Chemoprophylaxis Vaccination: Phase I Study to Explore Stage-specific Immunity to Plasmodium falciparum in US Adults

Author:

Healy Sara A123,Murphy Sean C145,Hume Jen C C13,Shelton Lisa1,Kuntz Steve6,Van Voorhis Wesley C56,Moodie Zoe7,Metch Barbara7,Wang Ruobing1,Silver-Brace Tiffany1,Fishbaugher Matthew1,Kennedy Mark1,Finney Olivia C1,Chaturvedi Richa1,Marcsisin Sean R8,Hobbs Charlotte V3,Warner-Lubin Margaret19,Talley Angela K1,Wong-Madden Sharon13,Stuart Ken1,Wald Anna46710,Kappe Stefan H1,Kublin James G17,Duffy Patrick E13

Affiliation:

1. Center for Infectious Disease Research, Seattle, Washington, USA

2. Department of Pediatrics, Division of Pediatric Infectious Diseases, University of Washington, Seattle, Washington, USA

3. Laboratory of Malaria Immunology and Vaccinology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, USA

4. Department of Laboratory Medicine and Microbiology, University of Washington, Seattle, Washington, USA

5. Center for Emerging and Re-emerging Infectious Diseases, University of Washington, Seattle, Washington, USA

6. Department of Medicine, Division of Allergy and Infectious Diseases, University of Washington, Seattle, Washington, USA

7. Vaccine and Infectious Diseases Division, Fred Hutchinson Cancer Research Center, Seattle, Washington, USA

8. Military Malaria Research Program, Division of Experimental Therapeutics, Walter Reed Army Institute of Research, Silver Spring, Maryland, USA

9. C3 Research Associates, Seattle, Washington, USA

10. Department of Epidemiology, Division of Allergy and Infectious Diseases, University of Washington, Seattle, Washington, USA

Abstract

Abstract Background Chemoprophylaxis vaccination with sporozoites (CVac) with chloroquine induces protection against a homologous Plasmodium falciparum sporozoite (PfSPZ) challenge, but whether blood-stage parasite exposure is required for protection remains unclear. Chloroquine suppresses and clears blood-stage parasitemia, while other antimalarial drugs, such as primaquine, act against liver-stage parasites. Here, we evaluated CVac regimens using primaquine and/or chloroquine as the partner drug to discern whether blood-stage parasite exposure impacts protection against homologous controlled human malaria infection. Methods In a Phase I, randomized, partial double-blind, placebo-controlled study of 36 malaria-naive adults, all CVac subjects received chloroquine prophylaxis and bites from 12–15 P. falciparum–infected mosquitoes (CVac-chloroquine arm) at 3 monthly iterations, and some received postexposure primaquine (CVac-primaquine/chloroquine arm). Drug control subjects received primaquine, chloroquine, and uninfected mosquito bites. After a chloroquine washout, subjects, including treatment-naive infectivity controls, underwent homologous, PfSPZ controlled human malaria infection and were monitored for parasitemia for 21 days. Results No serious adverse events occurred. During CVac, all but 1 subject in the study remained blood-smear negative, while only 1 subject (primaquine/chloroquine arm) remained polymerase chain reaction–negative. Upon challenge, compared to infectivity controls, 3/3 chloroquine arm subjects displayed delayed patent parasitemia (P = .01) but not sterile protection, while 3/11 primaquine/chloroquine subjects remained blood-smear negative. Conclusions CVac-primaquine/chloroquine is safe and induces sterile immunity to P. falciparum in some recipients, but a single 45 mg dose of primaquine postexposure does not completely prevent blood-stage parasitemia. Unlike previous studies, CVac-chloroquine did not produce sterile immunity. Clinical Trials Registration NCT01500980.

Funder

Bill and Melinda Gates Foundation

National Institute of Allergy and Infectious Diseases

National Institutes of Health

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Microbiology (medical)

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