Yannick Chantran, Hélène Renaudin, Michel Arock, Tamazoust Guiddir, A. Nemni
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引用次数: 0
摘要
遗传性α-胰蛋白酶血症(HαT)与基础血清胰蛋白酶(bST)升高有关,并与患有克隆肥大细胞疾病或 IgE 介导的膜翅目昆虫毒液诱发过敏性休克的患者发生严重过敏反应的风险较高有关。在这里,我们描述了一个四口之家的三例花生过敏病例:其中两例与 HαT 有关,第三例与胰蛋白酶野生型基因型有关。TPSAB1/TPSB2 基因型是通过数字 PCR 测定的。在对病例进行描述后,我们回顾了有关过敏性休克的 bST 水平和胰蛋白酶基因型的文献,尤其是有关食物过敏的文献。与传统胰蛋白酶基因型的兄弟姐妹相比,HαT 基因型的两个兄弟姐妹在初次口服食物挑战时的花生阈值较低,花生皮肤点刺试验反应性较高,花生、Ara h 2 和 Ara h 6 特异性 IgE 水平较高,口服免疫疗法 10 年后的 IgG4/IgE 比率较低。
Case Report: A family history of peanut allergy and hereditary alpha-tryptasemia
Hereditary alpha-tryptasemia (HαT) is associated with elevated basal serum tryptase (bST) and is associated with a higher risk of severe anaphylactic reactions in patients with clonal mast cell disorders or IgE-mediated Hymenoptera venom-induced anaphylaxis. The consequence of this genetic trait remains to be determined in other allergic diseases and food allergy in particular.Here, we describe three cases of peanut allergy among siblings from a single family of four: two of them were associated with HαT, and the third one was associated with the tryptase wild-type genotype.TPSAB1/TPSB2 genotypes were determined by digital PCR. After the case description, we provided a review of the literature regarding bST levels and tryptase genotypes in anaphylaxis, with a particular focus on food allergy.Compared to the sibling with the conventional tryptase genotype, the two siblings with HαT presented a lower peanut threshold at the initial oral food challenge, higher peanut skin prick test reactivity, higher levels of specific IgE to peanut, Ara h 2, and Ara h 6, and a lower IgG4/IgE ratio after 10 years of oral immunotherapy.The tryptase genotype and HαT status might modify the clinical presentation and biological features of food allergy.