Sadchikov Pavel E.过敏性疾病风险婴儿的分子致敏特征

Irina A. Belyayeva, T. Turti, L. Namazova-Baranova, E. Bombardirova, E. Vishneva, E. Kaytukova, K. Efendieva, R. A. Shukenbaeva, Pavel E. Sadchikov
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The hereditary atopy risk was observed in 74% of cases (37/50) in Group 1 and in 71% of cases (25/35) in Group 2. 38% of children (19/50) in Group 1 were breastfed, in Group 2 — 60% of children (21/35). Supplemental feeding was implemented in 5.5 [5.0–6.0] months. Sensitisation was reported in 10% and 37% of children. Children of Group 1 were sensitised to food allergen antigens: cow's milk/meat (Bos d 6, Bos d 8), egg-white (Gal d 1, Gal d 2, Gal d 3), soybeans (Gly m 6), shrimps (Pen m 4); airborne allergens: house dust mite (Blo t 5, Der h 10), Anisakidae (Ani s 3), cockroach (Bla g 7). Children of Group 2 were sensitised to food allergen antigens: cow's milk (Bos d 6), egg-white (Gal d 1, Gal d 2), soybeans (Gly m 6), peanut (Ara h 1, Ara h 2, Ara h 6), kiwi (Act d 1), corn (Tri a 19); airborne allergens: cat (Fel d 1, Fel d 4), birch pollen (Bet v 1). Polyvalent sensitisation was revealed in 4% and 6% of cases, respectively.Conclusion. 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摘要

背景。目前,关于初始过敏表现的婴儿对特定过敏原抗原的敏感性特征的数据很少。该研究的目的是根据出生后年龄确定具有特应性疾病风险的婴儿的主要分子致敏特征。有沉重的家族过敏史和/或皮肤/胃肠道过敏症状的足月婴儿进行检查:1 - 50组儿童,年龄- 2.0[1.0-3.0]个月;组2 ~ 35例,年龄- 9.0[8.0 ~ 11.0]个月。第1组有74%(37/50)的病例存在遗传性特应性风险,第2组有71%(25/35)的病例存在遗传性特应性风险。第1组38%的儿童(19/50)母乳喂养,第2组60%的儿童(21/35)母乳喂养。在5.5[5.0-6.0]月龄时进行补充喂养。据报道,10%和37%的儿童过敏。1组患儿对食物过敏原抗原敏感:牛奶/肉类(bos6、bos8)、蛋白(gald1、gald2、gald3)、大豆(gly6)、虾(peng4);空气致敏原:屋尘螨(Blo t 5、Der h 10)、异螨科(Anisakidae)、蟑螂(Bla g 7)。2组儿童对食物致敏原抗原:牛奶(bod 6)、蛋白(gald 1、gald 2)、大豆(Gly m 6)、花生(Ara h 1、Ara h 2、Ara h 6)、猕猴桃(Act d 1)、玉米(Tri a 19);空气致敏原:猫(Fel d 1, Fel d 4),桦树花粉(betv 1)。多价致敏分别为4%和6%。婴儿对过敏原的敏感范围比通常认为的要大得多。除了专性食物过敏原外,空气中的过敏原也可能引起致敏:室内尘螨、表皮、桦树花粉;交叉反应成分-原肌球蛋白。
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Sadchikov Pavel E. Features of Molecular Sensitisation Profile in Infants with Risk of Allergic Diseases
Background. For now, there is little data on sensitivity features to specific allergen antigens in infants with initial allergy manifestations.Objective. The aim of the study is to determine the features of the primary molecular sensitisation profile in infants with risk of atopic disease according to their postnatal age.Methods. Full-term infants with burdened familial allergic history and/or skin/gastrointestinal allergy symptoms were examined: Group 1 — 50 children, age — 2.0 [1.0–3.0] months; Group 2 — 35 children, age — 9.0 [8.0–11.0] months.Results. The hereditary atopy risk was observed in 74% of cases (37/50) in Group 1 and in 71% of cases (25/35) in Group 2. 38% of children (19/50) in Group 1 were breastfed, in Group 2 — 60% of children (21/35). Supplemental feeding was implemented in 5.5 [5.0–6.0] months. Sensitisation was reported in 10% and 37% of children. Children of Group 1 were sensitised to food allergen antigens: cow's milk/meat (Bos d 6, Bos d 8), egg-white (Gal d 1, Gal d 2, Gal d 3), soybeans (Gly m 6), shrimps (Pen m 4); airborne allergens: house dust mite (Blo t 5, Der h 10), Anisakidae (Ani s 3), cockroach (Bla g 7). Children of Group 2 were sensitised to food allergen antigens: cow's milk (Bos d 6), egg-white (Gal d 1, Gal d 2), soybeans (Gly m 6), peanut (Ara h 1, Ara h 2, Ara h 6), kiwi (Act d 1), corn (Tri a 19); airborne allergens: cat (Fel d 1, Fel d 4), birch pollen (Bet v 1). Polyvalent sensitisation was revealed in 4% and 6% of cases, respectively.Conclusion. Infants have much wider range of allergens to which they are sensitive than it is commonly believed. Beside obligate food allergens, sensitisation can be caused by airborne allergens: house dust mites, epidermal, birch pollen; crossreactive component — tropomyosin.
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