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Biologics in Pediatric Asthma: Controlling Symptoms, Maintaining Safety, and Improving Outcomes. 儿童哮喘的生物制剂:控制症状、维持安全性和改善预后。
IF 4.6 2区 医学 Q1 ALLERGY Pub Date : 2026-02-04 DOI: 10.1007/s11882-026-01252-x
Priya Chopra, William C Anderson Iii
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引用次数: 0
Inverted Sinonasal Papilloma: Pheno-endotyping and Predictive Markers of Recurrence and Malignancy - A Systematic Review. 内翻性鼻窦乳头状瘤:表型内分型和复发和恶性的预测标记-系统综述。
IF 4.6 2区 医学 Q1 ALLERGY Pub Date : 2026-01-28 DOI: 10.1007/s11882-025-01247-0
María Paola Aguilera, Daniela Pastene, Joan Lop, Concepció Marin, Joaquim Mullol, Isam Alobid

Purpose of review: This review aimed to summarize the inflammatory, microscopic, and histopathological features of inverted sinonasal papilloma (ISP) and to identify viral, molecular, and genetic predictors of recurrence and malignant transformation.

Recent findings: Recent studies describe a heterogeneous inflammatory microenvironment with mixed Th1/Th2/Th17 cytokine responses and epithelial neutrophilia as a defining hallmark. Considerable variability persists across studies evaluating viral and molecular markers. High-risk Human Papillomavirus type 18 (HR-HPV-18), Epidermal Growth Factor Receptor (EGFR) exon 20 mutations, p53 alterations, and p16 loss have been most consistently linked to recurrence and malignant progression. SNIP exhibits multifactorial biological behavior driven by inflammation, viral infection, and molecular dysregulation. These findings highlight the need for standardized histopathological and molecular criteria and prospective studies to refine recurrence prediction and early detection of malignant transformation.

综述目的:本综述旨在总结鼻窦内翻性乳头状瘤(ISP)的炎症、显微镜和组织病理学特征,并确定其复发和恶性转化的病毒、分子和遗传预测因素。最近的发现:最近的研究描述了一个异质性的炎症微环境,混合的Th1/Th2/Th17细胞因子反应和上皮嗜中性粒细胞是一个决定性的标志。在评估病毒和分子标记物的研究中,存在相当大的差异。高危人乳头瘤病毒18型(HR-HPV-18)、表皮生长因子受体(EGFR)外显子20突变、p53改变和p16缺失与复发和恶性进展最为一致。SNIP表现出由炎症、病毒感染和分子失调驱动的多因素生物学行为。这些发现强调需要标准化的组织病理学和分子标准以及前瞻性研究来完善恶性转化的复发预测和早期检测。
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引用次数: 0
Occupational Allergy to Rat and Mouse in Research Laboratories. 研究实验室对大鼠和小鼠的职业性过敏。
IF 4.6 2区 医学 Q1 ALLERGY Pub Date : 2026-01-25 DOI: 10.1007/s11882-026-01250-z
Juliette Caron, Anaïs Lemoine, Anne Herman, Florence Libon, Christine Delebarre-Sauvage
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引用次数: 0
Defining the Role and Clinical Relevance of Periostin in Chronic Rhinosinusitis with or without Nasal Polyps: a Systematic Review and Meta-analysis. 确定骨膜蛋白在伴或不伴鼻息肉的慢性鼻窦炎中的作用和临床相关性:一项系统综述和荟萃分析。
IF 4.6 2区 医学 Q1 ALLERGY Pub Date : 2026-01-15 DOI: 10.1007/s11882-025-01248-z
Baharudin Abdullah, Sakinah Mohamad, Intan Kartika Kamarudin, Tengku Ahmad Damitri Al-Astani Tengku Din, Nurul Asma Abdullah, Wan Faiziah Wan Abdul Rahman, Rohimah Mohmud
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引用次数: 0
Biologics in Chronic Rhinosinusitis with Nasal Polyps: The Otolaryngologist's Perspective. 生物制剂治疗慢性鼻窦炎伴鼻息肉:耳鼻喉科医生的观点。
IF 4.6 2区 医学 Q1 ALLERGY Pub Date : 2026-01-10 DOI: 10.1007/s11882-025-01243-4
Michael F Armstrong, Brent A Senior

Purpose of review: Monoclonal antibodies ("biologics") have increasingly been used to manage chronic sinusitis with nasal polyps (CRSwNP). The aim of this manuscript was to compare biologic outcomes to traditional management of CRSwNP with endoscopic sinus surgery (ESS).

