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Biomedical subjects

C A Cuba-Cuba

Publications and source records attributed to C A Cuba-Cuba.

6 recordsLinked to original sources

Dissemination of Leishmania (Viannia) braziliensis.

Destructive human mucocutaneous leishmaniasis may appear many years after the primary cutaneous infection with Leishmania (Viannia) braziliensis. Hamsters (Mesocricetus auratus) were infected with metacyclic L. braziliensis promastigotes. It was found that secondary metastatic visceral lesions could arise from a primary cutaneous lesion, or secondary cutaneous lesions from a primary visceral lesion. Parasites in the viscera were shown to be viable, multiplying and capable of metastasis to either secondary visceral or cutaneous sites. The finding of an early metastasis in the wall of a small cutaneous vessel indicates that dissemination can occur by the haematogenous route. Slow growing organisms in viscera may thus be a source for late metastasis to mucocutaneous sites or for systemic relapse after immunosuppression.

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Marmosets in New World leishmaniasis research.

In leishmaniasis, the search for a suitable experimental animal model is highly recommended, especially in Leishmania (Viannia) braziliensis (L. (V) b) research. Diverse species of neotropical primates have increasingly been used as experimental hosts of Leishmania. This article describes aspects of parasite L(V)b and marmoset, Callithrix penicillata (Primates, Callithricidae), interaction and summarizes the biology of parasitism in this primate model. Results of recent studies on primary infections with several strains of L(V)b as well as parasitism evolution, clinical outcome patterns and immunoprotection experiments, are summarily discussed. The relevance of homologous reinfection experiments for vaccine development in leishmaniasis is discussed.

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Clonal variation within a mucosal isolate derived from a patient with Leishmania (Viannia) braziliensis infection.

Three isolates over 5 years from a patient with persistent relapsing mucosal leishmaniasis due to Leishmania (Viannia) braziliensis and 7 clones from one of these isolates were studied by zymodemes and serodemes analysis. Results showed evidences of clonal phenotypic variation. Eight isoenzymes markers demonstrated clear differences on Cellulose Acetate (CA) and thin starch gel electrophoresis. Also a panel of specific monoclonal antibodies showed such differences. Our observations provide additional evidence that Leishmania (Viannia) braziliensis is composed by subpopulations of parasites with peculiar biochemical and antigenic characteristics.

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