首页 > 最新文献

World Allergy Organization Journal最新文献

英文 中文
Disparities in food allergy amongst British South Asian adult patients in central England 英格兰中部英国南亚成年患者食物过敏的差异
IF 4.3 2区 医学 Q2 ALLERGY Pub Date : 2025-09-01 DOI: 10.1016/j.waojou.2025.101099
Toni Osborne MSc , Gareth Walters PhD , Richard Baretto PhD , Mamidipudi Thirumala Krishna PhD

Background

Published evidence suggests an increased burden of food allergy (FA) amongst ethnic minority groups resident the United States of America and Australia, with limited data from the United Kingdom. The West Midlands Regional Allergy Service serves British Caucasian White and Ethnic Minority Groups with a large proportion being British South Asian, making it important to explore ethnicity—based differences in clinical outcomes for FA.

Aims

To compare clinical outcomes of FA and other atopic diseases between Caucasian White and South Asian patients attending the regional allergy service in West Midlands.

Methods

This prospective cross-sectional, observational study (N = 29 White and N = 21 South Asian) used a structured questionnaire with dichotomous, multiple-choice, and scaled questions to gather data on age, ethnicity, FA (including allergens, allergic reactions, adrenaline auto-injector use, and emergency department visits), and other atopic conditions.

Main results

1.) South Asians had significantly (p = 0.006) more frequent FA reactions. 2.) Poorly controlled eczema and asthma were significantly (eczema p = 0.015, asthma p = 0.022) more common amongst South Asians. 3.) The burden of asthma, eczema, and allergic rhinitis was similar between groups. 4.) Significantly more White patients (p = 0.027) with asthma were on higher treatment steps.

