Base de dados : HANSEN
Pesquisa : LINFOCITOS [Descritor de assunto]
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  1 / 232 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 / 232 HANSEN  
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Texto Completo-en
Id:27150
Autor:Ramos, Teresa; Zalcberg-Quintana, Ilana; Appelberg, Rui; Sarno, Euzenir N; Silva, Manuel T.
Título:T-helper cell subpopulations and the immune spectrum of leprosy.
Fonte:Int J Lep;57(1):73-81, Mar. 1989. .
Descritores:Hanseníase/genet
Hanseníase/imunol
Linfócitos T Auxiliares-Indutores/clas
Linfócitos T Auxiliares-Indutores/imunol
Limites:Humanos
Meio Eletrônico:http://hansen.bvs.ilsl.br/textoc/revistas/intjlepr/1989/pdf/v57n1/v57n1edt01.pdf - en.
Localização:Br191.1


  3 / 232 HANSEN  
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Texto Completo-en
Id:27141
Autor:Mustafa, Abu Salim; Qvigstad, Erik.
Título:HLA-DR-restricted antigen induced proliferation and cytotoxicity mediated by CD4+ T-cell clones from subjects vaccinated with killed M. leprae.
Fonte:Int J Lep;57(1):1-11, Mar. 1989. ^btab.
Resumo:Thirteen CD4+ T-cell clones raised against Mycobacterium leprae from three M. leprae-vaccinated subjects were studied for major histocompatibility complex (MHC) restriction in proliferative and cytotoxicity assays. These T-cell clones recognized at least nine different epitopes, ranging from M. leprae-specific to broadly crossreactive. Restriction studies with a panel of antigen-presenting cells (APCs) suggest that all of the T-cell clones recognized antigens in the context of the DR locus. Three T-cell clones with three different reactivities from a DR1, 2-positive subject responded to M. leprae in proliferation and cytotoxicity when the antigen was presented in the context of DR1-positive APCs. Four T-cell clones responding to M. leprae-specific or crossreactive epitopes from the second donor, who was DR4,DW4; DR4,Dw14-positive, and a single M. leprae-specific T-cell clone from the third subject, who was DR3,4:Dw4, recognized the antigens in the presence of Dw4 APCs. Four crossreactive T-cell clones from the second subject responded in the presence of Dw14-positive APCs, and one limited crossreactive clone recognized the antigen in the context of DR4 and DR7-positive cells, suggesting that its response was restricted by a common determinant. The T-cell clones that recognize the 65-kDa, 18-kDa, and 13B3 recombinant M. leprae antigens in proliferative assays were cytotoxic for autologous adherent cells pulsed with the respective antigens^ien.
Descritores:Hanseníase/imunol
Mycobacterium leprae/imunol
Linfócitos/imunol
Meio Eletrônico:http://hansen.bvs.ilsl.br/textoc/revistas/intjlepr/1989/pdf/v57n1/v57n1a01.pdf - en.
Localização:Br191.1


  4 / 232 HANSEN  
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Texto Completo-en
Id:26662
Autor:Huizar-López, Rosario; Santerre, Ann; Madrid-Marina, Vicente; Peralta-Zaragoza, Oscar; Villalobos-Arámbula, Alma; Islas-Rodríguez, Alfonso.
Título:AP-1 Is present in nuclear extracts of lymphocytes from lepromatous leprosy patients.
Fonte:Int. J. Lepr;70(4):274-277, Dec., 2002. ilus, tab.
Descritores:Hanseníase Virchowiana/imunol
Hanseníase Virchowiana/fisiopatol
Antígenos CD95/genet
Antígenos CD95/imunol
Linfócitos/imunol
Linfócitos/fisiol
Limites:Humanos
Meio Eletrônico:http://hansen.bvs.ilsl.br/textoc/revistas/intjlepr/2002/pdf/v70n4/v70n4cor.pdf - en.
Localização:BR191.1


