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Patients With Chronic Urticaria Have Higher Health-Care Resource Utilisation: A Danish Nationwide Case-Control Study. 慢性荨麻疹患者有较高的医疗资源利用率:丹麦全国病例对照研究。
IF 5.2 2区 医学 Q1 ALLERGY Pub Date : 2026-02-09 DOI: 10.1111/cea.70239
Jennifer Astrup Sørensen, Somaia Naassan, Christian Vestergaard, Nana Aviaaja Lippert Rosenø, Cæcilie Bachdal Johansen, Alexander Egeberg, Jacob P Thyssen, Panagiotis Orfanos, Nadine Chapman-Rothe, Tara Raftery, Simon Francis Thomsen, Zarqa Ali
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引用次数: 0
Perceived Acquired Resistance to Omalizumab in Obese Patients With Chronic Spontaneous Urticaria. 慢性自发性荨麻疹肥胖患者对Omalizumab的获得性耐药
IF 5.2 2区 医学 Q1 ALLERGY Pub Date : 2026-02-08 DOI: 10.1111/cea.70236
Francisco Martins, Ilaria Trave, Sofia Pereira, Margarida Gonçalo
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引用次数: 0
Identifying an At-Risk Asthma Phenotype: Allergy and Recurrent Infections Predict Severe Disease. 识别哮喘的危险表型:过敏和复发性感染预测严重疾病。
IF 5.2 2区 医学 Q1 ALLERGY Pub Date : 2026-02-08 DOI: 10.1111/cea.70230
Emilie Johanning Bari, Susanne Hansen, Patrik Sandin, Olivia Ernstsson, Kirk Geale, Apostolos Bossios, Lauri Lehtimäki, Christer Janson, Charlotte Ulrik, Hannu Kankaanranta, Bernt Bøgvald Aarli, Anna Von Bülow, Arja Viinanen, Asger Sverrild, Dóra Lúdvíksdóttir, Helena Backman, Johannes Martin Schmid, Jussi Karjalainen, Leif Bjermer, Maritta Kilpeläinen, Ole Hilberg, Paula Kauppi, Sverre Lehmann, Thomas Sandström, Tina Skjold, Unnur Steina Björnsdóttir, Valentyna Yasinska, Vibeke Backer, Alan Altraja, Celeste Porsbjerg

Background: Asthma severity is influenced by complex immunologic and environmental factors. While allergic asthma is linked to increased susceptibility to respiratory infections, the combined role of allergy and antibiotic-treated infections in progression to severe asthma has not been fully evaluated.

Objective: To evaluate whether allergic asthma and recurrent respiratory infections (RRI) requiring antibiotics are associated with increased risk of developing severe asthma.

Methods: We conducted a registry-based cohort study using Swedish national registry data. Adults with mild-to-moderate asthma were identified in 2014 (baseline) based on prescription records and absence of severe disease indicators. During a two-year exposure window (2015-2016), RRI was defined as ≥ 2 antibiotic prescriptions for lower respiratory tract infections. The outcome was development of severe asthma during 2017-2019, based on ERS/ATS treatment criteria. Allergic asthma was defined by ≥ 2 prescriptions for anti-allergic medications at baseline.

Results: Among 113,393 patients, 24,692 (21.8%) had allergic asthma. RRI occurred more frequently in allergic versus non-allergic asthma (7.5% vs. 5.9%, p < 0.001). A total of 869 patients (0.77%) developed severe asthma. Incidence was higher in those with RRI and highest among patients with both allergic asthma and RRI (2.0%), corresponding to a relative risk of 3.47 (95% CI: 2.49-4.83) versus patients with neither exposure. Results were consistent after adjustment for age, sex and comorbidities.

Conclusion: Allergic asthma and antibiotic-treated respiratory infections were independent and additive predictors of severe asthma progression. These findings support a clinically actionable risk profile and may inform targeted preventive strategies in asthma management.

