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SEVERE ANEMIA AFFECTS BOTH SPLENECTOMIZED AND NON-SPLENECTOMIZED PLASMODIUM FALCIPARUM-INFECTED AOTUS INFULATUS MONKEYS
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Fundação Oswaldo Cruz. Instituto Oswaldo Cruz. Departamento de Imunologia, WHO-collaborating Centre for Research and Training in Immunology of Parasitic Diseases. Laboratório de Pesquisas em Malária. Rio de Janeiro, RJ, Brasil.
Fundação Oswaldo Cruz. Instituto Oswaldo Cruz. Centro Nacional de Primatas. Rio de Janeiro, RJ, Brasil.
Instituto Evandro Chagas. Funasa, Belém, PA, Brasil.
Fundação Oswaldo Cruz. Instituto Oswaldo Cruz. Centro Nacional de Primatas. Rio de Janeiro, RJ, Brasil.
Fundação Oswaldo Cruz. Instituto Oswaldo Cruz. Departamento de Imunologia, WHO-collaborating Centre for Research and Training in Immunology of Parasitic Diseases. Laboratório de Pesquisas em Malária. Rio de Janeiro, RJ, Brasil.
Fundação Oswaldo Cruz. Instituto Oswaldo Cruz. Centro Nacional de Primatas. Rio de Janeiro, RJ, Brasil.
Fundação Oswaldo Cruz. Instituto Oswaldo Cruz. Departamento de Imunologia, WHO-collaborating Centre for Research and Training in Immunology of Parasitic Diseases. Laboratório de Pesquisas em Malária. Rio de Janeiro, RJ, Brasil.
Fundação Oswaldo Cruz. Instituto Oswaldo Cruz. Centro Nacional de Primatas. Rio de Janeiro, RJ, Brasil.
Instituto Evandro Chagas. Funasa, Belém, PA, Brasil.
Fundação Oswaldo Cruz. Instituto Oswaldo Cruz. Centro Nacional de Primatas. Rio de Janeiro, RJ, Brasil.
Fundação Oswaldo Cruz. Instituto Oswaldo Cruz. Departamento de Imunologia, WHO-collaborating Centre for Research and Training in Immunology of Parasitic Diseases. Laboratório de Pesquisas em Malária. Rio de Janeiro, RJ, Brasil.
Fundação Oswaldo Cruz. Instituto Oswaldo Cruz. Centro Nacional de Primatas. Rio de Janeiro, RJ, Brasil.
Fundação Oswaldo Cruz. Instituto Oswaldo Cruz. Departamento de Imunologia, WHO-collaborating Centre for Research and Training in Immunology of Parasitic Diseases. Laboratório de Pesquisas em Malária. Rio de Janeiro, RJ, Brasil.
Abstract
Severe anemia is the earliest and a frequently fatal complication of Plasmodium falciparum infection. Here we
describe Aotus infulatus as a primate model suitable to study this malaria complication. Both non-splenectomized
and splenectomized monkeys receiving different inocula of P. falciparum FVO strain presented large (> 50%)
decreases in hematocrit values during infection. Non-splenectomized animals were able to control parasite growth
(parasitemia did not exceed 4%), but they had to be treated because of severe anemia. Three of 4 splenectomized
monkeys did not control parasitemia and were treated, but developed severe anemia after treatment when presenting
a negative blood film. Destruction of parasitized red blood cells alone cannot account for the degree of anemia.
Non-splenectomized monkeys repeatedly infected with homologous parasites became rapidly and progressively
resistant to reinfection and to the development of severe anemia. The data presented here point to A. infulatus as a
suitable model for studying the pathogenesis of severe malarial infection.
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