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1.
Nihon Hansenbyo Gakkai Zasshi ; 73(1): 15-21, 2004 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-15035064

RESUMO

The deciphering of the genomic sequence of Mycobacterium leprae has made possible to predict the possible lipoproteins. The consensus sequence at the N-terminal region of the protein, including the cysteine residue to which the lipid moiety gets attached, provides a clue to the search. As such, more than 20 putative lipoproteins have been identified from Mycobacterium leprae genomic sequence. Lipoprotein LpK (Accession no. ML0603) which encodes for 371 amino acid precursor protein, was identified. Expression of the protein, in Escherichia coli revealed a 33 kD protein, and metabolic labeling experiments proved that the protein was lipidated. The purified lipoprotein was found to induce production of IL-12 in human peripheral blood monocytes which may imply that M. leprae LpK is involved in protective immunity against leprosy. Pursuit of such lipoproteins may reveal insights into the pathogenesis of the disease.


Assuntos
Proteínas de Bactérias/fisiologia , Hanseníase/imunologia , Lipoproteínas/fisiologia , Mycobacterium leprae/genética , Proteínas de Bactérias/análise , Proteínas de Bactérias/genética , Proteínas de Bactérias/isolamento & purificação , Genoma Bacteriano , Humanos , Interleucina-12/biossíntese , Interleucina-12/imunologia , Lipoproteínas/análise , Lipoproteínas/genética , Lipoproteínas/isolamento & purificação , Peso Molecular , Monócitos/metabolismo , Mycobacterium leprae/química
2.
Nat Med ; 9(5): 525-32, 2003 May.
Artigo em Inglês | MEDLINE | ID: mdl-12692544

RESUMO

The expression and activation of Toll-like receptors (TLRs) was investigated in leprosy, a spectral disease in which clinical manifestations correlate with the type of immune response mounted toward Mycobacterium leprae. TLR2-TLR1 heterodimers mediated cell activation by killed M. leprae, indicating the presence of triacylated lipoproteins. A genome-wide scan of M. leprae detected 31 putative lipoproteins. Synthetic lipopeptides representing the 19-kD and 33-kD lipoproteins activated both monocytes and dendritic cells. Activation was enhanced by type-1 cytokines and inhibited by type-2 cytokines. In addition, interferon (IFN)-gamma and granulocyte-macrophage colony-stimulating factor (GM-CSF) enhanced TLR1 expression in monocytes and dendritic cells, respectively, whereas IL-4 downregulated TLR2 expression. TLR2 and TLR1 were more strongly expressed in lesions from the localized tuberculoid form (T-lep) as compared with the disseminated lepromatous form (L-lep) of the disease. These data provide evidence that regulated expression and activation of TLRs at the site of disease contribute to the host defense against microbial pathogens.


Assuntos
Hanseníase/imunologia , Glicoproteínas de Membrana/fisiologia , Receptores de Superfície Celular/fisiologia , Animais , Citocinas/fisiologia , Humanos , Imunidade Inata , Lipoproteínas/análise , Glicoproteínas de Membrana/análise , Camundongos , Receptores de Superfície Celular/análise , Receptor 1 Toll-Like , Receptor 2 Toll-Like , Receptores Toll-Like
3.
s.l; s.n; 2003. 8 p. ilus, graf.
Não convencional em Inglês | SES-SP, HANSEN, HANSENIASE, SESSP-ILSLACERVO, SES-SP | ID: biblio-1241191

RESUMO

The expression and activation of Toll-like receptors (TLRs) was investigated in leprosy, a spectral disease in which clinical manifestations correlate with the type of immune response mounted toward Mycobacterium leprae. TLR2-TLR1 heterodimers mediated cell activation by killed M. leprae, indicating the presence of triacylated lipoproteins. A genome-wide scan of M. leprae detected 31 putative lipoproteins. Synthetic lipopeptides representing the 19-kD and 33-kD lipoproteins activated both monocytes and dendritic cells. Activation was enhanced by type-1 cytokines and inhibited by type-2 cytokines. In addition, interferon (IFN)-gamma and granulocyte-macrophage colony-stimulating factor (GM-CSF) enhanced TLR1 expression in monocytes and dendritic cells, respectively, whereas IL-4 downregulated TLR2 expression. TLR2 and TLR1 were more strongly expressed in lesions from the localized tuberculoid form (T-lep) as compared with the disseminated lepromatous form (L-lep) of the disease. These data provide evidence that regulated expression and activation of TLRs at the site of disease contribute to the host defense against microbial pathogens.