背景:哮喘的严重程度受复杂的免疫和环境因素的影响。虽然过敏性哮喘与呼吸道感染易感性增加有关,但过敏和抗生素治疗感染在进展为严重哮喘中的综合作用尚未得到充分评估。目的:评价过敏性哮喘和需要抗生素的复发性呼吸道感染(RRI)是否与发生严重哮喘的风险增加相关。方法:我们使用瑞典国家登记数据进行了一项基于登记的队列研究。根据处方记录和缺乏严重疾病指标,于2014年(基线)确定患有轻中度哮喘的成人。在为期两年的暴露窗口(2015-2016)中,RRI定义为下呼吸道感染的抗生素处方≥2。根据ERS/ATS治疗标准,结果是2017-2019年期间发生严重哮喘。过敏性哮喘定义为基线抗过敏药物处方≥2张。结果:113393例患者中有24692例(21.8%)发生过敏性哮喘。过敏性哮喘患者的RRI发生率高于非过敏性哮喘患者(7.5% vs. 5.9%, p)。结论:过敏性哮喘和抗生素治疗的呼吸道感染是严重哮喘进展的独立和附加预测因素。这些发现支持临床可操作的风险概况,并可能为哮喘管理提供有针对性的预防策略。
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引用次数: 0
Pro-Inflammatory Dietary Patterns Are Associated With Atopic but Not Non-Atopic Dermatitis in Asian Adults: Evidence From a Cross-Sectional Study. 促炎饮食模式与亚洲成年人特应性皮炎有关,但与非特应性皮炎无关:来自横断面研究的证据
IF 5.2 2区 医学 Q1 ALLERGY Pub Date : 2026-02-08 DOI: 10.1111/cea.70232
Jun Jie Lim, Jia Yi Karen Wong, Zongxun Huang, Kavita Reginald, Yee-How Say, Mei Hui Liu, Fook Tim Chew
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引用次数: 0
Featured Cover 了封面
IF 5.2 2区 医学 Q1 ALLERGY Pub Date : 2026-02-06 DOI: 10.1111/cea.70225
Eric M. Rodríguez-López, Rachel L. Clement, Megha Lal, Yusen Zhou, Stephen D. Carro, Charles-Antoine Assenmacher, Ravi Gautam, Jarad Beers, Amanda B. Muir, Jonathan M. Spergel, Melanie A. Ruffner, Laurence C. Eisenlohr, David A. Hill

The cover image is based on the article Oesophageal Epithelial Cell-Intrinsic MHCII Regulates Food Antigen-Dependent Eosinophilic Esophagitis in an IFNγ-Dependent Manner by Eric M. Rodríguez-López et al., https://doi.org/10.1111/cea.70205.

封面图片基于Eric M. Rodríguez-López等人,https://doi.org/10.1111/cea.70205的文章《食道上皮细胞内在MHCII以ifn γ依赖的方式调节食物抗原依赖性嗜酸性食管炎》。
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引用次数: 0
Differential Expression Profile of Circulating microRNAs and Regulatory Cytokines in Infants With Cow's Milk Allergy. 牛奶过敏婴儿循环microrna和调节细胞因子的差异表达谱。
IF 5.2 2区 医学 Q1 ALLERGY Pub Date : 2026-02-04 DOI: 10.1111/cea.70231
Rebeca López-Gómez, Álvaro Arranz-Fragua, Marta Gil-Martínez, Jose Manuel Rodrigo-Muñoz, Daniel Rodríguez-González, Gema Guillén-Sánchez, Antonio Serrano-Santiago, Ana Ladrón-Guevara, Nerea Ruiz-García, José Antonio Cañas, Genoveva Del Río Camacho, Victoria Del Pozo
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引用次数: 0
Effectiveness and Predictors of House Dust Mite Subcutaneous Immunotherapy in Polysensitised Patients With Allergic Rhinitis: A Multicentre Retrospective Study. 多敏化变应性鼻炎患者屋尘螨皮下免疫治疗的有效性和预测因素:一项多中心回顾性研究。
IF 5.2 2区 医学 Q1 ALLERGY Pub Date : 2026-02-03 DOI: 10.1111/cea.70229
Zhouxian Pan, Shengyang Yao, Lisha Li, Yongshi Yang, Wenchao Guan, Yin Wang, Xiaoshang Lou, Chuanhe Liu, Yanmin Bao, Shijie Zhuang, Li Sha, Ruonan Chai, Rongfei Zhu, Kai Guan

Background: In China, therapeutic options are limited by the narrow availability of allergen preparations, with house dust mite (HDM) allergen immunotherapy (AIT) as the main choice for most patients. However, polysensitization is highly prevalent, and the benefit of HDM AIT in such patients remains uncertain. The study aims to evaluate the effectiveness of single-allergen HDM AIT on both perennial and coexisting allergen-specific symptoms in polysensitised allergic rhinitis (AR) patients and to explore predictors of treatment response.