Recent findings: There are now four approved biologics for the treatment of CRSwNP in the United States: dupilumab, mepolizumab, omalizumab, and tezepelumab. Cost analysis and comparison between phase 3 clinical trial results of biologics and ESS show ESS is at least as effective as biologics in controlling symptoms with significantly less cost to the healthcare system. Recent guidelines published by the European Position paper on Rhinosinusitis and Nasal Polyps (EPOS) and the American Academy of Otolaryngology continue to support ESS in the management of CRSwNP when traditional medical therapy has failed. Biologics may be considered an option for severe uncontrolled CRSwNP that has failed comprehensive ESS. Future studies are needed to assess long-term efficacy and cost of biologics compared to ESS in CRSwNP.

综述目的:单克隆抗体(“生物制剂”)越来越多地用于治疗慢性鼻窦炎伴鼻息肉(CRSwNP)。这篇文章的目的是比较传统治疗CRSwNP与内镜鼻窦手术(ESS)的生物学结果。最近的发现:目前在美国有四种生物制剂被批准用于治疗CRSwNP: dupilumab, mepolizumab, omalizumab和tezepelumab。成本分析和生物制剂与ESS三期临床试验结果的比较表明,ESS在控制症状方面至少与生物制剂一样有效,而医疗系统的成本却明显更低。最近由欧洲鼻窦炎和鼻息肉立场文件(EPOS)和美国耳鼻喉学会发布的指南继续支持在传统药物治疗失败时使用ESS治疗CRSwNP。对于综合ESS失败的严重不受控制的CRSwNP,生物制剂可被视为一种选择。未来的研究需要评估与ESS相比,生物制剂在CRSwNP中的长期疗效和成本。
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引用次数: 0
Chronic Rhinosinusitis Optimisation of Nasal Outcomes and Scores (CHRONOS): An Italian Delphi Consensus on Long-Term Management with Biologics. 慢性鼻窦炎鼻腔预后和评分的优化(CHRONOS):意大利德尔菲共识对生物制剂的长期管理。
IF 4.6 2区 医学 Q1 ALLERGY Pub Date : 2026-01-09 DOI: 10.1007/s11882-025-01246-1
Eugenio De Corso, Frank Rikki Mauritz Canevari, Marco Caminati, Carlotta Pipolo, Enrico Heffler, Matteo Lazzeroni, Veronica Seccia, Massimiliano Garzaro, Giancarlo Ottaviano, Elena Cantone, Fabio Pagella, Giulia Gramellini, Ignazio La Mantia, Stefania Gallo, Antonio Moffa, Ernesto Pasquini, Antonella Loperfido, Sara Torretta, Lorenzo Cecchi, Gian Luca Fadda, Giandomenico Maggiore, Stefano Pelucchi, Lucia Iannuzzi, Daniela Lucidi, Alberto Macchi, Roberto Padoan, Vincenzo Patella, Giulia Dané, Jan Schroeder, Claudio Montuori, Marco Corbò, Giorgio Walter Canonica, Gianenrico Senna

Purpose of review: This review synthesizes current evidence and expert consensus on the long-term management of severe chronic rhinosinusitis with nasal polyps (CRSwNP) treated with biologics, as established by the Italian CHRONOS project.

