Characterization of a major house dust mite allergen Der p 22 among Malaysian adult population
Year: 2025
Type: article
Study design: Observational Study
Abstract: Background: House dust mites (HDM) are a major trigger factor of allergic diseases worldwide. Objective: among Malaysian atopic adults. Methods: and purified. Specific IgE levels to group 22 allergens were measured in serum samples from a combined cohort of Malaysian adults (n = 176) and participants from the SMCGES sub-cohort (n = 755), with responses classified by ImmunoCAP classes. Age- and gender-adjusted multivariate logistic regression was used to assess associations between Class 3+ group 22-specific IgE responses (>3.5 IU/mL) and clinical diagnoses of asthma, allergic rhinitis (AR), and atopic dermatitis (AD). IgE inhibition assays were performed to evaluate the presence of unique epitopes in Der p 22 relative to its homologue Der p 2. Epitope mapping was performed using 33 single-alanine substitution mutants of Der p 22. Statistical analyses were carried out using GraphPad Prism and logistic regression models. Results: Recombinant Der p 22 was expressed and purified as a 17.2 kDa protein. Among 149 atopic Malaysian adults, 54% had detectable sIgE to Der p 22. IgE inhibition assays demonstrated partial cross-reactivity between Der p 22 and Der p 2. High-level group 22-specific IgE responses (Class 3+) were associated with an increased risk of asthma (OR = 1.73, 95% CI = 0.98-3.00, p = 0.0524) and significantly associated with the presence of atopic comorbidities including AR and AD (all p < 0.05). Epitope mapping identified to 6 critical residues, K10, H35, R43, D106, R117 and R130, where alanine substitution led to a marked reduction in IgE binding (median reduction >95%). Conclusion: Der p 22 is a clinically relevant HDM allergen in the Malaysian adult population. It harbours both unique and shared IgE epitopes with Der p 2, highlighting its value for inclusion in molecular diagnostic panels to improve allergen sensitization profiling. Alanine mutation to 6 amino acid residues of Der p 22 significantly reduced IgE binding, suggesting its potential as a candidate hypoallergen molecule in allergen-specific immunotherapy.
Institutions: Sunway University, National University of Singapore
Language: English
Subfield: Immunology and Allergy
Field: Medicine
Domain: Health Sciences
Open Access status: gold
Estimated APC paid: $3,508
Funders: Singapore Food Agency, National Research Foundation, Agency for Science, Technology and Research, Ministry of Health -Singapore, National University of Singapore, National Research Foundation Singapore, Economic Development Board - Singapore, Ministry of Education - Singapore, Ministry of Higher Education, Malaysia, National Medical Research Council, Sunway University, Biomedical Research Council, Singapore Immunology Network
Awards: G1039587875, G1300787965, G1334985092, G1428925201, G1788000084, G1882880913, G1915093512, G1974073535, G1991588944, G2064790790, G3150745450, G3263134948, G3510775757, G3529637569, G3635921226, G386625895, G4082020776, G4674587860, G471023165, G5782863272, G5787215903, G6205900255, G627303337, G6520984640, G6931770012, G7365156025, G8040322890, G815687687, G8576646137, G8649121184, G912430096, G921128766
OpenAlex ID: W4414444442