  5 / 232 HANSEN  
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Id:25255
Autor:Reinherz, Ellis L; Schlossman, Stuart F
Título:The differentiation and function of human T lymphocytes
..-
Fonte:s.l; s.n; 1980. 7 p. tab, graf.
Descritores:ANTIGENOS DE DIFERENCIACAO DE LINFOCITOS B/anal
ANTIGENOS DE DIFERENCIACAO DE LINFOCITOS B/sangue
ANTIGENOS DE DIFERENCIACAO DE LINFOCITOS B/imunol
ANTIGENOS DE DIFERENCIACAO DE LINFOCITOS T/anal
ANTIGENOS DE DIFERENCIACAO DE LINFOCITOS T/sangue
ANTIGENOS DE DIFERENCIACAO DE LINFOCITOS T/imunol
ANTIGENOS SECUNDARIOS DE ESTIMULACAO DE LINFOCITOS/anal
ANTIGENOS SECUNDARIOS DE ESTIMULACAO DE LINFOCITOS/sangue
ANTIGENOS SECUNDARIOS DE ESTIMULACAO DE LINFOCITOS/imunol
LINFOCITOS/sangue
LINFOCITOS/clas
LINFOCITOS/imunol
INTERLEUCINA-1/anal
 INTERLEUCINA-1/sangue
 INTERLEUCINA-1/imunol
 ANTICORPOS MONOCLONAIS/bios
 ANTICORPOS MONOCLONAIS/isol
 ANTICORPOS MONOCLONAIS/farmacocin
 IMUNOFLUORESCÊNCIA/util
Limites:HUMANO
ANIMAL
Localização:BR191.1; 00799/s


  6 / 232 HANSEN  
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Id:25126
Autor:Quiroga, Maria F; Martinez, Gustavo J; Pasquinelli, Virginia; Costas, Monica A; Bracco, Maria M; Malbran, Aleajndro; Olivares, Liliana M; Sieling, Peter A; Garcia, Veronica E
Título:Activation of signaling lymphocytic activation molecule triggers a signaling cascade that enhances Th1 responses in human intracellular infection
..-
Fonte:s.l; s.n; 2004. 10 p. graf.
Resumo:T cell production of IFN-gamma contributes to host defense against infections by intracellular pathogens, including mycobacteria. Lepromatous leprosy, the dissminated from of infection caused by Mycobacterium leprae, is characterized by loss of cellular response against the pathogen and diminished Th1 cytokine production. Relieving bacterial burden in Ag-unresponsive patients might be achieved through alternative receptors that stimulate IFN-gamma production. We have previously shown that ligation of signaling lymphocytic activation molecule (SLAM) enhances IFN-gamma in mycobacterial infection; therefore, we investigated molecular pathways leading from SLAM activation to IFN-gamma production in human leprosy. The expression of the SLAM-associated protein (an inhibitory factor for IFN-gamma induction) on M. leprae-stimulated cells from leprosy patients was inversely correlated to IFN-gamma production. Howevwe, SLAM ligation or exposure of cell from lepromatous patients to a proinflammatory microenvironment down-regulated SLAM-associated protein expression. Moreover. SALAM activation induced a sequence of signaling proteins, including activation of the NF-kB complex, phosphorylation of Stat1, and induction of T-bet expression, resulting in the promotion a cascade of molecular events during signaling through SLAM in leprosy that cooperate to induce INF-gamma production and strongly suggest that SLAM might be a focal point for therapeutic modulation of the cell cytokine responses in diseases characterized by dysfunctional Th2 responses (AU).
Descritores:HANSENIASE/imunol
HANSENIASE/microbiol
LINFOCITOS T/imunol
LINFOCITOS T/microbiol
INTERLEUCINAS/sangue
INTERLEUCINAS/imunol
LINFOCITOS/imunol
 LINFOCITOS/microbiol
 MYCOBACTERIUM LEPRAE/imunol
 MYCOBACTERIUM LEPRAE/patogen
Limites:HUMANO
Localização:BR191.1; 09192/s


