Interleukin-18 Is a Potential Biomarker to Discriminate Active Adult-Onset Still’s Disease From COVID-19
BackgroundHyperinflammation with dysregulated production of galectins and cytokines may develop in COVID-19 or adult-onset Still’s disease (AOSD). Given the similar clinical features in both diseases, it is necessary to identify biomarkers that can differentiate COVID-19 from AOSD. However, the rela...
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doaj-f30916835a134af6901e500eea779db82021-07-23T12:55:10ZengFrontiers Media S.A.Frontiers in Immunology1664-32242021-07-011210.3389/fimmu.2021.719544719544Interleukin-18 Is a Potential Biomarker to Discriminate Active Adult-Onset Still’s Disease From COVID-19Po-Ku Chen0Po-Ku Chen1Po-Ku Chen2Joung-Liang Lan3Joung-Liang Lan4Joung-Liang Lan5Po-Hao Huang6Po-Hao Huang7Jye-Lin Hsu8Jye-Lin Hsu9Ching-Kun Chang10Ching-Kun Chang11Ni Tien12Hui-Ju Lin13Der-Yuan Chen14Der-Yuan Chen15Der-Yuan Chen16Der-Yuan Chen17Rheumatology and Immunology Center, China Medical University Hospital, Taichung, TaiwanCollege of Medicine, China Medical University, Taichung, TaiwanTranslational Medicine Laboratory, China Medical University Hospital, Taichung, TaiwanRheumatology and Immunology Center, China Medical University Hospital, Taichung, TaiwanCollege of Medicine, China Medical University, Taichung, TaiwanRheumatic Diseases Research Center, China Medical University Hospital, Taichung, TaiwanRheumatology and Immunology Center, China Medical University Hospital, Taichung, TaiwanCollege of Medicine, China Medical University, Taichung, TaiwanCollege of Medicine, China Medical University, Taichung, TaiwanGraduate Institute of Biomedical Sciences, China Medical University, Taichung, TaiwanRheumatology and Immunology Center, China Medical University Hospital, Taichung, TaiwanCollege of Medicine, China Medical University, Taichung, TaiwanDepartment of Laboratory Medicine, China Medical University Hospital, Taichung, TaiwanDepartment of Laboratory Medicine, China Medical University Hospital, Taichung, TaiwanRheumatology and Immunology Center, China Medical University Hospital, Taichung, TaiwanCollege of Medicine, China Medical University, Taichung, TaiwanTranslational Medicine Laboratory, China Medical University Hospital, Taichung, TaiwanPh.D. Program in Translational Medicine and Rong Hsing Research Center for Translational Medicine, National Chung Hsing University, Taichung, TaiwanBackgroundHyperinflammation with dysregulated production of galectins and cytokines may develop in COVID-19 or adult-onset Still’s disease (AOSD). Given the similar clinical features in both diseases, it is necessary to identify biomarkers that can differentiate COVID-19 from AOSD. However, the related data remain scarce currently.MethodsIn this cross-sectional study, plasma levels of galectin-3, galectin-9, and soluble TIM-3 (sTIM-3) were determined by ELISA in 55 COVID-19 patients (31 non-severe and 24 severe), 23 active AOSD patients, and 31 healthy controls (HC). The seropositivity for SARS-CoV-2 was examined using an immunochromatographic assay, and cytokine profiles were determined with the MULTIPLEX platform.ResultsSignificantly higher levels of galectin-3, galectin-9, IL-1β, IL-1Ra, IL-10, IFN-α2, IL-6, IL-18, and TNF-α were observed in severe COVID-19 and active AOSD patients compared with HC (all p<0.001). AOSD, but not COVID-19, showed significantly higher IFN-γ and IL-17A compared with HC (both p<0.01). Moreover, active AOSD patients had 68-fold higher IL-18 levels and 5-fold higher ferritin levels than severe COVID-19 patients (both p<0.001). IL-18 levels at the cut-off value 190.5pg/mL had the highest discriminative power for active AOSD and severe COVID-19, with AUC 0.948, sensitivity 91.3%, specificity 95.8%, and accuracy of 91.5% (p<0.005). Multivariate regression analysis revealed IL-18 as a significant predictor of active AOSD (p<0.05).ConclusionActive AOSD patients share features of hyperinflammation and cytokine storm with severe COVID-19 patients but possess a distinct cytokine profile, including elevated IL-18, IL-6, IFN-γ, and IL-17A. IL-18 is a potential discriminator between AOSD and COVID-19 and may significantly predict active AOSD.https://www.frontiersin.org/articles/10.3389/fimmu.2021.719544/fullgalectinscytokine profileferritinCOVID-19adult-onset Still’s disease (AOSD) |
