Database : HANSEN
Search on : LINFOCITOS T CD4-POSITIVOS/*IM [Subject descriptor]
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Id:17315
Author:Kirkaldy, A. A; Musonda, A. C; Khanolkhar-Young, S; Suneetha, S; Lockwood, D. N. J
Title:Expression of CC and CXC chemokines and chemokine receptors in human in human leprosy skin lesions ..-
Source:s.l; s.n; 2003. 7 p. ilus, tab, graf.
Abstract: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).
Descriptors: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
Limits:Humano
Pele/*IM
Estatísticas não Paramétricas
Location:BR191.1; 00253/s


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Id:13709
Author: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
Title:T-cell responses to the Mycobacterium tuberculosis-specific antigen ESAT-6 in Brazilian tuberculosis patients ..-
Source:s.l; s.n; 2002. 8 p. tab, graf.
Abstract: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).
Descriptors: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
Limits:FEMININO
HUMANO
MASCULINO
SUPPORT, NON-U.S. GOV'T
Location:BR191.1; 09070/s


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Id:11755
Author:Adams, Linda B; Scollard, David M; Ray, Nashone A; Cooper, Andrea M; Frank, Anthony A; Orne, Ian M; Krahenbuhl, James L
Title:The study of Mycobacterium leprae infection in interferon-y gene-disrupted mice as a model to explore the immunopathologic spectrum of leprosy ..-
Source:s.l; s.n; 2002. 8 p. ilus, graf.
Descriptors: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
Limits:ANIMAL
Location:BR191.1; 08511/s


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Id:11678
Author:Phillips, Peter
Title:Immunoresititution disease in relation to infection with Mycobacterium avium complex and to leprosy (Correspondence) ..-
Source:s.l; s.n; 2001. 3 p. .
Descriptors:HANSENIASE
HANSENIASE
LINFOCITOS T CD4-POSITIVOS
HOSPEDEIRO IMUNOCOMPROMETIDO
COMPLEXO MYCOBACTERIUM AVIUM
INFECÇAO POR MYCOBACTERIUM AVIUM-INTRACELLULARE
INFECÇAO POR MYCOBACTERIUM AVIUM-INTRACELLULARE
MYCOBACTERIUM LEPRAE
INFECCOES OPORTUNISTAS RELACIONADAS COM A AIDS/*IM/MI
Location:BR191.1; 08469/s



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