Author: Pape, Constantin; Remme, Roman; Wolny, Adrian; Olberg, Sylvia; Wolf, Steffen; Cerrone, Lorenzo; Cortese, Mirko; Klaus, Severina; Lucic, Bojana; Ullrich, Stephanie; Andersâ€Ã–sswein, Maria; Wolf, Stefanie; Cerikan, Berati; Neufeldt, Christopher J.; Ganter, Markus; Schnitzler, Paul; Merle, Uta; Lusic, Marina; Boulant, Steeve; Stanifer, Megan; Bartenschlager, Ralf; Hamprecht, Fred A.; Kreshuk, Anna; Tischer, Christian; Kräusslich, Hansâ€Georg; Müller, Barbara; Laketa, Vibor
                    Title: Microscopyâ€based assay for semiâ€quantitative detection of SARSâ€CoVâ€2 specific antibodies in human sera: A semiâ€quantitative, high throughput, microscopyâ€based assay expands existing approaches to measure SARSâ€CoVâ€2 specific antibody levels in human sera  Cord-id: jwe2csvh  Document date: 2020_12_30
                    ID: jwe2csvh
                    
                    Snippet: Emergence of the novel pathogenic coronavirus SARSâ€CoVâ€2 and its rapid pandemic spread presents challenges that demand immediate attention. Here, we describe the development of a semiâ€quantitative highâ€content microscopyâ€based assay for detection of three major classes (IgG, IgA, and IgM) of SARSâ€CoVâ€2 specific antibodies in human samples. The possibility to detect antibodies against the entire viral proteome together with a robust semiâ€automated image analysis workflow resulted 
                    
                    
                    
                     
                    
                    
                    
                    
                        
                            
                                Document: Emergence of the novel pathogenic coronavirus SARSâ€CoVâ€2 and its rapid pandemic spread presents challenges that demand immediate attention. Here, we describe the development of a semiâ€quantitative highâ€content microscopyâ€based assay for detection of three major classes (IgG, IgA, and IgM) of SARSâ€CoVâ€2 specific antibodies in human samples. The possibility to detect antibodies against the entire viral proteome together with a robust semiâ€automated image analysis workflow resulted in specific, sensitive and unbiased assay that complements the portfolio of SARSâ€CoVâ€2 serological assays. Sensitive, specific and quantitative serological assays are urgently needed for a better understanding of humoral immune response against the virus as a basis for developing public health strategies to control viral spread. The procedure described here has been used for clinical studies and provides a general framework for the application of quantitative highâ€throughput microscopy to rapidly develop serological assays for emerging virus infections.
 
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