牛奶蛋白过敏婴儿的牛奶梯与早期口服免疫疗法。

IF 4.6 2区 医学 Q2 ALLERGY
Yurika Matsumoto, Mayumi Fujita, Tsukahara Ayumi, Tetsuya Takamasu, Chisato Inuo
{"title":"牛奶蛋白过敏婴儿的牛奶梯与早期口服免疫疗法。","authors":"Yurika Matsumoto,&nbsp;Mayumi Fujita,&nbsp;Tsukahara Ayumi,&nbsp;Tetsuya Takamasu,&nbsp;Chisato Inuo","doi":"10.1002/clt2.12388","DOIUrl":null,"url":null,"abstract":"<p>Cow's milk protein allergy (CMPA) significantly decreases the quality of life of infants and their families, necessitating effective management. Avoidance of cow's milk protein (CMP) has been the primary approach, awaiting the development of a natural tolerance.<span><sup>1</sup></span></p><p>Oral immunotherapy (OIT) for CMPA gradually increases the use of pure CMP, such as milk, to enhance tolerance. A previous study demonstrated the efficacy and safety of early OIT (E-OIT) for infants with CMPA.<span><sup>2</sup></span> The Milk Ladder (ML) method modifies the OIT strategy and enhances CMP tolerance through stepwise exposure to milk-containing foods.<span><sup>1, 3-5</sup></span> Despite growing adoption, ML lacks extensive validation and requires further research.<span><sup>4</sup></span> To the best of our knowledge, there have been no comparative studies of E-OIT and ML in infants with CMPA. This study aimed to compare the efficacy and safety of ML and E-OIT in infants with CMPA.</p><p>We retrospectively analyzed infants younger than 2 years who started intervention for CMPA at the Department of Allergy at Kanagawa Children's Medical Center from April 2016 to March 2022, with a treatment protocol shift in April 2018 from E-OIT to ML. Inclusion criteria included a CMPA diagnosis based on parent-reported immediate allergic reaction to CMP ingestion or a serum milk-specific IgE level greater than 5 kU<sub>A</sub>/L.<span><sup>3</sup></span> Patients with only gastrointestinal symptoms were excluded due to different CMPA types. The ML protocol started with baked milk (BM), advancing toward less processed forms, while E-OIT began with controlled doses of milk or yogurt. For detailed protocols, see the Supplementary materials in Supporting Information S1.</p><p>CMP tolerance was defined as the ability to consume 100 mL of milk or an equivalent amount of approximately 3300 mg of CMP daily without experiencing symptoms. Low dairy tolerance for processed foods was defined as the ability to consume processed foods. Products high in dairy ingredients, such as cheese, yogurt, and pizza were excluded. These were confirmed through repeated intake at home. All patients underwent treatment review and assessment through interviews approximately every 3 months to assess progress and adjust care, as necessary.</p><p>This study conformed to the guidelines established by the Declaration of Helsinki and was approved by the Kanagawa Children's Medical Center Research Ethics Committee (approval no. 2105-4). Informed consent was obtained from the parents of all patients.</p><p>The analyses were performed according to the intention-to-treat principle (ITT) 2 years post intervention. The Mann–Whitney <i>U</i> test was used to compare continuous variables, while the Chi-squared test or Fisher's exact test was used for categorical variables. To evaluate the progression of CMP tolerance over time, Kaplan–Meier analysis with a log-rank test was performed. Statistical significance was set at <i>p</i> &lt; 0.05. Statistical analyses were performed using GraphPad Prism 10.2.2 (GraphPad Software Inc.).</p><p>We analyzed 89 patients (ML, 38; E-OIT, 51). The ML group had higher baseline CM-specific IgE levels and was younger. Patients with a history of anaphylaxis were exclusively found in the ML group (Table 1).</p><p>The ML and E-OIT groups showed no significant difference in CMP tolerance (<i>p</i> = 0.28). However, the ML group exhibited higher tolerance to processed foods with low amounts of dairy products than the E-OIT group (<i>p</i> = 0.007). On Kaplan–Meier analysis, there was no difference in CMP tolerance over time (Figure 1A; <i>p</i> = 0.29), although a significantly lower avoidance of CMP-containing products was observed in the ML group (Figure 1B; <i>p</i> = 0.0030).</p><p>Adverse event rates were similar in both groups (<i>p</i> = 0.51). One case of anaphylaxis was reported in the ML group. The affected child initially started the ML protocol with BM but discontinued it owing to taste issues. Consequently, the child deviated from the ML group and was switched to yogurt intake, which induced anaphylaxis.</p><p>This result suggests that the contribution of ML to CMP tolerance is the same as that of E-OIT, which is consistent with a previous report indicating that low-dose OIT may provide a similar therapeutic effect with much greater safety than conventional OIT.<span><sup>6</sup></span> Furthermore, ML facilitates the intake of processed foods, such as bread, cookies, ham, chocolate, and butter, better than E-OIT. An elimination diet affects the meals of the entire family, necessitating all members to follow dietary restrictions and experience dietary monotony.