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Chemoprophylaxis Vaccination: Phase I Study to Explore Stage-specific Immunity to Plasmodium falciparum in US Adults.
Healy, Sara A; Murphy, Sean C; Hume, Jen C C; Shelton, Lisa; Kuntz, Steve; Van Voorhis, Wesley C; Moodie, Zoe; Metch, Barbara; Wang, Ruobing; Silver-Brace, Tiffany; Fishbaugher, Matthew; Kennedy, Mark; Finney, Olivia C; Chaturvedi, Richa; Marcsisin, Sean R; Hobbs, Charlotte V; Warner-Lubin, Margaret; Talley, Angela K; Wong-Madden, Sharon; Stuart, Ken; Wald, Anna; Kappe, Stefan H; Kublin, James G; Duffy, Patrick E.
Afiliação
  • Healy SA; Center for Infectious Disease Research, Seattle, Washington, USA.
  • Murphy SC; Department of Pediatrics, Division of Pediatric Infectious Diseases, University of Washington, Seattle, Washington, USA.
  • Hume JCC; Laboratory of Malaria Immunology and Vaccinology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, USA.
  • Shelton L; Center for Infectious Disease Research, Seattle, Washington, USA.
  • Kuntz S; Department of Laboratory Medicine and Microbiology, University of Washington, Seattle, Washington, USA.
  • Van Voorhis WC; Center for Emerging and Re-emerging Infectious Diseases, University of Washington, Seattle, Washington, USA.
  • Moodie Z; Center for Infectious Disease Research, Seattle, Washington, USA.
  • Metch B; Laboratory of Malaria Immunology and Vaccinology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, USA.
  • Wang R; Center for Infectious Disease Research, Seattle, Washington, USA.
  • Silver-Brace T; Department of Medicine, Division of Allergy and Infectious Diseases, University of Washington, Seattle, Washington, USA.
  • Fishbaugher M; Center for Emerging and Re-emerging Infectious Diseases, University of Washington, Seattle, Washington, USA.
  • Kennedy M; Department of Medicine, Division of Allergy and Infectious Diseases, University of Washington, Seattle, Washington, USA.
  • Finney OC; Vaccine and Infectious Diseases Division, Fred Hutchinson Cancer Research Center, Seattle, Washington, USA.
  • Chaturvedi R; Vaccine and Infectious Diseases Division, Fred Hutchinson Cancer Research Center, Seattle, Washington, USA.
  • Marcsisin SR; Center for Infectious Disease Research, Seattle, Washington, USA.
  • Hobbs CV; Center for Infectious Disease Research, Seattle, Washington, USA.
  • Warner-Lubin M; Center for Infectious Disease Research, Seattle, Washington, USA.
  • Talley AK; Center for Infectious Disease Research, Seattle, Washington, USA.
  • Wong-Madden S; Center for Infectious Disease Research, Seattle, Washington, USA.
  • Stuart K; Center for Infectious Disease Research, Seattle, Washington, USA.
  • Wald A; Military Malaria Research Program, Division of Experimental Therapeutics, Walter Reed Army Institute of Research, Silver Spring, Maryland, USA.
  • Kappe SH; Laboratory of Malaria Immunology and Vaccinology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, USA.
  • Kublin JG; Center for Infectious Disease Research, Seattle, Washington, USA.
  • Duffy PE; C3 Research Associates, Seattle, Washington, USA.
Clin Infect Dis ; 71(6): 1481-1490, 2020 09 12.
Article em En | MEDLINE | ID: mdl-31621832
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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Malária Falciparum / Antimaláricos Tipo de estudo: Clinical_trials Limite: Adult / Animals / Humans Idioma: En Revista: Clin Infect Dis Assunto da revista: DOENCAS TRANSMISSIVEIS Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Malária Falciparum / Antimaláricos Tipo de estudo: Clinical_trials Limite: Adult / Animals / Humans Idioma: En Revista: Clin Infect Dis Assunto da revista: DOENCAS TRANSMISSIVEIS Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Estados Unidos