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1.
Mem. Inst. Oswaldo Cruz ; 95(3): 363-5, May-Jun. 2000. graf
Article in English | LILACS | ID: lil-258190

ABSTRACT

Aotus is one of the WHO-recommended primate models for studies in malaria, and several species can be infected with Plasmodium falciparum or P. vivax. Here we describe the successful infection of the species A. infulatus from eastern Amazon with blood stages of P. falciparum. Both intact and splenectomized animals were susceptible to infection; the intact ones were able to keep parasitemias at lower levels for several days, but developed complications such as severe anemia; splenectomized monkeys developed higher parasitemias but no major complications. We conclude that A. infulatus is susceptible to P. falciparum infection and may represent an alternative model for studies in malaria.


Subject(s)
Animals , Male , Female , Disease Models, Animal , Haplorhini/parasitology , Malaria, Falciparum/parasitology , Monkey Diseases/parasitology , Plasmodium falciparum/immunology , Body Temperature , Disease Susceptibility , Haplorhini/immunology , Monkey Diseases/immunology , Parasitemia/parasitology , Splenectomy
2.
Mem. Inst. Oswaldo Cruz ; 92(supl.2): 69-73, Dec. 1997. tab, graf
Article in English | LILACS | ID: lil-202017

ABSTRACT

Interleukin 5 (IL-5) is a critical cytokine for the maturation of eosinophil precursors to eosinophils in the bone marrow and those eosinophils then accumulate in the lungs during asthma. We have studied anti-bodies on allergic responses in mice, guinea pigs anf monkeys and are extending this experiment into humans with a humanized antibody. In a monkey model of pulmonary inflammation and airway hyperreactivity, we found that the TRFK-5 antibody blocked both responses for three months following a single dose of 0.3 mg/kg i.v. This antibody also blocked lung eosinophilia in mice by inhibiting release from the bone marrow. To facilitate multiple dosing and to reduce immunogenicity in humans, we prepared Sch 55700, humanized antibody against IL-5. Sch 55700 was also active against lung eosinophilia in allergic monkeys and mice and against pulmonary eosinophilia and airway hyperresponsiveness in guinea pigs. Furthermore, as opposed to steroids, Sch 55700 dis not cause immunosuppression in guinea pigs. Studies with antibody in humans will be critical to establishing the therapeutic potential of IL-5 inhibition.


Subject(s)
Animals , Guinea Pigs , Humans , Mice , Antibodies , Interleukin-5/immunology , Lung/physiopathology , Asthma/immunology , Eosinophils , Haplorhini/immunology , Bronchial Hyperreactivity/physiopathology , Respiratory Hypersensitivity
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