Base de dados : HANSEN
Pesquisa : LINFOCITOS T CD8-POSITIVOS/IMUNOL [Descritor de assunto]
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  1 / 10 HANSEN  
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Id:27279
Autor:Barrera, Silvia de la; Finiasz, Marta; Fink, Susana; Valdez, Raul; Bottasso, Oscar; Balina, Luis Maria; Sasiain, Maria del Carmen.
Título:Differential development of CD4 and CD8 cytotoxic T cells (CTL) in PBMC across the leprosy spectrum IL-6 with IFN-gamma or IL-2 generate CTL in multibacillary patients.
Fonte:Int. J. Lepr;65(1):45-55, Mar., 1997. tab, graf.
Resumo:In the present study we evaluated the contribution of CD4 and CD8 T cells on the antigen-specific cytotoxic activity induced by whole Mycobacterium leprae in leprosy patients and normal controls (N) as well as the modulation of this activity by some cytokines. Peripheral blood mononuclear cells (PBMC) from N or from leprosy patients were stimulated with antigen in the presence or absence of cytokines for 7 days. M. leprae-stimulated PBMC were depleted of CD4 or CD8 antigen-bearing cells and employed as effector cells in a 4-hr [31Cr]-release assay against autologous M. leprae-pulsed macrophages. Our results demonstrate that both CD4 and CD8 T cells contribute to M. leprae-induced cytotoxic activity, with differences observed in paucibacillary (PB) and multibacillary (MB) patients. CD8-mediated cytotoxic activity is higher than that of CD4 cells in PB patients, while in MB patients CD4 cytotoxicity is predominant. Our data also demonstrate that the generation of CD4 and CD8 cytotoxic T lymphocytes (CTL) can be modulated differentially by interleukin-4 (IL-4), IL-6, gamma interferon (IFN-gamma), or IL-2. Although MB patients developed the lowest CTL response, cytokines such as IL-6 plus IL-2 or IFN-gamma were able to generate both CD4 and CD8 cytotoxic T cells from MB patients. In PB patients, IL-6 plus IFN-gamma displayed the highest stimulation on CD8 effector cells. Thus, an important role may be assigned to IL-6, together with IL-2 or IFN-gamma, in the differentiation of M. leprae-specific CTL effector cells. (AU)^ien.
Descritores:Linfócitos T CD4-Positivos/imunol
Linfócitos T CD8-Positivos/imunol
Hanseníase Dimorfa/imunol
Hanseníase Virchowiana/imunol
Hanseníase Tuberculóide/imunol
Localização:BR191.1


  2 / 10 HANSEN  
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Id:22738
Autor:Kirkaldy, A. A; Musonda, A. C; Khanolkhar-Young, S; Suneetha, S; Lockwood, D. N. J
Título:Expression of CC and CXC chemokines and chemokine receptors in human in human leprosy skin lesions
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Fonte:s.l; s.n; 2003. 7 p. ilus, tab, graf.
Resumo:We have investigated the expression of chemokines and their receptors in leprosy skin lesions using immunohistochemistry. Skin biopsies from 25 leprosy patients across the leprosy spectrum, 11 patients undergoing type I reversal reactions and four normal donors were immunostained by ABC peroxidase method using antibodies against CC and CXC chemokines and their receptors. Using an in situ hybridization technique we have also studied the expression of monocyte chemoattractant protein 1 (MCP-1), RANTES and interleukin (IL)-8 chemokines mRNA in leprosy skin lesions. Chemokines and receptor expression was detected in all leprosy skin biopsies. Expression of CC chemokines MCP-1 (P < 0.01) and RANTES (P < 0.01) were elevated significantly in borderline tuberculoid leprosy in reversal reaction compared to non-reactional borderline tuberculoid leprosy, but there was no difference in the expression of IL-8 chemokine. Surprisingly, there was no significant difference in the expression of CC (CCR2 and CCR5) and CXC (CXCR2) chemokine receptors across the leprosy spectrum. Similarly, there was no significant difference in the expression of mRNA for MCP-1, regulated upon activation normal T cell expressed and secreted (RANTES) and IL-8 chemokines. Here, the presence of a neutrophil chemoattractant IL-8 in leprosy lesions, which do not contain neutrophils, suggests strongly a role of IL-8 as a monocyte and lymphocyte recruiter in leprosy lesions. These results suggest that the chemokines and their receptors, which are known to chemoattract T lymphocytes and macrophages, are involved in assembling the cellular infiltrate found in lesions across the leprosy spectrum. (AU).
Descritores:Linfócitos T CD4-Positivos/IM
Linfócitos T CD8-Positivos/IM
Quimiocinas/*AN/GE
Imunohistoquímica/MT
Hibridização In Situ/MT
Interleucina-8/GE
Hanseníase/*IM
Macrófagos/IM
Proteína-1 Quimioatraente de Monócito/GE
RANTES/GE
RNA Mensageiro/AN
Receptores CCR5/AN
Receptores de Quimiocinas/*AN/GE
Receptores de Interleucina-8B/AN
Limites:Humano
Pele/*IM
Estatísticas não Paramétricas
Localização:BR191.1; 00253/s