Conclusion

British South Asian patients with FA attending the West Midlands regional allergy service had more frequent allergic reactions and poorly controlled asthma and eczema compared to British Caucasian White patients. This highlights the need for improved education and compliance. Larger multi-centre studies are needed to gain further insight into ethnicity-based disparities in FA.
已发表的证据表明,居住在美利坚合众国和澳大利亚的少数民族群体的食物过敏(FA)负担增加,而来自英国的数据有限。西米德兰兹地区过敏服务中心服务于英国白种人、白人和少数民族群体,其中很大一部分是英国南亚人,因此探索基于种族的FA临床结果差异非常重要。目的比较在西米德兰兹郡参加区域过敏服务的高加索白人和南亚患者的FA和其他特应性疾病的临床结果。方法本前瞻性横断面观察性研究(N = 29名白人和N = 21名南亚人)采用结构化问卷,采用二分法、多项选择和量表问题收集年龄、种族、FA(包括过敏原、过敏反应、肾上腺素自动注射器使用和急诊就诊)和其他特应性疾病的数据。主要其中回答。)南亚人的FA反应明显(p = 0.006)更频繁。2)。控制不良的湿疹和哮喘(湿疹p = 0.015,哮喘p = 0.022)在南亚人群中更为常见。哮喘、湿疹和变应性鼻炎的负担在两组之间相似。4)。白人哮喘患者在更高的治疗步骤中显著增加(p = 0.027)。结论在西米德兰地区过敏服务中心就诊的英属南亚裔FA患者的过敏反应发生率高于英国白种人患者,哮喘和湿疹控制较差。这突出了改进教育和遵守的必要性。需要更大规模的多中心研究来进一步了解FA中基于种族的差异。
{"title":"Disparities in food allergy amongst British South Asian adult patients in central England","authors":"Toni Osborne MSc ,&nbsp;Gareth Walters PhD ,&nbsp;Richard Baretto PhD ,&nbsp;Mamidipudi Thirumala Krishna PhD","doi":"10.1016/j.waojou.2025.101099","DOIUrl":"10.1016/j.waojou.2025.101099","url":null,"abstract":"<div><h3>Background</h3><div>Published evidence suggests an increased burden of food allergy (FA) amongst ethnic minority groups resident the United States of America and Australia, with limited data from the United Kingdom. The West Midlands Regional Allergy Service serves British Caucasian White and Ethnic Minority Groups with a large proportion being British South Asian, making it important to explore ethnicity—based differences in clinical outcomes for FA.</div></div><div><h3>Aims</h3><div>To compare clinical outcomes of FA and other atopic diseases between Caucasian White and South Asian patients attending the regional allergy service in West Midlands.</div></div><div><h3>Methods</h3><div>This prospective cross-sectional, observational study (N = 29 White and N = 21 South Asian) used a structured questionnaire with dichotomous, multiple-choice, and scaled questions to gather data on age, ethnicity, FA (including allergens, allergic reactions, adrenaline auto-injector use, and emergency department visits), and other atopic conditions.</div></div><div><h3>Main results</h3><div>1.) South Asians had significantly (p = 0.006) more frequent FA reactions. 2.) Poorly controlled eczema and asthma were significantly (eczema p = 0.015, asthma p = 0.022) more common amongst South Asians. 3.) The burden of asthma, eczema, and allergic rhinitis was similar between groups. 4.) Significantly more White patients (p = 0.027) with asthma were on higher treatment steps.</div></div><div><h3>Conclusion</h3><div>British South Asian patients with FA attending the West Midlands regional allergy service had more frequent allergic reactions and poorly controlled asthma and eczema compared to British Caucasian White patients. This highlights the need for improved education and compliance. Larger multi-centre studies are needed to gain further insight into ethnicity-based disparities in FA.</div></div>","PeriodicalId":54295,"journal":{"name":"World Allergy Organization Journal","volume":"18 9","pages":"Article 101099"},"PeriodicalIF":4.3,"publicationDate":"2025-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144997187","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
From cockpit to community: Time to stop the use of first-generation H1-antihistamines 从驾驶舱到社区:是时候停止使用第一代h1 -抗组胺药了
IF 4.3 2区 医学 Q2 ALLERGY Pub Date : 2025-09-01 DOI: 10.1016/j.waojou.2025.101112
Mário Morais-Almeida MD , Raquel Baptista-Pestana MD , Sandra N. González-Dĺaz MD, PhD , Bryan L. Martin DO , Gary W.K. Wong MD
{"title":"From cockpit to community: Time to stop the use of first-generation H1-antihistamines","authors":"Mário Morais-Almeida MD ,&nbsp;Raquel Baptista-Pestana MD ,&nbsp;Sandra N. González-Dĺaz MD, PhD ,&nbsp;Bryan L. Martin DO ,&nbsp;Gary W.K. Wong MD","doi":"10.1016/j.waojou.2025.101112","DOIUrl":"10.1016/j.waojou.2025.101112","url":null,"abstract":"","PeriodicalId":54295,"journal":{"name":"World Allergy Organization Journal","volume":"18 9","pages":"Article 101112"},"PeriodicalIF":4.3,"publicationDate":"2025-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144997188","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Wildfire and asthma - The prospective interventions 野火和哮喘-前瞻性干预
IF 4.3 2区 医学 Q2 ALLERGY Pub Date : 2025-09-01 DOI: 10.1016/j.waojou.2025.101110
Xingxing Yuan PhD , Liuxin Yang MD , Chaofan Li MD , Ousman Bajinka MSc, PhD , Zhuying Li PhD
The increasing global warming trend has led to a drier landscape, which has in turn resulted in an increased incidence of wildfires. The smoke emanating from these fires has consequences that extend beyond the loss of property. This comes with the wildfire season whose smoke emanations have implications beyond loss of property. Among the health concerns regarding wildfires and smoke are respiratory diseases, such as asthma. Asthma, as a heterogeneous disease, is directly linked to other types of smoke rather than cigarettes, traffic exhaust, and industrial chemicals. Wildfires have been shown to be associated with particulate matter that act as pollutants to human life. The unprecedented increase in emergency visits during wildfire seasons is of clinical significance for its association with asthma and other pulmonary disorders. Despite the efforts of wealthy communities or nations, which have faced episodes of wildfires in recent years, the most effective protocol is yet to be developed. Given the vulnerability of individuals, including asthmatics, to the smoke from wildfires, interventions should extend beyond emergency measures. This review aims to provide a comprehensive overview of the relationship between wildfires and asthma symptoms, exploring the underlying mechanisms both in vitro and in vivo. It also delves into the potential implications for science policies, communication strategies, research directions, and management strategies for asthma cases, emphasizing the importance of preventive measures. Furthermore, this review serves as a guideline for various sectors, offering a clear conceptual rationale for preventing and managing wildfire smoke-related asthma and other pulmonary diseases. The interventions are multi-sectoral and multidisciplinary concerns, and given the transboundary nature of smoke, it is imperative for all relevant parties to collaborate to minimize preventable deaths.
日益加剧的全球变暖趋势导致了更干燥的景观,这反过来又导致了野火的发生率增加。这些火灾产生的烟雾所造成的后果超出了财产损失。这是在野火季节发生的,其烟雾散发的影响不仅仅是财产损失。与野火和烟雾有关的健康问题包括呼吸系统疾病,如哮喘。哮喘作为一种异质性疾病,与其他类型的烟雾直接相关,而不是香烟、交通废气和工业化学品。野火已被证明与颗粒物有关,这些颗粒物对人类生活起着污染物的作用。在野火季节,急诊人数空前增加,这与哮喘和其他肺部疾病有关,具有临床意义。尽管富裕的社区或国家在近年来面临野火事件的努力,但最有效的协议尚未制定出来。考虑到包括哮喘患者在内的个人容易受到野火烟雾的伤害,干预措施应超出紧急措施的范围。本文旨在全面概述野火与哮喘症状之间的关系,并在体内和体外探讨其潜在机制。探讨了哮喘病例的科学政策、传播策略、研究方向和管理策略的潜在意义,强调了预防措施的重要性。此外,本综述可作为各部门的指导方针,为预防和管理野火烟雾相关的哮喘和其他肺部疾病提供明确的概念依据。这些干预措施涉及多部门和多学科问题,鉴于吸烟的跨界性质,所有相关各方必须进行合作,尽量减少可预防的死亡。
{"title":"Wildfire and asthma - The prospective interventions","authors":"Xingxing Yuan PhD ,&nbsp;Liuxin Yang MD ,&nbsp;Chaofan Li MD ,&nbsp;Ousman Bajinka MSc, PhD ,&nbsp;Zhuying Li PhD","doi":"10.1016/j.waojou.2025.101110","DOIUrl":"10.1016/j.waojou.2025.101110","url":null,"abstract":"<div><div>The increasing global warming trend has led to a drier landscape, which has in turn resulted in an increased incidence of wildfires. The smoke emanating from these fires has consequences that extend beyond the loss of property. This comes with the wildfire season whose smoke emanations have implications beyond loss of property. Among the health concerns regarding wildfires and smoke are respiratory diseases, such as asthma. Asthma, as a heterogeneous disease, is directly linked to other types of smoke rather than cigarettes, traffic exhaust, and industrial chemicals. Wildfires have been shown to be associated with particulate matter that act as pollutants to human life. The unprecedented increase in emergency visits during wildfire seasons is of clinical significance for its association with asthma and other pulmonary disorders. Despite the efforts of wealthy communities or nations, which have faced episodes of wildfires in recent years, the most effective protocol is yet to be developed. Given the vulnerability of individuals, including asthmatics, to the smoke from wildfires, interventions should extend beyond emergency measures. This review aims to provide a comprehensive overview of the relationship between wildfires and asthma symptoms, exploring the underlying mechanisms both <em>in vitro</em> and <em>in vivo</em>. It also delves into the potential implications for science policies, communication strategies, research directions, and management strategies for asthma cases, emphasizing the importance of preventive measures. Furthermore, this review serves as a guideline for various sectors, offering a clear conceptual rationale for preventing and managing wildfire smoke-related asthma and other pulmonary diseases. The interventions are multi-sectoral and multidisciplinary concerns, and given the transboundary nature of smoke, it is imperative for all relevant parties to collaborate to minimize preventable deaths.</div></div>","PeriodicalId":54295,"journal":{"name":"World Allergy Organization Journal","volume":"18 9","pages":"Article 101110"},"PeriodicalIF":4.3,"publicationDate":"2025-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144988005","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A preliminary investigation of the differences in immune responses in different strains of mice with localized allergic rhinitis tolerance models 不同品系小鼠局部变应性鼻炎耐受模型免疫应答差异的初步研究
IF 4.3 2区 医学 Q2 ALLERGY Pub Date : 2025-09-01 DOI: 10.1016/j.waojou.2025.101115
Qidi Zhang MD , Wanting Zhu MD , Zhixin Zou MD , Wenting Yu PhD , Pei Gao PhD , Ziyi Long MD , Ying Wang PhD , Jianjun Chen PhD

Objectives

This study aimed to compare systematically strain-specific immune differences between BALB/c and C57BL/6 mice in a local tolerance model and explore the underlying mechanisms.

Methods

BALB/c and C57BL/6 mice received daily intranasal ovalbumin (OVA; 25 mg/ml, 10μl/nostril) or PBS for 15 weeks. Systemic responses (serum OVA-specific IgE, IgG1, IgG2a; splenocyte cytokine secretion: IL-4, IL-10, IFN-γ) and local nasal responses (symptoms, histopathology: polymorphonuclear/goblet cell infiltration; immunohistochemistry: TGF-β, IL-10, eotaxin; RNA-seq transcriptomics of nasal mucosa) were assessed at the 8th and 15th weeks.