Recent findings: Accumulating real-world and clinical trial data confirm the sustained efficacy and safety of biologics targeting type 2 inflammation, enabling durable control and remission in a significant proportion of patients. Personalized dosing regimens, including dose-spacing strategies, appear feasible. The CHRONOS project provides practical guidance for optimizing long-term biologic therapy in severe CRSwNP. Response assessment should combine subjective and objective measures, especially for olfactory testing. Biologics may be considered before surgery only in selected complex cases. Dose-spacing strategies may be appropriate in stable patients but require multidisciplinary oversight in those with comorbid asthma. Adverse events are uncommon. The concept of disease modification is endorsed, recognizing biologics' potential to alter the natural history of CRSwNP.

综述目的:本综述综合了意大利CHRONOS项目建立的重度慢性鼻窦炎伴鼻息肉(CRSwNP)生物制剂长期治疗的现有证据和专家共识。最近的发现:不断积累的现实世界和临床试验数据证实了针对2型炎症的生物制剂的持续有效性和安全性,使相当比例的患者能够持久控制和缓解。个性化给药方案,包括剂量间隔策略,似乎是可行的。CHRONOS项目为优化重度CRSwNP的长期生物治疗提供了实践指导。反应评价应主客观结合,尤其是嗅觉检测。只有在特定的复杂病例中,才能在手术前考虑使用生物制剂。剂量间隔策略可能适用于病情稳定的患者,但对于合并哮喘的患者则需要多学科监督。不良事件并不常见。疾病修饰的概念得到认可,认识到生物制剂改变CRSwNP自然历史的潜力。
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引用次数: 0
Sublingual Immunotherapy for Food Allergy: Updates in Safety, Efficacy, and Future Considerations. 食物过敏的舌下免疫疗法:安全性、有效性和未来考虑的最新进展。
IF 4.6 2区 医学 Q1 ALLERGY Pub Date : 2026-01-03 DOI: 10.1007/s11882-025-01244-3
Anna A Ilyasova, Edwin H Kim

Purpose of the review: With the continued increase in the prevalence of food allergy and its significant associated medical and financial burden, there is a need for safe and effective treatment options for patients. The goal of this review is to summarize published data on the safety and efficacy of peanut sublingual immunotherapy (SLIT) as a potential treatment option for children with food allergy.

Recent findings: Peanut SLIT has demonstrated clinically significant desensitization across 2 cohorts of children ages 1-11 years. In a study focused on 1-4-year-old peanut-allergic toddlers, even greater levels of desensitization as well as the potential for 3-month remission has been demonstrated. Small studies have also demonstrated potential efficacy with SLIT for other foods such as milk, hazelnut, and peach. Evidence to date supports SLIT as effective and safe and a potential future treatment option for children with food allergy.

回顾的目的:随着食物过敏患病率的持续增加及其相关的重大医疗和经济负担,需要为患者提供安全有效的治疗选择。本综述的目的是总结已发表的关于花生舌下免疫疗法(SLIT)作为食物过敏儿童潜在治疗选择的安全性和有效性的数据。最近发现:花生SLIT在2组1-11岁儿童中显示出临床显着的脱敏作用。在一项针对1-4岁花生过敏幼儿的研究中,已经证明了更高水平的脱敏以及3个月缓解的潜力。小型研究也证明了SLIT对牛奶、榛子和桃子等其他食物的潜在功效。迄今为止的证据支持SLIT是有效和安全的,并且是未来治疗食物过敏儿童的潜在选择。
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引用次数: 0
A Review of Adenosine Deaminase 2 (ADA2) as a Biomarker of Monocyte/Macrophage Activation. 腺苷脱氨酶2 (ADA2)作为单核细胞/巨噬细胞活化的生物标志物的研究进展
IF 4.6 2区 医学 Q1 ALLERGY Pub Date : 2026-01-03 DOI: 10.1007/s11882-025-01249-y
Jamie Lim, Jayanth Doss, Jeffrey Shen, Michael Hershfield, Teresa Tarrant

Purpose of review: Adenosine deaminase 2 (ADA2) is predominantly expressed by and secreted from activated monocytes and macrophages into plasma. This review explores the utility of ADA2 as a biomarker of monocyte/macrophage activation in a range of conditions and suggests potential applications for its clinical use.