  7 / 232 HANSEN  
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Id:24504
Autor:Brennan, Patrick J.
Título:Mycobacterium leprae: the significance of our knowledge of its composition and antigenicity.
Fonte:Hansen. int;(n.esp):103-110, Jun. 1998. .
Conferência:Apresentado em: Congresso da Associação Brasileira de Hansenologia, IX, Foz do Iguaçu, 04-08 junho 1997.
Descritores:MYCOBACTERIUM LEPRAE/cresc
MYCOBACTERIUM LEPRAE/genet
MYCOBACTERIUM LEPRAE/fisiol
LINFOCITOS T CD4-POSITIVOS/citol
LINFOCITOS T CD4-POSITIVOS/fisiol
Limites:ESTUDO COMPARATIVO
HUMANO
Localização:BR191.1


  8 / 232 HANSEN  
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Id:23970
Autor:Geluk, Annemieke; Ottenhoff, Tom H. M
Título:HLA and leprosy in the pre and postgenomic eras
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Fonte:s.l; s.n; 2006. 7 p. graf.
Resumo:Leprosy has intrigued immunologists for many decades. Despite minimal genetic variation between Mycobacterium leprae isolates worldwide, two completely different forms of the disease can develop in the susceptible human host: localized, tuberculoid, or paucibacillary leprosy, which can heal spontaneously, and disseminating, lepromatous, or multibacillary leprosy, which is progressive if untreated. The questions which host factors regulate these very different outcomes of infection, by what mechanisms, and whether these can be used to combat disease remain unanswered. Leprosy has been one of the very first human diseases in which human leukocyte antigen (HLA) genes were demonstrated to codetermine disease outcome. Jon van Rood was among the earliest researchers to recognize the potential of this ancient disease as a human model to dissect the role of HLA in disease. Decades later, it is now clear that HLA molecules display highly allele-specific peptide binding capacity. This restricts antigen presentation to M. leprae-reactive T cells and controls the magnitude of the ensuing immune response. Furthermore, specific peptide/HLA class II complexes can also determine the quality of the immune response by selectively activating regulatory (suppressor) T cells. All these factors are believed to contribute to leprosy disease susceptibility. Despite the global reduction in leprosy disease prevalence, new case detection rates remain invariably high, demonstrating that treatment alone does not block transmission of leprosy. Better tools for early detection of preclinical M. leprae infection, likely the major source of unidentified transmission, therefore is a priority. Newly developed HLA-based bioinformatic tools now provide novel opportunities to help combat this disease. Here, we describe recent work using HLA-DR peptide binding algorithms in combination with recently elucidated genome sequences of several different mycobacteria. Using this postgenomic HLA-based approach, we were able to identify 12 candidate genes that were unique to M. leprae and were predicted to contain T cell epitopes restricted via several major HLA-DR alleles. Five of these antigens (ML0576, ML1989, ML1990, ML2283, ML2567) were indeed able to induce significant T cell responses in paucibacillary leprosy patients and M. leprae-exposed healthy controls but not in most multibacillary leprosy patients, tuberculosis patients, or endemic controls...(AU).
Descritores:Motivos de Aminoácidos
Anticorpos Antibacterianos/BL
Antígenos de Bactérias/IM
Sítios de Ligação
Epitopos de Linfócito T
Genes Classe II do Complexo de Histocompatibilidade (MHC)
Genoma Bacteriano
Glicolipídeos/IM
Antígenos HLA-DR/*GE/IM
Hanseníase/DI/*IM/MI
Hanseníase Virchowiana/DI/IM/MI
Hanseníase Tuberculóide/DI/IM/MI
Mycobacterium leprae/GE/*IM
Linfócitos T/IM/MI
Limites:HUMANO
Research Support, Non-U.S. Gov´t
Localização:BR191.1; 09362/S