Results

BALB/c mice initially exhibited worsening nasal symptoms, which was followed by significant alleviation. In contrast, C57BL/6 mice showed a significant worsening of symptoms. Serum levels of IgE, IgG1, and IgG2a increased significantly over time in BALB/c mice. In C57BL/6 mice, serum IgE and IgG1 levels also increased significantly, while IgG2a levels showed no significant changes. In splenocyte supernatants, BALB/c mice showed IL-4 levels that initially increased significantly but later decreased significantly, whereas IL-10 levels were significantly elevated and sustained. Conversely, C57BL/6 mice exhibited no significant changes in these splenocyte cytokines. Within nasal mucosa, BALB/c mice displayed polymorphonuclear cell infiltration and significantly elevated eotaxin levels, which subsequently stabilized, alongside significant upregulation of TGF-β and IL-10 expression. At 15th week, C57BL/6 mice demonstrated significantly higher nasal PMN infiltration and eotaxin levels compared to BALB/c mice, but showed no significant increase in TGF-β or IL-10 compared to controls. RNA-seq analysis of nasal mucosa revealed that BALB/c mice at 15th week exhibited significant upregulation of genes involved in biological processes, tolerance-related signaling pathways, and negative regulatory pathways. Conversely, C57BL/6 mice showed significant upregulation of genes associated with cell synthesis- and secretion-related pathways.

