新生儿和婴儿胃肠道牛奶过敏的特点、自然病程及口服免疫疗法的疗效

H. Arakawa, H. Yagi, H. Koyama, N. Nakajima, T. Takizawa
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摘要

胃肠道(GI)过敏主要影响婴幼儿,其特征和自然过程尚未完全确定。我们研究了新生儿和婴儿胃肠道过敏的性质,以及慢性口服免疫疗法对持续症状患者的疗效。我们观察了12名患者(5名男孩,7名女孩),年龄在出生后0天至8个月首次出现。详细的访谈、外周血嗜酸性粒细胞计数、抗原特异性IgE抗体水平、抗原特异性淋巴细胞刺激试验(LST)、粪便潜血嗜酸性细胞计数和皮肤试验结合牛奶消除试验进行。5名患者接受了肠粘膜活检。挑衅测试用于评估耐受性获得。6名患者的唯一临床症状是便血,6名患者出现呕吐、发烧、体重增加不良或肝功能障碍。在11例检测病例中,有10例为牛奶特异性LSTs阳性。下消化道内窥镜检查显示,五名肠粘膜活检患者中有四名出现大量浸润性嗜酸性粒细胞。对三名患者进行了激发试验以确认耐受性获得。有趣的是,一名患者在激发试验中出现IgE介导的胃肠道过敏反应。一名患者的LST指数持续偏高,并继续消除乳制品。4岁时,她接受了口腔挑战测试。在摄入5毫升牛奶后,她出现发烧、便便稀、外观不佳和白细胞计数增加,这被认为是一种阳性激发测试。因此,使用阈值剂量的1/20开始缓慢口服免疫疗法,每周至少摄入四次脂肪。这在两周内稳定增加了20%,没有引起症状。新生儿和婴儿胃肠道过敏的特点多种多样,通常会自行缓解。然而,没有产生耐受性的患者可能是口服免疫疗法的合适选择。
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Characteristics and natural course of neonatal and infantile gastrointestinal milk allergy and the efficacy of oral immunotherapy

The characteristics and natural course of gastrointestinal (GI) allergies, which mainly affect infants and young children, are not fully determined. We investigated the nature of neonatal and infantile GI allergies and the efficacy of slow oral immunotherapy in patients with persistent symptoms. We observed 12 patients (five boys, seven girls) aged at first presentation from 0 days to 8 months after birth. Detailed interviews, peripheral blood eosinophil counts, antigen-specific IgE antibody levels, antigen-specific lymphocyte stimulation tests (LSTs), stool occult blood eosinophil counts and skin tests were performed in combination with milk elimination tests. Five patients underwent an intestinal mucosal biopsy. Provocation testing was used to assess tolerance acquisition. The only clinical symptom in six patients was bloody stool, while vomiting, fever, poor weight gain or hepatic dysfunction developed in six patients. Milk-specific LSTs were positive in 10 of 11 cases tested. Lower GI endoscopy showed large numbers of infiltrating eosinophils in four of five patients with an intestinal mucosal biopsy. Provocation tests to confirm tolerance acquisition were performed in three patients. Interestingly, one patient suffered IgE-mediated GI anaphylaxis during the provocation test. One patient had a sustained high LST index, and elimination of dairy milk products was continued. At 4 years of age, she underwent an oral challenge test. On ingestion of 5 mL of milk, she exhibited fever, loose stool, poor appearance and increased white blood cell counts, which was considered a positive provocation test. Therefore, slow oral immunotherapy was started using 1/20 of the threshold dose, with fat intake at least four times per week. This was steadily increased by 20% over 2 weeks without inducing symptoms. The characteristics of neonatal and infantile GI allergies are diverse, and they generally remit spontaneously. However, patients who do not develop tolerance may be suitable choices for oral immunotherapy.

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