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language |
English |
format |
Article |
sources |
DOAJ |
author |
Po-Ku Chen Po-Ku Chen Po-Ku Chen Joung-Liang Lan Joung-Liang Lan Joung-Liang Lan Po-Hao Huang Po-Hao Huang Jye-Lin Hsu Jye-Lin Hsu Ching-Kun Chang Ching-Kun Chang Ni Tien Hui-Ju Lin Der-Yuan Chen Der-Yuan Chen Der-Yuan Chen Der-Yuan Chen |
spellingShingle |
Po-Ku Chen Po-Ku Chen Po-Ku Chen Joung-Liang Lan Joung-Liang Lan Joung-Liang Lan Po-Hao Huang Po-Hao Huang Jye-Lin Hsu Jye-Lin Hsu Ching-Kun Chang Ching-Kun Chang Ni Tien Hui-Ju Lin Der-Yuan Chen Der-Yuan Chen Der-Yuan Chen Der-Yuan Chen Interleukin-18 Is a Potential Biomarker to Discriminate Active Adult-Onset Still’s Disease From COVID-19 Frontiers in Immunology galectins cytokine profile ferritin COVID-19 adult-onset Still’s disease (AOSD) |
author_facet |
Po-Ku Chen Po-Ku Chen Po-Ku Chen Joung-Liang Lan Joung-Liang Lan Joung-Liang Lan Po-Hao Huang Po-Hao Huang Jye-Lin Hsu Jye-Lin Hsu Ching-Kun Chang Ching-Kun Chang Ni Tien Hui-Ju Lin Der-Yuan Chen Der-Yuan Chen Der-Yuan Chen Der-Yuan Chen |
author_sort |
Po-Ku Chen |
title |
Interleukin-18 Is a Potential Biomarker to Discriminate Active Adult-Onset Still’s Disease From COVID-19 |
title_short |
Interleukin-18 Is a Potential Biomarker to Discriminate Active Adult-Onset Still’s Disease From COVID-19 |
title_full |
Interleukin-18 Is a Potential Biomarker to Discriminate Active Adult-Onset Still’s Disease From COVID-19 |
title_fullStr |
Interleukin-18 Is a Potential Biomarker to Discriminate Active Adult-Onset Still’s Disease From COVID-19 |
title_full_unstemmed |
Interleukin-18 Is a Potential Biomarker to Discriminate Active Adult-Onset Still’s Disease From COVID-19 |
title_sort |
interleukin-18 is a potential biomarker to discriminate active adult-onset still’s disease from covid-19 |
publisher |
Frontiers Media S.A. |
series |
Frontiers in Immunology |
issn |
1664-3224 |
publishDate |
2021-07-01 |
description |
BackgroundHyperinflammation with dysregulated production of galectins and cytokines may develop in COVID-19 or adult-onset Still’s disease (AOSD). Given the similar clinical features in both diseases, it is necessary to identify biomarkers that can differentiate COVID-19 from AOSD. However, the related data remain scarce currently.MethodsIn this cross-sectional study, plasma levels of galectin-3, galectin-9, and soluble TIM-3 (sTIM-3) were determined by ELISA in 55 COVID-19 patients (31 non-severe and 24 severe), 23 active AOSD patients, and 31 healthy controls (HC). The seropositivity for SARS-CoV-2 was examined using an immunochromatographic assay, and cytokine profiles were determined with the MULTIPLEX platform.ResultsSignificantly higher levels of galectin-3, galectin-9, IL-1β, IL-1Ra, IL-10, IFN-α2, IL-6, IL-18, and TNF-α were observed in severe COVID-19 and active AOSD patients compared with HC (all p<0.001). AOSD, but not COVID-19, showed significantly higher IFN-γ and IL-17A compared with HC (both p<0.01). Moreover, active AOSD patients had 68-fold higher IL-18 levels and 5-fold higher ferritin levels than severe COVID-19 patients (both p<0.001). IL-18 levels at the cut-off value 190.5pg/mL had the highest discriminative power for active AOSD and severe COVID-19, with AUC 0.948, sensitivity 91.3%, specificity 95.8%, and accuracy of 91.5% (p<0.005). Multivariate regression analysis revealed IL-18 as a significant predictor of active AOSD (p<0.05).ConclusionActive AOSD patients share features of hyperinflammation and cytokine storm with severe COVID-19 patients but possess a distinct cytokine profile, including elevated IL-18, IL-6, IFN-γ, and IL-17A. IL-18 is a potential discriminator between AOSD and COVID-19 and may significantly predict active AOSD. |
topic |
galectins cytokine profile ferritin COVID-19 adult-onset Still’s disease (AOSD) |
url |
https://www.frontiersin.org/articles/10.3389/fimmu.2021.719544/full |
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