对 "牛奶蛋白过敏婴儿的牛奶阶梯疗法与早期口服免疫疗法 "评论的回应。

IF 4.6 2区 医学 Q2 ALLERGY
Chisato Inuo, Yurika Matsumoto
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引用次数: 0

摘要

亲爱的编辑,感谢作者们对我们的出版物《牛奶阶梯疗法与早期口服免疫疗法在牛奶蛋白过敏婴儿中的应用》所提出的周到而富有建设性的意见。我们感谢他们对这篇关于牛奶蛋白过敏(CMPA)治疗的临床讨论的关注和参与。在全球过敏界,牛奶和鸡蛋阶梯等膳食促进疗法(DATs)的使用正变得越来越广泛。正如作者正确指出的那样,我们的研究是在真实世界的临床环境中进行的,由于各种实际限制,我们对大多数患者使用了家长报告的临床病史和过敏标记物,而不是黄金标准的口服食物挑战(OFC)。表 S1 列出了仅因摄入牛奶蛋白而立即发生过敏反应的患者的数据。其余患者的牛奶特异性 IgE 水平较高(>5 kUA/L),超过了诊断 CMPA 预测值的 95%。我们承认这是一个局限性,并同意由于缺乏经挑战证实的过敏症,可能会将一些无症状的致敏儿童或家长报告症状但无 OFC 的儿童纳入其中。我们也同意作者对一级、二级和三级过敏预防的精辟区分,以及根据临床病史和过敏状态对接受牛奶导入的患者进行仔细分类的必要性。在我们的研究中,有些患者可能接受了一级或二级预防,这是一个重要的考虑因素。与作者的观点一致,我们认识到必须仔细标注耐受和再引入的结果,尤其是在没有通过 OFC 事先确认过敏的情况下。我们相信,采用更严格的诊断标准进行进一步研究对于完善治疗方案和确保在干预措施中解决真正的过敏反应至关重要。我们再次感谢作者的宝贵反馈意见,并感谢我们有机会进一步澄清和讨论 CMPA 管理的重要方面。我们希望我们的研究能为DATs(如牛奶阶梯疗法和早期口服免疫疗法)的不断进步做出有意义的贡献,并欢迎在这一领域提出更多的意见和讨论:写作-原稿。松本百合香撰写-审阅和编辑。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Response to comments on ‘Milk ladder versus early oral immunotherapy in infants with cow's milk protein allergy’

Dear Editor,

We would like to thank the authors for their thoughtful and constructive comments on our publication, “Milk ladder versus early oral immunotherapy in infants with cow's milk protein allergy.” We appreciate their interest and engagement in this clinical discussion on the management of cow milk protein allergy (CMPA).

The use of dietary advancement therapies (DATs) such as milk and egg ladders is becoming widespread in the global allergy community. It is important to collect and share local data on these practices to expand our collective knowledge of the treatment of food allergies.

As the authors rightly pointed out, our study was conducted in a real-world clinical setting where, due to various practical constraints, we used parent-reported clinical histories and sensitization markers instead of the gold-standard Oral Food Challenge (OFC) for most patients. Data on patients who only had previous immediate allergic reactions due to the ingestion of cow milk protein is shown Table S1. The remaining patients had high levels of cow milk-specific IgE (>5 kUA/L), which exceeded 95% of the predicted value for diagnosing CMPA. We acknowledge that this is a limitation and agree that the absence of a challenge-proven allergy could have led to the inclusion of some children with asymptomatic sensitization or those with parent-reported symptoms without OFC. Nonetheless, we aimed to reflect the reality of clinical practice in which OFC is not always feasible or conducted in every case.

We also concur with the authors' insightful differentiation between the primary, secondary, and tertiary allergy prevention and the need to carefully classify patients undergoing milk introduction based on their clinical history and sensitization status. The suggestion that some patients in our study may have undergone the primary or secondary prevention is an important consideration. This underscores the complexity of managing food allergies in clinical settings where treatment protocols often overlap.

In agreement with the authors, we recognize that tolerance and reintroduction outcomes must be carefully labeled, particularly in the absence of prior confirmation of allergy through the OFC. We believe that further studies employing more rigorous diagnostic criteria will be crucial to refine treatment protocols and ensure that true allergic responses are addressed in our interventions.

Once again, we appreciate the authors' valuable feedback and our opportunity to further clarify and discuss the important aspects of CMPA management. We hope that our study contributes meaningfully to the ongoing advancement of DATs, such as Milk Ladder and Early Oral Immunotherapy, and we welcome further comments and discussions in this field.

Chisato Inuo: Writing—original draft. Yurika Matsumoto: Writing—review and editing.

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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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