Targeted Proteomics Reveals Inflammatory Pathways that Classify Immune Dysregulation in Common Variable Immunodeficiency

التفاصيل البيبلوغرافية
العنوان: Targeted Proteomics Reveals Inflammatory Pathways that Classify Immune Dysregulation in Common Variable Immunodeficiency
المؤلفون: Joris M. van Montfrans, Baerbel Keller, Pauline M. Ellerbroek, Annick A. J. M. van de Ven, Julia Drylewicz, Stefan Nierkens, Klaus Warnatz, P. Martin van Hagen, Jaap M van Laar, Roos-Marijn Berbers, Helen L. Leavis, Virgil A. S. H. Dalm
المساهمون: Immunology, Internal Medicine
المصدر: Journal of Clinical Immunology, 41(2), 362-373. Springer New York
Journal of Clinical Immunology
Journal of Clinical Immunology, 41. SPRINGER/PLENUM PUBLISHERS
بيانات النشر: SPRINGER/PLENUM PUBLISHERS, 2021.
سنة النشر: 2021
مصطلحات موضوعية: Adult, Male, Proteomics, Chemokine, LAG3, DISORDERS, medicine.medical_treatment, Common variable immunodeficiency (CVID), Immunology, PROTEIN, chemical and pharmacologic phenomena, INTERSTITIAL LUNG-DISEASE, medicine.disease_cause, Autoimmunity, Cohort Studies, ACTIVATION, Immune system, MARKERS, LAG-3, Immunology and Allergy, Medicine, Humans, Inflammation, Primary immunodeficiency, biology, RECEPTOR, business.industry, Common variable immunodeficiency, Immune dysregulation, Middle Aged, Th1 Cells, medicine.disease, DEFICIENCY, Cytokine, Common Variable Immunodeficiency, biology.protein, T-CELLS, Th17 Cells, Cytokines, Original Article, Female, Chemokines, business, Prediction, Biomarkers, Signal Transduction
الوصف: Patients with common variable immunodeficiency (CVID) can develop immune dysregulation complications such as autoimmunity, lymphoproliferation, enteritis, and malignancy, which cause significant morbidity and mortality. We aimed to (i) assess the potential of serum proteomics in stratifying patients with immune dysregulation using two independent cohorts and (ii) identify cytokine and chemokine signaling pathways that underlie immune dysregulation in CVID. A panel of 180 markers was measured in two multicenter CVID cohorts using Olink Protein Extension Assay technology. A classification algorithm was trained to distinguish CVID with immune dysregulation (CVIDid, n = 14) from CVID with infections only (CVIDio, n = 16) in the training cohort, and validated on a second testing cohort (CVIDid n = 23, CVIDio n = 24). Differential expression in both cohorts was used to determine relevant signaling pathways. An elastic net classifier using MILR1, LILRB4, IL10, IL12RB1, and CD83 could discriminate between CVIDid and CVIDio patients with a sensitivity of 0.83, specificity of 0.75, and area under the curve of 0.73 in an independent testing cohort. Activated pathways (fold change > 1.5, FDR-adjusted p
وصف الملف: application/pdf
اللغة: English
تدمد: 0271-9142
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::19d3ecb85b241cd84dc58061789872d9Test
https://research.rug.nl/en/publications/bd83922a-fae5-44ec-8649-fb3ce7e70a5fTest
حقوق: OPEN
رقم الانضمام: edsair.doi.dedup.....19d3ecb85b241cd84dc58061789872d9
قاعدة البيانات: OpenAIRE