  3 / 10 HANSEN  
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Id:18951
Autor:Maeda, Yumi; Gidoh, Masaichi; Ishii, Norihisa; Mukai, Chifumi; Makino, Masahiko
Título:Assessment of cell mediated immunogenicity of Mycobacterium leprae-derived antigens
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Fonte:s.l; s.n; 2003. 9 p. tab, graf.
Resumo:The antigenicity of Mycobacterium leprae (M. leprae)-derived cell membrane fraction was examined using human dendritic cells (DCs). Immature DCs internalized and processed the cell membrane components, and expressed M. leprae-derived antigens (Ags) on their surface. The expression of MHC class II, CD86, and CD83 Ags on DCs and CD40 ligand (L)-associated IL-12 p70 production from DCs were up-regulated by the membrane Ags. Moreover these stimulated DCs induced significantly higher level of interferon-gamma (IFN-gamma) production by autologous CD4(+) and CD8(+) T cells than those pulsed with equivalent doses of live M. leprae or its cytosol fraction. Both subsets of T cells from tuberculoid leprosy patients also produced several fold more IFN-gamma than those from normal individuals. Furthermore, the intracellular perforin production in CD8(+) T cells was up-regulated in an Ag-dose dependent manner. These results suggest that M. leprae membrane Ags might be useful as the vaccinating agents against leprosy. (AU).
Descritores:ANTIGENOS DE BACTERIAS/imunol
ANTIGENOS DE SUPERFÍCIE/imunol
LINFOCITOS T CD4-POSITIVOS/imunol
LIGANTE A CD40/fisiol
LINFOCITOS T CD8-POSITIVOS/imunol
CELULAS DENDRITICAS/imunol
INTERFERON TIPO II/bios
INTERLEUCINA-12/bios
TRANSFORMACAO LINFOCITICA
GLICOPROTEINAS DE MEMBRANA/bios
MYCOBACTERIUM LEPRAE/imunol
Limites:HUMANO
SUPPORT, NON-U.S. GOV'T
SUPPORT, U.S. GOV'T, P.H.S.
Meio Eletrônico: - .
Localização:BR191.1; 09083/s


  4 / 10 HANSEN  
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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


