Year: 2024
Type: article
Study design: Observational Study
Abstract: BACKGROUND: Allergen-specific immunotherapy (AIT) is a disease-modifying therapy and is effective to reduce the symptoms of grass pollen-allergy. The airway epithelium of these patients releases inflammatory mediators including type-2 cytokines, which are associated with cellular processes involved in the symptomatic response of the affected tissue. Aim of the study was to identify epithelial biomarkers indicating AIT progress. METHODS: In an exploratory, observational allergy cohort, we longitudinally phenotyped 56 grass pollen-allergic patients undergoing AIT for over three years and 18 controls using nasal secretions at critical time windows during therapy to assess peak-season responses along the course of therapy. Type-2 cytokine protein levels were analyzed using the high-sensitivity multiplex electrochemiluminescence mesoscale technique. RESULTS: The type-2 cytokines CCL26 and POSTN oscillated seasonally, in contrast to TSLP and IL-33. However, only POSTN was reduced over the three-year AIT progression. In addition to POSTN, IL-24 and IL-37 levels were continuously reduced during AIT, while IFN-g and CCL27 were increased. Compared to healthy individuals, AIT did not restore healthy secretion levels but rather induced a novel homeostasis CONCLUSION: Nasal secretions trace the epithelial response during different phases of AIT. We demonstrate that AIT only partially controls the epithelial type 2 cytokine CCL26, which also adapts to seasonal changes, while POSTN and IL-24 are potential indicators of therapy success. Therefore, nasal secretions represent a promising, non-invasive tool for monitoring seasonal progress of AIT.
Source: Rhinology Journal
DOI: 10.4193/rhin24.038
Authors: C A Jakwerth, U M Zissler, M Oelsner, L Pechtold, L zur Bonsen, M Plaschke, J Kau, M Davidovic, M Mootz, B Haller, A M Chaker, C B Schmidt-Weber
Language: English
Subfield: Immunology and Allergy
Field: Medicine
Domain: Health Sciences
Open Access status: bronze
Awards: G1401711827, Divergente E1 und E2 Epithelzelldifferenzierung und damit assoziierte regulatorische Mechanismen der IL20 Superfamilie, ESCAPE - Angriffspunkte der Invasionsstrategie von SARS-CoV-2 in bronchialen Epithelzellen - Teilvorhaben A, Technische Universität München, Mechanismen der epithelialen Virusantwort
OpenAlex ID: W4405296786