<span><sup>7</sup></span> The ability to consume processed products containing milk protein without allergic symptoms may alleviate anxiety about hidden allergens and reduce the family burden.<span><sup>4</sup></span> Our safety data are consistent with those of previous ML reports.<span><sup>4, 5, 8</sup></span> The use of food ladders is often associated with isolated skin reactions. However, the sole anaphylaxis case in the ML group underscores the need for careful monitoring of dietary interventions. Considering the high rate of protocol discontinuation among both groups, further improvements in the methods are required for the food ladder.<span><sup>9</sup></span></p><p>Our study has several limitations. First, the sample size was small, lacking randomized and blinding. We analyzed the data using the ITT technique to reduce selection bias. The ML group had higher baseline CM-specific IgE levels and was younger, potentially influencing the result. Prospective, randomized, blinded studies are warranted. Second, we did not conduct a double-blind oral food challenge test, which is the gold standard for diagnosing and tolerance CMPA. Third, this was a single-center study, and the results cannot be generalized to other populations.</p><p>In conclusion, ML is as effective and safe as E-OIT for the management of CMPA in infants. Furthermore, ML facilitates the intake of processed foods in infants with CMPA better than E-OIT.</p><p><b>Yurika Matsumoto</b>: Writing – original draft; investigation; formal analysis. <b>Mayumi Fujita</b>: Investigation; data curation; supervision. <b>Tsukahara Ayumi</b>: Investigation; data curation. <b>Tetsuya Takamasu</b>: Investigation. <b>Chisato Inuo</b>: Conceptualization; writing – review &amp; editing; funding acquisition; investigation; supervision; project administration; visualization.</p><p>The authors have no conflict of interest to declare.</p>","PeriodicalId":10334,"journal":{"name":"Clinical and Translational Allergy","volume":null,"pages":null},"PeriodicalIF":4.6000,"publicationDate":"2024-08-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11309850/pdf/","citationCount":"0","resultStr":"{\"title\":\"Milk ladder versus early oral immunotherapy in infants with cow's milk protein allergy\",\"authors\":\"Yurika Matsumoto,&nbsp;Mayumi Fujita,&nbsp;Tsukahara Ayumi,&nbsp;Tetsuya Takamasu,&nbsp;Chisato Inuo\",\"doi\":\"10.1002/clt2.12388\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Cow's milk protein allergy (CMPA) significantly decreases the quality of life of infants and their families, necessitating effective management. Avoidance of cow's milk protein (CMP) has been the primary approach, awaiting the development of a natural tolerance.<span><sup>1</sup></span></p><p>Oral immunotherapy (OIT) for CMPA gradually increases the use of pure CMP, such as milk, to enhance tolerance. A previous study demonstrated the efficacy and safety of early OIT (E-OIT) for infants with CMPA.<span><sup>2</sup></span> The Milk Ladder (ML) method modifies the OIT strategy and enhances CMP tolerance through stepwise exposure to milk-containing foods.<span><sup>1, 3-5</sup></span> Despite growing adoption, ML lacks extensive validation and requires further research.<span><sup>4</sup></span> To the best of our knowledge, there have been no comparative studies of E-OIT and ML in infants with CMPA. This study aimed to compare the efficacy and safety of ML and E-OIT in infants with CMPA.</p><p>We retrospectively analyzed infants younger than 2 years who started intervention for CMPA at the Department of Allergy at Kanagawa Children's Medical Center from April 2016 to March 2022, with a treatment protocol shift in April 2018 from E-OIT to ML. Inclusion criteria included a CMPA diagnosis based on parent-reported immediate allergic reaction to CMP ingestion or a serum milk-specific IgE level greater than 5 kU<sub>A</sub>/L.<span><sup>3</sup></span> Patients with only gastrointestinal symptoms were excluded due to different CMPA types. The ML protocol started with baked milk (BM), advancing toward less processed forms, while E-OIT began with controlled doses of milk or yogurt. For detailed protocols, see the Supplementary materials in Supporting Information S1.</p><p>CMP tolerance was defined as the ability to consume 100 mL of milk or an equivalent amount of approximately 3300 mg of CMP daily without experiencing symptoms. Low dairy tolerance for processed foods was defined as the ability to consume processed foods. Products high in dairy ingredients, such as cheese, yogurt, and pizza were excluded. These were confirmed through repeated intake at home. All patients underwent treatment review and assessment through interviews approximately every 3 months to assess progress and adjust care, as necessary.