Baculovirus produced Plasmodium falciparum vaccine
AssigneeUniversity of Hawaii
InventorsSandra P. Chang, Kenton J. Kramer, William L. Gosnell, Tani Nishimura
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Abstract
Compositions and methods are provided for the induction of a protective immunize response in primates against lethal challenge of Plasmodium.
Claims19
A pharmaceutical composition for treating plasmodium parasitemia in a mammal, said composition comprising:
- an isolated p42 polypeptide comprising at least a portion of the 42 kDa C-terminal processing fragment of major merozoite surface protein gp195 from a Plasmodium falciparum isolate, wherein said isolated p42 polypeptide shares at least 80% sequence identity with a polypeptide according to any one of SEQ ID NOs. 2-5, in combination with an adjuvant selected from the group consisting of QS-21 and ISA51 and mixtures thereof, and
- wherein the combination of said adjuvant and said isolated p42 polypeptide is capable of inducing an effective immune response against a Plasmodium infection in said mammal.
An anti-plasmodium vaccine comprising an immunogenic amount of an isolated p42 polypeptide comprising at least a portion of the C-terminal processing fragment of major merozoite surface protein gp195 from a Plasmodium falciparum isolate, wherein said isolated p42 polypeptide shares at least 80% sequence identity with a polypeptide according to any one of SEQ ID NOs. 2-5, said p42 polypeptide being expressed by an insect cell which contains a vector that encodes said polypeptide, in combination with an adjuvant selected from the group consisting of QS21 and ISA51 and mixtures thereof,
- wherein said isolated p42 polypeptide is more immunogenic in a mammalian host than is the same polypeptide expressed in yeast, and
- wherein the combination of said adjuvant and said isolated p42 polypeptide is capable of inducing an effective immune response against a Plasmodium infection in said mammal.
A pharmaceutical composition for treating plasmodium parasitemia in a mammal, said composition comprising:
- an isolated p42 polypeptide comprising at least a portion of the 42 kDa C-terminal processing fragment of major merozoite surface protein gp195 from a Plasmodium falciparum isolate, wherein said isolated p42 polypeptide shares at least 80% sequence identity with a polypeptide according to SEQ ID NO:
- 8, in combination with an adjuvant selected from the group consisting of QS-21 and ISA51 and mixtures thereof, and
- wherein the combination of said adjuvant and said isolated p42 polypeptide is capable of inducing effective immune response against a Plasmodium infection in said mammal.
Dependencies are inferred from the claim text.