Most-cited articles · 2024

The 50 most-cited articles in Journal of Allergy and Clinical Immunology, 2024

Ranked by OpenAlex citation count on 29 October 2026, out of 1,248 eligible articles Journal of Allergy and Clinical Immunology published in 2024. Ranks are frozen; this page will not change. Number one, with 171 citations: Dupilumab in patients with chronic spontaneous urticaria (LIBERTY-CSU CUPID): Two randomized, double-blind, placebo-controlled, phase 3 trials.

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2026-10-29

The most-cited articles from the Journal of Allergy and Clinical Immunology in 2024 cluster around several themes, including biologic therapies for allergic and inflammatory disease, mechanisms of airway and skin inflammation, and consensus definitions for clinical conditions. The top paper, with 171 citations, reports two phase 3 trials of dupilumab in chronic spontaneous urticaria. Other highly cited works examine airway hyperresponsiveness in asthma and the role of the epithelium, and present a consensus definition and classification of angioedema.

Readers can use this ranked list to identify the articles that attracted the most citation attention in 2024 across allergy and clinical immunology. The entries span clinical trials, mechanistic studies, biomarker evaluations, and consensus statements, reflecting the range of research published in the journal. Citation counts are drawn from OpenAlex and are based on the titles and abstracts provided here.

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  1. 1
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    Dupilumab in patients with chronic spontaneous urticaria (LIBERTY-CSU CUPID): Two randomized, double-blind, placebo-controlled, phase 3 trials

    Marcus Maurer, Thomas B. Casale, Sarbjit S. Saini, Moshe Ben‐Shoshan, Ana Maria Giménez‐Arnau and 14 more

    171 citationsOpen access (CC-BY-NC-ND)doi:10.1016/j.jaci.2024.01.028OpenAlex

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    BACKGROUND: antihistamines (H1-AH) or anti-IgE (omalizumab) treatment. Dupilumab blocks IL-4/IL-13 signaling and is approved for multiple type 2/atopic indications. OBJECTIVE: We conducted two phase 3, randomized, placebo-controlled, double-blind trials comparing dupilumab with placebo in patients with symptomatic CSU despite H1-AH. METHODS: In LIBERTY-CSU CUPID Study A, patients were omalizumab-naive (n = 138, aged ≥6 years). In Study B, patients were omalizumab-intolerant/incomplete responders (n = 108, aged ≥12 years). The primary end point was either change from baseline over 7 days in the Urticaria Activity Score (UAS7) or Itch Severity Score (ISS7) at week 24, with the other as a key secondary end point, depending on regional regulatory requirements. Studies were pooled for safety assessment. RESULTS: In Study A, UAS7 and ISS7 improved with dupilumab versus placebo (difference -8.5 [95% CI, -13.2 to -3.9; P = .0003] and -4.2 [95% CI, -6.6 to -1.8; P = .0005]). In Study B, tested at α = 0.043 after interim analysis, UAS7 improved (difference -5.8 [95% CI, -11.4 to -0.3; P =…

  2. 2
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    Airway hyperresponsiveness in asthma: The role of the epithelium

    Peter H. Bradding, Celeste Michala Porsbjerg, Andréanne Côté, Sven‐Erik Dahlén, Teal S. Hallstrand and 1 more

    133 citationsOpen access (CC-BY)doi:10.1016/j.jaci.2024.02.011OpenAlex

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    Airway hyperresponsiveness (AHR) is a key clinical feature of asthma. The presence of AHR in people with asthma provides the substrate for bronchoconstriction in response to numerous diverse stimuli, contributing to airflow limitation and symptoms including breathlessness, wheeze and chest tightness. Dysfunctional airway smooth muscle (ASM) significantly contributes to AHR and is displayed as increased sensitivity to direct pharmacological bronchoconstrictor stimuli, such as inhaled histamine and methacholine (direct AHR), or to endogenous mediators released by activated airway cells such as mast cells (indirect AHR). Research in in vivo human models has shown that the disrupted airway epithelium plays an important role in driving inflammation that mediates indirect AHR in asthma, through the release of cytokines such as TSLP and IL-33. These cytokines upregulate type 2 cytokines promoting airway eosinophilia and induce the release of bronchoconstrictor mediators from mast cells such as histamine, prostaglandin D 2 and cysteine leukotrienes. While bronchoconstriction is largely due…

  3. 3
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    Definition, acronyms, nomenclature, and classification of angioedema (DANCE): AAAAI, ACAAI, ACARE, and APAAACI DANCE consensus

    Avner Reshef, Thomas Buttgereit, Stephen Betschel, Teresa Caballero, Henriette Farkas and 25 more

    118 citationsOpen accessdoi:10.1016/j.jaci.2024.03.024OpenAlex

  4. 4
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    JAK-STAT signaling pathway, immunodeficiency, inflammation, immune dysregulation, and inborn errors of immunity

    Simran Samra, Jenna Bergerson, Alexandra F. Freeman, Stuart E. Turvey

    94 citationsOpen access (CC-BY-NC-ND)doi:10.1016/j.jaci.2024.09.020OpenAlex

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    The Janus kinase-signal transducer and activator of transcription (JAK-STAT) signaling cascade is an evolutionarily conserved signal transduction pathway that regulates many vital cellular processes, including immune function and hematopoiesis. Human genetic variants that disrupt JAK-STAT signaling are being found to cause a rapidly increasing number of diseases, including both germline-encoded inborn errors of immunity (IEI) and acquired somatic variants, causing a so-called phenocopy of the IEI. Multiple genetic mechanisms are responsible for this growing group of JAK-STAT diseases including loss-of-function, gain-of-function, and dominant negative effects. In this review, we discuss the clinical presentation and pathogenesis of all currently described JAK-STAT defects, as well as provide an overview of the guiding principles to consider in diagnosing and treating these conditions.

