4.7 Article

Targeted isolation of diverse human protective broadly neutralizing antibodies against SARS-like viruses

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NATURE IMMUNOLOGY
卷 23, 期 6, 页码 960-+

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NATURE PORTFOLIO
DOI: 10.1038/s41590-022-01222-1

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资金

  1. National Institutes of Health (NIH) [CHAVD UM1 AI44462]
  2. International AIDS Vaccine Initiative Neutralizing Antibody Center
  3. Bill and Melinda Gates Foundation [INV-004923]
  4. Translational Virology Core of the San Diego Center for AIDS research grant NIH [NIH AI036214, NIH 5T32AI007384, NIH AI149644, AI157155, NIH R21 AI145372]
  5. John and Mary Tu Foundation
  6. James B. Pendleton Charitable Trust
  7. Pfizer NCBiotech Distinguished Postdoctoral Fellowship in Gene Therapy
  8. Burroughs Wellcome Fund Postdoctoral Enrichment Program Award
  9. Howard Hughes Medical Institute

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This study isolated and characterized a large panel of sarbecovirus broadly neutralizing antibodies (bnAbs) that were able to neutralize all SARS-CoV-2 variants of concern (VOCs), including Omicron. These antibodies also demonstrated prophylaxis in mice infected with diverse sarbecoviruses, suggesting their potential use in next-generation antibody-based prophylactic and therapeutic applications.
The emergence of current severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variants of concern (VOCs) and potential future spillovers of SARS-like coronaviruses into humans pose a major threat to human health and the global economy. Development of broadly effective coronavirus vaccines that can mitigate these threats is needed. Here, we utilized a targeted donor selection strategy to isolate a large panel of human broadly neutralizing antibodies (bnAbs) to sarbecoviruses. Many of these bnAbs are remarkably effective in neutralizing a diversity of sarbecoviruses and against most SARS-CoV-2 VOCs, including the Omicron variant. Neutralization breadth is achieved by bnAb binding to epitopes on a relatively conserved face of the receptor-binding domain (RBD). Consistent with targeting of conserved sites, select RBD bnAbs exhibited protective efficacy against diverse SARS-like coronaviruses in a prophylaxis challenge model in vivo. These bnAbs provide new opportunities and choices for next-generation antibody prophylactic and therapeutic applications and provide a molecular basis for effective design of pan-sarbecovirus vaccines. A broadly neutralizing antibody (bnAb) response is required to combat SARS-CoV-2 variants of concern (VOCs). The authors isolated and characterized a large panel of sarbecovirus bnAbs from vaccinated individuals who had recovered from COVID-19, finding that many of these antibodies were able to neutralize all VOCs, including Omicron, and demonstrate prophylaxis in mice infected with diverse sarbecoviruses.

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