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J Clin Invest ; 82(3): 825-32, 1988 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-2458387

RESUMO

Allergic contact dermatitis to Toxicodendron radicans (poison ivy) is mediated by the hapten urushiol. An urushiol-specific, interleukin 2 (IL-2)-dependent T cell clone (RLB9-7) was generated from the peripheral blood of a patient with a history of allergic contact dermatitis to T. radicans. This clone proliferated specifically to both leaf extract and pure urushiol. Although the clone had the phenotype CD3+CD4+CD8+, proliferation to antigen was blocked by anti-CD8 and anti-HLA-A, B, C, but not by anti-CD4, suggesting that CD4 was not functionally associated with the T cell receptor. Furthermore, studies with antigen-presenting cells from MHC-typed donors indicated that the clone was MHC class 1 restricted. RLB9-7 was WT31 positive, indicating it bears the alpha beta T cell receptor. The clone lacked significant natural killer cell activity and produced only low levels of IL-2 or gamma-interferon upon antigen stimulation. Addition of RLB9-7 to autologous peripheral blood mononuclear cells in the presence of urushiol inhibited the pokeweed mitogen-driven IgG synthesis. This suppression was resistant to irradiation (2,000 rad) and was not seen when RLB9-7 was added to allogeneic cells, even in the presence of irradiated autologous antigen-presenting cells, suggesting that suppression was MHC restricted and not mediated by nonspecific soluble factors. However, RLB9-7 cells in the presence of urushiol inhibited the synthesis of tetanus toxoid-specific IgG by autologous lymphocytes, indicating that the suppression, although triggered specifically by urushiol, was nonspecific.


Assuntos
Catecóis/imunologia , Dermatite por Toxicodendron/imunologia , Ativação Linfocitária , Linfócitos T Citotóxicos/imunologia , Linfócitos T Reguladores/imunologia , Especificidade de Anticorpos , Células Apresentadoras de Antígenos/imunologia , Células Clonais/imunologia , Dermatite por Toxicodendron/sangue , Epitopos/imunologia , Humanos , Imunoglobulina G/biossíntese , Ativação Linfocitária/efeitos dos fármacos , Linfocinas/biossíntese , Toxoide Tetânico/imunologia
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