laurence Lemiale
Thomas C. Stabler
Tooba Murshedkar
Mei-Chun Chen
Christopher Schwabe
Josea Ratsirarson
Matilde Riloha Rivas
Mitoha Ondo’o Ayekaba
Diosdado Vicente Nsué Milang
Carlos Cortés Falla
Wonder P. Phiri
Guillermo A. García
Carl D. Maas
Bonifacio Manguire Nlavo
Marcel Tanner
Peter F. Billingsley
B. Kim Lee Sim
Claudia Daubenberger
Stephen L. Hoffman
Salim Abdulla
Thomas L. Richie
Source :
The American journal of tropical medicine and hygiene.
Publication Year :
2021

Abstract

Plasmodium falciparum sporozoite (PfSPZ) Vaccine is composed of radiation-attenuated, aseptic, purified cryopreserved PfSPZ. Multiple clinical trials empirically assessing two to six doses have shown multi-dose priming (two to four doses the first week) to be optimal for protection in both 4- and 16-week regimens. In this randomized, double-blind, normal saline (NS) placebo-controlled trial, four groups (G) of 18- to 32-year-old Equatoguineans received multi-dose priming regimens with or without a delayed final dose at 4 or 16 weeks. The regimens were G1: days 1, 3, 5, 7, and 113; G2: days 1, 3, 5, and 7; G3: days 1, 3, 5, 7, and 29; and G4: days 1, 8, and 29. All doses were 9 × 105 PfSPZ. Tolerability, safety, immunogenicity, and vaccine efficacy (VE) against homologous controlled human malaria infection (CHMI) 6–7 weeks after vaccination were assessed to down-select the best regimen. All four regimens were safe and well tolerated, with no significant differences in adverse events (AEs) between vaccinees (N = 84) and NS controls (N = 20) or between regimens. Out of 19 controls, 13 developed Pf parasitemia by quantitative polymerase chain reaction (qPCR) after CHMI. Only the vaccine regimen administered on study days 1, 8, and 29 gave significant protection (7/21 vaccinees versus 13/19 controls infected, VE 51.3%, P = 0.03, Barnard’s test, two-tailed). There were no significant differences in antibodies against Pf circumsporozoite protein (PfCSP), a major SPZ antigen, between protected and nonprotected vaccinees or controls pre-CHMI. The six controls not developing Pf parasitemia had significantly higher antibodies to blood stage antigens Pf exported protein 1 (PfEXP1) and Pf merozoite surface protein 1 (PfMSP1) than the controls who developed parasitemia, suggesting naturally acquired immunity against Pf limited infections in controls. This study identified a safe, protective, 4-week, multi-dose prime vaccination regimen for assessment in future trials of PfSPZ Vaccine.

Details

ISSN :
14761645
Database :
OpenAIRE
Journal :
The American journal of tropical medicine and hygiene
Accession number :
edsair.doi.dedup.....084dea569c63a6d438e84d6df3f96b9a