Aotus lemunnus is currently accepted to be one of the most appropriate animal models for human malaria parasite infection (1-3). This species is susceptible to infection by P. falciparum (4-6), P. vivax (2, 7-10) and P. malariae (11-12)and unlike chimpanzees, it is available in sufficient numbers to carry out studies with adequate sample sizes. Based on this susceptibility, the model has been extensively used to study the immunogenicity and protective efficacy of malaria vaccine candidates. However, during the past several years there has been concern that monkey models may not reproduce the immune response of humans to specific antigens, leading to results in pre-clinical trials that do not predict the outcome in humans. Despite this concern, we have conducted an important number of pre-clinical trials using this primate model during the last decade, and the results of many of our studies suggest that the Aotus model is a reliable system for testing the immunogenicity and protective efficacy of candidate malaria vaccines. Thus we propose that the Aotus model has the potential to play a critical role in malaria vaccine development, and for this reason, we plan to conduct systematic analyses in order to validate the model. These analyses are the subject of project 3. We plan to approach this issue by studying the response of Aotus monkeys to different P. vivax candidate antigens and vaccine formulations, and compare these to the responses induced in humans exposed to P. vivax through immunizations with irradiated sporozoites (project 2), or exposed to the parasite under natural conditions or immunized with candidate vaccines by ourselves and by our collaborators (not part of this proposal). This project will cover analyses of both preerythrocytic and erythrocytic asexual stage antigens available from different collaborators. We will use different fragments of the P. vivax CSP and SSP-2, as well as different regions of the MSP-1 and the DBP. The response of Aotus monkeys to different parasite antigens and gene constructs will be determined.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Specialized Center (P50)
Project #
1P50AI049486-01
Application #
6477693
Study Section
Special Emphasis Panel (ZAI1)
Project Start
2001-07-01
Project End
2006-06-30
Budget Start
Budget End
Support Year
1
Fiscal Year
2001
Total Cost
Indirect Cost
Name
University of Valle
Department
Type
DUNS #
City
Cali
State
Country
Colombia
Zip Code
Arévalo-Herrera, Myriam; Solarte, Yezid; Marin, Catherin et al. (2011) Malaria transmission blocking immunity and sexual stage vaccines for interrupting malaria transmission in Latin America. Mem Inst Oswaldo Cruz 106 Suppl 1:202-11
Rodríguez, Julio Cesar Padilla; Uribe, Gilberto Álvarez; Araújo, Roberto Montoya et al. (2011) Epidemiology and control of malaria in Colombia. Mem Inst Oswaldo Cruz 106 Suppl 1:114-22
Jordán-Villegas, Alejandro; Perdomo, Anilza Bonelo; Epstein, Judith E et al. (2011) Immune responses and protection of Aotus monkeys immunized with irradiated Plasmodium vivax sporozoites. Am J Trop Med Hyg 84:43-50
Valencia, Sócrates Herrera; Rodríguez, Diana Carolina; Acero, Diana Lucía et al. (2011) Platform for Plasmodium vivax vaccine discovery and development. Mem Inst Oswaldo Cruz 106 Suppl 1:179-92
Herrera, Sócrates; Fernández, Olga; Manzano, María R et al. (2009) Successful sporozoite challenge model in human volunteers with Plasmodium vivax strain derived from human donors. Am J Trop Med Hyg 81:740-6
Castellanos, Angelica; Arevalo-Herrera, Myriam; Restrepo, Nora et al. (2007) Plasmodium vivax thrombospondin related adhesion protein: immunogenicity and protective efficacy in rodents and Aotus monkeys. Mem Inst Oswaldo Cruz 102:411-6
Llanos, Cesar; Quintero, Gustavo; Castellanos, Alejandro et al. (2006) Surgical bone marrow aspiration in Aotus lemurinus griseimembra. J Med Primatol 35:131-5
Arevalo-Herrera, Myriam; Castellanos, Angelica; Yazdani, Syed S et al. (2005) Immunogenicity and protective efficacy of recombinant vaccine based on the receptor-binding domain of the Plasmodium vivax Duffy binding protein in Aotus monkeys. Am J Trop Med Hyg 73:25-31
Jordan-Villegas, Alejandro; Zapata, Judith Constanza; Perdomo, Anilza Bonelo et al. (2005) Aotus lemurinus griseimembra monkeys: a suitable model for Plasmodium vivax sporozoite infection. Am J Trop Med Hyg 73:10-5
Terrientes, Zilka I; Vergara, Juana; Kramer, Kenton et al. (2005) Restricted genetic diversity of Plasmodium falciparum major merozoite surface protein 1 in isolates from Colombia. Am J Trop Med Hyg 73:55-61

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