Abstract |
A blood-stage vaccine based on Plasmodium falciparum merozoite surface protein 3 (MSP3) was tested for efficacy in a primate model. Aotus nancymai monkeys were vaccinated with yeast-expressed MSP3 before a lethal challenge with Plasmodium falciparum parasites. Five of 7 control monkeys had acute infections and required treatment to control parasitemia. Only 1 of 7 monkeys vaccinated with MSP3 required this treatment. The efficacy of the MSP3 vaccination appeared to be comparable to that of MSP1(42), a leading asexual vaccine candidate, in response to which 2 monkeys experienced acute infections. In the MSP3-vaccinated group, protection correlated with prechallenge titers of antibody to MSP3. In the MSP1 and control groups, protection correlated with antibody to MSP3 raised by challenge infection.
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Authors | Hajime Hisaeda, Allan Saul, Joshua J Reece, Michael C Kennedy, Carole A Long, Louis H Miller, Anthony W Stowers |
Journal | The Journal of infectious diseases
(J Infect Dis)
Vol. 185
Issue 5
Pg. 657-64
(Mar 01 2002)
ISSN: 0022-1899 [Print] United States |
PMID | 11865423
(Publication Type: Journal Article, Research Support, U.S. Gov't, P.H.S.)
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Chemical References |
- Antibodies, Protozoan
- Antigens, Bacterial
- Bacterial Proteins
- Malaria Vaccines
- Vaccines, Synthetic
- major surface protein 3, Anaplasma marginale
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Topics |
- Animals
- Antibodies, Protozoan
(blood)
- Antigens, Bacterial
- Aotidae
- Bacterial Proteins
(administration & dosage, genetics, immunology)
- Malaria Vaccines
(administration & dosage, immunology)
- Malaria, Falciparum
(prevention & control)
- Plasmodium falciparum
(immunology)
- Saccharomyces cerevisiae
(genetics, metabolism)
- Vaccination
- Vaccines, Synthetic
(administration & dosage, immunology)
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