</p><p>This study conformed to the guidelines established by the Declaration of Helsinki and was approved by the Kanagawa Children's Medical Center Research Ethics Committee (approval no. 2105-4). Informed consent was obtained from the parents of all patients.</p><p>The analyses were performed according to the intention-to-treat principle (ITT) 2 years post intervention. The Mann–Whitney <i>U</i> test was used to compare continuous variables, while the Chi-squared test or Fisher's exact test was used for categorical variables. To evaluate the progression of CMP tolerance over time, Kaplan–Meier analysis with a log-rank test was performed. Statistical significance was set at <i>p</i> &lt; 0.05. Statistical analyses were performed using GraphPad Prism 10.2.2 (GraphPad Software Inc.).</p><p>We analyzed 89 patients (ML, 38; E-OIT, 51). The ML group had higher baseline CM-specific IgE levels and was younger. Patients with a history of anaphylaxis were exclusively found in the ML group (Table 1).</p><p>The ML and E-OIT groups showed no significant difference in CMP tolerance (<i>p</i> = 0.28). However, the ML group exhibited higher tolerance to processed foods with low amounts of dairy products than the E-OIT group (<i>p</i> = 0.007). On Kaplan–Meier analysis, there was no difference in CMP tolerance over time (Figure 1A; <i>p</i> = 0.29), although a significantly lower avoidance of CMP-containing products was observed in the ML group (Figure 1B; <i>p</i> = 0.0030).</p><p>Adverse event rates were similar in both groups (<i>p</i> = 0.51). One case of anaphylaxis was reported in the ML group. The affected child initially started the ML protocol with BM but discontinued it owing to taste issues. Consequently, the child deviated from the ML group and was switched to yogurt intake, which induced anaphylaxis.</p><p>This result suggests that the contribution of ML to CMP tolerance is the same as that of E-OIT, which is consistent with a previous report indicating that low-dose OIT may provide a similar therapeutic effect with much greater safety than conventional OIT.<span><sup>6</sup></span> Furthermore, ML facilitates the intake of processed foods, such as bread, cookies, ham, chocolate, and butter, better than E-OIT. An elimination diet affects the meals of the entire family, necessitating all members to follow dietary restrictions and experience dietary monotony.<span><sup>7</sup></span> The ability to consume processed products containing milk protein without allergic symptoms may alleviate anxiety about hidden allergens and reduce the family burden.<span><sup>4</sup></span> Our safety data are consistent with those of previous ML reports.<span><sup>4, 5, 8</sup></span> The use of food ladders is often associated with isolated skin reactions. However, the sole anaphylaxis case in the ML group underscores the need for careful monitoring of dietary interventions. Considering the high rate of protocol discontinuation among both groups, further improvements in the methods are required for the food ladder.<span><sup>9</sup></span></p><p>Our study has several limitations. First, the sample size was small, lacking randomized and blinding. We analyzed the data using the ITT technique to reduce selection bias. The ML group had higher baseline CM-specific IgE levels and was younger, potentially influencing the result. Prospective, randomized, blinded studies are warranted. Second, we did not conduct a double-blind oral food challenge test, which is the gold standard for diagnosing and tolerance CMPA. Third, this was a single-center study, and the results cannot be generalized to other populations.</p><p>In conclusion, ML is as effective and safe as E-OIT for the management of CMPA in infants. Furthermore, ML facilitates the intake of processed foods in infants with CMPA better than E-OIT.</p><p><b>Yurika Matsumoto</b>: Writing – original draft; investigation; formal analysis. <b>Mayumi Fujita</b>: Investigation; data curation; supervision. <b>Tsukahara Ayumi</b>: Investigation; data curation. <b>Tetsuya Takamasu</b>: Investigation. <b>Chisato Inuo</b>: Conceptualization; writing – review &amp; editing; funding acquisition; investigation; supervision; project administration; visualization.</p><p>The authors have no conflict of interest to declare.</p>\",\"PeriodicalId\":10334,\"journal\":{\"name\":\"Clinical and Translational Allergy\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":4.6000,\"publicationDate\":\"2024-08-08\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11309850/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Clinical and Translational Allergy\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/clt2.12388\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"ALLERGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Clinical and Translational Allergy","FirstCategoryId":"3","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/clt2.12388","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ALLERGY","Score":null,"Total":0}
引用次数: 0

