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首页> 外文期刊>International journal of clinical & laboratory research >Cytokine production by allergen (Der pI)-specific CD4+T cell clones derived from a patient with severe atopic disease
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Cytokine production by allergen (Der pI)-specific CD4+T cell clones derived from a patient with severe atopic disease

机译:来自严重特应性疾病患者的变应原 (Der pI) 特异性 CD4+T 细胞克隆产生的细胞因子

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Twenty-four T cell clones (TCC) specific for purifiedDermatophagoides pteronyssinusgroup I allergen (Der pI) were established from the peripheral blood of a patient with severe atopic disease and assessed for cytokine production in response to stimulation with both phorbol 12-myristate 13-acetate and anti-CD3 monoclonal antibody. All Der pI-specific TCC produced high amounts of interleukin (IL)-4 in association with IL-3, IL-5 and granulocyte monocyte-colony stimulating factor (GM-CSF), whereas they produced variable amounts of IL-2 and virtually no interferon-γ. These data support the hypothesis that atopy is associated with preferential activation of type 2 T helper cells and suggest a deregulation in the function of the IL-3, IL-4, IL-5 and GM-CSF gene cluster in subjects with severe atopic disorders
机译:从一名严重特应性疾病患者的外周血中建立了 24 个对纯化的 Dermatophagoides pteronyssinusgroup I 过敏原 (Der pI) 具有特异性的 T 细胞克隆 (TCC),并评估了佛波醇 12-肉豆蔻酸酯 13-乙酸酯和抗 CD3 单克隆抗体刺激下的细胞因子产生。所有 Der pI 特异性 TCC 都产生大量与 IL-3、IL-5 和粒细胞单核细胞集落刺激因子 (GM-CSF) 相关的白细胞介素 (IL)-4,而它们产生不同量的 IL-2,几乎没有干扰素γ。这些数据支持特应性与 2 型辅助性 T 细胞的优先激活相关的假设,并表明严重特应性疾病受试者的 IL-3、IL-4、IL-5 和 GM-CSF 基因簇功能失调

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