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Regulatory activity of human CD4+ CD25+ T cells depends on allergen concentration type of allergen and atopy status of the donor

机译:人CD4 + CD25 + T细胞的调节活性取决于过敏原浓度过敏原类型和供体的过敏状态

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摘要

Regulatory CD4+ CD25+ FoxP3-positive T cells (Treg) are functional in most atopic patients with allergic rhinitis and are able to inhibit T helper type 1 (Th1) and Th2 cytokine production of CD4+ CD25 T cells. This study was designed to analyse the following additional aspects: influence of allergen concentration, influence of the type of allergen, and influence of the atopy status of the donor on the strength of the regulatory activity. CD4+ CD25 T cells from healthy non-atopic controls or from grass-pollen-allergic or wasp-venom-allergic donors were stimulated alone or in the presence of Treg with autologous mature monocyte-derived dendritic cells which were pulsed with different concentrations of the respective allergens. Treg from grass-pollen-allergic donors failed to inhibit proliferation but not cytokine production of CD4+ CD25 T cells at high antigen doses while Treg from non-atopic donors did not fail at these allergen concentrations. Proliferative responses and cytokine production of CD4+ CD25 T cells from most of the examined wasp-venom-allergic patients were not inhibited at any concentration of wasp venom. The use of wasp venom- or phospholipase A2-pulsed dendritic cells for stimulation of CD4+ CD25 T cells from donors who were not allergic to wasp stings only resulted in an inhibited proliferation and Th2 cytokine production by Treg at 10-fold lower than the optimal concentration, while interferon-γ production was inhibited at all concentrations investigated. These data demonstrate that in allergic diseases the function of Treg is dependent on the concentration and the type of the respective allergen with different thresholds for individual allergens and patients.
机译:调节性CD4 + CD25 + FoxP3阳性T细胞(Treg)在大多数特应性过敏性鼻炎患者中发挥功能,并能够抑制1型T辅助细胞(Th1)和Th2 CD4 + CD25 T细胞的细胞因子产生。本研究旨在分析以下其他方面:过敏原浓度的影响,过敏原类型的影响以及供体过敏状态对调节活性强度的影响。来自健康的非异位对照或来自花粉过敏或黄蜂毒液过敏的供体的CD4 + CD25 T细胞被单独刺激或在Treg存在下刺激自体成熟单核细胞衍生的树突状细胞,用不同浓度的相应变应原脉冲处理。来自花粉过敏性供体的Treg不能抑制增殖,但不能抑制高抗原剂量的CD4 + CD25 - T细胞的细胞因子产生,而来自非特应性供体的Treg则不能在这些过敏原浓度下失败。在任何浓度的黄蜂毒液中,大多数接受检查的黄蜂毒液过敏性患者的CD4 + CD25 T细胞的增殖反应和细胞因子产生均不受抑制。使用黄蜂毒液或磷脂酶A2刺激的树突状细胞刺激对黄蜂st过敏的供体的CD4 + CD25 - T细胞,只会导致抑制作用Treg的增殖和Th2细胞因子的产生比最佳浓度低10倍,而在所有研究的浓度下,γ干扰素的产生均受到抑制。这些数据表明,在变应性疾病中,Treg的功能取决于各自的变应原的浓度和类型,且对个体变应原和患者的阈值不同。

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