Comment on: Matsumoto et al.

IF 4.6 2区 医学 Q2 ALLERGY Clinical and Translational Allergy Pub Date : 2024-11-09 DOI:10.1002/clt2.70000
Molly Cremin, Sadhbh Hurley, Juan Trujillo
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This practice has been deemed safe and successful in Irish settings.<span><sup>2</sup></span> As the use of Dietary advancement therapies (DATs) including MLs and OIT become more widespread in the global allergy community we strongly support the recollection of local data and thank the authors for publishing this paper which adds to the collective knowledge on the treatment of CMPA. This paper led us to consider our practice for patient selection and the differences between what is possible and practical in the clinical setting versus what is best practice.</p><p>In clinical practice the use of clinical history of parental reported immediate symptoms and proof of sensitisation is used to confirm milk allergy instead of the gold-standard Oral Food Challenge (OFC). Prior to the initiation of OIT international guidelines indicates the use of OFC to confirm the diagnosis.<span><sup>3</sup></span> In the protocol described by Matsumoto et al. they included patients with either parent reported immediate symptoms or proof of sensitisation (Milk specific IgE &gt; 5 kUA/L). We agree with the authors that this is a limitation of the study. 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引用次数: 0

Abstract

Dear Editor,

We would like to respond to the recent publication by Matsumoto et al. “Milk ladder versus early oral immunotherapy in infants with cow's milk protein (CMP) allergy” which we read with interest1 In this single center retrospective observational study the authors compared the efficacy and safety of milk ladder (ML) with early-oral immunotherapy (E-OIT) in children under the age of 2 years.

For over 10 years, milk ladders have been used as the mainstay of treatment for both IgE and non-IgE mediated cow’s milk protein allergy (CMPA) in Ireland. As described in this publication, the ML involves the home-based graded reintroduction of CMP containing foods in a stepwise fashion from least to most allergenic forms. This practice has been deemed safe and successful in Irish settings.2 As the use of Dietary advancement therapies (DATs) including MLs and OIT become more widespread in the global allergy community we strongly support the recollection of local data and thank the authors for publishing this paper which adds to the collective knowledge on the treatment of CMPA. This paper led us to consider our practice for patient selection and the differences between what is possible and practical in the clinical setting versus what is best practice.

In clinical practice the use of clinical history of parental reported immediate symptoms and proof of sensitisation is used to confirm milk allergy instead of the gold-standard Oral Food Challenge (OFC). Prior to the initiation of OIT international guidelines indicates the use of OFC to confirm the diagnosis.3 In the protocol described by Matsumoto et al. they included patients with either parent reported immediate symptoms or proof of sensitisation (Milk specific IgE > 5 kUA/L). We agree with the authors that this is a limitation of the study. We feel that in the absence of a challenge proven allergy, it is likely that this cohort included children with parent reported symptoms alone (with no sensitisation or allergy) or asymptomatic sensitisation.

Previous studies comparing the use of OIT with total milk avoidance identified approximately half of children screened with parent reported symptoms AND evidence of sensitisation (IgE > 0.35) had a negative double-blind placebo-controlled food challenge to milk.4

The same limitations were discussed in research from our Irish team, we compared the use of ML and milk avoidance in real-life diagnosed CMPA patients (positive clinical history and allergy tests without OFC) and decided to label the primary outcome as reintroduction of milk instead of tolerance.5

DATs can be used in high-risk patients for the first introduction of CMP. This may be helpful when there is hesitation to introduce milk and can enable and empower families to introduce it at home in a graded way. For example, in high risk allergy patients that have no history of reaction or sensitisation to milk this practice for allergen introduction would be classified as Primary allergy prevention. In the case of patients milk sensitised with no history of reaction an introduction of milk using the ML could prevent the development of milk allergy and subsequently be classified as Secondary allergy prevention.6 In this study by Matsumoto et al, we wonder if some patients reported as tolerant following ML or E-OIT could have instead undergone a primary or secondary CMPA prevention management.

This article made us re-evaluate our own treatment outcomes and reflect that while DATs encompass different active treatments, in clinical practice we often do not differentiate between a graded re-introduction and oral immune tolerance induction of an allergy.6

For us, this paper by Matsumoto et al. was an excellent study to remind us that without prior confirmation of allergy (with OFC) before commencing DAT or E-OIT that we cannot label that this intervention targets an already allergic patient (tertiary prevention) and claim tolerance was achieved.6

Molly Cremin: Writing—original draft; writing—review and editing. Sadhbh Hurley: Writing—original draft; writing—review and editing. Juan Trujillo: Writing—original draft; Writing—review and editing; supervision.