  5 / 10 HANSEN  
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Id:18557
Autor:Cardoso, Fernando L. L; Antas, Paulo R. Z; Milagres, Alexandre S; Geluk, Annemieke; Franken, Kees L. M. C; Oliveira, Eliane B; Teixeira, Henrique C; Nogueira, Susie A; Sarno, Euzenir N; Klatser, Paul; Ottenhoff, Tom H. M; Sampaio, Elizabeth P
Título:T-cell responses to the Mycobacterium tuberculosis-specific antigen ESAT-6 in Brazilian tuberculosis patients
..-
Fonte:s.l; s.n; 2002. 8 p. tab, graf.
Resumo:The Mycobacterium tuberculosis-specific ESAT-6 antigen induces highly potent T-cell responses and production of gamma interferon (IFN-gamma), which play a critical role in protective cell-mediated immunity against tuberculosis (TB). In the present study, IFN-gamma secretion by peripheral blood mononuclear cells (PBMCs) in response to M. tuberculosis ESAT-6 in Brazilian TB patients was investigated in relation to clinical disease types, such as pleurisy and cavitary pulmonary TB. Leprosy patients, patients with pulmonary diseases other than TB, and healthy donors were assayed as control groups. Sixty percent of the TB patients indeed recognized M. tuberculosis ESAT-6, as did 50 per cent of the leprosy patients and 60 per cent of the non-TB controls. Nevertheless, the levels of IFN-gamma in response to the antigen ESAT, but not to antigen 85B (Ag85B) and purified protein derivative (PPD), were significantly lower in controls than in patients with treated TB or pleural or cavitary TB. Moreover, according to Mycobacterium bovis BCG vaccination status, only 59 per cent of the vaccinated TB patients responded to ESAT in vitro, whereas 100 per cent of them responded to PPD. Both CD4 and CD8 T cells were able to release IFN-gamma in response to ESAT. The present data demonstrate the specificity of ESAT-6 of M. tuberculosis and its ability to discriminate TB patients from controls, including leprosy patients. However, to obtain specificity, it is necessary to include quantitative IFN-gamma production in response to the antigen as well, and this might limit the use of ESAT-6-based immunodiagnosis of M. tuberculosis infection in an area of TB endemicity. (AU).
Descritores:ANTIGENOS DE BACTERIAS/DU/GE/*IM
LINFOCITOS T CD4-POSITIVOS/*IM
LINFOCITOS T CD8-POSITIVOS/*IM
INTERFERON TIPO II/BI
MYCOBACTERIUM TUBERCULOSIS/*IM
PROTEINAS RECOMBINANTES/IM
TUBERCULINA/IM
TUBERCULOSE PLEURAL/DI/*IM/MI
TUBERCULOSE PULMONAR/DI/*IM/MI
Limites:FEMININO
HUMANO
MASCULINO
SUPPORT, NON-U.S. GOV'T
Localização:BR191.1; 09070/s


  6 / 10 HANSEN  
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Id:16381
Autor:Adams, Linda B; Scollard, David M; Ray, Nashome A; Cooper, Andrea M; Frank, Anthony A; Orme, Ian M; Krahenbuhl, James L
Título:The study of mycobacterium leprae infection in interferon-gamma gene - disrupted mice as a model to explore the immunopathologic spectrum of leprosy
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Fonte:s.l; s.n; 2002. 8 p. ilus, graf.
Descritores:LINFOCITOS T CD4-POSITIVOS
LINFOCITOS T CD8-POSITIVOS
CITOCINAS
MODELOS ANIMAIS DE DOENÇAS
CITOMETRIA DE FLUXO
PELE
PELE
DELEÇAO DE GENES
IMUNOHISTOQUIMICA
INTERFERON TIPO II
HANSENIASE
HANSENIASE
HANSENIASE
TRANSFORMAÇAO LINFOCITICA
MACROFAGOS PERITONEAIS
CAMUNDONGOS
CAMUNDONGOS ENDOGAMICOS BALB C
CAMUNDONGOS KNOCKOUT
MYCOBACTERIUM LEPRAE
MYCOBACTERIUM LEPRAE
MYCOBACTERIUM LEPRAE
Limites:ANIMAL
Localização:BR191.1; 08655/s