  5. 5
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    Inflammatory memory in psoriasis: From remission to recurrence

    Luc Francis, Francesca Capon, Catherine H. Smith, Muzlifah A. Haniffa, Satveer K. Mahil

    87 citationsOpen access (CC-BY)doi:10.1016/j.jaci.2024.05.008OpenAlex

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    The routine use of targeted systemic immunomodulatory therapies has transformed outcomes for people with severe psoriasis, with skin clearance (clinical remission) rates up to 60% at 1 year of biologic treatment. However, psoriasis may recur following drug withdrawal, and as a result, patients tend to continue receiving costly treatment indefinitely. Here, we review research into the "inflammatory memory" in resolved psoriasis skin and the potential mechanisms leading to psoriasis recurrence following drug withdrawal. Research has implicated immune cells such as tissue resident memory T cells, Langerhans cells, and dermal dendritic cells, and there is growing interest in keratinocytes and fibroblasts. A better understanding of the interactions between these cell populations, enabled by single cell technologies, will help to elucidate the events underpinning the shift from remission to recurrence. This may inform the development of personalized strategies for sustaining remission while reducing long-term drug burden.

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    Inhibition of mast cell degranulation by novel small molecule MRGPRX2 antagonists

    Joshua Wollam, Michelle Solomon, Christiane Villescaz, Marion C. Lanier, Samantha Evans and 22 more

    75 citationsOpen access (CC-BY-NC-ND)doi:10.1016/j.jaci.2024.07.002OpenAlex

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    BACKGROUND: Mas-related G protein-coupled receptor X2 (MRGPRX2) is a promiscuous receptor on mast cells that mediates IgE-independent degranulation and has been implicated in multiple mast cell-mediated disorders, including chronic urticaria, atopic dermatitis, and pain disorders. Although it is a promising therapeutic target, few potent, selective, small molecule antagonists have been identified, and functional effects of human MRGPRX2 inhibition have not been evaluated in vivo. OBJECTIVE: We sought to identify and characterize novel, potent, and selective orally active small molecule MRGPRX2 antagonists for potential treatment of mast cell-mediated disease. METHODS: transgenic human MRGPRX2 knock-in mice by assessment of agonist-induced skin vascular permeability. Ex vivo skin mast cell degranulation and associated histamine release was evaluated by microdialysis of human skin tissue samples. RESULTS: MRGPRX2 antagonists potently inhibited agonist-induced MRGPRX2 activation and mast cell degranulation in all mast cell types tested in an IgE-independent manner. Orally administered…

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    Exploring the skin microbiome in atopic dermatitis pathogenesis and disease modification

    Claudia Hülpüsch, Robin Rohayem, Matthias Reiger, Claudia Traidl‐Hoffmann

    74 citationsOpen accessdoi:10.1016/j.jaci.2024.04.029OpenAlex

  8. 8
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    Impact of climate change on immune responses and barrier defense

    Chrysanthi L. Skevaki, Kari Christine Nadeau, Marc E. Rothenberg, Barrak Alahmad, Blandina Theophil Mmbaga and 5 more

    71 citationsOpen access (CC-BY-NC-ND)doi:10.1016/j.jaci.2024.01.016OpenAlex

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    Climate change is not just jeopardizing the health of our planet but is also increasingly affecting our immune health. There is an expanding body of evidence that climate-related exposures such as air pollution, heat, wildfires, extreme weather events, and biodiversity loss significantly disrupt the functioning of the human immune system. These exposures manifest in a broad range of stimuli, including antigens, allergens, heat stress, pollutants, microbiota changes, and other toxic substances. Such exposures pose a direct and indirect threat to our body's primary line of defense, the epithelial barrier, affecting its physical integrity and functional efficacy. Furthermore, these climate-related environmental stressors can hyperstimulate the innate immune system and influence adaptive immunity-notably, in terms of developing and preserving immune tolerance. The loss or failure of immune tolerance can instigate a wide spectrum of noncommunicable diseases such as autoimmune conditions, allergy, respiratory illnesses, metabolic diseases, obesity, and others. As new evidence unfolds,…

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    Blood eosinophils and fractional exhaled nitric oxide are prognostic and predictive biomarkers in childhood asthma

    Leonard B. Bacharier, Ian Douglas Pavord, Jorge Fernando Maspero, Daniel J. Jackson, Alessandro Giovanni Fiocchi and 10 more

    68 citationsOpen access (CC-BY-NC-ND)doi:10.1016/j.jaci.2023.09.044OpenAlex

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    BACKGROUND: Blood eosinophils and fractional exhaled nitric oxide (Feno) are prognostic biomarkers for exacerbations and predict lung function responses to dupilumab in adolescents and adults with asthma. OBJECTIVE: We evaluated the relationship between baseline blood eosinophils and Feno and response to dupilumab in children with asthma. METHODS: ) at week 12 were assessed according to cutoff baseline levels for Feno (<20 ppb vs ≥20 ppb) and blood eosinophil count (<150, ≥150 to <300, ≥300 to <500, and ≥500 cells/μL). Quadrant analyses in populations defined by biomarker thresholds and spline models across continuous end points assessed the relationship with Feno and eosinophil count. Interaction testing evaluated the independent roles of Feno and blood eosinophils as predictive markers. RESULTS: Exacerbation risk and magnitude of AER reduction increased in subgroups with higher baseline biomarker levels. Quadrant analyses revealed that disease of patients with either elevated Feno or eosinophil counts demonstrated a clinical response to dupilumab. Interaction testing indicated…