Assuntos
Humanos , Animais , Camundongos , Citocinas/fisiologia , Glicoproteínas de Membrana/análise , Glicoproteínas de Membrana/fisiologia , Hanseníase/imunologia , Imunidade Inata , Lipoproteínas/análise , Receptores de Superfície Celular/análise , Receptores de Superfície Celular/fisiologia
4.
Hansen. int ; 22(2): 20-30, jul.-dez. 1997. tab
Artigo em Português | LILACS, SES-SP | ID: lil-222029

RESUMO

Muitos portadores de hanseníase virchoviana, após longo tempo de evoluçäo, apresentam alterações dérmicas muito semelhantes aos xantonas e seus exames histológicos mostram numerosos macrófagos carregados de material lipídico. Esses fatos, associados a alteraçöes humorais dos lipídios descritas na literatura, sugerindo alteraçöes no metabolismo dos mesmos, levou-nos a estudos, visando a estabelecer valores médios em pacientes, utilizando-se de novas determinaçöes lipoprotêicas e de apoproteínas muito mais precisas. A lipoproteína(a) apresentou valor médio acima de 20 mg/dl em 64,6(por cento) dos pacientes, contra 33,3(por cento) no grupo controle. O encontro de lipoproteína(a) aumentada em pacientes portadores de hanseníase virchoviana é importante, porque existe uma comprovada relaçäo entre esta lipoproteína e alteraçöes vasculares tipo ateroscleróticas e distúrbios na fibrinólise


Assuntos
Aterosclerose/complicações , Hanseníase , Lipídeos/análise , Lipoproteínas/análise , Técnicas Histológicas/classificação
5.
Exp Pathol ; 42(2): 81-93, 1991.
Artigo em Inglês | MEDLINE | ID: mdl-1879516

RESUMO

The search for leptospiral antigens (L. interrogans serogroup icterohaemorrhagiae) was carried out in 24 guinea pigs experimentally inoculated with 1 ml of culture containing 10(7)-10(8) leprospires and sequentially sacrificed from the first until the 6th day of infection. Semiquantitative analysis of histopathological variables comprising kidney interstitium, tubules and glomeruli was done in 1 micron sections of tissue embedded in glycolmetacrylate. Leptospiral antigen (LAg) and its glycolipoprotein (GLP) expression were detected through PAP in paraffin embedded tissue. The mild interstitial involvement of the kidney, manifested chiefly by oedema and focal interstitial nephritis seen at the 4th day, progressed to tubular damage at the 6th day, characterized by either swelling or cytoplasmic acidophilia of epithelial cells with loss of cell cohesion and sloughing of cells into the tubular lumina. Brush border alterations and mitochondrial changes were observed. Endothelial cell injury was noted in the interstitial vessels. LAg expression was parallel to the kidney changes: small deposits of elongated forms of LAg were detected at the 4th day either within the vascular lumen or free in the interstitium. A rise in the antigen expression was observed at the 5th day when it was seen either around tubules or in their walls. LAg was detected inside the tubular lumina at the 6th day of infection when granular LAg and GLP were abundant. This sequence reproduces the pathway of leptospires in the kidney and the crescent amounts of antigens detected toward the end of the experiment, with antigen concentration in cases of major tissue damage suggesting a direct action of the microorganisms and/or their products in the pathogesis of the lesions.


Assuntos
Antígenos de Bactérias/análise , Rim/patologia , Leptospira interrogans/isolamento & purificação , Nefrite Intersticial/patologia , Doença de Weil/patologia , Animais , Glicoproteínas/análise , Glicoproteínas/imunologia , Cobaias , Imuno-Histoquímica , Rim/microbiologia , Glomérulos Renais/microbiologia , Glomérulos Renais/patologia , Túbulos Renais/microbiologia , Túbulos Renais/patologia , Cinética , Leptospira interrogans/imunologia , Lipoproteínas/análise , Lipoproteínas/imunologia , Masculino , Nefrite Intersticial/microbiologia , Doença de Weil/imunologia , Doença de Weil/microbiologia
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