Conclusion

Based on the criteria defining “local tolerance” in this model—significant symptom attenuation despite allergen escalation coupled with downregulation of nasal inflammatory markers (eotaxin, polymorphonuclear cell infiltration)—local tolerance was successfully induced in BALB/c mice by long-term OVA stimulation, but not in C57BL/6 mice. The normal function of T regulatory cells is key to establishing local tolerance.
目的系统比较BALB/c和C57BL/6小鼠在局部耐受模型下的株特异性免疫差异,并探讨其机制。方法balb /c和C57BL/6小鼠每日经鼻注射卵白蛋白(OVA, 25 mg/ml, 10μl/鼻孔)或PBS,连续15周。在第8周和第15周评估全身反应(血清ova特异性IgE、IgG1、IgG2a;脾细胞细胞因子分泌:IL-4、IL-10、IFN-γ)和局部鼻腔反应(症状、组织病理学:多形核/杯状细胞浸润;免疫组织化学:TGF-β、IL-10、eotaxin;鼻黏膜RNA-seq转录组学)。结果balb /c小鼠最初表现为鼻症状加重,随后症状明显缓解。相比之下,C57BL/6小鼠表现出明显的症状恶化。BALB/c小鼠血清中IgE、IgG1和IgG2a水平随时间显著升高。C57BL/6小鼠血清IgE和IgG1水平也显著升高,而IgG2a水平无明显变化。在脾细胞上清液中,BALB/c小鼠IL-4水平先显著升高后显著降低,而IL-10水平则显著升高并持续。相反,C57BL/6小鼠的这些脾细胞因子没有明显变化。在鼻黏膜内,BALB/c小鼠出现多形核细胞浸润,eotaxin水平显著升高,随后趋于稳定,TGF-β和IL-10表达显著上调。在第15周,C57BL/6小鼠的鼻腔PMN浸润和eotaxin水平明显高于BALB/c小鼠,但TGF-β和IL-10水平与对照组相比无显著升高。鼻黏膜RNA-seq分析显示,BALB/c小鼠在第15周时表现出参与生物过程、耐受相关信号通路和负调控通路的基因显著上调。相反,C57BL/6小鼠显示与细胞合成和分泌相关通路相关的基因显著上调。结论根据该模型中定义“局部耐受”的标准——尽管过敏原增加,鼻腔炎症标志物(eotaxin,多形核细胞浸润)下调,但症状明显减轻——BALB/c小鼠通过长期卵细胞刺激成功诱导了局部耐受,而C57BL/6小鼠则没有。T调节细胞的正常功能是建立局部耐受的关键。
{"title":"A preliminary investigation of the differences in immune responses in different strains of mice with localized allergic rhinitis tolerance models","authors":"Qidi Zhang MD ,&nbsp;Wanting Zhu MD ,&nbsp;Zhixin Zou MD ,&nbsp;Wenting Yu PhD ,&nbsp;Pei Gao PhD ,&nbsp;Ziyi Long MD ,&nbsp;Ying Wang PhD ,&nbsp;Jianjun Chen PhD","doi":"10.1016/j.waojou.2025.101115","DOIUrl":"10.1016/j.waojou.2025.101115","url":null,"abstract":"<div><h3>Objectives</h3><div>This study aimed to compare systematically strain-specific immune differences between BALB/c and C57BL/6 mice in a local tolerance model and explore the underlying mechanisms.</div></div><div><h3>Methods</h3><div>BALB/c and C57BL/6 mice received daily intranasal ovalbumin (OVA; 25 mg/ml, 10μl/nostril) or PBS for 15 weeks. Systemic responses (serum OVA-specific IgE, IgG1, IgG2a; splenocyte cytokine secretion: IL-4, IL-10, IFN-γ) and local nasal responses (symptoms, histopathology: polymorphonuclear/goblet cell infiltration; immunohistochemistry: TGF-β, IL-10, eotaxin; RNA-seq transcriptomics of nasal mucosa) were assessed at the 8th and 15th weeks.</div></div><div><h3>Results</h3><div>BALB/c mice initially exhibited worsening nasal symptoms, which was followed by significant alleviation. In contrast, C57BL/6 mice showed a significant worsening of symptoms. Serum levels of IgE, IgG1, and IgG2a increased significantly over time in BALB/c mice. In C57BL/6 mice, serum IgE and IgG1 levels also increased significantly, while IgG2a levels showed no significant changes. In splenocyte supernatants, BALB/c mice showed IL-4 levels that initially increased significantly but later decreased significantly, whereas IL-10 levels were significantly elevated and sustained. Conversely, C57BL/6 mice exhibited no significant changes in these splenocyte cytokines. Within nasal mucosa, BALB/c mice displayed polymorphonuclear cell infiltration and significantly elevated eotaxin levels, which subsequently stabilized, alongside significant upregulation of TGF-β and IL-10 expression. At 15th week, C57BL/6 mice demonstrated significantly higher nasal PMN infiltration and eotaxin levels compared to BALB/c mice, but showed no significant increase in TGF-β or IL-10 compared to controls. RNA-seq analysis of nasal mucosa revealed that BALB/c mice at 15th week exhibited significant upregulation of genes involved in biological processes, tolerance-related signaling pathways, and negative regulatory pathways. Conversely, C57BL/6 mice showed significant upregulation of genes associated with cell synthesis- and secretion-related pathways.</div></div><div><h3>Conclusion</h3><div>Based on the criteria defining “local tolerance” in this model—significant symptom attenuation despite allergen escalation coupled with downregulation of nasal inflammatory markers (eotaxin, polymorphonuclear cell infiltration)—local tolerance was successfully induced in BALB/c mice by long-term OVA stimulation, but not in C57BL/6 mice. The normal function of T regulatory cells is key to establishing local tolerance.</div></div>","PeriodicalId":54295,"journal":{"name":"World Allergy Organization Journal","volume":"18 9","pages":"Article 101115"},"PeriodicalIF":4.3,"publicationDate":"2025-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145026644","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Drug hypersensitivity reactions in children in clinical practice: A WAO Statement 临床实践中儿童药物超敏反应:WAO声明
IF 4.3 2区 医学 Q2 ALLERGY Pub Date : 2025-08-29 DOI: 10.1016/j.waojou.2025.101087
Steering Committee Authors, M. Pilar Berges-Gimeno MD, PhD , Emilio Alvarez-Cuesta MD, PhD, MQM , Marina Atanaskovic-Markovic MD, PhD , Marina Attanassi MD, PhD , Carlo Caffareli MD, PhD , Jean-Christoph Caubet MD , George du Toit MBBCh, MRCPCH , Antonieta Guzman-Melendez MD, PhD , Semanur Kuyucu MD, PhD , Ricardo Madrigal-Burgaleta PhD, FRCP , Lina Mayorga MD, PhD , Elizabeth Powell MBChB, PhD , Michelle Ramien MD, MSc , Eva Rebelo Gomes MD, PhD , Francesca Mori MD, PhD , Andrew A. White MD , Ignacio J. Ansotegui MD, PhD , Review Panel Authors, Marcelo Vivolo Aun MD, PhD , Masao Yamaguchi MD, PhD
Drug hypersensitivity reactions (DHRs) in children and adolescents are less common than in adults but can have serious consequences if mismanaged. Mislabeling children as drug-allergic due to incomplete diagnostic evaluations leads to unnecessary medication restrictions, increased healthcare costs, and suboptimal treatment choices. This Statement from the World Allergy Organization (WAO) provides evidence-based recommendations for evaluating and managing pediatric DHRs, emphasizing accurate diagnosis through in vivo and in vitro testing, risk stratification, and personalized approaches. Antibiotics, particularly β-lactams, and non-steroidal anti-inflammatory drugs (NSAIDs) are the most frequently implicated drugs, with non-immediate reactions, such as maculopapular exanthema, being the most common presentation. The document also addresses emerging concerns, including monoclonal antibody-induced anaphylaxis and drug-induced enterocolitis syndrome. It underscores the need for specialized care in allergy centers with expertise in pediatric populations and advocates for multidisciplinary programs to manage complex cases, such as chemotherapy hypersensitivity and perioperative drug allergy. By addressing diagnostic challenges and clinical uncertainties, this document aims to improve the management of DHRs in children, reduce mislabeling, and enhance patient outcomes worldwide.
药物超敏反应(DHRs)在儿童和青少年中不像在成人中那么常见,但如果处理不当可能会造成严重后果。由于不完整的诊断评估而错误地将儿童标记为药物过敏,导致不必要的药物限制,增加医疗保健费用和次优治疗选择。世界过敏组织(WAO)的这份声明为评估和管理儿科dhr提供了基于证据的建议,强调通过体内和体外测试、风险分层和个性化方法进行准确诊断。抗生素,特别是β-内酰胺类药物和非甾体抗炎药(NSAIDs)是最常见的相关药物,非立即反应,如黄斑丘疹,是最常见的表现。该文件还解决了新出现的问题,包括单克隆抗体诱导的过敏反应和药物诱导的小肠结肠炎综合征。它强调了过敏中心对儿科人群专业护理的需求,并倡导多学科项目来管理复杂病例,如化疗超敏反应和围手术期药物过敏。通过解决诊断挑战和临床不确定性,本文件旨在改善儿童dhr的管理,减少错误标签,并提高全球患者的预后。
{"title":"Drug hypersensitivity reactions in children in clinical practice: A WAO Statement","authors":"Steering Committee Authors,&nbsp;M. Pilar Berges-Gimeno MD, PhD ,&nbsp;Emilio Alvarez-Cuesta MD, PhD, MQM ,&nbsp;Marina Atanaskovic-Markovic MD, PhD ,&nbsp;Marina Attanassi MD, PhD ,&nbsp;Carlo Caffareli MD, PhD ,&nbsp;Jean-Christoph Caubet MD ,&nbsp;George du Toit MBBCh, MRCPCH ,&nbsp;Antonieta Guzman-Melendez MD, PhD ,&nbsp;Semanur Kuyucu MD, PhD ,&nbsp;Ricardo Madrigal-Burgaleta PhD, FRCP ,&nbsp;Lina Mayorga MD, PhD ,&nbsp;Elizabeth Powell MBChB, PhD ,&nbsp;Michelle Ramien MD, MSc ,&nbsp;Eva Rebelo Gomes MD, PhD ,&nbsp;Francesca Mori MD, PhD ,&nbsp;Andrew A. White MD ,&nbsp;Ignacio J. Ansotegui MD, PhD ,&nbsp;Review Panel Authors,&nbsp;Marcelo Vivolo Aun MD, PhD ,&nbsp;Masao Yamaguchi MD, PhD","doi":"10.1016/j.waojou.2025.101087","DOIUrl":"10.1016/j.waojou.2025.101087","url":null,"abstract":"<div><div>Drug hypersensitivity reactions (DHRs) in children and adolescents are less common than in adults but can have serious consequences if mismanaged. Mislabeling children as drug-allergic due to incomplete diagnostic evaluations leads to unnecessary medication restrictions, increased healthcare costs, and suboptimal treatment choices. This Statement from the World Allergy Organization (WAO) provides evidence-based recommendations for evaluating and managing pediatric DHRs, emphasizing accurate diagnosis through <em>in vivo</em> and <em>in vitro</em> testing, risk stratification, and personalized approaches. Antibiotics, particularly β-lactams, and non-steroidal anti-inflammatory drugs (NSAIDs) are the most frequently implicated drugs, with non-immediate reactions, such as maculopapular exanthema, being the most common presentation. The document also addresses emerging concerns, including monoclonal antibody-induced anaphylaxis and drug-induced enterocolitis syndrome. It underscores the need for specialized care in allergy centers with expertise in pediatric populations and advocates for multidisciplinary programs to manage complex cases, such as chemotherapy hypersensitivity and perioperative drug allergy. By addressing diagnostic challenges and clinical uncertainties, this document aims to improve the management of DHRs in children, reduce mislabeling, and enhance patient outcomes worldwide.</div></div>","PeriodicalId":54295,"journal":{"name":"World Allergy Organization Journal","volume":"18 9","pages":"Article 101087"},"PeriodicalIF":4.3,"publicationDate":"2025-08-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144913768","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Allergic diseases are signalling a public health crisis — It is time for a global allergy health plan 过敏性疾病是一场公共卫生危机的信号——现在是制定全球过敏健康计划的时候了
IF 4.3 2区 医学 Q2 ALLERGY Pub Date : 2025-08-25 DOI: 10.1016/j.waojou.2025.101106
Tari Haahtela MD, PhD
{"title":"Allergic diseases are signalling a public health crisis — It is time for a global allergy health plan","authors":"Tari Haahtela MD, PhD","doi":"10.1016/j.waojou.2025.101106","DOIUrl":"10.1016/j.waojou.2025.101106","url":null,"abstract":"","PeriodicalId":54295,"journal":{"name":"World Allergy Organization Journal","volume":"18 9","pages":"Article 101106"},"PeriodicalIF":4.3,"publicationDate":"2025-08-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144895085","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Discontinuation of biologic therapy in severe asthma: Evidence and strategies for safe withdrawal: A scoping review 严重哮喘生物治疗的停药:安全停药的证据和策略:一项范围综述
IF 4.3 2区 医学 Q2 ALLERGY Pub Date : 2025-08-22 DOI: 10.1016/j.waojou.2025.101107
Johanna Ramirez-Villamizar MD , Ciro D. Ibarra-Enríquez MD , Juan Sebastián Galindo-Sánchez MD , Carlos Serrano-Reyes MD , Liliana Fernández-Trujillo MD

