| Literature DB >> 32434847 |
Meta Roestenberg1,2, Jona Walk3,4, Saskia C van der Boor3, Marijke C C Langenberg1, Marie-Astrid Hoogerwerf1, Jacqueline J Janse1, Mikhael Manurung1, X Zen Yap3, Amanda Fabra García3, Jan Pieter R Koopman1, Pauline Meij5, Els Wessels6, Karina Teelen3, Youri M van Waardenburg3, Marga van de Vegte-Bolmer3, Geert Jan van Gemert3, Leo G Visser2, André J A M van der Ven4, Quirijn de Mast4, K C Natasha7, Yonas Abebe7, Tooba Murshedkar7, Peter F Billingsley7, Tom L Richie7, B Kim Lee Sim7, Chris J Janse1, Stephen L Hoffman7, Shahid M Khan1, Robert W Sauerwein8.
Abstract
Immunization with attenuated Plasmodium sporozoites can induce protection against malaria infection, as shown by Plasmodium falciparum (Pf) sporozoites attenuated by radiation in multiple clinical trials. As alternative attenuation strategy with a more homogeneous population of Pf sporozoites (PfSPZ), genetically engineered Plasmodium berghei sporozoites (SPZ) lacking the genes b9 and slarp induced sterile protection against malaria in mice. Consequently, PfSPZ-GA1 Vaccine, a Pf identical double knockout (Pf∆b9∆slarp), was generated as a genetically attenuated malaria parasite vaccine and tested for safety, immunogenicity, and preliminary efficacy in malaria-naïve Dutch volunteers. Dose-escalation immunizations up to 9.0 × 105 PfSPZ of PfSPZ-GA1 Vaccine were well tolerated without breakthrough blood-stage infection. Subsequently, groups of volunteers were immunized three times by direct venous inoculation with cryopreserved PfSPZ-GA1 Vaccine (9.0 × 105 or 4.5 × 105 PfSPZ, N = 13 each), PfSPZ Vaccine (radiation-attenuated PfSPZ, 4.5 × 105 PfSPZ, N = 13), or normal saline placebo at 8-week intervals, followed by exposure to mosquito bite controlled human malaria infection (CHMI). After CHMI, 3 of 25 volunteers from both PfSPZ-GA1 groups were sterilely protected, and the remaining 17 of 22 showed a patency ≥9 days (median patency in controls, 7 days; range, 7 to 9). All volunteers in the PfSPZ Vaccine control group developed parasitemia (median patency, 9 days; range, 7 to 12). Immunized groups exhibited a significant, dose-related increase in anti-Pf circumsporozoite protein (CSP) antibodies and Pf-specific interferon-γ (IFN-γ)-producing T cells. Although no definite conclusion can be drawn on the potential strength of protective efficacy of PfSPZ-GA1 Vaccine, the favorable safety profile and induced immune responses by PfSPZ-GA1 Vaccine warrant further clinical evaluation.Entities:
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Year: 2020 PMID: 32434847 DOI: 10.1126/scitranslmed.aaz5629
Source DB: PubMed Journal: Sci Transl Med ISSN: 1946-6234 Impact factor: 17.956