Immunization of
Saimiri sciureus
Monkeys with a Recombinant Hybrid Protein Derived from the
Plasmodium falciparum
Antigen Glutamate-Rich Protein and Merozoite Surface Protein 3 Can Induce Partial Protection with Freund and Montanide ISA720 Adjuvants
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Published:2005-02
Issue:2
Volume:12
Page:242-248
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ISSN:1556-6811
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Container-title:Clinical and Vaccine Immunology
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language:en
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Short-container-title:Clin Vaccine Immunol
Author:
Carvalho Leonardo J. M.12345, Alves Francisco A.12345, Bianco Cesare12345, Oliveira Salma G.12345, Zanini Graziela M.12345, Soe Soe12345, Druilhe Pierre12345, Theisen Michael12345, Muniz José A. P. C.12345, Daniel-Ribeiro Cláudio T.12345
Affiliation:
1. Laboratory of Malaria Research, Department of Immunology, Instituto Oswaldo Cruz 2. Evandro Chagas Institute for Clinical Research, Fiocruz, Rio de Janeiro 3. National Primate Center 4. Instituto Evandro Chagas, SVS, Belém, Brazil 5. Biomedical Parasitology, Institute Pasteur, Paris, France
Abstract
ABSTRACT
The immunogenicity and efficacy of a hybrid recombinant protein derived from the N-terminal end of the glutamate-rich protein (GLURP) and the C-terminal portion of the merozoite surface protein 3 (MSP3) of
Plasmodium falciparum
was evaluated in
Saimiri sciureus
monkeys. The GLURP/MSP3 hybrid protein, expressed in
Lactococcus lactis
, was administered in association with alum, Montanide ISA720, or complete or incomplete Freund adjuvant (CFA/IFA) in groups of five animals each. The three formulations were shown to be immunogenic, but the one with alum was shown to be weak compared to the other two, particularly CFA/IFA, which provided very high antibody titers (enzyme-linked immunosorbent assay titers of >3,000,000 and immunofluorescence antibody test titers of 6,400). After a challenge infection with
P. falciparum
FUP strain, all five monkeys from the GLURP/MSP3-alum group showed a rapid increase in parasitemia, reaching 10% and were treated early. The two monkeys with the highest antibody titers in group GLURP/MSP3-Montanide ISA720 had a delay in the course of parasitemia and were treated late due to a low hematocrit. In the GLURP/MSP3-CFA/IFA group, parasitemia remained below this threshold in four of the five animals and, after it reached a peak, parasitemia started to decrease and monkeys were treated late. When all animals were grouped according to the outcome, a statistically significant association between high antibody titers and partial protection was observed. The challenge infection boosted the antibody titers, and the importance of this event for vaccine efficacy in areas where this parasite is endemic is discussed. In conclusion, these data suggest that GLURP and MSP3 can induce protection against malaria infection if antibodies are induced at properly high titers.
Publisher
American Society for Microbiology
Subject
Microbiology (medical),Clinical Biochemistry,Immunology,Immunology and Allergy
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