Introduction

Severe asthma is characterized by poor disease control despite the use of high-dose inhaled corticosteroids and long-acting bronchodilators. Biologic therapies have revolutionized its management, allowing some patients to achieve remission. However, uncertainty remains regarding the optimal duration of treatment and the safest strategies for discontinuation. This study reviews the available evidence on the withdrawal of biologic therapy in patients with severe asthma in remission, evaluating their clinical outcomes.

Methods

A literature review was conducted in PubMed, EMBASE, Epistemonikos, and LILACS up to May 2024, using terms related to severe asthma and discontinuation of biologic therapies. Studies evaluating asthma control after dose reduction or withdrawal of biologic treatment were included, considering outcomes such as exacerbations, lung function, and inflammatory biomarkers.

Results

Of the 2494 studies identified, 23 articles were included after full-text review. Discontinuation of tezepelumab led to a gradual loss of clinical control in most patients, although baseline levels of inflammation were not reached. Regarding mepolizumab, 59% of patients experienced at least 1 significant exacerbation within the first year after withdrawal, suggesting the need for prolonged use. For omalizumab, results were heterogeneous: 67% of patients who continued treatment remained exacerbation-free, compared to 47.7 of those who discontinued it. Studies that implemented gradual tapering strategies showed higher success rates in discontinuation without loss of clinical control.

Conclusion

Evidence suggests that discontinuation of biologic therapy should be individualized, and a minimum treatment duration of 5 years may be appropriate before considering withdrawal. Optimal candidates include those with sustained clinical control, stable lung function, suppressed inflammatory biomarkers, and no need for oral corticosteroids. Gradual decreasing strategies may optimize treatment withdrawal while minimizing the risk of relapse.
尽管使用了大剂量吸入皮质类固醇和长效支气管扩张剂,但严重哮喘的特点是疾病控制不佳。生物疗法已经彻底改变了其管理,使一些患者达到缓解。然而,关于最佳治疗持续时间和最安全的停药策略仍然存在不确定性。本研究回顾了严重哮喘缓解期患者停止生物治疗的现有证据,评估了他们的临床结果。方法对截至2024年5月的PubMed、EMBASE、Epistemonikos和LILACS进行文献综述,使用与严重哮喘和停止生物治疗相关的术语。纳入了评估减少剂量或停止生物治疗后哮喘控制的研究,考虑了诸如恶化、肺功能和炎症生物标志物等结果。结果在纳入的2494项研究中,23篇文章在全文审查后被纳入。停用tezepelumab导致大多数患者逐渐失去临床控制,尽管炎症未达到基线水平。关于mepolizumab, 59%的患者在停药后的第一年内至少经历了一次显著恶化,这表明需要长期使用。对于omalizumab,结果是不均匀的:67%继续治疗的患者仍然没有恶化,而停止治疗的患者为47.7%。实施逐渐减量策略的研究显示,在不失去临床控制的情况下,停药成功率更高。结论有证据表明,停止生物治疗应个体化,在考虑停药前至少治疗5年为宜。最佳候选者包括那些持续的临床控制,稳定的肺功能,抑制炎症生物标志物,不需要口服皮质类固醇。逐渐减少的策略可以优化治疗停药,同时最小化复发的风险。
{"title":"Discontinuation of biologic therapy in severe asthma: Evidence and strategies for safe withdrawal: A scoping review","authors":"Johanna Ramirez-Villamizar MD ,&nbsp;Ciro D. Ibarra-Enríquez MD ,&nbsp;Juan Sebastián Galindo-Sánchez MD ,&nbsp;Carlos Serrano-Reyes MD ,&nbsp;Liliana Fernández-Trujillo MD","doi":"10.1016/j.waojou.2025.101107","DOIUrl":"10.1016/j.waojou.2025.101107","url":null,"abstract":"<div><h3>Introduction</h3><div>Severe asthma is characterized by poor disease control despite the use of high-dose inhaled corticosteroids and long-acting bronchodilators. Biologic therapies have revolutionized its management, allowing some patients to achieve remission. However, uncertainty remains regarding the optimal duration of treatment and the safest strategies for discontinuation. This study reviews the available evidence on the withdrawal of biologic therapy in patients with severe asthma in remission, evaluating their clinical outcomes.</div></div><div><h3>Methods</h3><div>A literature review was conducted in PubMed, EMBASE, Epistemonikos, and LILACS up to May 2024, using terms related to severe asthma and discontinuation of biologic therapies. Studies evaluating asthma control after dose reduction or withdrawal of biologic treatment were included, considering outcomes such as exacerbations, lung function, and inflammatory biomarkers.</div></div><div><h3>Results</h3><div>Of the 2494 studies identified, 23 articles were included after full-text review. Discontinuation of tezepelumab led to a gradual loss of clinical control in most patients, although baseline levels of inflammation were not reached. Regarding mepolizumab, 59% of patients experienced at least 1 significant exacerbation within the first year after withdrawal, suggesting the need for prolonged use. For omalizumab, results were heterogeneous: 67% of patients who continued treatment remained exacerbation-free, compared to 47.7 of those who discontinued it. Studies that implemented gradual tapering strategies showed higher success rates in discontinuation without loss of clinical control.</div></div><div><h3>Conclusion</h3><div>Evidence suggests that discontinuation of biologic therapy should be individualized, and a minimum treatment duration of 5 years may be appropriate before considering withdrawal. Optimal candidates include those with sustained clinical control, stable lung function, suppressed inflammatory biomarkers, and no need for oral corticosteroids. Gradual decreasing strategies may optimize treatment withdrawal while minimizing the risk of relapse.</div></div>","PeriodicalId":54295,"journal":{"name":"World Allergy Organization Journal","volume":"18 9","pages":"Article 101107"},"PeriodicalIF":4.3,"publicationDate":"2025-08-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144887026","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Methodology of the international cross-sectional prevalence and severity study of pediatric and adult IgE-mediated food allergies (ASSESS FA) 儿童和成人ige介导的食物过敏的国际横断面患病率和严重程度研究方法(ASSESS FA)
IF 4.3 2区 医学 Q2 ALLERGY Pub Date : 2025-08-22 DOI: 10.1016/j.waojou.2025.101105
Ruchi Gupta MD, MPH , Tarek Mnif PharmD , Suzanne Reed PhD , Mira Hleyhel PhD , Stefani Dritsa PhD , Perrine LeCalvé MSc , Alissar Moussallem PharmD, MPH , Paolo Tassinari MD , Jessica Marvel MPH , Alessandro Fiocchi MD

Background

The burden and prevalence of food allergy (FA), a condition known to negatively impact the quality of life (QoL) of patients and their families, vary across countries due to cultural habits and clinical practices and have been assessed differently among previous studies. To date, no validated scale exists to measure FA severity risk.

