Base de dados : HANSEN
Pesquisa : FATOR DE NECROSE TUMORAL/IM [Descritor de assunto]
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Id:18575
Autor:Cheadle, Eleanor J; Selby, Peter J; Jackson, Andrew M
Título:Mycobacterium bovis bacillus Calmette-Guérin-infected dendritic cells potently activate autologous T cells via a B7 and interleukin-12-dependent mechanism
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Fonte:s.l; s.n; 2003. 10 p. graf.
Resumo:Mycobacteria are potent adjuvants, can survive intracellularly and have been safely used for many years as vaccines against tuberculosis and leprosy. They are thus important potential vectors for recombinant vaccines. Many of their adjuvant properties are mediated following phagocytosis by dendritic cells (DC), which are in turn critical for priming naïve T cells. Although the maturation of DC in response to mycobacteria, such as Mycobacterium bovis bacillus Calmette-Guérin (BCG), is well described the subsequent responses of autologous T cells to mycobacterium-infected DC remains uncharacterized. In our experiments DC infected with BCG expressed more co-stimulatory molecules than tumour-necrosis factor-alpha (TNF-alpha) -treated DC and stimulated more potent mixed leucocyte reactions. When autologous T cells were co-cultured with BCG-exposed DC they became highly activated, as determined by display of CD25, CD54 and CD71 on both CD4+ and CD8+ cells. In contrast, the response of T cells to TNF-alpha-matured DC was significantly less. Cytokine production from T cells cultured with BCG-exposed DC was enhanced with elevated secretion of interleukin-2 (IL-2), IL-10 and interferon-gamma (IFN-gamma) and was produced by both CD4+ and CD8+ lymphocytes as determined by intracellular staining. In particular, IFN-gamma secretion was increased from 50 pg/ml to 25 000 pg/ml and IL-10 secretion increased from 20 pg/ml to 300 pg/ml in BCG-exposed DC co-cultures. Blocking antibodies to B7.1 and B7.2 or IL-12 significantly reduced the secretion of IFN-gamma and reductions were also seen in the expression of CD25 and CD71 by CD4+ cells. These data demonstrate that mycobacterially infected DC are particularly potent activators of autologous T cells compared to TNF-alpha-exposed DC and that the resultant T cells are functionally superior. (AU).
Descritores:ANTIGENOS CD/metab
ANTIGENOS CD80/imunol
ANTIGENOS DE DIFERENCIACAO DE LINFOCITOS B/metab
LINFOCITOS T CD4-POSITIVOS/imunol
LINFOCITOS T CD8-POSITIVOS/imunol
CITOCINAS/bios
CELULAS DENDRITICAS/imunol
CELULAS DENDRITICAS/microbiol
MOLECULA 1 DE ADESAO INTERCELULAR
IMUNOFENOTIPAGEM
INTERLEUCINA-12/imunol
TRANSFORMACAO LINFOCITICA/imunol
MYCOBACTERIUM BOVIS/imunol
RECEPTORES DA INTERLEUCINA-2/metab
LINFOCITOS T/imunol
FATOR DE NECROSE TUMORAL/imunol
REGULACAO PARA CIMA/imunol
Limites:HUMANO
SUPPORT, NON-U.S. GOV'T
Meio Eletrônico: - .
Localização:BR191.1; 08996/s


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Id:18498
Autor:Hernandez, M. O; Neves Junior, I; Sales, J. S; Carvalho, D. S; Sarno, E. N; Sampaio, E. P
Título:Induction of apoptosis in monocytes by Mycobacterium leprae in vitro: a possible role for tumour necrosis factor-alpha
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Fonte:s.l; s.n; 2003. 9 p. graf.
Resumo:A diverse range of infectious organisms, including mycobacteria, have been reported to induce cell death in vivo and in vitro. Although morphological features of apoptosis have been identified in leprosy lesions, it has not yet been determined whether Mycobacterium leprae modulates programmed cell death. For that purpose, peripheral blood mononuclear cells obtained from leprosy patients were stimulated with different concentrations of this pathogen. Following analysis by flow cytometry on 7AAD/CD14+ cells, it was observed that M. leprae induced apoptosis of monocyte-derived macrophages in a dose-dependent manner in both leprosy patients and healthy individuals, but still with lower efficiency as compared to M. tuberculosis. Expression of tumour necrosis factor-alpha (TNF-alpha), Bax-alpha, Bak mRNA and TNF-alpha protein was also detected in these cultures; in addition, an enhancement in the rate of apoptotic cells (and of TNF-alpha release) was noted when interferon-gamma was added to the wells. On the other hand, incubation of the cells with pentoxifylline impaired mycobacterium-induced cell death, the secretion of TNF-alpha, and gene expression in vitro. In addition, diminished bacterial entry decreased both TNF-alpha levels and the death of CD14+ cells, albeit to a different extent. When investigating leprosy reactions, an enhanced rate of spontaneous apoptosis was detected as compared to the unreactive lepromatous patients. The results demonstrated that M. leprae can lead to apoptosis of macrophages through a mechanism that could be at least partially related to the expression of pro-apoptotic members of the Bcl-2 protein family and of TNF-alpha. Moreover, while phagocytosis may be necessary, it seems not to be crucial to the induction of cell death by the mycobacteria. (AU).
Descritores:APOPTOSE/ef drogas
APOPTOSE/imunol
CELULAS CULTIVADAS
REGULACAO DA EXPRESSÃO GÊNICA
INTERFERON TIPO II/farmacol
HANSENIASE/imunol
PROTEINAS DE MEMBRANA/genet
MONOCITOS/imunol
MONOCITOS/patol
MYCOBACTERIUM LEPRAE/imunol
PENTOXIFILINA/farmacol
FAGOCITOSE/imunol
PROTEINAS PROTO-ONCOGÊNICAS/genet
FATOR DE NECROSE TUMORAL/imunol
Limites:HUMANO
MASCULINO
FEMININO
ADULTO
MEIA-IDADE
IDOSO
SUPPORT, NON-U.S. GOV'T
Meio Eletrônico: - .
Localização:BR191.1; 09128/s


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Id:15024
Autor:Griffin, George; Krishna, Sanjeev
Título:Infectious diseases
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Fonte:s.l; s.n; may-jun. 1998. 4 p. ilus, tab.
Descritores:QUIMIOCINAS
QUIMIOCINAS
DOENÇAS TRANSMISSIVEIS
CITOCINAS
CITOCINAS
CITOCINAS
INTERLEUCINA-1
HANSENIASE
MALARIA
RECEPTORES, CITOCINA
LINFOCITOS T AUXILIADORES-INDUTORES
TUBERCULOSE
VIROSES
FATOR DE NECROSE TUMORAL/IM
Limites:ESTUDO COMPARATIVO
Localização:BR191.1; 07296/s



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