摘要

考虑到两组中方案中止率都很高,因此需要进一步改进食物阶梯的方法。首先,样本量较小,缺乏随机性和盲法。我们采用 ITT 技术分析数据,以减少选择偏差。ML组的基线CM特异性IgE水平较高,而且更年轻,可能会影响结果。有必要进行前瞻性、随机、盲法研究。其次,我们没有进行双盲口服食物挑战试验,而这是诊断和耐受 CMPA 的金标准。总之,在治疗婴儿 CMPA 方面,ML 与 E-OIT 一样有效、安全。此外,ML 比 E-OIT 更有利于 CMPA 患儿摄入加工食品:写作--原稿;调查;正式分析。藤田真由美:调查;数据整理;监督。冢原步美调查;数据整理。Tetsuya Takamasu:调查。猪尾千里构思;撰写-审阅&amp;编辑;资金获取;调查;监督;项目管理;可视化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Milk ladder versus early oral immunotherapy in infants with cow's milk protein allergy

Milk ladder versus early oral immunotherapy in infants with cow's milk protein allergy

Cow's milk protein allergy (CMPA) significantly decreases the quality of life of infants and their families, necessitating effective management. Avoidance of cow's milk protein (CMP) has been the primary approach, awaiting the development of a natural tolerance.1

Oral immunotherapy (OIT) for CMPA gradually increases the use of pure CMP, such as milk, to enhance tolerance. A previous study demonstrated the efficacy and safety of early OIT (E-OIT) for infants with CMPA.2 The Milk Ladder (ML) method modifies the OIT strategy and enhances CMP tolerance through stepwise exposure to milk-containing foods.1, 3-5 Despite growing adoption, ML lacks extensive validation and requires further research.4 To the best of our knowledge, there have been no comparative studies of E-OIT and ML in infants with CMPA. This study aimed to compare the efficacy and safety of ML and E-OIT in infants with CMPA.

We retrospectively analyzed infants younger than 2 years who started intervention for CMPA at the Department of Allergy at Kanagawa Children's Medical Center from April 2016 to March 2022, with a treatment protocol shift in April 2018 from E-OIT to ML. Inclusion criteria included a CMPA diagnosis based on parent-reported immediate allergic reaction to CMP ingestion or a serum milk-specific IgE level greater than 5 kUA/L.3 Patients with only gastrointestinal symptoms were excluded due to different CMPA types. The ML protocol started with baked milk (BM), advancing toward less processed forms, while E-OIT began with controlled doses of milk or yogurt. For detailed protocols, see the Supplementary materials in Supporting Information S1.