  9 / 232 HANSEN  
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Id:23196
Autor:Geluk, A; van Meijgaarden, K. E; Franken, K. L. M. C; Wieles, B; Arend, S. M; Faber, W. R; Naafs, B; Ottenhoff, T. H. M
Título:Immunological crossreactivity of the Mycobacterium leprae CFP-10 with its homologue in Mycobacterium tuberculosis
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Fonte:s.l; s.n; 2004. 5 p. tab, graf.
Resumo:Mycobacterium tuberculosis culture filtrate protein-10 (CFP-10) (Rv3874) is considered a promising antigen for the immunodiagnosis of tuberculosis (TB) together with early secreted antigens of M. tuberculosis (ESAT-6). Both ESAT-6 and CFP-10 are encoded by the RD1 region that is deleted from all tested M. bovis bacille Calmette-Guérin (BCG) strains but present in M. leprae, M. tuberculosis, M. bovis, M. kansasii, M. africanum and M. marinum. In this study, the homologue of CFP-10 in M. leprae (ML0050) is identified and characterized. Interferon-gamma production in response to this homologue by T cells from leprosy patients, TB patients and unexposed controls shows that CFP-10 of M. leprae is a potent antigen that crossreacts with CFP-10 of M. tuberculosis at the T-cell level. This crossreactivity has implications for the use of CFP-10 of these mycobacterial species as diagnostic tool in areas endemic for both the diseases. (AU).
Descritores:Sequência de Aminoácidos
Antígenos de Bactérias/IM
Proteínas de Bactérias/*IM
Reações Cruzadas/IM
Interferon Tipo II/IM/SE
Hanseníase/*IM
Ativação Linfocítica/IM
Dados de Sequência Molecular
Mycobacterium leprae/*IM
Mycobacterium tuberculosis/*IM
Homologia de Sequência
Linfócitos T/IM/ME
Tuberculose/*IM
Limites:Research Support, Non-U.S. Gov't
Humanos
Estudo Comparativo
Animais
Localização:BR191.1; 09340/s


  10 / 232 HANSEN  
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Id:23106
Autor:Kennedy, Cornelis; Lien, Roel A. M. Chin; Stolz, Ernst; Joost, Theodoor; Naafs, Bernard
Título:Leprosy and human immunodeficiency virus infection: a closer look at the lesions
..-
Fonte:s.l; s.n; 1990. 2 p. .
Descritores:Síndrome de Imunodeficiência Adquirida/*CO/PA
Infecções por HIV/*CO/PA
Ceratinócitos/PA
Células de Langerhans/PA
Hanseníase Dimorfa/CO/*PA
Hanseníase Virchowiana/CO/*PA
Linfócitos T Citotóxicos/PA
Linfócitos T Auxiliadores-Indutores/PA
Linfócitos T Supressores-Efetores/PA
Limites:FEMININO
ADULTO
Humanos
Localização:BR191.1; 09234/s


