首页> 美国卫生研究院文献>The Journal of Experimental Medicine >Allergen-responsive CD4+CD25+ Regulatory T Cells in Children who Have Outgrown Cows Milk Allergy
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Allergen-responsive CD4+CD25+ Regulatory T Cells in Children who Have Outgrown Cows Milk Allergy

机译:对牛奶过敏症已超过儿童的过敏原反应性CD4 + CD25 +调节性T细胞

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摘要

Cow's milk allergy in children is often of short duration, which makes this disorder an interesting clinical model for studies of tolerance to dietary antigens. Here, we studied T cell responses in 21 initially allergic children who, after a milk-free period of >2 mo, had cow's milk reintroduced to their diet. Children who outgrew their allergy (tolerant children) had higher frequencies of circulating CD4+CD25+ T cells and decreased in vitro proliferative responses to bovine β-lactoglobulin in peripheral blood mononuclear cells (PBMCs) compared with children who maintained clinically active allergy. No significant difference in proliferative activity stimulated by the polyclonal mitogen phytohemagglutinin was observed between the two groups. Depletion of CD25+ cells from PBMCs of tolerant children led to a fivefold increase in in vitro proliferation against β-lactoglobulin. This suggests that tolerance is associated with the appearance of circulating CD4+CD25+ regulatory T (Treg) cells that are capable of suppressing the effector T cells generated 1 wk after reintroduction of cow's milk. The suppressive function of the CD4+CD25+ Treg cells was shown to be partly cell contact dependent. Collectively, our study provides human data to suggest that mucosal induction of tolerance against dietary antigens is associated with the development of CD4+CD25+ Treg cells.
机译:儿童对牛奶的过敏通常持续时间很短,这使得这种疾病成为研究膳食抗原耐受性的有趣临床模型。在这里,我们研究了21名最初过敏儿童的T细胞反应,这些儿童在无奶期超过2个月后将牛奶重新摄入饮食中。变态反应过敏的孩子(宽容的孩子)循环CD4 + CD25 + T细胞的频率更高,并且对外周血单个核细胞中的牛β-乳球蛋白的体外增殖反应降低(PBMC)与维持临床活跃过敏症的儿童进行比较。两组之间没有观察到多克隆促分裂素植物血凝素刺激的增殖活性有显着差异。耐受性儿童PBMC CD25 + 细胞的耗竭导致抗β-乳球蛋白的体外增殖增加了五倍。这表明耐受性与循环CD4 + CD25 + 调节性T细胞(Treg)的出现有关,该调节性T细胞能够抑制再引入1周后产生的效应T细胞。牛奶。 CD4 + CD25 + Treg细胞的抑制功能显示部分依赖细胞接触。总的来说,我们的研究提供了人类数据,表明粘膜诱导对饮食抗原的耐受性与CD4 + CD25 + Treg细胞的发育有关。

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