  7 / 10 HANSEN  
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Id:15813
Autor:Adams, Linda B; Scollard, David M; Ray, Nashone A; Cooper, Andrea M; Frank, Anthony A; Orne, Ian M; Krahenbuhl, James L
Título:The study of Mycobacterium leprae infection in interferon-y gene-disrupted mice as a model to explore the immunopathologic spectrum of leprosy
..-
Fonte:s.l; s.n; 2002. 8 p. ilus, graf.
Descritores:LINFOCITOS T CD4-POSITIVOS
LINFOCITOS T CD8-POSITIVOS
CITOCINAS
MODELOS ANIMAIS DE DOENÇAS
CITOMETRIA DE FLUXO


DELEÇAO DE GENES
IMUNOHISTOQUIMICA
INTERFERON TIPO II
HANSENIASE
HANSENIASE
HANSENIASE
TRANSFORMAÇAO LINFOCITICA
MACROFAGOS PERITONEAIS
CAMUNDONGOS
CAMUNDONGOS ENDOGAMICOS BALB C
CAMUNDONGOS KNOCKOUT
MYCOBACTERIUM LEPRAE
MYCOBACTERIUM LEPRAE
MYCOBACTERIUM LEPRAE
ANIMAL
LINFONODOS/IM
Limites:ANIMAL
Localização:BR191.1; 08511/s


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Id:14244
Autor:Sieling, Peter A; Wang, Xiao-Hong; Gately, Maurice K; Oliveros, Jennifer L; McHugh, Teresa; Barnes, Peter F; Wolf, Stanley F; Golkar, Linda; Yamamura, Masahiro; Yogi, Yasuko; Uyemura, Koichi; Rea, Thomas H; Modlin, Robert L
Título:IL-12 regulates T helper type 1 cytokine responses in human infectious disease
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Fonte:s.l; s.n; 1994. 9 p. ilus, graf.
Descritores:SEQUENCIA DE BASES
LINFOCITOS T CD8-POSITIVOS
PRIMERS DO DNA
EXPRESSAO GENICA
INTERFERON TIPO II
INTERLEUCINA-10
INTERLEUCINA-12
INTERLEUCINA-4
INTERLEUCINA-4
HANSENIASE
TRANSFORMAÇAO LINFOCITICA
DADOS DE SEQUENCIA MOLECULAR
MYCOBACTERIUM LEPRAE
RNA MENSAGEIRO
SUB-POPULAÇOES DE LINFOCITOS T
CÉLULAS TH1
Localização:BR191.1; 06955/s


  9 / 10 HANSEN  
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Id:14169
Autor:Sieling, Peter A; Modlin, Robert L
Título:Cytokine patterns at the site of mycobacterial infection
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Fonte:s.l; s.n; 1994. 10 p. ilus, graf.
Descritores:HANSENIASE
LINFOCITOS T CD4-POSITIVOS
LINFOCITOS T CD8-POSITIVOS
CITOCINAS
CITOCINAS
ATIVAÇAO DE MACROFAGOS
MODELOS BIOLOGICOS
RNA MENSAGEIRO
RNA MENSAGEIRO
Limites:ANIMAL
CAMUNDONGOS
Localização:BR191.1; 07083/s


  10 / 10 HANSEN  
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Id:14154
Autor:Ottenhoff, Tom H. M; Spierings, Eric; Nibbering, Peter H; Jong, Rolien de
Título:Modulation of protective and pathological immunity in mycobacterial infections
..-
Fonte:s.l; s.n; 1997. 9 p. graf.
Descritores:ANTIGENOS CD4
ANTIGENOS CD4
CITOCINAS
CITOCINAS
LINFOCITOS T CD8-POSITIVOS
IMUNIDADE ATIVA
IMUNIDADE CELULAR
HANSENIASE
HANSENIASE
HANSENIASE
CAMUNDONGOS
MICOBACTERIOSE
MICOBACTERIOSE
MICOBACTERIOSE
CÉLULAS TH1
CÉLULAS TH1
TUBERCULOSE
TUBERCULOSE
TUBERCULOSE
VACINAS
Limites:ANIMAL
Localização:BR191.1; 07128/s



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