CMP tolerance was defined as the ability to consume 100 mL of milk or an equivalent amount of approximately 3300 mg of CMP daily without experiencing symptoms. Low dairy tolerance for processed foods was defined as the ability to consume processed foods. Products high in dairy ingredients, such as cheese, yogurt, and pizza were excluded. These were confirmed through repeated intake at home. All patients underwent treatment review and assessment through interviews approximately every 3 months to assess progress and adjust care, as necessary.

This study conformed to the guidelines established by the Declaration of Helsinki and was approved by the Kanagawa Children's Medical Center Research Ethics Committee (approval no. 2105-4). Informed consent was obtained from the parents of all patients.

The analyses were performed according to the intention-to-treat principle (ITT) 2 years post intervention. The Mann–Whitney U test was used to compare continuous variables, while the Chi-squared test or Fisher's exact test was used for categorical variables. To evaluate the progression of CMP tolerance over time, Kaplan–Meier analysis with a log-rank test was performed. Statistical significance was set at p < 0.05. Statistical analyses were performed using GraphPad Prism 10.2.2 (GraphPad Software Inc.).

We analyzed 89 patients (ML, 38; E-OIT, 51). The ML group had higher baseline CM-specific IgE levels and was younger. Patients with a history of anaphylaxis were exclusively found in the ML group (Table 1).

The ML and E-OIT groups showed no significant difference in CMP tolerance (p = 0.28). However, the ML group exhibited higher tolerance to processed foods with low amounts of dairy products than the E-OIT group (p = 0.007). On Kaplan–Meier analysis, there was no difference in CMP tolerance over time (Figure 1A; p = 0.29), although a significantly lower avoidance of CMP-containing products was observed in the ML group (Figure 1B; p = 0.0030).

Adverse event rates were similar in both groups (p = 0.51). One case of anaphylaxis was reported in the ML group. The affected child initially started the ML protocol with BM but discontinued it owing to taste issues. Consequently, the child deviated from the ML group and was switched to yogurt intake, which induced anaphylaxis.

This result suggests that the contribution of ML to CMP tolerance is the same as that of E-OIT, which is consistent with a previous report indicating that low-dose OIT may provide a similar therapeutic effect with much greater safety than conventional OIT.6 Furthermore, ML facilitates the intake of processed foods, such as bread, cookies, ham, chocolate, and butter, better than E-OIT. An elimination diet affects the meals of the entire family, necessitating all members to follow dietary restrictions and experience dietary monotony.7 The ability to consume processed products containing milk protein without allergic symptoms may alleviate anxiety about hidden allergens and reduce the family burden.4 Our safety data are consistent with those of previous ML reports.4, 5, 8 The use of food ladders is often associated with isolated skin reactions. However, the sole anaphylaxis case in the ML group underscores the need for careful monitoring of dietary interventions. Considering the high rate of protocol discontinuation among both groups, further improvements in the methods are required for the food ladder.9

Our study has several limitations. First, the sample size was small, lacking randomized and blinding. We analyzed the data using the ITT technique to reduce selection bias. The ML group had higher baseline CM-specific IgE levels and was younger, potentially influencing the result. Prospective, randomized, blinded studies are warranted. Second, we did not conduct a double-blind oral food challenge test, which is the gold standard for diagnosing and tolerance CMPA. Third, this was a single-center study, and the results cannot be generalized to other populations.

In conclusion, ML is as effective and safe as E-OIT for the management of CMPA in infants. Furthermore, ML facilitates the intake of processed foods in infants with CMPA better than E-OIT.

Yurika Matsumoto: Writing – original draft; investigation; formal analysis. Mayumi Fujita: Investigation; data curation; supervision. Tsukahara Ayumi: Investigation; data curation. Tetsuya Takamasu: Investigation. Chisato Inuo: Conceptualization; writing – review & editing; funding acquisition; investigation; supervision; project administration; visualization.

The authors have no conflict of interest to declare.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
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.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信