{"title":"用于检测SARS-CoV-2中和抗体的快速减焦中和试验方法的建立","authors":"Abigail Vanderheiden, Venkata Viswanadh Edara, Katharine Floyd, Robert C. Kauffman, Grace Mantus, Evan Anderson, Nadine Rouphael, Sri Edupuganti, Pei-Yong Shi, Vineet D. Menachery, Jens Wrammert, Mehul S. Suthar","doi":"10.1002/cpim.116","DOIUrl":null,"url":null,"abstract":"SARS‐CoV‐2 is a recently emerged human coronavirus that has escalated to a pandemic. There are currently no approved vaccines for SARS‐CoV‐2, which causes severe respiratory illness or death. Defining the antibody response to SARS‐CoV‐2 will be essential for understanding disease progression, long‐term immunity, and vaccine efficacy. Here we describe two methods for evaluating the neutralization capacity of SARS‐CoV‐2 antibodies. The basic protocol is a focus reduction neutralization test (FRNT), which involves immunostaining infected cells with a chromogen deposit readout. The alternate protocol is a modification of the FRNT that uses an infectious clone−derived SARS‐CoV‐2 virus expressing a fluorescent reporter. These protocols are adapted for use in a high‐throughput setting, and are compatible with large‐scale vaccine studies or clinical testing. © 2020 Wiley Periodicals LLC","PeriodicalId":10733,"journal":{"name":"Current Protocols in Immunology","volume":"131 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2020-11-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/cpim.116","citationCount":"101","resultStr":"{\"title\":\"Development of a Rapid Focus Reduction Neutralization Test Assay for Measuring SARS-CoV-2 Neutralizing Antibodies\",\"authors\":\"Abigail Vanderheiden, Venkata Viswanadh Edara, Katharine Floyd, Robert C. Kauffman, Grace Mantus, Evan Anderson, Nadine Rouphael, Sri Edupuganti, Pei-Yong Shi, Vineet D. Menachery, Jens Wrammert, Mehul S. Suthar\",\"doi\":\"10.1002/cpim.116\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"SARS‐CoV‐2 is a recently emerged human coronavirus that has escalated to a pandemic. There are currently no approved vaccines for SARS‐CoV‐2, which causes severe respiratory illness or death. Defining the antibody response to SARS‐CoV‐2 will be essential for understanding disease progression, long‐term immunity, and vaccine efficacy. Here we describe two methods for evaluating the neutralization capacity of SARS‐CoV‐2 antibodies. The basic protocol is a focus reduction neutralization test (FRNT), which involves immunostaining infected cells with a chromogen deposit readout. The alternate protocol is a modification of the FRNT that uses an infectious clone−derived SARS‐CoV‐2 virus expressing a fluorescent reporter. These protocols are adapted for use in a high‐throughput setting, and are compatible with large‐scale vaccine studies or clinical testing. © 2020 Wiley Periodicals LLC\",\"PeriodicalId\":10733,\"journal\":{\"name\":\"Current Protocols in Immunology\",\"volume\":\"131 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2020-11-20\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1002/cpim.116\",\"citationCount\":\"101\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Current Protocols in Immunology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/cpim.116\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"Immunology and Microbiology\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Protocols in Immunology","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/cpim.116","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"Immunology and Microbiology","Score":null,"Total":0}
引用次数: 101