85 resultados para CIRROSIS HEPATICA
Resumo:
Os autores observam que após a inactivação de sôro de cobaya a 54° durante 30 minutos permanecem no sôro as fracções thermolabeis em quantidade apreciavel; um tal sôro conservado na temperatura de 6°, por espaço de 18 horas, regenera parte da sua actividade alexica perdida. 2° Confirma-se a existencia de 4 componentes do complemento. 3° O chamado terceiro componente de Ritz e Coca é na verdade constituidos por dois elementos, pelos menos, differentes: um destructivel pelo formol e outro destructivel pelo hydrosulphito de sodio. 4° A ammonia, o formol e o hydrosulpito de sodio são capazes de destruir os constituintes thermoresistentes da alexina do sôro inactivado a 56° 30 minutos, ao passo que as emulsões de levedos, de orgãos ou de gelose não o são. 5° As emulsões de levedo addicionadas a uma mistura em partes eguaes de sôro fresco de cobaya e de sôro aquecido a 56°, 30 m., são capazes de retirar não só o terceiro componente contido no sôro fresco da mistura, mas tambem o terceiro componente contido no sôro inactivado pelo calor. 6° Sem excluir a hypothese de uma floculação em que o sôro aquecido exerça o papel de um colloide protector, os autores admittem que a inactivação do complemento pelas emulsões de levedo ou pela gelose seja devida a substancias thermolabeis, do sôro, depois de adsorpção por essas emulsões, de substancias anti-tripticas. 7° Os diversos elementos que constituem a alexina são adsorvidos pelos globulos sensibilizados na seguinte ordem: Globulos-sensibilizadora-Fracção thermo-resistente sensivel á ammonia-Fracção thermolabil Globulina-Fracção thermolabil albumina-Fracção thermoresistente sensivel ao formol-Fracção thermoresistente sensivel ao hydrosulphito de sodio. 8° Na reacção de Bordet-Wassermann fortemente positiva é fixada sobretudo a fracção globulina thermolabil do complemento e não sómente o terceiro componente como seria licito esperar; a fracção thermolabil albumina permanece de regra livre e activa no liquido. 9° Os autores acham que se deve considerar como demonstrada a origem hepatica da alexina. Segundo experiencias procedidas em cães intoxicados pelo chloroformio não só baixa consideravelmente o titulo alexico global do sôro mas tambem os titulos, de todos os constituintes da alexina separadamente, soffrem, com a excepção da fracção thermolabil globulina, uma reducção muito accentuada.
Resumo:
Estudamos 25 casos escolhidos de Ancylostomose, procurando determinar quaes os factores que provocam a regeneração hematica, procurando o mechanismo desta regeneração e o desenvolver do processo anemiante. Preferimos seleccionar um numero pequeno de casos e acompanhal-o durante um largo tempo, observando alguns delles durante 1 a 1 anno e meio. A parte hematologica constou, além de 568 exames rotineiros (numeração das hematias, dosagem de Hb., determinação do hematocrito, e na maioria das vezes, determinação da taxa de reticulocytose verificação do aspecto morphologico do sangue em esfregaços), de pesquisas sobre a resistencia globular, sobre a taxa de proteinas no sôro, e em alguns casos, contagem de plaquetas, determinação da viscosidade, etc. Empregamos para estas pesquizas os methodos usuaes, a não ser na determinação da resistencia globular, para a qual descrevemos detalhadamente um processo pouco usado. Durante todo o transcorrer das observações, a actividade biologica dos helminthos parasitos foi controlada por numerosos exames de fezes, que constavam da pesquiza de ovos eliminados, de reacções chimicas que demonstrassem a presença de sangue. Exames de urina foram feitos periodicamente e outros exames foram praticados quando sobrevinha uma complicação ou qualquer facto inesperado. Observamos nos casos graves da doença, uma anemia de caracteristicas fixas. E' uma anemia hypochromica, microcytica, fracamente regenerativa. Verificamos que a degeneração dos indices hematicos, isto é, que o grau de hypochromia e micocytose, não se apresentam nestes casos extremos de modo variavel, mas sim, de maneira particularmente constante; e verificamos mais que estes indices assim degenerados (Ind. Vol. 53 uc., Ind. Hb. 13 yy, Ind. Sat. 23%) tambem são encontrados segundo observações de outros autores, em varias anemias hypochromicas humanas ou de outros mammiferos. No exame de esfregaços, são extremamente raros ou mesmo ausentes, os normoblastos, as hematias com restos nucleares e as hematias polychromaticas. A reticulose oscilla em torno de 3%. Este aspecto é constante nos casos graves, sendo entretanto variavel na unidade de volume o numero destas hematias acima caracterisadas. A média dessa ultima cifra