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    Phase 2b randomized clinical trial of amlitelimab, an anti-OX40 ligand antibody, in patients with moderate-to-severe atopic dermatitis

    Stephan Weidinger, Andrew Blauvelt, Kim Alexander Papp, Adam Reich, Chih‐Hung Lee and 15 more

    67 citationsOpen access (CC-BY)doi:10.1016/j.jaci.2024.10.031OpenAlex

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    BACKGROUND: Amlitelimab, a fully human nondepleting mAb targeting OX40 ligand on antigen-presenting cells, could prevent T-cell-driven inflammation seen in atopic dermatitis (AD). OBJECTIVE: This trial evaluated the efficacy and safety of amlitelimab in adults with AD. METHODS: In this 2-part, phase 2b, randomized, double-blinded placebo-controlled trial (ClinicalTrials.gov identifier NCT05131477), patients received subcutaneous amlitelimab every 4 weeks at doses of 250 mg plus a 500-mg loading dose, 250 mg, 125 mg, or 62.5 mg or placebo for 24 weeks in Part 1 (1:1:1:1:1 randomization). In Part 2, clinical responders were reallocated 3:1 to stop taking amlitelimab or continue the previous dose regimen for 28 weeks. The primary end point was percentage of change in Eczema Area and Severity Index (EASI) from baseline to week 16. RESULTS: In all, 390 and 190 patients enrolled in Part 1 and Part 2, respectively. A significant percentage of change decrease in EASI was observed with amlitelimab doses versus with placebo (P < .001). Clinical responses at week 24 (Investigator Global…

  12. 12
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    Effect of mepolizumab in airway remodeling in patients with late-onset severe asthma with an eosinophilic phenotype

    Kalliopi Domvri, Ioanna Tsiouprou, Petros Bakakos, Paschalis Steiropoulos, Κonstantinos Κatsoulis and 12 more

    67 citationsOpen access (CC-BY)doi:10.1016/j.jaci.2024.10.024OpenAlex

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    BACKGROUND: Clinical trials and real-world experience have provided evidence for the clinical benefits of mepolizumab, an anti-IL-5 biologic, in severe asthma. However, limited data exist regarding the impact of mepolizumab on airway remodeling. OBJECTIVE: We sought to investigate the effect of mepolizumab on airway structural remodeling in patients treated for severe asthma in routine clinical care. METHODS: The MESILICO (Efficacy of Mepolizumab in patients with latE-onset Severe eosInophiLic asthma and fIxed obstruCtiOn) study is a multicenter study involving 8 pulmonology departments in Greece. This study focused on patients who initiated mepolizumab for severe asthma with an eosinophilic phenotype and had late-onset disease with obstructive patterns (impaired reversibility). Forty-seven patients were recruited, of whom 41 were enrolled in the bronchoscopy substudy. The findings were related to clinical outcome. RESULTS: After 12 months, mepolizumab treatment was associated with significant improvements in lung function and Asthma Control Test score, along with a significant…

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    Trained innate immunity: Concept, nomenclature, and future perspectives

    Mihai Gheorghe Netea, Leo A. B. Joosten

    61 citationsOpen access (CC-BY)doi:10.1016/j.jaci.2024.09.005OpenAlex

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    During the past decade, compelling evidence has accumulated demonstrating that innate immune cells can mount adaptive characteristics, leading to long-term changes in their function. This de facto innate immune memory has been termed trained immunity. Trained immunity, which is mediated through extensive metabolic rewiring and epigenetic modifications, has important effects in human diseases. Although the upregulation of trained immunity by certain vaccines provides heterologous protection against infections, the inappropriate activation of trained immunity by endogenous stimuli contributes to the pathogenesis of inflammatory and neurodegenerative disorders. Development of vaccines that can induce both classical adaptive immunity and trained immunity may lead to a new generation of vaccines with increased efficacy. Activation of trained immunity can also lead to novel strategies for the treatment of cancer, whereas modulation of trained immunity can provide new approaches to the treatment of inflammatory diseases.

  14. 14
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    Bronchiectasis and asthma: Data from the European Bronchiectasis Registry (EMBARC)

    Eva Polverino, Katerina Dimakou, Letizia Traversi, Apostolos Bossios, CHARLES S. HAWORTH and 25 more

    61 citationsOpen access (CC-BY)doi:10.1016/j.jaci.2024.01.027OpenAlex

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    BACKGROUND: Asthma is commonly reported in patients with a diagnosis of bronchiectasis. OBJECTIVE: The aim of this study was to evaluate whether patients with bronchiectasis and asthma (BE+A) had a different clinical phenotype and different outcomes compared with patients with bronchiectasis without concomitant asthma. METHODS: A prospective observational pan-European registry (European Multicentre Bronchiectasis Audit and Research Collaboration) enrolled patients across 28 countries. Adult patients with computed tomography-confirmed bronchiectasis were reviewed at baseline and annual follow-up visits using an electronic case report form. Asthma was diagnosed by the local investigator. Follow-up data were used to explore differences in exacerbation frequency between groups using a negative binomial regression model. Survival analysis used Cox proportional hazards regression. RESULTS: Of 16,963 patients with bronchiectasis included for analysis, 5,267 (31.0%) had investigator-reported asthma. Patients with BE+A were younger, were more likely to be female and never smokers, and had a…

  15. 15
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    DAB2IP associates with hereditary angioedema: Insights into the role of VEGF signaling in HAE pathophysiology

    Maria D’Apolito, Rosa Santacroce, Daniel Vázquez, Giorgia Cordisco, Claudio Agustin Fantini and 7 more