The authors declare no conflicts of interest.

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亲爱的编辑,我们想对 Matsumoto 等人最近发表的《牛奶阶梯疗法与早期口服免疫疗法在牛奶蛋白(CMP)过敏婴儿中的应用》一文做出回应。在这项单中心回顾性观察研究中,作者比较了牛奶阶梯疗法(ML)与早期口服免疫疗法(E-OIT)在 2 岁以下儿童中的疗效和安全性。10 多年来,牛奶梯一直是爱尔兰治疗 IgE 和非 IgE 介导的牛奶蛋白过敏 (CMPA) 的主要方法。如本出版物所述,牛奶阶梯疗法包括在家中分级重新引入含有牛乳蛋白的食物,从过敏性最小的食物到过敏性最大的食物。2 随着膳食促进疗法(DAT)(包括 ML 和 OIT)在全球过敏社区的使用越来越广泛,我们强烈支持对当地数据的回顾,并感谢作者发表这篇论文,为治疗 CMPA 的集体知识添砖加瓦。在临床实践中,我们使用父母报告的直接症状临床病史和过敏证明来确认牛奶过敏,而不是黄金标准的口服食物挑战(OFC)。3 在 Matsumoto 等人描述的方案中,他们将父母报告的即刻症状或过敏证明(牛奶特异性 IgE > 5 kUA/L)的患者纳入其中。我们同意作者的观点,认为这是研究的局限性。我们认为,在缺乏过敏挑战证明的情况下,该队列很可能包括了仅有父母报告症状(无致敏或过敏)或无症状致敏的儿童。先前对使用 OIT 和完全避免喝牛奶进行比较的研究发现,在父母报告症状和致敏证据(IgE > 0.35)的筛查儿童中,约有半数对牛奶进行了阴性双盲安慰剂对照食物挑战。4 我们爱尔兰团队的研究也讨论了同样的局限性,我们比较了在现实生活中确诊的 CMPA 患者(临床病史和过敏测试呈阳性,无 OFC)中使用 ML 和牛奶回避的情况,并决定将主要结果标记为重新引入牛奶而非耐受。5DATs 可用于高风险患者首次引入 CMP 的治疗,这可能会在患者对引入牛奶犹豫不决时有所帮助,并能使患者家庭有能力在家中分级引入牛奶。例如,对于对牛奶没有反应或过敏史的高危过敏患者,这种引入过敏原的做法可归类为初级过敏预防。对于对牛奶过敏但无反应史的患者,使用 ML 导入牛奶可预防牛奶过敏的发生,因此被归类为二级过敏预防6。在 Matsumoto 等人的这项研究中,我们不禁要问,是否有些患者在接受 ML 或 E-OIT 治疗后出现了耐受,而不是接受了一级或二级 CMPA 预防管理。这篇文章让我们重新评估了自己的治疗结果,并反思道,虽然 DATs 包含不同的积极治疗方法,但在临床实践中,我们通常不会区分过敏的分级再引入和口服免疫耐受诱导。对我们来说,Matsumoto 等人的这篇论文是一项很好的研究,它提醒我们,在开始 DAT 或 E-OIT 之前,如果没有事先确认过敏(通过 OFC),我们就不能说这种干预措施针对的是已经过敏的患者(三级预防),并声称已经实现了耐受:写作-原稿;写作-审阅和编辑。Sadhbh Hurley:写作-原稿;写作-审阅和编辑。胡安-特鲁希略(Juan Trujillo):撰写-原稿;撰写-审阅和编辑;监督。
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来源期刊
Clinical and Translational Allergy
Clinical and Translational Allergy Immunology and Microbiology-Immunology
CiteScore
7.50
自引率
4.50%
发文量
117
审稿时长
12 weeks
期刊介绍: Clinical and Translational Allergy, one of several journals in the portfolio of the European Academy of Allergy and Clinical Immunology, provides a platform for the dissemination of allergy research and reviews, as well as EAACI position papers, task force reports and guidelines, amongst an international scientific audience. Clinical and Translational Allergy accepts clinical and translational research in the following areas and other related topics: asthma, rhinitis, rhinosinusitis, drug hypersensitivity, allergic conjunctivitis, allergic skin diseases, atopic eczema, urticaria, angioedema, venom hypersensitivity, anaphylaxis, food allergy, immunotherapy, immune modulators and biologics, animal models of allergic disease, immune mechanisms, or any other topic related to allergic disease.
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