Recent findings: Elevated ADA2 activity has been observed in conditions associated with granulomatous inflammation and macrophage activation, including tuberculosis, sarcoidosis, and macrophage activation syndrome. This finding has also been reported in liver fibrosis, malignancy, infection, and autoimmune diseases such as rheumatoid arthritis and systemic lupus erythematosus. Absent or near absent ADA2 activity is associated with deficiency of ADA2 (DADA2), an autosomal recessive inborn error of immunity. Increased ADA2 activity correlates with monocyte/macrophage activity, making it a potential biomarker in diseases characterized by excessive macrophage activation. Although ADA2 activity is relatively easy to measure in plasma and may assist with diagnosis when conventional approaches are unavailable, invasive, or carry additional risks, it lacks disease specificity. The absence of ADA2 activity in plasma combined with a characteristic clinical phenotype and biallelic genetic mutations inADA2 is diagnostic of DADA2.

综述目的:腺苷脱氨酶2 (ADA2)主要由活化的单核细胞和巨噬细胞表达并分泌到血浆中。这篇综述探讨了ADA2作为单核细胞/巨噬细胞激活的生物标志物在一系列条件下的效用,并提出了其临床应用的潜在应用。最近发现:在肉芽肿性炎症和巨噬细胞激活相关的疾病中,包括结核、结节病和巨噬细胞激活综合征,ADA2活性升高已被观察到。这一发现在肝纤维化、恶性肿瘤、感染和自身免疫性疾病(如类风湿关节炎和系统性红斑狼疮)中也有报道。ADA2活性缺失或接近缺失与ADA2缺陷(DADA2)有关,这是一种常染色体隐性先天性免疫错误。ADA2活性升高与单核细胞/巨噬细胞活性相关,使其成为巨噬细胞过度活化疾病的潜在生物标志物。虽然血浆中ADA2活性相对容易测量,并且在常规方法不可用、侵入性或有额外风险时可能有助于诊断,但它缺乏疾病特异性。血浆中缺乏ADA2活性,结合ADA2的特征性临床表型和双等位基因突变,可诊断为DADA2。
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引用次数: 0
A Review of Airborne Pollen and Its Interactions With Air Pollutants, Urbanization, and Climate Change: Implications for Human Health and Monitoring Gaps. 空气花粉及其与空气污染物、城市化和气候变化的相互作用:对人类健康和监测差距的影响
IF 4.6 2区 医学 Q1 ALLERGY Pub Date : 2025-12-27 DOI: 10.1007/s11882-025-01241-6
Sachin Dhawan, Anand Kumar, Dalip Singh Mehta, Mukesh Khare

Purpose of review: This review synthesizes interdisciplinary evidence on how environmental stressors-including climate change, urbanization, and air pollution-impact pollen dynamics and human health. We assess conventional and innovative monitoring methods to identify critical gaps in exposure evaluation and public health response.

Recent findings: Recent research confirms that climate change and urbanization are prolonging pollen seasons and increasing pollen potency. Pollutants such as O3, NOx, PM, SO2, and elevated CO2 along with urban heat island and vegetation changes further enhance pollen allergenicity. While monitoring technology is advancing, significant limitations persist, including poor spatial resolution, a lack of real-time capabilities, and severe underrepresentation of tropical regions. An integrated approach to pollen surveillance that combines climate, air quality, and health data is critically needed. Key challenges remain, including inadequate spatial coverage, a lack of standardized protocols, and poor integration with public health systems. The complex interactions between pollen as a bioaerosol and atmospheric processes represent a significant research gap, hindering our ability to predict and manage pollen-related health risks effectively.