Objective

The study objectives were to develop a standardized methodology to estimate FA point prevalence in children and adults in 9 countries, to assess FA impact on QoL, and to construct a framework to define FA severity risk based on QoL and FA clinical severity.

Methods

This was a cross-sectional, international study that collected self-reported data through an online quantitative survey. Participants were recruited from general population panels: parents/caregivers of children aged 6 months-17 years, and adults aged 18–65 years. The survey instrument was developed by a panel of clinical FA experts and epidemiologists.

Results

Weighted prevalence rates were calculated for the 4 generated case definitions of FA (self-reported, physician-diagnosed, symptom-convincing, and confirmed FA). Several validated scales, including the Food Allergy Quality of Life Questionnaire (FAQLQ) and the Food Allergy Independent Measure (FAIM), were used to assess FA impact on QoL in patients with symptom-convincing FA. Four FA severity risk profiles were generated: non-severe, at-risk, highly impacted QoL, and severe patients.

Conclusion

The ASSESS FA study developed a methodology to estimate the prevalence of FA and its impact on QoL consistently across countries, age groups, and food allergens. The severity risk framework was based on both the clinical severity and impact on QoL aspects of FA.
食物过敏(FA)是一种已知会对患者及其家庭的生活质量(QoL)产生负面影响的疾病,其负担和流行程度因文化习惯和临床实践而异,并且在以往的研究中进行了不同的评估。到目前为止,还没有有效的量表来衡量FA的严重程度风险。研究目的是建立一种标准化的方法来估计9个国家儿童和成人的FA点患病率,评估FA对生活质量的影响,并根据生活质量和FA临床严重程度构建一个框架来定义FA严重程度风险。方法这是一项横断面的国际研究,通过在线定量调查收集自我报告的数据。参与者是从一般人群中招募的:6个月至17岁儿童的父母/照顾者,以及18-65岁的成年人。该调查工具是由临床FA专家和流行病学家组成的小组开发的。结果计算了4种生成的FA病例定义(自我报告、医生诊断、症状可信和确诊FA)的加权患病率。几个有效的量表,包括食物过敏生活质量问卷(FAQLQ)和食物过敏独立测量(FAIM),用于评估FA对症状可信FA患者生活质量的影响。产生了四种FA严重程度风险概况:非严重、有风险、高度影响的生活质量和严重患者。结论:evaluate FA研究开发了一种方法来估计不同国家、年龄组和食物过敏原的FA患病率及其对生活质量的影响。严重性风险框架是基于FA的临床严重性和对生活质量的影响。
{"title":"Methodology of the international cross-sectional prevalence and severity study of pediatric and adult IgE-mediated food allergies (ASSESS FA)","authors":"Ruchi Gupta MD, MPH ,&nbsp;Tarek Mnif PharmD ,&nbsp;Suzanne Reed PhD ,&nbsp;Mira Hleyhel PhD ,&nbsp;Stefani Dritsa PhD ,&nbsp;Perrine LeCalvé MSc ,&nbsp;Alissar Moussallem PharmD, MPH ,&nbsp;Paolo Tassinari MD ,&nbsp;Jessica Marvel MPH ,&nbsp;Alessandro Fiocchi MD","doi":"10.1016/j.waojou.2025.101105","DOIUrl":"10.1016/j.waojou.2025.101105","url":null,"abstract":"<div><h3>Background</h3><div>The burden and prevalence of food allergy (FA), a condition known to negatively impact the quality of life (QoL) of patients and their families, vary across countries due to cultural habits and clinical practices and have been assessed differently among previous studies. To date, no validated scale exists to measure FA severity risk.</div></div><div><h3>Objective</h3><div>The study objectives were to develop a standardized methodology to estimate FA point prevalence in children and adults in 9 countries, to assess FA impact on QoL, and to construct a framework to define FA severity risk based on QoL and FA clinical severity.</div></div><div><h3>Methods</h3><div>This was a cross-sectional, international study that collected self-reported data through an online quantitative survey. Participants were recruited from general population panels: parents/caregivers of children aged 6 months-17 years, and adults aged 18–65 years. The survey instrument was developed by a panel of clinical FA experts and epidemiologists.</div></div><div><h3>Results</h3><div>Weighted prevalence rates were calculated for the 4 generated case definitions of FA (self-reported, physician-diagnosed, symptom-convincing, and confirmed FA). Several validated scales, including the Food Allergy Quality of Life Questionnaire (FAQLQ) and the Food Allergy Independent Measure (FAIM), were used to assess FA impact on QoL in patients with symptom-convincing FA. Four FA severity risk profiles were generated: non-severe, at-risk, highly impacted QoL, and severe patients.</div></div><div><h3>Conclusion</h3><div>The ASSESS FA study developed a methodology to estimate the prevalence of FA and its impact on QoL consistently across countries, age groups, and food allergens. The severity risk framework was based on both the clinical severity and impact on QoL aspects of FA.</div></div>","PeriodicalId":54295,"journal":{"name":"World Allergy Organization Journal","volume":"18 9","pages":"Article 101105"},"PeriodicalIF":4.3,"publicationDate":"2025-08-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144890620","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
LncRNA PELATON regulates Th2 cell differentiation by miR-10b-5p/GATA3 axis in allergic rhinitis LncRNA PELATON通过miR-10b-5p/GATA3轴调控变应性鼻炎中Th2细胞的分化
IF 4.3 2区 医学 Q2 ALLERGY Pub Date : 2025-08-21 DOI: 10.1016/j.waojou.2025.101108
Zhen Liu MD , Yumei Li PhD , Xiangkun Zhao MM , Qi Sun MD , Yu Zhang MD , Yaqi Wang MM , Han Fang MD , Yujuan Yang MD , Yakui Mou MD , Xicheng Song MD

Background

Long non-coding RNAs (lncRNAs) have been increasingly recognized as critical regulators in the pathogenesis of immunoinflammatory diseases. Nevertheless, their mechanistic contributions to Th2-driven allergic rhinitis (AR) remain unclear. This study investigated the immunomodulatory function of lncRNA PELATON in AR pathogenesis by exploring its regulatory effects on Th2 cell differentiation.