    57 citationsOpen accessdoi:10.1016/j.jaci.2024.05.017OpenAlex

  16. 16
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    Comparative safety of oral Janus kinase inhibitors versus dupilumab in patients with atopic dermatitis: A population-based cohort study

    Serena Yun‐Chen Tsai, Wanda Phipatanakul, Elena B. Hawryluk, Michiko K. Oyoshi, Lynda C. Schneider and 1 more

    55 citationsOpen accessdoi:10.1016/j.jaci.2024.07.019OpenAlex

  17. 17
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    One-food versus 4-food elimination diet for pediatric eosinophilic esophagitis: A multisite randomized trial

    Kara Kliewer, Juan Pablo Abonia, Seema Sharma Aceves, Dan Atkins, Peter A Bonis and 19 more

    49 citationsdoi:10.1016/j.jaci.2024.08.023OpenAlex

  18. 18
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    Validating inborn error of immunity prevalence and risk with nationally representative electronic health record data

    Nicholas L. Rider, Ahuva Truxton, Tracy L. Ohrt, Irene Margolin-Katz, Mary Horan and 9 more

    49 citationsOpen accessdoi:10.1016/j.jaci.2024.01.011OpenAlex

  19. 19
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    Indoor air pollution and airway health

    Jared M. Radbel, Meghan E. Rebuli, Howard M. Kipen, Emily Pfeil Brigham

    48 citationsOpen access (CC-BY)doi:10.1016/j.jaci.2024.08.013OpenAlex

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    Because of the disproportionate amount of time that people spend indoors and the complexities of air pollutant exposures found there, indoor air pollution is a growing concern for airway health. Both infiltration of outdoor air pollution into the indoor space and indoor sources (such as smoke from tobacco products, cooking or heating practices and combustion of associated fuels, and household materials) contribute to unique exposure mixtures. Although there is substantial literature on the chemistry of indoor air pollution, research focused on health effects is only beginning to emerge and remains an important area of need to protect public health. We provide a review of emerging literature spanning the past 3 years and relating indoor air exposures to airway health, with a specific focus on the impact of either individual pollutant exposures or common combustion sources on the lower airways. Factors defining susceptibility and/or vulnerability are reviewed with consideration for priority populations and modifiable risk factors that may be targeted to advance health equity.

  20. 20
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    Utility of eosinophil peroxidase as a biomarker of eosinophilic inflammation in asthma

    Monica C. Tang, Annabelle R. Charbit, Mats W. Johansson, Nizar N. Jarjour, Loren C. Denlinger and 19 more

    47 citationsOpen access (CC-BY)doi:10.1016/j.jaci.2024.03.023OpenAlex

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    BACKGROUND: The relative utility of eosinophil peroxidase (EPX) and blood and sputum eosinophil counts as disease biomarkers in asthma is uncertain. OBJECTIVE: We sought to determine the utility of EPX as a biomarker of systemic and airway eosinophilic inflammation in asthma. METHODS: EPX protein was measured by immunoassay in serum and sputum in 110 healthy controls to establish a normal reference range and in repeated samples of serum and sputum collected during 3 years of observation in 480 participants in the Severe Asthma Research Program 3. RESULTS: values of 0.74 and 0.43, respectively), and high sputum EPX levels occurred in 27% of participants with blood eosinophil counts less than 150 cells/μL and 42% of participants with blood eosinophil counts between 150 and 299 cells/μL. Patients with persistently high sputum EPX values for 3 years were characterized by severe airflow obstruction, frequent exacerbations, and high mucus plug scores. In 59 patients with asthma who started mepolizumab during observation, serum EPX levels normalized in 96% but sputum EPX normalized in only…

  21. 21
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    The mucosal concept in chronic rhinosinusitis: Focus on the epithelial barrier

    Bing Yan, Feng Lan, Jingyun Li, Chengshuo Wang, Luo Zhang

    47 citationsOpen accessdoi:10.1016/j.jaci.2024.01.015OpenAlex

  22. 22
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    Omalizumab safety concerns

    Thanai Pongdee, James T. Li

    46 citationsdoi:10.1016/j.jaci.2024.11.005OpenAlex

  23. 23
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    Antibiotics taken within the first year of life are linked to infant gut microbiome disruption and elevated atopic dermatitis risk

    Courtney Hoskinson, Maria Medeleanu, Myrtha E. Reyna, Darlene Liying Dai, Biswajit Chowdhury and 8 more

    45 citationsOpen access (CC-BY-NC-ND)doi:10.1016/j.jaci.2024.03.025OpenAlex

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    Background Atopic dermatitis (AD) is the most common chronic inflammatory skin disease in both pediatric and adult populations. The development of AD has been linked to antibiotic usage, which causes perturbation of the microbiome and has been associated with abnormal immune system function. However, imbalances in the gut microbiome itself associated with antibiotic usage have been inconsistently linked to AD. Objectives This study aimed to elucidate the timing and specific factors mediating the relationship between systemic (oral or intravenous) antibiotic usage and AD. Methods We used statistical modeling and differential analysis to link CHILD Cohort Study participants' history of antibiotic usage and early-life gut microbiome alterations to AD. Results Here we report that systemic antibiotics during the first year of life, as compared to later, are associated with AD risk (adjusted odds ratio [aOR] = 1.81; 95% CI: 1.28-2.57; P < .001), with an increased number of antibiotic courses corresponding to a dose response–like increased risk of AD risk (1 course: aOR: 1.67; 95% CI:…

  24. 24
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    Interactions between skin-resident dendritic and Langerhans cells and pain-sensing neurons

