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Immunogenicity of Plasmodium falciparum circumsporozoite protein multiple antigen peptide vaccine formulated with different adjuvants

Only low antibody levels were obtained from vaccinating human volunteers with singlechain peptide from the Plasmodium falciparum circumsporozoite protein (PfCSP). This resulted in modest protection against sporozoite challenge. In addition, HLA restriction limits the probability of synthesis of a va...

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Bibliographic Details
Published in:Vaccine 1998-01, Vol.16 (2), p.305-312
Main Authors: Le, Thong P., Preston Church, L.W., Corradin, Giampietro, Hunter, Robert L., Charoenvit, Yupin, Wang, Ruobing, de la Vega, Patricia, Sacci, John, Ripley Ballou, W., Kolodny, Nelly, Kitov, Svetlana, Glenn, Gregory M., Richards, Roberta L., Alving, Carl R., Hoffman, Stephen L.
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Language:English
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Summary:Only low antibody levels were obtained from vaccinating human volunteers with singlechain peptide from the Plasmodium falciparum circumsporozoite protein (PfCSP). This resulted in modest protection against sporozoite challenge. In addition, HLA restriction limits the probability of synthesis of a vaccine effective for a diverse population. We report immunization studies with a multiple antigen peptide (MAP) system consisting of multiple copies of a B-cell epitope from the central repeat region of the PfCSP in combination with a universal T-cell epitope, the P2P30 portion of tetanus toxin. This MAP4(NANP) 6P2P30 vaccine was highly immunogenic in four different strains of mice when used with various safe and nontoxic adjuvants. When this MAP vaccine was encapsulated in liposomes with lipid A and adsorbed to aluminum hydroxide and given three times at 4-week intervals, the resultant antibody prevented 100% of sporozoites from invading and developing into liver stage infection. This high degree of immunogenicity of MAP4(NANP) 6P2P30 vaccine formulated in liposomes, lipid A and aluminum hydroxide provides the foundation for consideration of human trials with this formulation.
ISSN:0264-410X
1873-2518
DOI:10.1016/S0264-410X(97)00165-5