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      Multiplexed High-Throughput Serological Assay for Human Enteroviruses

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          Abstract

          Immunological assays detecting antibodies against enteroviruses typically use a single enterovirus serotype as antigen. This limits the ability of such assays to detect antibodies against different enterovirus types and to detect possible type-specific variation in antibody responses. We set out to develop a multiplexed assay for simultaneous detection of antibodies against multiple enterovirus and rhinovirus types encompassing all human infecting species. Seven recombinant VP1 proteins from enteroviruses EV-A to EV-D and rhinoviruses RV-A to RV-C species were produced. Using Meso Scale Diagnostics U-PLEX platform we were able to study antibody reactions against these proteins as well as non-structural enterovirus proteins in a single well with 140 human serum samples. Adults had on average 33-fold stronger antibody responses to these antigens ( p < 10 −11) compared to children, but children had less cross-reactivity between different enterovirus types. The results suggest that this new high-throughput assay offers clear benefits in the evaluation of humoral enterovirus immunity in children, giving more exact information than assays that are based on a single enterovirus type as antigen.

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          Most cited references35

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          Pancreatic cancer in chronic pancreatitis; aetiology, incidence, and early detection.

          Acute pancreatitis, chronic pancreatitis and pancreatic cancer are responsible for most of the burden of exocrine pancreatic disease. Glandular damage from recurrent bouts of acute pancreatitis can lead to irreversible changes characteristic of chronic pancreatitis. In recent decades accumulating evidence has defined longstanding pre-existing chronic pancreatitis as a strong risk factor for pancreatic cancer. The lag period between diagnosis of chronic pancreatitis and pancreatic cancer is usually one or two decades: pancreatitis appearing a year or two before the diagnosis of pancreatic cancer is often the result of tumour-related ductal obstruction. The risk of developing pancreatic cancer appears to be highest in rare types of pancreatitis with an early onset, such as hereditary pancreatitis and tropical pancreatitis. Even though there is a strong link between chronic pancreatitis and pancreatic cancer, over a 20 year period only around five percent of patients with chronic pancreatitis will develop pancreatic cancer. Until the development of more sophisticated screening procedures, screening is not recommended for patients with chronic pancreatitis. 2010 Elsevier Ltd. All rights reserved.
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            On the doctrine of original antigenic sin

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              Isolation of a virus from the pancreas of a child with diabetic ketoacidosis.

              A healthy 10-year-old boy was admitted to the hospital in diabetic ketoacidosis within three days of onset of symptoms of a flu-like illness. He died seven days later and post-mortem examination showed lymphocytic infiltration of the islets of Langerhans and necrosis of beta cells. Inoculation of mouse, monkey and human cell cultures with homogenates from the patient's pancreas led to isolation of a virus. Serologic studies revealed a rise in the titer of neutralizing antibody to this virus from less than 4 on the second hospital day to 32 on the day of death. Neutralization data showed that the virus was related to a diabetogenic variant derived from Coxsackievirus B4. Inoculation of mice with the human isolate produced hyperglycemia, inflammatory cells in the islets of Langerhans and beta-cell necrosis. Staining of mouse pancreatic sections with fluorescein-labeled antiviral antibody revealed viral antigens in beta cells. Both the clinical picture and animal studies suggested that the patient's diabetes was virus induced.
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                Author and article information

                Journal
                Microorganisms
                Microorganisms
                microorganisms
                Microorganisms
                MDPI
                2076-2607
                26 June 2020
                June 2020
                : 8
                : 6
                : 963
                Affiliations
                [1 ]Faculty of Medicine and Health Technology, Tampere University, 33520 Tampere, Finland; niila.saarinen@ 123456tuni.fi (N.V.V.S.); jussi.lehtonen@ 123456tuni.fi (J.L.); heikki.hyoty@ 123456tuni.fi (H.H.); olli.laitinen@ 123456tuni.fi (O.H.L.)
                [2 ]Department of Paediatrics, University of Oulu, 90570 Oulu, Finland; riitta.veijola@ 123456oulu.fi
                [3 ]Department of Paediatrics, University of Turku, 20520 Turku, Finland; johanna.lempainen@ 123456utu.fi
                [4 ]Pediatric Research Center, Children’s Hospital, University of Helsinki and Helsinki University Hospital, 00029 Helsinki, Finland; mikael.knip@ 123456helsinki.fi
                [5 ]Research Program for Clinical and Molecular Metabolism, Faculty of Medicine, University of Helsinki, 00029 Helsinki, Finland
                [6 ]Fimlab Laboratories, 33520 Tampere, Finland
                Author notes
                [* ]Correspondence: vesa.hytonen@ 123456tuni.fi ; Tel.: +358-401901517
                Author information
                https://orcid.org/0000-0001-5029-974X
                https://orcid.org/0000-0003-0474-0033
                https://orcid.org/0000-0002-3751-9952
                https://orcid.org/0000-0002-9357-1480
                Article
                microorganisms-08-00963
                10.3390/microorganisms8060963
                7355947
                32604930
                07b47b4a-3908-429f-9c3e-906d4e7c6c9b
                © 2020 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 08 June 2020
                : 24 June 2020
                Categories
                Article

                enterovirus,rhinovirus,multiplex immunoassay
                enterovirus, rhinovirus, multiplex immunoassay

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