Möller C, Magnusson K E, Sundqvist T, Stenling R, Björkstén B
Allergy. 1986 May;41(4):280-5. doi: 10.1111/j.1398-9995.1986.tb02029.x.
Twenty-four children with rhinoconjunctivitis due to birch pollinosis were treated in a double-blind manner with enteric-coated capsules containing either a high dose of a birch pollen preparation (n = 11) or placebo (n = 13). The permeability of the small intestine was analysed at three different occasions with a mixture of differently sized polyethyleneglycols (PEG 400 and PEG 1000), before the start of oral immunotherapy (OIT), at the moment of maximum allergen dose, and after 3 months of therapy which was at the beginning of the pollen season. The actively treated children did not significantly change their permeability characteristics as determined from PEG recovery in the urine. By contrast, in the control group of patients the recovery of larger PEG molecules was decreased after 3 months of therapy, possibly due to the commencing pollen season. In addition, small bowel biopsies were taken at the time of maximum allergen dose from two children openly treated with OIT. Both specimens were normal.
24名因桦树花粉症导致鼻结膜炎的儿童接受了双盲治疗,分别服用含有高剂量桦树花粉制剂的肠溶胶囊(n = 11)或安慰剂(n = 13)。在口服免疫疗法(OIT)开始前、过敏原剂量最大时以及治疗3个月后(花粉季节开始时),使用不同大小的聚乙二醇混合物(PEG 400和PEG 1000)在三个不同时间点分析小肠通透性。根据尿液中PEG的回收率测定,接受积极治疗的儿童其通透性特征没有明显变化。相比之下,在对照组患者中,治疗3个月后较大PEG分子的回收率降低,这可能是由于花粉季节开始所致。此外,在过敏原剂量最大时,对两名接受OIT公开治疗的儿童进行了小肠活检。两份标本均正常。