  11 / 232 HANSEN  
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Id:22741
Autor:Black, Gillian F; Weir, Rosemari E; Chaguluka, Steven D; Warndorff, David; Crampin, Amelia C; Mwaungulu, Lorren; Sichali, Lifted; Floyd, Sian; Bliss, Lyn; Jarman, Elizabeth; Docovan, Linda; Andersen, Peter; Britton, Warwick; Hewinson, Glyn; Huygen, Kris; Paulsen, Jean; Sing, Mahavir; Prestidge, Ross; Fine, Paul E. M; Dockrell, Hazel M
Título:Gama interferon responses induced by a panel of recombinant and purified mycobacterial antigens in healthy, non-Mycobacterium bovis BCG-vaccinated Malawian young adults
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Fonte:s.l; s.n; 2003. 10 p. graf.
Resumo:We have previously shown that young adults living in a rural area of northern Malawi showed greater gamma interferon (IFN-gamma) responses to purified protein derivatives (PPD) prepared from environmental mycobacteria than to PPD from Mycobacterium tuberculosis. In order to define the mycobacterial species to which individuals living in a rural African population have been exposed and sensitized, we tested T-cell recognition of recombinant and purified antigens from M. tuberculosis (38 kDa, MPT64, and ESAT-6), M. bovis (MPB70), M. bovis BCG (Ag85), and M. leprae (65 kDa, 35 kDa, and 18 kDa) in >600 non-M. bovis BCG-vaccinated young adults in the Karonga District of northern Malawi. IFN-gamma was measured by enzyme-linked immunosorbent assay (ELISA) in day 6 supernatants of diluted whole-blood cultures. The recombinant M. leprae 35-kDa and 18-kDa and purified native M. bovis BCG Ag85 antigens induced the highest percentages of responders, though both leprosy and bovine tuberculosis are now rare in this population. The M. tuberculosis antigens ESAT-6 and MPT64 and the M. bovis antigen MPB70 induced the lowest percentages of responders. One of the subjects subsequently developed extrapulmonary tuberculosis; this individual had a 15-mm-diameter reaction to the Mantoux test and responded to M. tuberculosis PPD, Ag85, MPT64, and ESAT-6 but not to any of the leprosy antigens. We conclude that in this rural African population, exposure to M. tuberculosis or M. bovis is much less frequent than exposure to environmental mycobacteria such as M. avium, which have antigens homologous to the M. leprae 35-kDa and 18-kDa antigens. M. tuberculosis ESAT-6 showed the strongest association with the size of the Mantoux skin test induration, suggesting that among the three M. tuberculosis antigens tested it provided the best indication of exposure to, or infection with, M. tuberculosis. (AU).
Descritores:Antígenos de Bactérias/*IM
Vacina BCG/*IM
Interferon Tipo II/*BI
Hanseníase/EP
Malauí/EP
Mycobacterium/GE/*IM
Mycobacterium bovis/IM
Mycobacterium leprae/IM
Mycobacterium tuberculosis/IM
Proteínas Recombinantes de Fusão/IM
Especificidade de Espécies
Linfócitos T/IM
Teste Tuberculínico
Tuberculose/IM
Vacinação
Limites:Adolescente
Adulto
Criança
Estudo Comparativo
Feminino
Humano
Masculino
População Rural
Localização:BR191.1; 00224/s


  12 / 232 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


  13 / 232 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
..-
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


  14 / 232 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
..-
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


  15 / 232 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


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Id:18514
Autor:Bala, Lakshmi; Anand, Sukumar; Sinha, Sudhir
Título:Enhancement of human T cell response to a peptide epitope of 38kDa antigen of Mycobacterium tuberculosis by liposomes
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Fonte:s.l; s.n; 2002. 9 p. graf.
Resumo:Diagnosis of tuberculosis a problem, specially in the regions harboring an abundance of both pathogenic and non-pathogenic mycobacteria. This study was undertaken to assess in such a situation the predictive value of proliferative T cell response to a peptide epitope ('38G') of the 38 kDa membrane protein of Mycobacterium tuberculosis. 3[H]-thymidine incorporation assays were done with peripheral blood mononuclear cells of tuberculoid leprosy and pulmonary tuberculosis patients. The donors were also classified as PPD responders (Stimulation Index, SI> 3) or non-responders (SI < or = 3) on the basis of their T cell response to the 'Purified Protein Derivative (PPD)' of M. tuberculosis. 38G peptide was used in either free or liposome-associated form prepared by the technique of 'Dehydration-rehydration Vesicles' (Kirby and Gregoriadis, 1984). While free peptide failed to induce a positive response in study subjects, its liposomal form was T cell stimulatory and distinguished, to certain extent, between PPD responders (corresponding SI > 3 in 54 per cent subjects) and non-responders (SI > 3 in 29 per cent subjects). However, it did not differentiate between leprosy and tuberculosis. The study supports use of liposomes as adjuvant vehicles for antigenic peptides designed to activate human T cells. (AU).
Descritores:ANTIGENOS DE BACTERIAS/admin
ANTIGENOS DE BACTERIAS/quim
ANTIGENOS DE BACTERIAS/genet
HANSENIASE TUBERCULOIDE/diag
HANSENIASE TUBERCULOIDE/imunol
EPITOPOS/admin
EPITOPOS/quim
EPITOPOS/genet
DIAGNOSTICO DIFERENCIAL
MYCOBACTERIUM TUBERCULOSIS/quim
MYCOBACTERIUM TUBERCULOSIS/genet
MYCOBACTERIUM TUBERCULOSIS/imunol
DADOS DE SEQUÊNCIA MOLECULAR
SEQUÊNCIA DE AMINOACIDOS
LINFOCITOS T/imunol
TESTE TUBERCULINICO
TUBERCULOSE PULMONAR/diag
TUBERCULOSE PULMONAR/imunol
TRANSFORMACAO LINFOCITICA
LIPOSSOMOS
 PESO MOLECULAR
Limites:ESTUDO COMPARATIVO
HUMANO
IN VITRO
SUPPORT, NON-U.S. GOV'T
Meio Eletrônico: - .
Localização:BR191.1; 09061/s


