Dupilumab 用于诱导对 SLIT-Melocotón® 的耐受。

IF 2.6 Q2 ALLERGY European annals of allergy and clinical immunology Pub Date : 2024-05-01 Epub Date: 2023-01-13 DOI:10.23822/EurAnnACI.1764-1489.280
M S Zamarro Parra, Y Petryk Petryk, S San Román Sirvent, C Navarro Garrido, A I Escudero Pastor, J C Miralles López, A Carbonell Martínez
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引用次数: 0

摘要

摘要:导言。食物过敏是一个日益严重的人口问题,目前正在研究利用舌下免疫疗法诱导耐受的治疗方法。病例介绍。作为过敏学家,我们的目标是通过舌下免疫疗法(SLIT-peach)实现对舌下过敏原特异性免疫疗法的耐受。我们提交的病例报告中,一名 40 岁的女性在食用水果和其他植物性食物后,因对非特异性脂质转移蛋白(nsLTP)过敏而出现过敏反应。她被诊断为 LTP 综合征。这种蛋白质是我们地区的主要泛过敏原,会引起对多种植物性食物的交叉反应。这种综合症的主要过敏原是 rPru p3,存在于桃子、大多数蔬菜、水果、坚果和谷物中。使用微阵列检测血清特异性 IgE 水平,结果显示七种 nsLTPs 呈阳性:rAra h9、rCor a8、nJug r3、rPru p3、rTri a 14、nArt v3 和 rPla a3。在维持剂量的第四个月,患者对 SLIT 立即出现反应,导致我们中断了 pru p3 免疫疗法。在医院使用奥马珠单抗第四剂时出现过敏性休克,促使我们改用杜匹单抗。在使用这种单克隆抗体四个月后,我们重新采用了pru p3 SLIT-peach®舌下免疫疗法,达到了每天四滴的维持剂量,并且没有出现任何临床反应。由于患者的饮食受限、反应严重,而且根据欧洲人生活质量调查问卷(Europevall questionnaire),SLIT-peach® 对她来说至关重要。我们的结论是,我们的目标是实现 SLIT。我们报告了一例由 nsLTP 介导的多种食物过敏综合征患者使用杜匹单抗的同情使用病例。目前还没有关于杜比鲁单抗用于这种用途的病例报道。
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Dupilumab to induce tolerance to SLIT-Melocotón®.

Summary: Food allergy is an increasing problem for population, and treatments inducing tolerance using sublingual immunotherapy is currently under study. Our aim as allergists is to achieve tolerance to sublingual allergen specific immunotherapy with sublingual immunotherapy (SLIT-peach). We present a case report consisting of a 40-year-old woman with anaphylactic reactions after eating fruit and other plant-foods due to sensitization to nonspecific lipid transfer proteins (nsLTP). Her diagnose was LTP-syndrome. This protein is the main pannallergen in our area and causes crossed reaction to multiple plant foods. The principal allergen in this syndrome is rPru p3, present in peach and most vegetables, fruits, nuts and grains. Serum specific IgE levels were performed using microarrays and positive for seven nsLTPs: rAra h9, rCor a8, nJug r3, rPru p3, rTri a 14, nArt v3 and rPla a3. Immediate reaction to SLIT in the fourth month of maintenance-dose led us to interrupt pru p3 immunotherapy. Immediate reaction to omalizumab in the fourth dose in hospital consisting in anaphylaxis prompted us to switch to dupilumab. After four months with this monoclonal antibody, we reintroduced sublingual immunotherapy with pru p3 SLIT-peach® achieving maintenance dose of four drops a day with no clinical reactions. SLIT-peach® in our patient is crucial for her due to her restricted diet, the severity of reactions and lack of quality of life measured by Europevall questionary. There are no cases reported for dupilumab in this use.

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