《Science,11月27日,Viral epitope profiling of COVID-19 patients》

  • 来源专题:COVID-19科研动态监测
  • 编译者: zhangmin
  • 发布时间:2020-12-22
  • Viral epitope profiling of COVID-19 patients reveals cross-reactivity and correlates of severity
    View ORCID ProfileEllen Shrock1,2,*, View ORCID ProfileEric Fujimura1,2,3,*, View ORCID ProfileTomasz Kula1,2,†, View ORCID ProfileRichard T. Timms1,2,†, View ORCID ProfileI-Hsiu Lee4, View ORCID ProfileYumei Leng1,2,...

    Science  27 Nov 2020:
    Vol. 370, Issue 6520, eabd4250
    DOI: 10.1126/science.abd4250

    Structured Abstract
    INTRODUCTION
    A systematic characterization of the humoral response to severe acute respiratory system coronavirus 2 (SARS-CoV-2) epitopes has yet to be performed. This analysis is important for understanding the immunogenicity of the viral proteome and the basis for cross-reactivity with the common-cold coronaviruses.

    Coronavirus disease 2019 (COVID-19), caused by SARS-CoV-2, is notable for its variable course, with some individuals remaining asymptomatic whereas others experience fever, respiratory distress, or even death. A comprehensive investigation of the antibody response in individuals with severe versus mild COVID-19—as well as an examination of past viral exposure history—is needed.

    RATIONALE
    An understanding of humoral responses to SARS-CoV-2 is critical for improving diagnostics and vaccines and gaining insight into variable clinical outcomes. To this end, we used VirScan, a high-throughput method to analyze epitopes of antiviral antibodies in human sera. We supplemented the original VirScan library with additional libraries of peptides spanning the proteomes of SARS-CoV-2 and all other human coronaviruses. These libraries enabled us to precisely map epitope locations and investigate cross-reactivity between SARS-CoV-2 and other coronavirus strains. The original VirScan library allowed us to simultaneously investigate antibody responses to prior infections and viral exposure history.

  • 原文来源:https://science.sciencemag.org/content/370/6520/eabd4250
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