The incidence of allergies is increasing, particularly in industrialized areas. Allergic inflammation can differ substantially in intensity. Traditional drug therapy such as antihistamines, corticosteroids, anticholinergic agents and leukotriene inhibitors is important in reducing and preventing symptoms and is essential in acute use. More recent therapies including anti-immunoglobin E (IgE) therapy, anti-interleukin (IL) monoclonal antibodies, and phosphodiesterase 4/phospholipaseA2 inhibitors, have improved outcomes. However, in order to develop more effective therapies, further research is needed into the molecular mechanisms underlying allergy onset, particularly in terms of intracellular reactions and the cytosolic Ca2+ balance.
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New clinical data presented at EAACI Congress 2026 highlighted the continued evolution of hereditary angioedema (HAE) management. Alongside established long-term prophylactic and on-demand treatment strategies, investigational therapies are aiming to reduce treatment burden through oral formulations, longer dosing intervals and, potentially, one-time disease-modifying approaches. Here, we summarise some of the key HAE clinical trial updates presented at this year's meeting.
Non-advanced systemic mastocytosis (NonAdvSM) is a rare disease characterized by clonal mast cell accumulation across multiple organ systems. In this interview, Dr Nathan Boggs discusses the clinical burden of NonAdvSM and explores data from the Phase 2 SUMMIT trial (NCT05186753), presented at AAAAI 2026, which investigated bezuclastinib, an oral, selective KIT D816V inhibitor, for the treatment of NonAdvSM.
In this interview, Dr José Clemente discusses recent findings presented at AAAAI 2026 from the ACTIVATE trial, exploring whether modifying the early microbiome in Caesarean-delivered infants at risk of allergy can influence food sensitization and how early microbial exposures may shape immune development.
Omalizumab-facilitated multi-allergen oral immunotherapy (mOIT) is an established therapy for the treatment of food allergies. The COMBINE trial (NCT03679676) was a Phase 2 randomized controlled trial investigating whether adjunct dupilumab would improve patient outcomes with mOIT. In this Q&A, Dr Sayantani B. Sindher explores the established efficacy and safety profile of mOIT, the aims and methodology of the COMBINE trial, and the key findings and the implications they could have on clinical practice.
As 2025 draws to a close, we’re celebrating another remarkable year of growth, collaboration and innovation at touchIMMUNOLOGY. From thought-provoking expert interviews and peer-reviewed research to dynamic conference coverage and an expanding portfolio of medical education, this year has been defined by meaningful conversations and impactful learning. We’ve had the privilege of engaging with leading clinicians, researchers and partner societies across the globe - bringing together diverse voices to support the immunology community with timely, accessible and authoritative content. As we reflect on the past 12 months, we’re proud to highlight the moments, milestones and stories that shaped our year. Here are just some of the standout highlights from 2025.
Eosinophilic esophagitis (EoE) is a chronic, often debilitating condition that can significantly impact children’s growth and quality of life. Dupilumab, a fully human monoclonal antibody that inhibits IL-4 and IL-13 signaling, has emerged as a promising treatment option. In this Q&A, Dr Margaret H. Collins, a pathologist at Cincinnati Children’s Hospital, discusses the burden of pediatric EoE, the mechanism of action of dupilumab, and key findings from the phase 3 EoE KIDS trial, which demonstrated meaningful improvements in disease activity and a safety profile consistent with prior studies.
Dermatologists now have a new tool to transform the treatment landscape for patients living with chronic spontaneous urticaria (CSU): the first and only oral Bruton’s tyrosine kinase inhibitor (BTKi) approved by the FDA for this condition. This oral therapy is indicated for adults with CSU who remain symptomatic despite treatment with H1 antihistamines. Taken twice daily, it requires no injections or routine laboratory monitoring, offering a convenient and targeted option for patients whose symptoms persist on standard care.
In this episode, we speak with leading paediatric allergist Prof. Helen Brough to explore the key factors behind why some children develop allergies to foods such as peanuts, and what we can do to help prevent them. We also examine the latest developments in managing food allergies and the innovations on the horizon that could transform how we treat them.
Physician burnout is at a critical point. In this episode, Nicky speaks with Dr Alfred Atanda about why so many physicians are burning out and what can be done to change the trend. From personal experience to system-wide solutions, Dr Atanda shares valuable insights on improving physician well-being and building a more effective healthcare culture.
In this episode, we explore the future of continuing medical education (CME) with the team behind touchIME. Hannah Fisher and Matthew Goodwin share insights into global and US trends, the importance of patient inclusivity and how educational outcomes are evolving to better measure the direct impact of learning on clinical practice and patient care.
The IMPACT-PLuS long-term follow-up trial found that children who underwent peanut oral immunotherapy in the earlier IMPACT trial maintained significant changes in their allergen-specific IgE and IgG4 profiles, which could have positive implications for long-term allergy management.
Epinephrine is the first-line treatment for severe allergic reactions, including anaphylaxis, where prompt intervention is crucial. Epinephrine sublingual film, a novel prodrug of epinephrine, is being developed to treat Type 1 allergic reactions, such as anaphylaxis. In the OASIS study, epinephrine sublingual film demonstrated equal or superior pharmacokinetics compared to intramuscular epinephrine in adult patients with oral allergy syndrome. The film led to rapid symptom resolution, with a median recovery time of 12 minutes. Additionally, stability tests showed that the film remained effective under extreme temperatures and real-world conditions, ensuring its reliability as an emergency treatment for anaphylaxis.
The FDA has approved a 1 mg epinephrine nasal spray for treating type I allergic reactions, including anaphylaxis, in children over 4 years old, weighing between 15 and 30 kg. This nasal spray offers a needle-free alternative to traditional epinephrine injections, which may be avoided due to fear, especially among children.
A globally recognized allergologist specializing in urticaria, drug allergies, and angioedema, Professor Luis FC Ensina has significantly advanced clinical care, research, and education. As a Professor at the Federal University of SĂŁo Paulo and coordinator of its specialized outpatient clinic, he leads Alergoalpha, a Center of Excellence for UCARE, ACARE, and ADCARE, where he has overseen over 20 clinical trials and authored more than 100 publications. A founder of the Brazilian Urticaria Network (RUBRA) and co-author of international urticaria guidelines, he has played a pivotal role in shaping global standards for allergy care. Active in organizations such as GA2LEN, AAAAI, and EAACI, he highlights the transformative potential of emerging therapies, gene therapy, and artificial intelligence to redefine allergy and immunology practice worldwide.
Multidisciplinary experts discuss the diagnosis and management of patients with systemic mastocytosis.
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