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Pilot-Scale Study Of Human Plasma Proteomics Identifies ApoE And IL33 As Markers In Atopic Asthma
Moumita Bhowmik1, Sreyashi Majumdar2, Angira Dasgupta3
1Division of Plant Biology, Bose Institute, Kolkata, West Bengal, India.
Journal of Asthma and Allergy
|October 2, 2019
Summary
Researchers identified potential biomarkers for atopic asthma. Apolipoprotein E (ApoE) was downregulated, while Interleukin 33 (IL33) was upregulated in atopic asthma patients, suggesting a new diagnostic approach.
Area of Science:
- * Respiratory Medicine
- * Immunology
- * Proteomics
Background:
- * Atopic asthma presents complex pathobiology with symptoms overlapping other respiratory conditions.
- * Identifying specific biomarkers is crucial for accurate diagnosis and effective management of atopic asthma.
Purpose of the Study:
- * To investigate plasma proteome and cytokine expression changes in atopic asthma.
- * To identify potential protein biomarkers for atopic asthma diagnosis and explore underlying aberrant pathways.
Main Methods:
- * Pilot study involving 5 healthy controls and 5 treatment-naïve atopic asthma patients.
- * Quantitative label-free liquid chromatography-tandem mass spectrometry proteomics.
- * Enzyme-Linked Immunosorbent Assay (ELISA) and immunoblotting for protein validation.
Main Results:
- * Apolipoprotein E (ApoE) significantly downregulated in atopic asthma patients (50.74% decrease).
- * Interleukin 33 (IL33) significantly upregulated in atopic asthma patients (3.84-fold increase).
- * ApoE levels were also lower in atopic asthma compared to COPD patients (36.33% decrease).
Conclusions:
- * Downregulation of ApoE and upregulation of IL33 are characteristic of atopic asthma.
- * These protein expression profiles differentiate atopic asthma from healthy controls and COPD.
- * ApoE and IL33 show promise as a two-protein classifier for prognostic biomarker development in atopic asthma.

