Malaria remains a serious global health problem for which there is no effective vaccine. Previous studies indicate that animals can be immunized with inactivated sporozoites. The genes coding for the circumsporozoite antigens of the malaria parasite Plasmodium knowlesi and P. falciparum were inserted into the vaccinia virus genome under the control of a defined vaccinia virus promoter. Tissue culture cells infected with the recombinant synthesized polypeptides that reacted with monoclonal antibody against the malaria protein. Studies on the sequence of the expressed P. falciparum CSP indicated that the NH2-terminus is blocked and COOH-terminus is not processed. Immunofluorescent staining demonstrated that the CSP was distributed primarily in the cytoplasm of infected cells. Rabbits vaccinated with the recombinant virus produced antibodies that bound specifically to sporozoites. The S antigen gene of P. falciparum also was expressed in a vaccinia virus recombinant. The protein was secreted from infected cells and reacted with specific antiserum. Vaccinated animals produced a low but detectable antibody response.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Intramural Research (Z01)
Project #
1Z01AI000393-02
Application #
4688513
Study Section
Project Start
Project End
Budget Start
Budget End
Support Year
2
Fiscal Year
1985
Total Cost
Indirect Cost
Name
Niaid Extramural Activities
Department
Type
DUNS #
City
State
Country
United States
Zip Code