Methods

A total of 32 participants were enrolled, comprising 16 patients diagnosed with AR and 16 control subjects. The allergy levels of the participants were assessed using the skin prick test (SPT), and the levels of PELATON expression in PBMCs were detected by qPCR. Spearman's correlation analysis was used to calculate the correlation between the 2 variables. Changes in GATA3, IL-4, IL-5, and IL-13 expression were examined, as well as changes in Th2 cell differentiation resulting from the overexpression of PELATON and miR-10b-5p. Modulation of miR-10b-5p and GATA3 expression by PELATON was studied via transcriptome sequencing, dual-luciferase reporter assays, and in vitro experiments.

Results

LncRNA PELATON expression was elevated in patients with AR and showed a significant correlation with allergy levels. PELATON was enriched in CD4+T cells. Overexpression of PELATON in PBMCs led to an increase in the proportion of Th2 cells and the levels of GATA3, IL-4, IL-5, and IL-13 expression, while the overexpression of miR-10b-5p reduced the expression levels of GATA3, IL-4, IL-5, and IL-13. PELATON bound directly to miR-10b-5p and inhibited the negative regulatory effect of miR-10b-5p on GATA3, thereby forming a ceRNA network that promoted Th2 cell differentiation.

Conclusion

LncRNA PELATON competitively binds to miR-10b-5p and promotes GATA3 expression, resulting in Th2 cell differentiation and activation in AR. Formation of the lncRNA PELATON/miR-10b-5p/GATA3 ceRNA network is a regulatory mechanism that offers new possibilities for finding therapeutic targets for AR.
长链非编码rna (lncRNAs)越来越被认为是免疫炎症疾病发病机制中的关键调控因子。然而,它们对th2驱动的过敏性鼻炎(AR)的机制作用尚不清楚。本研究通过探究lncRNA PELATON对Th2细胞分化的调控作用,探讨其在AR发病机制中的免疫调节功能。方法共纳入32名受试者,其中16名诊断为AR的患者和16名对照组。采用皮肤点刺试验(SPT)评估受试者的过敏水平,采用qPCR检测pbmc中PELATON的表达水平。采用Spearman相关分析计算两个变量之间的相关性。检测GATA3、IL-4、IL-5和IL-13表达的变化,以及过表达PELATON和miR-10b-5p导致的Th2细胞分化的变化。通过转录组测序、双荧光素酶报告基因测定和体外实验研究PELATON对miR-10b-5p和GATA3表达的调节。结果slncrna PELATON在AR患者中表达升高,且与过敏水平显著相关。PELATON在CD4+T细胞中富集。在PBMCs中,过表达PELATON导致Th2细胞比例和GATA3、IL-4、IL-5、IL-13表达水平升高,而过表达miR-10b-5p导致GATA3、IL-4、IL-5、IL-13表达水平降低。PELATON直接与miR-10b-5p结合,抑制miR-10b-5p对GATA3的负调控作用,从而形成促进Th2细胞分化的ceRNA网络。结论lncRNA PELATON与miR-10b-5p竞争性结合,促进GATA3表达,导致AR中Th2细胞分化和活化。lncRNA PELATON/miR-10b-5p/GATA3 ceRNA网络的形成是一种调控机制,为寻找AR的治疗靶点提供了新的可能性。
{"title":"LncRNA PELATON regulates Th2 cell differentiation by miR-10b-5p/GATA3 axis in allergic rhinitis","authors":"Zhen Liu MD ,&nbsp;Yumei Li PhD ,&nbsp;Xiangkun Zhao MM ,&nbsp;Qi Sun MD ,&nbsp;Yu Zhang MD ,&nbsp;Yaqi Wang MM ,&nbsp;Han Fang MD ,&nbsp;Yujuan Yang MD ,&nbsp;Yakui Mou MD ,&nbsp;Xicheng Song MD","doi":"10.1016/j.waojou.2025.101108","DOIUrl":"10.1016/j.waojou.2025.101108","url":null,"abstract":"<div><h3>Background</h3><div>Long non-coding RNAs (lncRNAs) have been increasingly recognized as critical regulators in the pathogenesis of immunoinflammatory diseases. Nevertheless, their mechanistic contributions to Th2-driven allergic rhinitis (AR) remain unclear. This study investigated the immunomodulatory function of lncRNA PELATON in AR pathogenesis by exploring its regulatory effects on Th2 cell differentiation.</div></div><div><h3>Methods</h3><div>A total of 32 participants were enrolled, comprising 16 patients diagnosed with AR and 16 control subjects. The allergy levels of the participants were assessed using the skin prick test (SPT), and the levels of PELATON expression in PBMCs were detected by qPCR. Spearman's correlation analysis was used to calculate the correlation between the 2 variables. Changes in GATA3, IL-4, IL-5, and IL-13 expression were examined, as well as changes in Th2 cell differentiation resulting from the overexpression of PELATON and miR-10b-5p. Modulation of miR-10b-5p and GATA3 expression by PELATON was studied via transcriptome sequencing, dual-luciferase reporter assays, and <em>in vitro</em> experiments.</div></div><div><h3>Results</h3><div>LncRNA PELATON expression was elevated in patients with AR and showed a significant correlation with allergy levels. PELATON was enriched in CD4<sup>+</sup>T cells. Overexpression of PELATON in PBMCs led to an increase in the proportion of Th2 cells and the levels of GATA3, IL-4, IL-5, and IL-13 expression, while the overexpression of miR-10b-5p reduced the expression levels of GATA3, IL-4, IL-5, and IL-13. PELATON bound directly to miR-10b-5p and inhibited the negative regulatory effect of miR-10b-5p on GATA3, thereby forming a ceRNA network that promoted Th2 cell differentiation.</div></div><div><h3>Conclusion</h3><div>LncRNA PELATON competitively binds to miR-10b-5p and promotes GATA3 expression, resulting in Th2 cell differentiation and activation in AR. Formation of the lncRNA PELATON/miR-10b-5p/GATA3 ceRNA network is a regulatory mechanism that offers new possibilities for finding therapeutic targets for AR.</div></div>","PeriodicalId":54295,"journal":{"name":"World Allergy Organization Journal","volume":"18 9","pages":"Article 101108"},"PeriodicalIF":4.3,"publicationDate":"2025-08-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144887025","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Prevalence and risk factors of de novo atopic diseases in pediatric liver transplant recipients: A retrospective cohort study. 儿童肝移植受者新发特应性疾病的患病率及危险因素:一项回顾性队列研究
IF 4.3 2区 医学 Q2 ALLERGY Pub Date : 2025-08-10 eCollection Date: 2025-08-01 DOI: 10.1016/j.waojou.2025.101102
Krittapaun Sombatwatthana, Watcharoot Kanchongkittiphon, Potjanee Kiewngam, Wanlapa Jotikasthira, Songpon Getsuwan, Napapat Butsriphum, Wiparat Manuyakorn, Suporn Treepongkaruna

Background: Atopic diseases are common in pediatric liver transplant (LT) recipients, yet their prevalence, remission, and risk factors remain unclear.

Objective: To investigate the prevalence, onset, remission, and risk factors for food allergy (FA), allergic rhinitis (AR), and asthma in pediatric LT recipients.