    Natalie C Wilcox, Golnar Taheri, Katherine Halievski, Sébastien Talbot, Jaqueline Raymondi Silva and 1 more

    44 citationsOpen access (CC-BY-NC-ND)doi:10.1016/j.jaci.2024.03.006OpenAlex

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    Various immune cells in the skin contribute to its function as a first line of defense against infection and disease, and the skin's dense innervation by pain-sensing sensory neurons protects the host against injury or damage signals. Dendritic cells (DCs) are a heterogeneous population of cells that link the innate immune response to the adaptive response by capturing, processing, and presenting antigens to promote T-cell differentiation and activation. DCs are abundant across peripheral tissues, including the skin, where they are found in the dermis and epidermis. Langerhans cells (LCs) are a DC subset located only in the epidermis; both populations of cells can migrate to lymph nodes to contribute to broad immune responses. Dermal DCs and LCs are found in close apposition with sensory nerve fibers in the skin and express neurotransmitter receptors, allowing them to communicate directly with the peripheral nervous system. Thus, neuroimmune signaling between DCs and/or LCs and sensory neurons can modulate physiologic and pathophysiologic pathways, including immune cell regulation,…

  25. 25
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    Mast cell activation syndrome: Current understanding and research needs

    Mariana Castells, Matthew P. Giannetti, Matthew J. Hamilton, Péter Novák, Olga Pozdnyakova and 19 more

    43 citationsOpen accessdoi:10.1016/j.jaci.2024.05.025OpenAlex

  26. 26
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    Intranasal antihistamines and corticosteroids in allergic rhinitis: A systematic review and meta-analysis

    Bernardo Sousa‐Pinto, Rafael José Vieira, Jan Brożek, António Cardoso‐Fernandes, Nuno Lourenço‐Silva and 9 more

    43 citationsOpen access (CC-BY-NC-ND)doi:10.1016/j.jaci.2024.04.016OpenAlex

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    BACKGROUND: There is insufficient systematized evidence on the effectiveness of individual intranasal medications in allergic rhinitis (AR). OBJECTIVES: We sought to perform a systematic review to compare the efficacy of individual intranasal corticosteroids and antihistamines against placebo in improving the nasal and ocular symptoms and the rhinoconjunctivitis-related quality of life of patients with perennial or seasonal AR. METHODS: The investigators searched 4 electronic bibliographic databases and 3 clinical trials databases for randomized controlled trials (1) assessing adult patients with seasonal or perennial AR and (2) comparing the use of intranasal corticosteroids or antihistamines versus placebo. Assessed outcomes included the Total Nasal Symptom Score, the Total Ocular Symptom Score, and the Rhinoconjunctivitis Quality-of-Life Questionnaire. The investigators performed random-effects meta-analyses of mean differences for each medication and outcome. The investigators assessed evidence certainty using the GRADE (Grading of Recommendations, Assessment, Development and…

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    Long COVID: Pathophysiology, current concepts, and future directions

    Chrysanthi L. Skevaki, Charalampos D. Moschopoulos, Paraskevi C. Fragkou, Karsten Grote, Elisabeth Schieffer and 1 more

    41 citationsdoi:10.1016/j.jaci.2024.12.1074OpenAlex

  29. 29
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    Newborn screening for SCID and severe T lymphocytopenia in Europe

    Maartje Blom, Maarja Soomann, Pere Soler‐Palacín, Anna Šedivá, Asbjørg Stray‐Pedersen and 4 more

    41 citationsOpen access (CC-BY)doi:10.1016/j.jaci.2024.10.018OpenAlex

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    Initiation of newborn screening (NBS) programs in Europe dates back to the 1960s. One of the most recent expansions of NBS programs was the addition of severe combined immunodeficiency (SCID) based on detection of T-cell receptor excision circles (TRECs). In this review, we present an overview of the current situation in Europe. To avoid a biased overview based on only published results, a 37-item survey on TREC-based NBS was sent to representatives of 46 European countries. With a response rate of 83%, we collected data of 38 countries. Seventeen of the 38 European countries that have completed the survey have nationally or regionally implemented TREC-based NBS. The survey results emphasize similarities and differences as well as common practices and challenges in TREC-based NBS. Because TRECs are a general surrogate marker for severe T lymphocytopenia, conditions other than SCID are also identified. Therefore, the initial definition of the target disease as "SCID" might need to be reconsidered and extended to "SCID and severe T lymphocytopenia." Even though complete harmonization…

  30. 30
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    Genetic, immunologic, and clinical features of 830 patients with Mendelian susceptibility to mycobacterial diseases (MSMD): A systematic review

    Armin Khavandegar, Seyed Alireza Mahdaviani, Majid Zaki‐Dizaji, Fereshteh Khalili-Moghaddam, Sarina Ansari and 6 more

    41 citationsOpen accessdoi:10.1016/j.jaci.2024.01.021OpenAlex

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    Single cell RNA sequencing of human eosinophils from nasal polyps reveals eosinophil heterogeneity in chronic rhinosinusitis tissue

    Naruhito Iwasaki, Julie A. Poposki, Aiko Oka, Masanori Kidoguchi, Aiko I. Klingler and 13 more

    40 citationsOpen accessdoi:10.1016/j.jaci.2024.05.014OpenAlex

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    Activated sputum eosinophils associated with exacerbations in children on mepolizumab

    Gabriella E. Wilson, James Knight, Qing Liu, Ashish Shelar, Emma Stewart and 16 more

