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      Serum calprotectin (S100A8/A9): a promising biomarker in diagnosis and follow-up in different subgroups of juvenile idiopathic arthritis

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          Abstract

          Introduction

          In the management of juvenile idiopathic arthritis (JIA), there is a lack of diagnostic and prognostic biomarkers. This study assesses the use of serum calprotectin (sCal) as a marker to monitor disease activity, and as a classification and prognosis tool of response to treatment or risk of flares in patients with JIA.

          Methods

          Eighty-one patients with JIA from the CAP48 multicentric cohort were included in this study, as well as 11 non-paediatric healthy controls. An ELISA method was used to quantify sCal with a commercial kit.

          Results

          Patients with an active disease compared with healthy controls and with patients with inactive disease showed an eightfold and a twofold increased level of sCal, respectively. sCal was found to be correlated with the C-reactive protein (CRP) and even more strongly with the erythrocyte sedimentation rate. Evolution of DAS28 scores correlated well with evolution of sCal, as opposed to evolution of CRP. With regard to CRP, sCal could differentiate forms with active oligoarthritis from polyarthritis and systemic forms. However, sCal brought an added value compared with the CRP as a prognosis marker. Indeed, patients with active disease and reaching minimal disease activity (according to Juvenile Arthritis Disease Activity Score) at 6 months following the test had higher sCal levels, while patients with inactive disease had higher sCal levels if a flare was observed up to 3–9 months following the test.

          Conclusions

          This study confirms the potential uses of sCal as a biomarker in the diagnosis and follow-up of JIA.

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          Most cited references39

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          International League of Associations for Rheumatology classification of juvenile idiopathic arthritis: second revision, Edmonton, 2001.

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            Elevated calprotectin and abnormal myeloid cell subsets discriminate severe from mild COVID-19

            Summary Blood myeloid cells are known to be dysregulated in the coronavirus disease 2019 (COVID-19) caused by SARS-CoV-2. It is unknown whether the innate myeloid response differs with disease severity, and whether markers of innate immunity discriminate high risk patients. Thus, we performed high dimensional flow cytometry and single cell RNA sequencing of COVID-19 patient peripheral blood cells and detected the disappearance of non-classical CD14LowCD16High monocytes, the accumulation of HLA-DRLow classical monocytes, and the release of massive amounts of calprotectin (S100A8/S100A9) in severe cases. Immature CD10LowCD101-CXCR4+/- neutrophils with an immuno-suppressive profile accumulated as well in blood and lungs, suggesting emergency myelopoiesis. We finally showed that calprotectin plasma level and a routine flow cytometry assay detecting decreased frequencies of non-classical monocytes could discriminate patients who develop a severe COVID-19 form, suggesting a predictive value that deserves prospective evaluation.
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              Juvenile idiopathic arthritis.

              Juvenile idiopathic arthritis is a broad term that describes a clinically heterogeneous group of arthritides of unknown cause, which begin before 16 years of age. This term encompasses several disease categories, each of which has distinct methods of presentation, clinical signs, and symptoms, and, in some cases, genetic background. The cause of disease is still poorly understood but seems to be related to both genetic and environmental factors, which result in the heterogeneity of the illness. Although none of the available drugs has a curative potential, prognosis has greatly improved as a result of substantial progresses in disease management. The most important new development has been the introduction of drugs such as anticytokine agents, which constitute a valuable treatment option for patients who are resistant to conventional antirheumatic agents. Further insights into the disease pathogenesis and treatment will be provided by the continuous advances in understanding of the mechanisms connected to the immune response and inflammatory process, and by the development of new drugs that are able to inhibit selectively single molecules or pathways.
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                Author and article information

                Journal
                RMD Open
                RMD Open
                rmdopen
                rmdopen
                RMD Open
                BMJ Publishing Group (BMA House, Tavistock Square, London, WC1H 9JR )
                2056-5933
                2021
                9 June 2021
                : 7
                : 2
                : e001646
                Affiliations
                [1 ]departmentDepartment of Rheumatology , CHU Brugmann , Bruxelles, Belgium
                [2 ]departmentDepartment of Pediatric Rheumatology , Hôpital Universitaire des Enfants Reine Fabiola , Bruxelles, Belgium
                [3 ]departmentDepartment of Rheumatology , Hôpital Erasme , Bruxelles, Belgium
                [4 ]departmentLaboratory of Bone and Metabolic Biochemistry , Université Libre de Bruxelles , Bruxelles, Belgium
                [5 ]departmentDepartment of Rheumatology , Cliniques universitaires Saint-Luc , Bruxelles, Belgium
                [6 ]departmentInstitut de Recherche expérimentale et Clinique (IREC) , Université catholique de Louvain Secteur des sciences de la santé , Bruxelles, Belgium
                Author notes
                [Correspondence to ] Dr Céline La; celine.la@ 123456ulb.be
                Author information
                http://orcid.org/0000-0002-6065-2970
                http://orcid.org/0000-0002-7156-2356
                Article
                rmdopen-2021-001646
                10.1136/rmdopen-2021-001646
                8191626
                34108235
                718edeca-0b37-4ef5-9161-19d282b8057e
                © Author(s) (or their employer(s)) 2021. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

                This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See:  http://creativecommons.org/licenses/by-nc/4.0/.

                History
                : 26 February 2021
                : 17 May 2021
                Funding
                Funded by: Radio-Télévision belge de la Communauté française (RTBF);
                Award ID: CAP48 program
                Categories
                Paediatric Rheumatology
                1506
                Original research
                Custom metadata
                unlocked

                juvenile idiopathic arthritis,inflammation,outcome assessment,health care

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