em numerosos casos é de 2,50 M., o que determina uma taxa de Hb. egual a 23%. Ao analysarmos certas observações, que descrevem aspectos hematologicos differentes daquelles aqui descriptos, concluimos pela existencia nesses casos anomalos, de superposições de outras doenças, cuja etio-pathogenia nada tem a ver com os factores que determinam o apparecimento da anemia ancylostomotica. A regeneração hematica processa-se na Ancylostomose unicamente após a administração de ferro em dóses variaveis, conforme o sal empregado. Mostraram-se inactivas nos casos aqui observados, as administrações de figado crú, triptophano, hystidina, lecithina, Vit. B, saes de arsenico, manganez, cobalto, cobre e a alimentação com dietas ricas em ferro. Em virtude dos resultados que obtivemos com a administração isolada de ferro, concluimos pela inefficiencia da administração de substancias pyrrholicas, da fracção hepatica sensivel nas anemias hypochromicas, e da associação ao ferro de acido chlorhydrico. Todas essas substancias, e tambem a elimanação simples dos helminthos parasitos, não só mostraram-se isoladamente sem acção sobre o sangue, como não auxiliaram a regeneração provocada pelo ferro...
Resumo:
Os autores descrevem um caso de pseudomyxoma do peritoneo, originario do appendice ileo-cecal, em individuo do sexo masculino, de 58 anos de edade. O processo teve evolução lenta, caracterizando-se clinicamente, por symptomas peritoneas (ventre augmentado, encerrando conteúdo gelatinoso e presença de um tumor palpavel ao nivel da região hepatica). O aspecto histologico do tumor corresponde ao do Pseudomyxoma peritonei. Levando em conta a systematização dos casos de pseudomyxoma do peritoneo, proposta por Trotter, o caso presente deve ser enquadrado entre aqueles que constituem o primeiro grupo (distribuição universal do tumor sobre o peritoneo).
Resumo:
The trematode and the cestode fauna was examined in 50 specimens of common shrews Sorex araneus L. (Insectivora: Soricidae) cillected in Valaam Island, URSS during 1988 and 1989. Two species of Trematoda and seven species of Cestoda were identified; prevalence of infection was as follows: Brachulaemus fulvus (86% ), Rubenstrema exasperatum (4% ), Hymenolepis scutigera (54% ), Neoskrjabinolepis schaldybini (26% ), Vigisolepis spinulosa (4% ), Choanotaenia crassiscolex (86% ), Choanotaenia hepatica (6% ), Dilepis undula (2% ) and Polycercus sp. (2% ).
Resumo:
Molecular cloning of components of protective antigenic preparations have suggested that related parasite fatty acid binding proteins could form the basis of the well documented protective, immune cross reactivity between the parasitic trematode worms Fasciola hepatica and Schistosoma mansoni. We have now confirmed the cross protective potential of parasite fatty acid binding proteins and suggest that it may be possible to produce a single vaccine that would be effective against at least two parasites, F. hepatica and S. mansoni of veterinary and human importance respectively.
Resumo:
In many helminth infected hosts the number of eosinophils increases dramatically, often without any concurrent increases in the number of other leukocytes, so that eosinophils become the dominant cell type. Many experimental investigations have shown that the eosinophilia is induced by interleukin-5 (IL-5) but its functional significance remains unclear. Mice genetically deficient in IL-5 (IL-5-/-) have been used to evaluate the functional consequences of the IL-5 dependent eosinophilia in helminth infected hosts. Host pathology and level of infection were determined in IL-5-/- and wild type mice infected with a range of species representative of each major group of helminths. The effects of IL-5 deficiency were very heterogeneous. Of the six species of helminth examined, IL-5 dependent immune responses had no detectable effect in infections with three species, namely the cestodes Mesocestoides corti and Hymenolepis diminuta and the trematode Fasciola hepatica. In contrast, IL-5 dependent immune responses were functionally important in mice infected with three species, notably all nematodes. Damage to the lungs caused by migrating larvae of Toxocara canis was reduced in IL-5-/- mice. Infections of the intestine by adult stages of either Strongyloides ratti or Heligmosomoides polygyrus were more severe in IL-5-/- mice. Adult intestinal nematodes were clearly deleteriously affected by IL-5 dependent processes since in its presence there were fewer worms which had reduced fecundity and longevity. The implications of these results for the viability of using inhibitors of IL-5 as a therapy for asthma are considered.