Methods: We performed a multicenter retrospective cohort study including 81 patients with AR who were polysensitised to HDM and at least one other inhalant allergen (e.g., pollens, mould or animal dander). All participants received HDM subcutaneous immunotherapy (SCIT) for 12 to 36 months. Baseline characteristics, including serum allergen-specific IgE (sIgE) levels and comorbidities, were collected. Symptom severity was assessed using the Visual Analog Scale (VAS), and treatment response was defined as a ≥ 30% reduction in VAS scores from baseline. Statistical comparisons between responders and non-responders were conducted using Fisher's exact test for categorical variables and Mann-Whitney U tests for continuous data. Firth logistic regression was used to identify predictors of treatment response.

Results: The overall response rate for perennial symptoms was 68.8%, and varied in patients with co-existing allergies: 72.7% for moulds, 70.0% for animal dander, 65.5% for tree pollen, 70.2% for weed pollens. Allergen-specific symptom response rates varied across allergens: 68.2% for moulds, 30.0% for animal dander, 56.7% for tree pollens, 74.5% for weed pollens. Higher sIgE levels to HDM and mould were significantly associated with lower response rates in patients co-sensitised to both. A predictive model incorporating both sIgEs showed good specificity.

Conclusion: Single-allergen HDM AIT is effective in many polysensitised AR patients; however, its efficacy varies by coexisting allergen type and sIgE level. Patients co-sensitised to mould with high HDM and mould sIgE appeared to have poorer outcomes. These preliminary findings require confirmation in larger prospective studies to guide tailored AIT strategies.