  17 / 232 HANSEN  
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Id:18512
Autor:Yassin, A; Shennawy, M. el; Enany G. el; Wassef, N. F; Shoeb, S
Título:Leprosy of the upper respiratory tract. A clinical bacteriological, histopathological and histochemical study of twenty cases
..-
Fonte:s.l; s.n; 1975. 7 p. ilus, tab.
Resumo:Twenty cases clinically diagnosed as leprosy were thoroughly examined for E.N.T. lesions. These lesions were subjected to bacteriological, histopathological and histochemical studies. The results have been tabulated and discussed with special stress on some findings which are of help in diagnosing the disease. (AU).
Descritores:EPITELIO/patol
PARALISIA FACIAL/etiol
HISTOCITOQUIMICA
HANSENIASE/diag
HANSENIASE/microbiol
HANSENIASE/patol
LARINGE/patol
LINFOCITOS
MYCOBACTERIUM LEPRAE/isol
METAPLASIA/etiol
MUCOSA NASAL/patol
INFECCOES RESPIRATORIAS/microbiol
INFECCOES RESPIRATORIAS/patol
FARINGE/patol
RINITE ATROFICA/etiol
 CELULAS PLASMATICAS
Limites:HUMANO
MASCULINO
FEMININO
CRIANÇA
ADULTO
MEIA-IDADE
IDOSO
ADOLESCENTE
Meio Eletrônico: - .
Localização:BR191.1. 9119/s


  18 / 232 HANSEN  
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Id:18511
Autor:Kalaiselvi, K; Rajaguru, P; Palanivel, M; Usharani, M. V; Ramu, G
Título:Chromosomal aberration, micronucleus and Comet assays on peripheral blood lymphocytes of leprosy patients undergoing multidrug treatment. (Mutagenesis, 17, 309-312, 2002)
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Fonte:s.l; s.n; 2003. 1 p. tab.
Resumo:To evaluate the genetic damage in leprosy patients, we carried out the alkaline Comet assay and chromosomal aberration (CA) and micronucleus (MN) tests in peripheral blood lymphocytes of 50 leprosy patients receiving multidrug treatment (MDT) and 50 healthy individuals. The Comet assay showed statistically higher mean values for length to width ratios of DNA mass (P < 0.01) and for mean frequencies of tailed cells (P < 0.001) in cells of leprosy patients than in those of controls. Similarly, the mean frequencies of micronucleated cells (per 1000 cytochalasin B-induced binucleated cells) were significantly greater (P < 0.001) in leprosy patients (19.92 +/- 2.564) than in controls (1.6 +/- 0.231). A statistically significant 10-fold increase in the frequency of CAs (11.16 +/- 0.411) was observed in leprosy patients compared with controls (1.28 +/- 0.242). In multiple regression analyses, when patients and controls were considered together, disease factor alone significantly influenced the genotoxicity markers. In the control group, age and alcohol consumption significantly influenced MN and length to width ratios and CA frequency, respectively. However, in MDT-treated leprosy patients none of the other confounding factors (sex, age, smoking and alcohol drinking) significantly affected the extent of genetic damage.(AU).
Descritores:ENSAIO EM COMETA
CONSUMO DE BEBIDAS ALCOOLICAS
ABERRACOES CROMOSSÔMICAS
HANSENIASE/sangue
HANSENIASE/quimioter
LINFOCITOS/ef drogas
LINFOCITOS/fisiol
TESTES PARA MICRONUCLEOS
FATORES SEXUAIS
TABAGISMO
Limites:MASCULINO
FEMININO
ADULTO
HUMANO
Meio Eletrônico: - .
Localização:BR191.1; 09120/s