Resumo:
Interferon-alpha is used in antiviral therapy in humans, mainly for viral hepatitis B and C. An anti-fibrotic effect of interferon has been postulated even in the absence of anti-viral response, which suggests that interferon directly inhibits fibrogenesis. Rats infected with the helminth Capillaria hepatica regularly develop diffuse septal fibrosis of the liver, which terminates in cirrhosis 40 days after inoculation. The aim of this study was to test the anti-fibrotic effect of interferon in this experimental model. Evaluation of fibrosis was made by three separate methods: semi-quantitative histology, computerized morphometry and hydroxyproline measurements. Treatment with interferon-alpha proved to inhibit the development of fibrosis in this model, especially when doses of 500,000 and 800,000 IU were used for 60 days. Besides confirming the anti-fibrotic potential of interferon-alpha on a non-viral new experimental model of hepatic fibrosis, a clear-cut dose-dependent effect was observed.
Resumo:
In previous studies it was shown that the recombinant molecule, r-Sm14, induces high levels of protection against Schistosoma mansoni infection in two outbred animal models and immune crossprotection against infection by Fasciola hepatica in Swiss outbred mice. r-Sm14 was derived from a living worm extract, called SE, and is being developed as the molecular basis of an anti-helminth bivalent vaccine against the two parasites, for medical and veterinary application. Present data refer to SDS-PAGE and Western Blotting analysis of four different preparations of S. mansoni adult worms focusing Sm14 identification. The extracts correspond to the initial fraction of the SE extraction process, containing products released by living worms (SEi); SE2, reextraction of adult worms in PBS; and SE of separated male and female adult worms. In all extracts it was possible to detect the component of 14 kDa, that was recognized by specific anti-rSm14 antibody raised in rabbits.
Resumo:
Previous studies carried out with Sm14 in experimental vaccination against Schistosoma mansoni or Fasciola hepatica infections were performed with recombinant Sm14 (rSm14) produced in Escherichia coli by the pGEMEX system (Promega). The rSm14 was expressed as a 40 kDa fusion protein with the major bacteriophage T7 capsid protein. Vaccination experiments with this rSm14 in animal models resulted in consistent high protective activity against S. mansoni cercariae challenge and enabled rSm14 to be included among the vaccine antigens endorsed by the World Health Organization for phase I/II clinical trials. Since the preparation of pGEMEX based rSm14 is time consuming and results in low yield for large scale production, we have tested other E. coli expression systems which would be more suitable for scale up and downstream processing. We expressed two different 6XHis-tagged Sm14 fusion proteins in a T7 promoter based plasmids. The 6XHis-tag fusions allowed rapid purification of the recombinant proteins through a Ni+2-charged resin. The resulted recombinant 18 and 16 kDa proteins were recognized by anti-Sm14 antibodies and also by antiserum against adult S. mansoni soluble secreted/excreted proteins in Western-Blot. Both proteins were also protective against S. mansoni cercariae infection to the same extent as the rSm14 expressed by the pGEMEX system.
Resumo:
A snail-conditioned water experiment was conducted in Pseudosuccinea columella to test the possible role of a chemical interaction between snails on the diminished growth and fecundity rates found for snails raised in pairs compared to those raised in complete isolation. The results permit to discard the hypothesis of an inhibition of growth and reproduction between snails due to factors released into the water.
Resumo:
Sm14 was the first fatty acid-binding protein homologue identified in helminths. Thereafter, members of the same family were identified in several helminth species, with high aminoacid sequence homology between them. In addition, immune crossprotection was also reported against Fasciola hepatica infection, in animals previously immunized with the Schistosoma mansoni vaccine candidate, r-Sm14. In the present study, data on preliminary sodium dodecyl sulphate-polyacrylamide gel electrophoresis and Western blotting analysis of nine different helminth extracts focusing the identification of Sm14 related proteins, is reported. Out of these, three extracts - Ascaris suum (males and females), Echinostoma paraensei, and Taenia saginata - presented components that comigrated with Sm14 in SDS-PAGE, and that were recognized by anti-rSm14 policlonal serum, in Western blotting tests.