    40 citationsOpen access (CC-BY-NC-ND)doi:10.1016/j.jaci.2024.01.031OpenAlex

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    Background MUPPITS-2 was a randomized, placebo-controlled clinical trial that demonstrated mepolizumab (anti-IL-5) reduced exacerbations and blood and airway eosinophils in urban children with severe eosinophilic asthma. Despite this reduction in eosinophilia, exacerbation risk persisted in certain patients treated with mepolizumab. This raises the possibility that subpopulations of airway eosinophils exist that contribute to breakthrough exacerbations. Objective We aimed to determine the effect of mepolizumab on airway eosinophils in childhood asthma. Methods Sputum samples were obtained from 53 MUPPITS-2 participants. Airway eosinophils were characterized using mass cytometry and grouped into subpopulations using unsupervised clustering analyses of 38 surface and intracellular markers. Differences in frequency and immunophenotype of sputum eosinophil subpopulations were assessed based on treatment arm and frequency of exacerbations. Results Median sputum eosinophils were significantly lower among participants treated with mepolizumab compared with placebo (58% lower, 0.35%…

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    Preparing Patients for Oral Immunotherapy (PPOINT): International Delphi consensus for procedural preparation and consent

    Douglas Paul Mack, Timothy E. Dribin, Paul Turner, Richard L. Wasserman, Mariam A. Hanna and 25 more

    39 citationsOpen access (CC-BY-NC-ND)doi:10.1016/j.jaci.2024.02.019OpenAlex

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    BACKGROUND: Despite the promise of oral immunotherapy (OIT) to treat food allergies, this procedure is associated with potential risk. There is no current agreement about what elements should be included in the preparatory or consent process. OBJECTIVE: We developed consensus recommendations about the OIT process considerations and patient-specific factors that should be addressed before initiating OIT and developed a consensus OIT consent process and information form. METHODS: We convened a 36-member Preparing Patients for Oral Immunotherapy (PPOINT) panel of allergy experts to develop a consensus OIT patient preparation, informed consent process, and framework form. Consensus for themes and statements was reached using Delphi methodology, and the consent information form was developed. RESULTS: The expert panel reached consensus for 4 themes and 103 statements specific to OIT preparatory procedures, of which 76 statements reached consensus for inclusion specific to the following themes: general considerations for counseling patients about OIT; patient- and family-specific factors…

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    Real-world effectiveness of dupilumab in a European cohort of chronic rhinosinusitis with nasal polyps (CHRINOSOR)

    Sven Seys, Sven Oliver Schneider, Joost de Kinderen, Sietze Reitsma, Carlo Cavaliere and 25 more

    38 citationsOpen accessdoi:10.1016/j.jaci.2024.10.016OpenAlex

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    Epithelial overexpression of IL-33 induces eosinophilic esophagitis dependent on IL-13

    Mia Y. Masuda, Grace C. Pyon, Huijun Luo, William E. LeSuer, Arina Putikova and 16 more

    38 citationsOpen accessdoi:10.1016/j.jaci.2024.01.017OpenAlex

  36. 36
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    Aggregated eosinophils and neutrophils characterize the properties of mucus in chronic rhinosinusitis

    Yui Miyabe, Mineyo Fukuchi, Hiroki Tomizawa, Yuka Nakamura, Mitsutoshi Jikei and 18 more

    37 citationsOpen accessdoi:10.1016/j.jaci.2023.11.925OpenAlex

  37. 37
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    Integrative epidemiology and immunotranscriptomics uncover a risk and potential mechanism for cutaneous lymphoma unmasking or progression with dupilumab therapy

    Javier S. Cabrera‐Perez, Vincent J. Carey, Oreofe Olukemi Odejide, Sonal Singh, Thomas Seth Kupper and 3 more

    36 citationsOpen access (CC-BY-NC-ND)doi:10.1016/j.jaci.2024.10.028OpenAlex

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    BACKGROUND: There have been multiple reports of the anti-IL-4Rα agent, dupilumab, being associated with the onset and/or progression of cutaneous T-cell lymphoma (CTCL). OBJECTIVE: We sought to evaluate safety signals associated with dupilumab, with a focus on CTCL, and to evaluate the possible underlying mechanism or mechanisms for the potential association. METHODS: First, we used the Food and Drug Administration's pharmacovigilance database, FAERS (FDA Adverse Event Reporting System), to evaluate whether dupilumab was associated with CTCL, including both positive outcome controls (conjunctivitis, eosinophilia, and arthralgia) and exposure controls (other medications with similar indications, including JAK inhibitors and the anti-IL-13 agent, tralokinumab) to evaluate confounding bias. Thereafter, we used publicly available bulk and single-cell RNA sequencing datasets to probe possible underlying mechanisms through which dupilumab might be associated with CTCL. RESULTS: Between January 2017 and the fourth quarter of 2023, there were 181,575 unique reports of dupilumab-related…

  38. 38
    top 3.1%

    Novel insights on the biology and immunologic effects of histamine: A road map for allergists and mast cell biologists

    Sima Heidarzadeh-Asl, Marcus Maurer, Amir Kiani, Dmitri Atiakshin, Per Stahl Skov and 1 more

    35 citationsOpen access (CC-BY)doi:10.1016/j.jaci.2024.12.1081OpenAlex

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    , molecular weight 111.15 g/mol) is a well-studied endogenous biogenic amine composed of an imidazole ring attached to an ethylamine side chain. It has a limited half-life of a few minutes within tissues and in circulation. Several cell types including mast cells (MCs), basophils, platelets, histaminergic neurons, and enterochromaffin cells produce varying amounts of histamine using histidine decarboxylase. However, only MCs and basophils have complex mechanisms to pack and store histamine in granules along with other mediators using serglycin and its carried glycosaminoglycan side chains. Relatively low granule pH (∼5.5) supports the binding of stored histamine to heparin, whereas exposure to neutral pH after degranulation weakens the binding and histamine becomes liberated. Histamine exerts multifaceted regulatory biofunctions by engaging its 4 types of heptahelical G protein-coupled receptors (H1R-H4R), which have different expression profiles and functions. MCs express H1R, H2R, and H4R, which gives them a dual role in histamine biology as producers and responsive target cells.…

