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Clinical Trial
. 1990 Jun;42(6):527-31.
doi: 10.4269/ajtmh.1990.42.527.

Safety and immunogenicity of a Plasmodium vivax sporozoite vaccine

Affiliations
Clinical Trial

Safety and immunogenicity of a Plasmodium vivax sporozoite vaccine

D M Gordon et al. Am J Trop Med Hyg. 1990 Jun.

Abstract

A recombinant DNA Plasmodium vivax sporozoite vaccine containing the repeating region of the Salvador I strain circumsporozoite (CS) protein was produced in Escherichia coli. This vaccine was tested in 13 naive volunteers at doses of 10-1,000 micrograms. No serious adverse reactions were noted. None of 4 volunteers receiving the 10 micrograms dose developed antibodies measurable by ELISA. Six of 9 volunteers in the other dose groups developed measurable antibodies: 5 of 5 volunteers receiving 100 micrograms and 1 of 4 receiving 1,000 micrograms. Antibody responses measured by immunofluorescence assays paralleled those seen by ELISA. None of the volunteers developed antisera that inhibited sporozoite invasion of human hepatoma cells in vitro. Lack of a classical anamnestic response and lack of a typical dose response to increasing amounts of antigen suggests the possible presence of an immunosuppressive epitope in the repetitive region of the CS protein.

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