背景:在中国,治疗选择受到过敏原制剂供应有限的限制,大多数患者的主要选择是屋尘螨(HDM)过敏原免疫治疗(AIT)。然而,多致敏是非常普遍的,HDM AIT对这类患者的益处仍不确定。本研究旨在评估单一过敏原HDM AIT对多致敏性变应性鼻炎(AR)患者常年性和共存的过敏原特异性症状的疗效,并探讨治疗反应的预测因素。方法:我们进行了一项多中心回顾性队列研究,包括81例对HDM和至少一种其他吸入性过敏原(如花粉、霉菌或动物皮屑)多敏化的AR患者。所有参与者接受HDM皮下免疫治疗(SCIT) 12至36个月。收集基线特征,包括血清过敏原特异性IgE (sIgE)水平和合并症。使用视觉模拟量表(VAS)评估症状严重程度,治疗反应定义为VAS评分较基线降低≥30%。对有反应者和无反应者进行统计比较,对分类变量采用Fisher精确检验,对连续数据采用Mann-Whitney U检验。第五,使用逻辑回归来确定治疗反应的预测因素。结果:常年性过敏症状的总有效率为68.8%,共存过敏患者的总有效率各不相同:霉菌过敏72.7%,动物皮屑过敏70.0%,树木花粉过敏65.5%,杂草花粉过敏70.2%。过敏原特异性症状反应率因过敏原而异:霉菌68.2%,动物皮屑30.0%,树木花粉56.7%,杂草花粉74.5%。对HDM和霉菌共同敏感的患者,sIgE水平越高,反应率越低。结合两种sIgEs的预测模型显示出良好的特异性。结论:单变应原HDM AIT对多致敏性AR患者有效;然而,其效果因同时存在的过敏原类型和sIgE水平而异。对高HDM和高sIgE霉菌共敏感的患者预后较差。这些初步发现需要在更大的前瞻性研究中得到证实,以指导量身定制的AIT策略。
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引用次数: 0
Type-2 Biomarkers, Asthma Diagnosis and Lung Function Impairment in the General Population. 普通人群中的2型生物标志物、哮喘诊断和肺功能损害。
IF 5.2 2区 医学 Q1 ALLERGY Pub Date : 2026-02-01 Epub Date: 2025-10-23 DOI: 10.1111/cea.70165
Sebastian Riemann, Andrei Malinovschi, Guy G Brusselle
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引用次数: 0
Advancing Allergy Research Through Innovative Methodologies and Epithelial Immunology 通过创新方法和上皮免疫学推进过敏研究。
IF 5.2 2区 医学 Q1 ALLERGY Pub Date : 2026-01-30 DOI: 10.1111/cea.70226
Mohamed H. Shamji, Robert J. Boyle
<p>In this month's editorial, the Editors of the journal are presenting three articles that exemplify how the field of allergy and clinical immunology is evolving through both methodological innovation and deeper mechanistic understanding of mucosal immunity. Together, these studies address fundamental questions about treatment effectiveness, diagnostic accuracy, and immune regulation across different allergic conditions.</p><p>The first article, ‘Oesophageal epithelial cell-intrinsic MHCII regulates food-antigen-dependent eosinophilic esophagitis in an IFNγ-dependent manner’, represents a significant advance in understanding the immunopathology of eosinophilic oesophagitis (EoE) [<span>1</span>]. This work by Rodriguez-López et al. demonstrates how oesophageal epithelial cells (EECs) expressing MHCII in an IFNγ-dependent manner challenge the traditional view of epithelia as passive barriers. Instead, EECs emerge as active immunological players capable of modulating adaptive immune responses through antigen presentation.</p><p>The finding that EEC-intrinsic MHCII attenuates rather than promotes eosinophilic inflammation is particularly noteworthy. Using epithelial-specific MHCII-deficient mice, the authors demonstrated that loss of epithelial MHCII resulted in exacerbated oesophageal eosinophilia in a food antigen-dependent model [<span>1</span>]. This protective role contrasts with traditional views of MHCII as purely pro-inflammatory and aligns with emerging evidence from intestinal models showing that epithelial MHCII can promote tolerance and regulate T cell responses [<span>2</span>].</p><p>The mechanistic insights regarding CIITA promoter IV-dependent regulation provide potential therapeutic targets. While EoE has been successfully treated with therapies targeting type 2 inflammation, such as duplimab [<span>3</span>], the identification of an IFNγ-dependent regulatory axis suggests that strategies to enhance epithelial MHCII expression might offer complementary approaches to current treatments. Figure 1 shows the graphical abstract illustrating that oesophageal epithelial cels upregulate MHCII expression during active EoE in humans and a mouse model.