  39. 39
    top 3.2%

    IL-4 acts on skin-derived dendritic cells to promote the TH2 response to cutaneous sensitization and the development of allergic skin inflammation

    Juan Manuel Leyva-Castillo, Mrinmoy Das, Maria Strakosha, Alexander I. McGurk, Emilie Artru and 7 more

    34 citationsOpen accessdoi:10.1016/j.jaci.2024.06.021OpenAlex

  40. 40
    top 3.3%

    Neutralizing IgG4 antibodies are a biomarker of sustained efficacy after peanut oral immunotherapy

    Tarun Keswani, Nicole A. LaHood, Orlee Marini‐Rapoport, Bijoya Karmakar, Léna Andrieux and 5 more

    34 citationsOpen accessdoi:10.1016/j.jaci.2024.02.017OpenAlex

  41. 41
    top 3.3%

    Association between allergic diseases and mental health conditions: An umbrella review

    Xianpeng Xu, Sha Li, Ying‐Jie Chen, Xinxing Deng, Jiongke Li and 2 more

    33 citationsdoi:10.1016/j.jaci.2024.10.030OpenAlex

  42. 42
    top 3.4%

    The nasal basal cell population shifts toward a diseased phenotype with impaired barrier formation capacity in allergic rhinitis

    Emma Ruysseveldt, Brecht Steelant, Tine Wils, Jonathan Cremer, Dominique M. A. Bullens and 2 more

    33 citationsOpen access (CC-BY-NC-ND)doi:10.1016/j.jaci.2024.04.021OpenAlex

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    BACKGROUND: The integrity of the airway epithelium is guarded by the airway basal cells that serve as progenitor cells and restore wounds in case of injury. Basal cells are a heterogenous population, and specific changes in their behavior are associated with chronic barrier disruption-mechanisms that have not been studied in detail in allergic rhinitis (AR). OBJECTIVE: We aimed to study basal cell subtypes in AR and healthy controls. METHODS: Single-cell RNA sequencing (scRNA-Seq) of the nasal epithelium was performed on nonallergic and house dust mite-allergic AR patients to reveal basal cell diversity and to identify allergy-related alterations. Flow cytometry, immunofluorescence staining, and in vitro experiments using primary basal cells were performed to confirm phenotypic findings at the protein level and functionally. RESULTS: The scRNA-Seq, flow cytometry, and immunofluorescence staining revealed that basal cells are abundantly and heterogeneously present in the nasal epithelium, suggesting specialized subtypes. The total basal cell fraction within the epithelium in AR is…

  43. 43
    top 3.5%

    Current status and future directions in food protein–induced enterocolitis syndrome: An NIAID workshop report of the June 22, 2022, virtual meeting

    Anna H Nowak-Wegrzyn, Scott Howard Sicherer, Cem Akin, Sara Anvari, Lisa M. Bartnikas and 18 more

    31 citationsOpen accessdoi:10.1016/j.jaci.2024.10.022OpenAlex

  44. 44
    top 3.6%

    European Society for Immunodeficiencies guidelines for the management of patients with congenital athymia

    Alexandra Y. Kreins, Fatima Dhalla, Aisling M. Flinn, Evey Howley, Olov Ekwall and 21 more

    31 citationsOpen access (CC-BY)doi:10.1016/j.jaci.2024.07.031OpenAlex

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    Congenital athymia is a life-limiting disorder due to rare inborn errors of immunity causing impaired thymus organogenesis or abnormal thymic stromal cell development and function. Athymic infants have a T-lymphocyte-negative, B-lymphocyte-positive, natural killer cell-positive immunophenotype with profound T-lymphocyte deficiency and are susceptible to severe infections and autoimmunity. Patients variably display syndromic features. Expanding access to newborn screening for severe combined immunodeficiency and T lymphocytopenia and broad genetic testing, including next-generation sequencing technologies, increasingly facilitate their timely identification. The recommended first-line treatment is allogeneic thymus transplantation, which is a specialized procedure available in Europe and the United States. Outcomes for athymic patients are best with early diagnosis and thymus transplantation before the development of infectious and inflammatory complications. These guidelines on behalf of the European Society for Immunodeficiencies provide a comprehensive review for clinicians who…

  45. 45
    top 3.7%

    Microbial intestinal dysbiosis drives long-term allergic susceptibility by sculpting an ILC2–B1 cell–innate IgE axis

    Ahmed Kabil, Natalia Nayyar, Julyanne Brassard, Yicong Li, Sameeksha Chopra and 2 more

    31 citationsOpen access (CC-BY-NC-ND)doi:10.1016/j.jaci.2024.07.023OpenAlex

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    BACKGROUND: The abundance and diversity of intestinal commensal bacteria influence systemic immunity with impact on disease susceptibility and severity. For example, loss of short chain fatty acid (SCFA)-fermenting bacteria in early life (humans and mice) is associated with enhanced type 2 immune responses in peripheral tissues including the lung. OBJECTIVE: Our goal was to reveal the microbiome-dependent cellular and molecular mechanisms driving enhanced susceptibility to type 2 allergic lung disease. METHODS: We used low-dose vancomycin to selectively deplete SCFA-fermenting bacteria in wild-type mice. We then examined the frequency and activation status of innate and adaptive immune cell lineages with and without SCFA supplementation. Finally, we used ILC2-deficient and signal transducer and activator of transcription 6 (STAT6)-deficient transgenic mouse strains to delineate the cellular and cytokine pathways leading to enhanced allergic disease susceptibility. RESULTS: Mice with vancomycin-induced dysbiosis exhibited a 2-fold increase in lung ILC2 primed to produce elevated…