综述目的:本文综合了气候变化、城市化和空气污染等环境压力因素如何影响花粉动态和人类健康的跨学科证据。我们评估传统和创新的监测方法,以确定暴露评估和公共卫生应对方面的关键差距。最近的发现:最近的研究证实,气候变化和城市化正在延长花粉季节,增加花粉的效力。O3、NOx、PM、SO2、CO2等污染物随着城市热岛和植被变化而升高,进一步增强了花粉的致敏性。虽然监测技术正在进步,但仍然存在重大限制,包括空间分辨率差、缺乏实时能力以及热带地区的代表性严重不足。迫切需要一种结合气候、空气质量和健康数据的花粉监测综合方法。主要挑战仍然存在,包括空间覆盖不足、缺乏标准化协议以及与公共卫生系统整合不良。花粉作为一种生物气溶胶与大气过程之间复杂的相互作用是一个重大的研究空白,阻碍了我们有效预测和管理花粉相关健康风险的能力。
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引用次数: 0
Acute Exacerbations of Chronic Rhinosinusitis. 慢性鼻窦炎的急性发作。
IF 4.6 2区 医学 Q1 ALLERGY Pub Date : 2025-12-20 DOI: 10.1007/s11882-025-01239-0
Robert M Frederick, Kent Lam, Joseph K Han

Purpose of review: We aim to highlight recent advancements on the evolving chronic rhinosinusitis (CRS) phenotype: acute exacerbations of chronic rhinosinusitis (AECRS). We focused on studies that expanded the current understanding of its pathophysiology, patient characteristics, and disease burden.

Recent findings: Defining AECRS has been a topic of discussion for many years. A recent regulatory definition of AECRS in the literature incorporates a > 3 day requirement of worsened symptoms and an escalation of treatment. It is important not to rely on patient-reported rescue medication frequency as it was recently demonstrated these are only obtained for 1/3 of reported AECRS episodes. The pathophysiology behind AECRS is still being evaluated but it appears irritants such as viral insult to the sinonasal microbiome can create a dysbiosis and worsens host immune system breakdown, facilitating a subsequent bacterial infection. Many studies are using loose definitions of AECRS because no formal definition has existed until recently. Clinical trials and other studies are relying on patient-reported illnesses, CRS-related antibiotics, and CRS-related corticosteroids to determine an episode of AECRS. Formally defining AECRS is vital in order to conduct future literature on its etiology and clinical outcomes so results may be translatable. Additionally, our review demonstrates that CRS patients with asthma and/or concomitant allergic rhinitis appear to be at an increased risk for developing AECRS and future research should continue to investigate their interplay. Many patients are being overprescribed antibiotics and corticosteroids for reported AECRS episodes. This increases total healthcare spending and increases the risk for adverse effects from corticosteroids and antibiotic resistance. Future research should investigate methods to mitigate this practice.

综述的目的:我们旨在强调慢性鼻窦炎(CRS)表型的最新进展:慢性鼻窦炎(AECRS)的急性加重。我们的研究重点是扩大目前对其病理生理学、患者特征和疾病负担的理解。最近的发现:定义AECRS是多年来讨论的话题。最近在文献中对AECRS的监管定义包含了症状恶化和治疗升级的bbb30天要求。重要的是不要依赖患者报告的抢救用药频率,因为最近的研究表明,只有1/3的AECRS事件报告获得了抢救用药频率。AECRS背后的病理生理学仍在评估中,但似乎刺激物,如病毒对鼻微生物群的损害,可以造成生态失调,恶化宿主免疫系统的崩溃,促进随后的细菌感染。由于直到最近才有正式的定义,许多研究都使用了AECRS的松散定义。临床试验和其他研究依赖于患者报告的疾病、crs相关抗生素和crs相关皮质类固醇来确定AECRS的发作。正式定义AECRS是至关重要的,以便进行未来的文献对其病因和临床结果,使结果可能是可翻译的。此外,我们的综述表明,伴有哮喘和/或过敏性鼻炎的CRS患者发生AECRS的风险增加,未来的研究应继续调查它们之间的相互作用。许多患者因报告的AECRS发作而被过量开具抗生素和皮质类固醇。这增加了总的医疗保健支出,并增加了皮质类固醇和抗生素耐药性的不良反应的风险。未来的研究应该调查减轻这种做法的方法。
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引用次数: 0
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Current Allergy and Asthma Reports
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