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1.
Rev. Inst. Med. Trop. Säo Paulo ; 35(6): 479-83, nov.-dez. 1993. ilus, tab
Artigo em Inglês | LILACS | ID: lil-140111

RESUMO

Toxoplasmose e uma infeccao zoonotica humana de lata prevalencia, causada por um protozoario Apicomplexa, Toxoplasma gondii. a evolucao da doenca aguda e geralmente leve ou assintomatica, exceto nas infeccoes agudas das gestantes, quando a infeccao fetal causa uma doenca devastadora. Para determinar se haveriam fatores de risco regionais, foi analisada a frequencia de titulos de anticorpos T. gondii em areas na regiao Metropolitana de Sao Paulo, comparando grupos etarios....


Assuntos
Humanos , Feminino , Gravidez , Adolescente , Adulto , Cuidado Pré-Natal/métodos , Toxoplasma/imunologia , Toxoplasmose/epidemiologia , Brasil , Imunoglobulina G/imunologia , Testes Sorológicos
2.
Mem. Inst. Oswaldo Cruz ; 87(4): 493-502, out.-dez. 1992. tab, ilus
Artigo em Inglês | LILACS | ID: lil-116361

RESUMO

Peritoneal macrophage activation as measured by H2O2 release and histopathology was compared between Swiss mice and Calomys callosus, a wild rodent, reservoir of Trypanosoma cruzi, during the course of infection with four strains of this parasite. In mice F and Y strain infections result in high parasitemia and mortality while with silvatic strains Costalimai and M226 parasitemia is sub-patent, with very low mortality. H2O2 release peaked at 33,6 and 59 nM/2 x 10(elevado a sexta potência) cells for strains Y and F, respectively, 48 and 50 nM/2 x 10 (elevado a sexta potência) for strains Costalimai and M226, at different days after infection. Histopathological findings of myositis, myocarditis, necrotizing artheritis and abscence of macrophage parasitism were foud for strains F and Costalimai. Y strain infection presented moderate myocarditis and myositis, with parasites multiplying within macrophages. In C. callosus all four strains resulted in patent parasitemia wich was eventually overcome, with scarce mortality. H2O2 release for strains Y or F was comparable to that of mice-peaks of 27 and 53 nM/2 x 10 (elevado a sexta potência) cells, with lower values for strains Costalimai and M226 - 16.5 and 4.6 nM/2 x 10(elevado a sexta potência)cells, respectively. Histopathological lesions with Y and F strain injected animals were comparable to those of mice at the onset of infections; they subsided completely at the later stages with Y strain and partially with F strain infected C. callosus. In Costalimai infected C. callosus practically no histopathological alterations were observed


Assuntos
Animais , Doença de Chagas/história , Ativação de Macrófagos , Roedores/parasitologia , Trypanosoma cruzi/isolamento & purificação
3.
Rev. Inst. Med. Trop. Säo Paulo ; 34(1): 1-8, Jan.-Feb. 1992.
Artigo em Inglês | LILACS | ID: lil-320637

RESUMO

Calomys callosus a wild rodent, previously described as harboring Trypanosoma cruzi, has a low susceptibility to infection by this protozoan. Experiments were designed to evaluate the contribution of the immune response to the resistance to T. cruzi infection exhibited by C. calossus. Animals were submitted to injections of high (200 mg/kg body weight) and low (20 mg/kg body weight) doses of cyclophosphamide on days -1 or -1 and +5, and inoculated with 4 x 10(3) T. cruzi on day O. Parasitemia, mortality and antibody response as measured by direct agglutination of trypomastigotes were observed. Two hundred mg doses of cyclophosphamide resulted in higher parasitemia and mortality as well as in suppression of the antibody response. A single dose of 20 mg enhanced antibody levels on the 20th day after infection, while an additional dose did not further increase antibody production. Parasitemia levels were not depressed, but rather increased in both these groups as compared to untreated controls. Passive transfer of hyperimmune C. callosus anti-T. cruzi serum to cyclophosphamide immunosuppressed animals resulted in lower parasitemia and mortality rates. These results indicate that the immune response plays an important role in the resistance of C. callossus to T. cruzi.


Assuntos
Animais , Feminino , Masculino , Anticorpos Antiprotozoários/imunologia , Arvicolinae , Ciclofosfamida , Doença de Chagas/imunologia , Trypanosoma cruzi , Testes de Aglutinação , Arvicolinae , Doença de Chagas/prevenção & controle , Fatores de Tempo
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