</p><p>The second article, ‘Macrolide hypersensitivity in a patient cohort’ by Hauge and colleagues, shows that with 97.7% of suspected macrolide allergies are rejected after drug provocation testing (DPT), and this work underscores the critical importance of confirmatory testing before labelling patients as allergic [<span>4</span>].</p><p>The consequences of incorrect antibiotic allergy labels extend beyond individual patient care [<span>5</span>]. Such labels restrict therapeutic options, may necessitate use of broader-spectrum or less effective alternatives, and can contribute to antimicrobial resistance [<span>6</span>]. The finding that symptoms, when present, were predominantly mild and cutaneous [<span>4</span>], should reassure clinicians about the safety of conducting DPTs in appropri
在本月的社论中,该杂志的编辑们发表了三篇文章,这些文章举例说明了过敏和临床免疫学领域是如何通过方法创新和对粘膜免疫的更深入的机制理解而发展的。总之,这些研究解决了关于治疗有效性、诊断准确性和不同过敏条件下免疫调节的基本问题。第一篇文章,“食道上皮细胞内在MHCII以ifn γ依赖的方式调节食物抗原依赖性嗜酸性食管炎”,代表了对嗜酸性食管炎(EoE)[1]免疫病理理解的重大进展。Rodriguez-López等人的这项工作证明了食管上皮细胞(EECs)如何以ifn γ依赖性的方式表达MHCII,挑战了将上皮视为被动屏障的传统观点。相反,eec作为主动免疫参与者出现,能够通过抗原呈递调节适应性免疫反应。EEC-intrinsic MHCII减弱而不是促进嗜酸性粒细胞炎症的发现特别值得注意。利用上皮特异性MHCII缺陷小鼠,作者证明,在食物抗原依赖模型[1]中,上皮性MHCII缺失导致食管嗜酸性粒细胞增多加剧。这种保护作用与MHCII纯粹促炎的传统观点形成对比,并与来自肠道模型的新证据一致,这些证据表明上皮MHCII可以促进耐受性并调节T细胞反应[2]。关于CIITA启动子iv依赖性调控的机制见解提供了潜在的治疗靶点。虽然针对2型炎症的治疗方法已经成功地治疗了EoE,如双单抗[3],但ifn γ依赖性调节轴的鉴定表明,增强上皮MHCII表达的策略可能为当前治疗提供补充方法。图1显示了在人类和小鼠模型中,食管上皮细胞在活动EoE期间上调MHCII表达的图形摘要。Hauge及其同事发表的第二篇文章《患者队列中的大环内酯超敏反应》显示,97.7%的疑似大环内酯过敏患者在药物激发试验(DPT)后被拒绝,这项工作强调了在将患者标记为过敏性bb0之前进行确证试验的重要性。不正确的抗生素过敏标签的后果超出了个别病人的护理范围。这样的标签限制了治疗选择,可能需要使用更广谱或效果较差的替代品,并可能导致抗菌素耐药性。当出现症状时,症状主要是轻微的和皮肤的,这一发现应该使临床医生对在适当的环境下进行dpt的安全性放心。这项研究与更广泛的证据一致,表明大多数报告的药物过敏,在经过适当调查后,无法得到证实。在接受检测的患者中,女性患者占主导地位(78%),这反映了其他药物过敏队列的模式,值得进一步调查药物过敏感知或报告中潜在的性别相关差异。第三篇文章,“基于移动医疗数据的目标试验模拟方法评估过敏性鼻炎药物的有效性”,由loren<s:1> - silva及其同事撰写,展示了移动医疗技术如何与严格的因果推理方法相结合,能够产生有意义的真实世界证据[8]。他们将目标轨迹模拟应用于MASK-air应用程序数据,这代表了一种方法学上的进步,可以改变我们在传统随机对照试验之外评估治疗效果的方式。鼻内治疗(INCS和INAH+INCS)在症状控制方面优于口服抗组胺药,这一发现支持了目前的指南建议,即局部治疗bb0。更有趣的是基于哮喘共病的差异反应,联合治疗(INAH+INCS)在哮喘患者中显示出更好的疗效,而在没有[8]的患者中则没有。虽然这仍然是一个需要证实的假设,但它表明鼻炎严重程度以外的表型特征应该为治疗选择提供信息。这项研究举例说明了移动健康平台如何实时捕获患者报告的结果,提供关于症状波动和治疗反应的细粒度数据,这些数据在传统研究中是不切实际的。使用逆概率加权来解决混淆表明,当用适当的因果推理方法分析观察数据时,可以补充随机试验的证据。这三个研究突出了不同研究方法的优势和局限性,Rodríguez-López等。 采用机械小鼠模型和基因操作,提供EEC-MHCII功能的因果证据,但提出了关于可翻译性的问题。Hauge等人使用了金标准DPT方法,但受样本量和缺乏主要反应数据的限制。lorenpado - silva等人利用了大规模的真实世界数据,但承认在控制未测量的混杂因素和药物类别之间不同的药效学方面存在局限性。未来的研究应继续整合这些互补的方法。对于EoE,将上皮MHCII发现转化为人类疾病将需要仔细地对患者进行表型分析,并潜在地开发反映上皮抗原递呈能力的生物标志物。对于药物过敏,更大的多中心DPT研究可以澄清交叉反应模式,并确定确诊反应的危险因素。对于变应性鼻炎,结合客观测量和详细表型数据的长期移动健康研究可以改进治疗算法。总的来说,这些研究通过对上皮免疫调节的机制见解、诊断方法的实用评估和数字健康数据的创新使用,推动了该领域的发展。他们提醒我们,过敏的进展既需要对免疫机制的还原研究,也需要对临床实践的务实评估。随着我们在过敏学领域向精准医学迈进,将分子理解与现实世界的治疗效果和准确诊断相结合,对于改善过敏性疾病患者的预后至关重要。Mohamed H. Shamji和Robert J. Boyle对这份手稿也做出了同样的贡献。作者声明无利益冲突。
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引用次数: 0
A Single-Nucleotide Polymorphism as a Surrogate Marker for Hereditary Alpha-Tryptasemia: Are We There Yet? 单核苷酸多态性作为遗传性α -胰蛋白酶血症的替代标记:我们还在那里吗?
IF 5.2 2区 医学 Q1 ALLERGY Pub Date : 2026-01-29 DOI: 10.1111/cea.70228
Yannick Chantran
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引用次数: 0
期刊
Clinical and Experimental Allergy
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