Childhood asthma: Novel endotyping by cytokines, validated through sensitization profiles and clinical characteristics

• Published in: Clinical and experimental allergy 2021-05, Vol.51 (5), p.654-665
• Main Authors: Salvermoser, Michael, Zeber, Kathrin, Boeck, Andreas, Klucker, Elisabeth, Schaub, Bianca
• Format: Article
• Language: English
• Subjects: Allergens; Animals; Antigens, Dermatophagoides - immunology; Asthma; Asthma - classification; Asthma - immunology; Asthma - physiopathology; Betula - immunology; Cats; Child; Childhood; childhood allergy; childhood asthma; Children; cytokine; Cytokines; Cytokines - immunology; Dander - immunology; Dogs; endotypes; Female; Food allergies; Food Hypersensitivity - immunology; Forced Expiratory Volume; Humans; Immunoglobulin E; Immunoglobulin E - immunology; Immunology; Interferon; Interferon-gamma - immunology; Interleukin-17 - immunology; Interleukin-5 - immunology; Lung - physiopathology; Lymphocytes T; Male; Malus - immunology; Phenotype; Phenotypes; Phleum - immunology; Reproducibility of Results; Respiratory function; Respiratory Hypersensitivity - immunology; Respiratory Hypersensitivity - physiopathology; sensitization; Th2 Cells - immunology; unsupervised learning; validation; Vital Capacity
• ISSN: 0954-7894; 1365-2222
• DOI: 10.1111/cea.13858

Background Specific allergy sensitization pattern, using “component‐resolved diagnosis” (CRD), is a central component of allergy and asthma in childhood. Besides this, allergic asthma has been characterized by a Th2‐shifted endotype with elevation of classical Th2 cytokines. Recently, other endotypes with distinct mechanisms focusing on cytokine regulation evolved, yet those pathways are still not well understood. Objective (a) To define reproducible immunological endotypes using cytokine expression in an asthma cohort and (b) to characterize their sensitization profile and clinical phenotype. Methods Supernatants from PBMCs of 234 children (median age 10 years) of an asthma cohort were analysed for cytokine expressions. The children were split into a training (n = 49) and validation (n = 185) group. The training group was used to identify immunological endotypes by clustering cytokine expressions, which were then assessed regarding clinical characteristics and specific IgE of recombinant allergen components. Next, our findings were validated in the validation group. Results We identified novel endotypes based on primarily unstimulated cytokine expression. One endotype showed an IFN‐γ/Interleukin (IL)‐17/IL‐5 predominance, a different sensitization pattern (high in birch/apple; p