  46. 46
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    Leukotriene receptor antagonists as add-on therapy to antihistamines for urticaria: Systematic review and meta-analysis of randomized clinical trials

    Daniel G. Rayner, Ming Liu, Alexandro W. L. Chu, Xiajing Chu, Gordon Henry Guyatt and 24 more

    31 citationsOpen access (CC-BY-NC-ND)doi:10.1016/j.jaci.2024.05.026OpenAlex

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    BACKGROUND: antihistamines (AHs) for the management of urticaria (hives, itch, and/or angioedema) remain unclear. OBJECTIVE: We sought to systematically synthesize the treatment outcomes of antileukotrienes in combination with AHs versus AHs alone for acute and chronic urticaria. METHODS: As part of updating American Academy of Allergy, Asthma & Immunology and American College of Allergy, Asthma, and Immunology Joint Task Force on Practice Parameters urticaria guidelines, we searched Medline, Embase, Central, LILACS, WPRIM, IBECS, ICTRP, CBM, CNKI, VIP, Wanfang, US Food and Drug Administration, and European Medicines Agency databases from inception to December 18, 2023, for randomized controlled trials (RCTs) evaluating antileukotrienes and AHs versus AHs alone in patients with urticaria. Paired reviewers independently screened citations, extracted data, and assessed risk of bias. Random effects models pooled effect estimates for urticaria activity, itch, wheal, sleep, quality of life, and harms. The GRADE approach informed certainty of evidence ratings. The study was registered at…

  47. 47
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    A practical guide for implementing omalizumab therapy for food allergy

    Thomas B. Casale, Alessandro Giovanni Fiocchi, Matthew Greenhawt

    31 citationsOpen accessdoi:10.1016/j.jaci.2024.03.019OpenAlex

  48. 48
    top 3.9%

    Blocking CD226 regulates type 2 innate lymphoid cell effector function and alleviates airway hyperreactivity

    Yoshihiro Sakano, Kei Sakano, Benjamin P. Hurrell, Doumet Georges Helou, Pedram Shafiei-Jahani and 8 more

    31 citationsOpen access (OTHER-OA)doi:10.1016/j.jaci.2024.01.003OpenAlex

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    Background Type 2 innate lymphoid cells (ILC2s) play a pivotal role in type 2 asthma. CD226 is a costimulatory molecule involved in various inflammatory diseases. Objective We aimed to investigate CD226 expression and function within human and mouse ILC2s, and to assess the impact of targeting CD226 on ILC2-mediated airway hyperreactivity (AHR). Methods We administered IL-33 intranasally to wild-type mice, followed by treatment with anti-CD226 antibody or isotype control. Pulmonary ILC2s were sorted for ex vivo analyses through RNA sequencing and flow cytometry. Next, we evaluated the effects of CD226 on AHR and lung inflammation in wild-type and Rag2 −/− mice. Additionally, we compared peripheral ILC2s from healthy donors and asthmatic patients to ascertain the role of CD226 in human ILC2s. Results Our findings demonstrated an inducible expression of CD226 in activated ILC2s, enhancing their cytokine secretion and effector functions. Mechanistically, CD226 alters intracellular metabolism and enhances PI3K/AKT and MAPK signal pathways. Blocking CD226 ameliorates ILC2-dependent AHR…

  49. 49
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    Association of CD19+-targeted chimeric antigen receptor (CAR) T-cell therapy with hypogammaglobulinemia, infection, and mortality

    Natalia M. Sutherland, Baijun Zhou, Lingxiao Zhang, Mei‐Sing Ong, Joseph Hong and 9 more

    30 citationsOpen accessdoi:10.1016/j.jaci.2024.10.021OpenAlex

  50. 50
    top 4.1%

    Update on inborn errors of immunity

    Hanna IJspeert, Emily S.J. Edwards, Robyn E. O’Hehir, Virgil A. S. H. Dalm, Menno C. van Zelm

    29 citationsOpen access (CC-BY)doi:10.1016/j.jaci.2024.12.1075OpenAlex

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    Ever since the first description of an inherited immunodeficiency in 1952 in a boy with gammaglobulin deficiency, new insights have progressed rapidly in disorders that are now referred to as inborn errors of immunity. In a field where fundamental molecular biology, genetics, immune signaling, and clinical care are tightly intertwined, 2022-24 saw a multitude of advances. Here we report a selection of research updates with a main focus on (1) diagnosis and screening, (2) new genetic defects, (3) susceptibility to severe coronavirus disease 2019 infection and impact of vaccination, and (4) treatment. Importantly, new pathogenic insights more rapidly affect treatment outcomes, either through an earlier and more precise diagnosis or through implementation of novel, personalized treatment. The field is growing rapidly, so awareness, communication, and collaboration are key to improving treatment outcomes.

How to read this list

The cohort is every article, review and book chapter OpenAlex attributes to Journal of Allergy and Clinical Immunology with publication year 2024, excluding retracted works and paratext such as editorials and errata. The top 50 by citation count are listed; the percentile is the rank divided by the cohort size. 27 of the 50 entries have an abstract in OpenAlex. Counts were read on 29 October 2026 and will not be updated on this page, so a quoted rank stays verifiable. Full rules on the methodology page.

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