30-Second Takeaway
- Allergic sensitisation is often dynamic across the life course, not always fixed.
- Cough severity predicts poor asthma control independently of airflow or inflammation.
- Current evidence does not support routine allergen immunotherapy for eosinophilic esophagitis.
Week ending June 20, 2026
Selected recent evidence for allergy/immunology practice — sensitisation dynamics, cough in asthma, AIT for EoE, arthropod allergy, and irAE research trends
Allergic sensitisation is dynamic across ages in a 5,046-person Austrian cohort
In 5,046 participants with three skin-prick test visits over a mean 4.25 years, 54.4% remained non‑sensitised and 30.6% remained sensitised. Resolution occurred in 5.6%, new onset in 4.8%, and fluctuation in 4.6% of participants. New sensitisation clustered to outdoor allergens and occurred into adulthood, while fluctuation related to seasonal pollens, environmental exposures, and adult adiposity. Stable sensitisation associated with parental allergy and blood eosinophils; cumulative smoking modestly reduced stability.
Cough-predominant phenotypes common and linked to poor control in 20,683 Chinese hospital asthma patients
Among 20,683 outpatients, 22.8% had uncontrolled and 39.5% had partially controlled asthma; cough was present in 80.0%. Cough-dominant and cough-variant phenotypes were common (14.6% and 11.4%, respectively). Cough severity independently predicted poor control, with stronger associations in patients using inhaled corticosteroids. Only 21.4% had used ICS in the prior year despite high exacerbation and hospitalization rates.
Systematic review finds insufficient evidence to support allergen immunotherapy for eosinophilic esophagitis
EAACI review identified four studies evaluating AIT in EoE, mainly pediatric milk EPIT from the SMILEE program. The randomized EPIT trial did not show a significant difference in tissue eosinophilia versus placebo, though 47% of treated patients tolerated milk without recurrence in follow-up. Open‑label and mechanistic data suggested immunologic changes but clinical benefit was inconsistent and not definitive. SCIT evidence was limited and retrospective, producing inconclusive results.
References
Numbered in order of appearance. Click any reference to view details.
Additional Reads
Optional additional studies from this edition.