  19 / 232 HANSEN  
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Id:18482
Autor:Kalaiselvi, K; Rajaguru, P; Palanivel, M; Usharani, M. V; Ramu, G
Título:Chromosomal aberration, micronucleus and Comet assays on peripheral blood lymphocytes of leprosy patients undergoing multidrug treatment
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Fonte:s.l; s.n; 2002. 4 p. ilus, tab.
Resumo:To evaluate the genetic damage in leprosy patients, we carried out the alkaline Comet assay and chromosomal aberration (CA) and micronucleus (MN) tests in peripheral blood lymphocytes of 50 leprosy patients receiving multidrug treatment (MDT) and 50 healthy individuals. The Comet assay showed statistically higher mean values for length to width ratios of DNA mass (P < 0.01) and for mean frequencies of tailed cells (P < 0.001) in cells of leprosy patients than in those of controls. Similarly, the mean frequencies of micronucleated cells (per 1000 cytochalasin B-induced binucleated cells) were significantly greater (P < 0.001) in leprosy patients (19.92 +/- 2.564) than in controls (1.6 +/- 0.231). A statistically significant 10-fold increase in the frequency of CAs (11.16 +/- 0.411) was observed in leprosy patients compared with controls (1.28 +/- 0.242). In multiple regression analyses, when patients and controls were considered together, disease factor alone significantly influenced the genotoxicity markers. In the control group, age and alcohol consumption significantly influenced MN and length to width ratios and CA frequency, respectively. However, in MDT-treated leprosy patients none of the other confounding factors (sex, age, smoking and alcohol drinking) significantly affected the extent of genetic damage. (AU).
Descritores:CONSUMO DE BEBIDAS ALCOOLICAS
ABERRACOES CROMOSSÔMICAS
ENSAIO EM COMETA
HANSENIASE/sangue
HANSENIASE/quimioter
LINFOCITOS/ef drogas
LINFOCITOS/fisiol
TESTES PARA MICRONUCLEOS
FATORES SEXUAIS
TABAGISMO
Limites:HUMANO
MASCULINO
FEMININO
ADULTO
Meio Eletrônico: - .
Localização:BR191.1; 09045/s


  20 / 232 HANSEN  
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Id:18428
Autor:Bjune, Gunnar
Título:Significance of immune reactions in leprosy
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Fonte:s.l; s.n; Jun-Jul. 1980. 20 p. .
Resumo:The disease Leprosy is a chronic infectious disease caused by Mycobacterium leprae. The only known natural host for this mycobacterium is the human being. A mycobacterial disease described in wild armadillos in Louisiana as being indistinguishable from leprosy (walsh et al. 1975), is of questionable significance for the epidemiology in humans (Fillice et al. 1977).(AU).
Descritores:IMUNOSSUPRESSAO
TECNICAS IMUNOLOGICAS
LINFOCITOS T/imunol
ERITEMA NODOSO/imunol
HANSENIASE/genet
HANSENIASE/imunol
HANSENIASE/microbiol
MYCOBACTERIUM LEPRAE/cresc
Limites:HUMANO
Meio Eletrônico: - .
Localização:BR191.1; 00262/s



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