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牛奶过敏患者经烘焙牛奶口服免疫疗法随机试验后的临床和免疫结果

Clinical and immunological outcomes after randomized trial of baked milk oral immunotherapy for milk allergy.

作者信息

Dantzer Jennifer A, Lewis Sloan A, Psoter Kevin J, Sutherland Aaron, Frazier April, Richardson Eve, Maiche Synaida, Seumois Gregory, Peters Bjoern, Wood Robert A

机构信息

Division of Pediatric Allergy, Immunology, and Rheumatology, Department of Pediatrics, John Hopkins University School of Medicine, Baltimore, Maryland, USA.

La Jolla Institute for Immunology, La Jolla, California, USA.

出版信息

JCI Insight. 2025 Jan 9;10(1):e184301. doi: 10.1172/jci.insight.184301.

Abstract

BACKGROUNDCow's milk (CM) allergy is the most common food allergy in young children. Treatment with oral immunotherapy (OIT) has shown efficacy, but high rates of adverse reactions. The aim of this study was to determine whether baked milk OIT (BMOIT) could reduce adverse reactions while still inducing desensitization, and to identify immunological correlates of successful BMOIT.METHODSThis phase II, randomized trial evaluated the safety and efficacy of BMOIT in milk-allergic children 3-18 years old. After the initial placebo-controlled first year of treatment, placebo-treated participants crossed over to active BMOIT. Double-blind, placebo-controlled oral food challenges (OFCs) were conducted with BM after year 1 and to both BM and unheated milk (UM) after year 2. IgG and IgE antibodies were measured along with CM-specific (CM+) CD4+ memory T cell populations, profiled using flow cytometry and scRNA-Seq.RESULTSTwenty-one of 30 (70%) reached the primary endpoint of tolerating 4044 mg of BM protein at month 24, and 11 of 30 tolerated 2000 mg or more of UM protein. Dosing symptoms were common, but more than 98% were mild, with no severe reactions. Immunological changes associated with desensitization included increased CM IgG4, CM+ FOXP3+ cells, and Tregs and corresponding decreases in CM IgE, CM+ Th2A cells, and CD154+ cells. T cell and antibody measurements were combined to build a model that predicted UM OFC outcomes.CONCLUSIONBMOIT was well tolerated and induced desensitization to BM and UM. This desensitization corresponded to redistribution within antigen-specific antibody and T cell compartments that provided insight into the mechanistic changes that occur with OIT treatment.TRIAL REGISTRATIONClinicalTrials.gov NCT03462030.FUNDING: Myra Reinhardt Family Foundation (grant number 128388), NIH/NIAID (U19AI135731, T32AI125179, S10OD025052).

摘要

背景

牛奶(CM)过敏是幼儿中最常见的食物过敏。口服免疫疗法(OIT)治疗已显示出疗效,但不良反应发生率较高。本研究的目的是确定烘焙牛奶OIT(BMOIT)是否能在诱导脱敏的同时减少不良反应,并确定成功的BMOIT的免疫相关性。

方法

这项II期随机试验评估了BMOIT在3至18岁牛奶过敏儿童中的安全性和有效性。在最初的安慰剂对照治疗的第一年之后,接受安慰剂治疗的参与者交叉接受活性BMOIT治疗。在第1年后对烘焙牛奶进行双盲、安慰剂对照口服食物激发试验(OFC),在第2年后对烘焙牛奶和未加热牛奶(UM)均进行该试验。使用流式细胞术和scRNA-Seq对IgG和IgE抗体以及CM特异性(CM+)CD4+记忆T细胞群体进行测量。

结果

30名参与者中有21名(70%)在第24个月达到了耐受4044毫克烘焙牛奶蛋白的主要终点,30名中有11名耐受2000毫克或更多的未加热牛奶蛋白。给药症状很常见,但超过98%为轻度,无严重反应。与脱敏相关的免疫变化包括CM IgG4增加、CM+ FOXP3+细胞和调节性T细胞增加,以及CM IgE、CM+ Th2A细胞和CD154+细胞相应减少。结合T细胞和抗体测量结果建立了一个预测未加热牛奶OFC结果的模型。

结论

BMOIT耐受性良好,并诱导对烘焙牛奶和未加热牛奶脱敏。这种脱敏对应于抗原特异性抗体和T细胞区室内的重新分布,这为OIT治疗中发生的机制变化提供了见解。

试验注册

ClinicalTrials.gov NCT03462030。

资助

迈拉·莱因哈特家族基金会(资助编号128388),美国国立卫生研究院/国家过敏和传染病研究所(U19AI135731、T32AI125179、S10OD025052)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3f1/11721308/a89297cb9c73/jciinsight-10-184301-g205.jpg

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