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Lipopeptide-Based Oral Vaccine Against Hookworm Infection.
Bartlett, Stacey; Eichenberger, Ramon M; Nevagi, Reshma J; Ghaffar, Khairunnisa Abdul; Marasini, Nirmal; Dai, Yang; Loukas, Alex; Toth, Istvan; Skwarczynski, Mariusz.
Afiliação
  • Bartlett S; The University of Queensland, School of Chemistry and Molecular Biosciences, St Lucia, Australia.
  • Eichenberger RM; James Cook University, Centre for Molecular Therapeutics, Australian Institute of Tropical Health & Medicine, Cairns, Australia.
  • Nevagi RJ; The University of Queensland, School of Chemistry and Molecular Biosciences, St Lucia, Australia.
  • Ghaffar KA; The University of Queensland, School of Chemistry and Molecular Biosciences, St Lucia, Australia.
  • Marasini N; The University of Queensland, School of Chemistry and Molecular Biosciences, St Lucia, Australia.
  • Dai Y; James Cook University, Centre for Molecular Therapeutics, Australian Institute of Tropical Health & Medicine, Cairns, Australia.
  • Loukas A; James Cook University, Centre for Molecular Therapeutics, Australian Institute of Tropical Health & Medicine, Cairns, Australia.
  • Toth I; The University of Queensland, School of Chemistry and Molecular Biosciences, St Lucia, Australia.
  • Skwarczynski M; The University of Queensland, School of Pharmacy, Woolloongabba, Australia.
J Infect Dis ; 221(6): 934-942, 2020 03 02.
Article em En | MEDLINE | ID: mdl-31621864
BACKGROUND: The human hookworm, Necator americanus, is a parasite that infects almost half a billion people worldwide. Although treatment is available, vaccination is favorable to combat the spread of this parasite due to its wide distribution and continuous reinfection cycle in endemic communities. METHODS: We have designed a lipopeptide oral delivery system using a B-cell epitope derived from the aspartic protease Na-APR-1 from N americanus, attached to a T-helper epitope. Lipopeptides were self-assembled into nanoparticles or entrapped in liposomes that were electrostatically coated with alginate and trimethyl chitosan polymer shields. The adjuvant-free vaccine candidates were orally administered to mice and generated a humoral immune response against both peptide antigen, and the parent protein in the hookworm gut. RESULTS: The vaccine candidates were evaluated in a rodent hookworm challenge model, resulting in up to 98% and 99% decreases in mean intestinal worm and egg burdens in immunized mice, respectively. CONCLUSIONS: Lipopeptide survived the gastrointestinal conditions, induced humoral immune responses and drived protection against parasite challenge infection.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Vacinas / Lipopeptídeos / Infecções por Uncinaria Limite: Animals Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Vacinas / Lipopeptídeos / Infecções por Uncinaria Limite: Animals Idioma: En Ano de publicação: 2020 Tipo de documento: Article