Resumo:
Previous studies in mice with hypervitaminosis A have demonstrated that fat-storing cells (hepatic stellate cells-HSCs) participate in schistosomal granuloma fibrogenesis. The origin of such cells in portal areas, away from the Disse spaces, was herein investigated. HSCs were identified in frozen sections of the liver by means of Sudan III staining. They appeared as red-stained cells disposed along the sinusoids of normal mice, but were never found within portal spaces. However, in the chronically inflamed portal spaces of Capillaria hepatica-infected mice, Sudan III-positive cells were frequently present among leukocytes and fibroblast-like cells. Thus, there are no resident HSCs in portal spaces, but their presence there in chronic inflammatory processes indicates that they are able to migrate from peri-sinusoidal areas in order to reach the portal areas.
Resumo:
An evaluation of the sensitivity and the specificity of the Anisakis simplex antigens purified by affinity chromatography was performed using sera from patients diagnosed with Anisakis sensitisation and sera from patients previously diagnosed with different helminthic infections. Only the sera of the patients diagnosed with Schistosoma mansoni or Onchocerca volvulus parasitic infections were negative against the A. simplex antigen and its purified fractions (PAK antigen: A. simplex antigen purified using columns prepared with anti-A. simplex rabbit IgG and PAS antigen: PAK antigen purified using columns prepared with anti-Ascaris suum rabbit IgG). However all the sera were positive against the A. suum antigen. In all the sera from the patients diagnosed with Anisakis sensitisation, the antibody levels detected using the purified antigens (PAK and PAS antigens) were lower than the observed using the A. simplex crude extract with the highest diminution in the case of the IgG. When these same sera were tested against the A. simplex crude extract by Western blot, several bands of high molecular masses were observed as well as, intense bands at 60 and/or 40 kDa. A concentration of these last proteins was observed in the PAK and the PAS antigens. When the sensitivity and the specificity determinations were performed, only seven of the 38 patients diagnosed of Anisakis sensitisation were positive, as well as, the sera from the patients diagnosed with parasitisms by Echinococcus granulosus or Fasciola hepatica.
Resumo:
Schistosomes have a comparatively large genome, estimated for Schistosoma mansoni to be about 270 megabase pairs (haploid genome). Recent findings have shown that mobile genetic elements constitute significant proportions of the genomes of S. mansoni and S. japonicum. Much less information is available on the genome of the third major human schistosome, S. haematobium. In order to investigate the possible evolutionary origins of the S. mansoni long terminal repeat retrotransposons Boudicca and Sinbad, several genomes were searched by Southern blot for the presence of these retrotransposons. These included three species of schistosomes, S. mansoni, S. japonicum, and S. haematobium, and three related platyhelminth genomes, the liver flukes Fasciola hepatica and Fascioloides magna and the planarian, Dugesia dorotocephala. In addition, Homo sapiens and three snail host genomes, Biomphalaria glabrata, Oncomelania hupensis, and Bulinus truncatus, were examined for possible indications of a horizontal origin for these retrotransposons. Southern hybridization analysis indicated that both Boudicca and Sinbad were present in the genome of S. haematobium. Furthermore, low stringency Southern hybridization analyses suggested that a Boudicca-like retrotransposon was present in the genome of B. truncatus, the snail host of S. haematobium.
Resumo:
Biomphalaria glabrata can react through different pathways to Schistosoma mansoni miracidium penetration, according to the degree of resistance/susceptibility presented by different snail strains, which is a genetically determined character, resistance being the dominant feature. However, it has been observed that previous susceptible snail strain may change its reactive behavior along the course of infection, exhibiting later a pattern of cercarial shedding and histopatopathological picture compatible with high resistance. Such observation suggests the possibility of B. glabrata to develop a sort of adaptative immunity face a schistosome infection. To explore on this aspect, the present investigation looked for the behavior of S. mansoni infection in B. glabrata previously subjected to different means of artificial stimulation of its internal defense system. Snails previously inoculated with irradiated miracídia (Group I); treated with S. mansoni antigens (Group II) or with a non-related parasite antigen (Group III) were challenged with 20 viable S. mansoni miracidia, and later looked for cercarial shedding and histopathologic changes at different times from exposition. Nodules of hemocyte accumulations were found at the site of antigen injection. These nodules resembled solid granulomas, and were larger and more frequent in snails injected with S. mansoni products as compared to those injected with Capillaria hepatica. However, the presence of such granulomas did not avoid the S. mansoni challenge infection from developing in a similar way as that seen in controls. The data are indicative that hemocytes are able to proliferate locally when stimulated, such capacity also remaining localized, not being shared by the population of hemocytes located elsewhere within the snail body.