Results: Among 118 pediatric LT recipients, 71 (60.2%) developed atopic diseases post-transplant. De novo FA was the most common (40.7%), with a median onset of 9.5 months after LT. Most cases were IgE-mediated, with cow's milk and egg as the most common allergens. Over 3 years, 56.3% outgrew at least one allergic food. AR was diagnosed in 24.4%, with house dust mites as the primary sensitizing allergens. Asthma was less frequent (3.4%). Younger age at LT (<2 years) significantly increased FA risk (OR: 5.5, 95% CI: 2.0-15.2), as did Epstein-Barr virus (EBV) reactivation (OR: 6.5, 95% CI: 1.2-33.8). AR risk was higher in those with a first-degree family history of atopy (OR: 5.6, 95% CI: 2.1-14.7) or an atopic organ donor (OR: 4.6, 95% CI: 1.3-16.2).

Conclusion: De novo FA and AR are common in pediatric LT recipients, with significant associations with age at transplant, EBV reactivation, and genetic predisposition. Early monitoring and intervention are crucial to managing atopic diseases in this population.

背景:特应性疾病在儿童肝移植(LT)受者中很常见,但其患病率、缓解程度和危险因素尚不清楚。目的:调查儿童肝移植受者食物过敏(FA)、变应性鼻炎(AR)和哮喘的患病率、发病、缓解和危险因素。结果:118名儿童肝移植受者中,71名(60.2%)在移植后发生特应性疾病。新发FA最常见(40.7%),中位发病时间为lt后9.5个月。大多数病例是ige介导的,牛奶和鸡蛋是最常见的过敏原。超过3年,56.3%的人至少摆脱了一种过敏食物。诊断为AR的占24.4%,屋尘螨是主要致敏变应原。哮喘发病率较低(3.4%)。结论:新生FA和AR在儿童肝移植受者中很常见,与移植年龄、EBV再激活和遗传易感显著相关。早期监测和干预对于控制这一人群的特应性疾病至关重要。
{"title":"Prevalence and risk factors of <i>de novo</i> atopic diseases in pediatric liver transplant recipients: A retrospective cohort study.","authors":"Krittapaun Sombatwatthana, Watcharoot Kanchongkittiphon, Potjanee Kiewngam, Wanlapa Jotikasthira, Songpon Getsuwan, Napapat Butsriphum, Wiparat Manuyakorn, Suporn Treepongkaruna","doi":"10.1016/j.waojou.2025.101102","DOIUrl":"10.1016/j.waojou.2025.101102","url":null,"abstract":"<p><strong>Background: </strong>Atopic diseases are common in pediatric liver transplant (LT) recipients, yet their prevalence, remission, and risk factors remain unclear.</p><p><strong>Objective: </strong>To investigate the prevalence, onset, remission, and risk factors for food allergy (FA), allergic rhinitis (AR), and asthma in pediatric LT recipients.</p><p><strong>Results: </strong>Among 118 pediatric LT recipients, 71 (60.2%) developed atopic diseases post-transplant. <i>De novo</i> FA was the most common (40.7%), with a median onset of 9.5 months after LT. Most cases were IgE-mediated, with cow's milk and egg as the most common allergens. Over 3 years, 56.3% outgrew at least one allergic food. AR was diagnosed in 24.4%, with house dust mites as the primary sensitizing allergens. Asthma was less frequent (3.4%). Younger age at LT (<2 years) significantly increased FA risk (OR: 5.5, 95% CI: 2.0-15.2), as did Epstein-Barr virus (EBV) reactivation (OR: 6.5, 95% CI: 1.2-33.8). AR risk was higher in those with a first-degree family history of atopy (OR: 5.6, 95% CI: 2.1-14.7) or an atopic organ donor (OR: 4.6, 95% CI: 1.3-16.2).</p><p><strong>Conclusion: </strong><i>De novo</i> FA and AR are common in pediatric LT recipients, with significant associations with age at transplant, EBV reactivation, and genetic predisposition. Early monitoring and intervention are crucial to managing atopic diseases in this population.</p>","PeriodicalId":54295,"journal":{"name":"World Allergy Organization Journal","volume":"18 8","pages":"101102"},"PeriodicalIF":4.3,"publicationDate":"2025-08-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12357041/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144876813","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
World Allergy Organization Journal
全部 Acc. Chem. Res. ACS Applied Bio Materials ACS Appl. Electron. Mater. ACS Appl. Energy Mater. ACS Appl. Mater. Interfaces ACS Appl. Nano Mater. ACS Appl. Polym. Mater. ACS BIOMATER-SCI ENG ACS Catal. ACS Cent. Sci. ACS Chem. Biol. ACS Chemical Health & Safety ACS Chem. Neurosci. ACS Comb. Sci. ACS Earth Space Chem. ACS Energy Lett. ACS Infect. Dis. ACS Macro Lett. ACS Mater. Lett. ACS Med. Chem. Lett. ACS Nano ACS Omega ACS Photonics ACS Sens. ACS Sustainable Chem. Eng. ACS Synth. Biol. Anal. Chem. BIOCHEMISTRY-US Bioconjugate Chem. BIOMACROMOLECULES Chem. Res. Toxicol. Chem. Rev. Chem. Mater. CRYST GROWTH DES ENERG FUEL Environ. Sci. Technol. Environ. Sci. Technol. Lett. Eur. J. Inorg. Chem. IND ENG CHEM RES Inorg. Chem. J. Agric. Food. Chem. J. Chem. Eng. Data J. Chem. Educ. J. Chem. Inf. Model. J. Chem. Theory Comput. J. Med. Chem. J. Nat. Prod. J PROTEOME RES J. Am. Chem. Soc. LANGMUIR MACROMOLECULES Mol. Pharmaceutics Nano Lett. Org. Lett. ORG PROCESS RES DEV ORGANOMETALLICS J. Org. Chem. J. Phys. Chem. J. Phys. Chem. A J. Phys. Chem. B J. Phys. Chem. C J. Phys. Chem. Lett. Analyst Anal. Methods Biomater. Sci. Catal. Sci. Technol. Chem. Commun. Chem. Soc. Rev. CHEM EDUC RES PRACT CRYSTENGCOMM Dalton Trans. Energy Environ. Sci. ENVIRON SCI-NANO ENVIRON SCI-PROC IMP ENVIRON SCI-WAT RES Faraday Discuss. Food Funct. Green Chem. Inorg. Chem. Front. Integr. Biol. J. Anal. At. Spectrom. J. Mater. Chem. A J. Mater. Chem. B J. Mater. Chem. C Lab Chip Mater. Chem. Front. Mater. Horiz. MEDCHEMCOMM Metallomics Mol. Biosyst. Mol. Syst. Des. Eng. Nanoscale Nanoscale Horiz. Nat. Prod. Rep. New J. Chem. Org. Biomol. Chem. Org. Chem. Front. PHOTOCH PHOTOBIO SCI PCCP Polym. Chem.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
×
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
现在去查看 取消
×
提示
确定
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1