4.8 Article

Naturally enhanced neutralizing breadth against SARS-CoV-2 one year after infection

期刊

NATURE
卷 595, 期 7867, 页码 426-+

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NATURE PORTFOLIO
DOI: 10.1038/s41586-021-03696-9

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资金

  1. NIH [P01-AI138398-S1, 2U19AI111825, R37-AI64003, R01AI78788]
  2. HHMI Hanna Gray and Burroughs Wellcome PDEP fellowships
  3. National Center for Advancing Translational Sciences (National Institutes of Health Clinical and Translational Science Award program [UL1 TR001866]
  4. Shapiro-Silverberg Fund for the Advancement of Translational Research
  5. Bulgari Women & Science Fellowship in COVID-19 Research
  6. George Mason University Fast Grants [3 R01-AI091707-10S1]
  7. Robert S. Wennett Post-Doctoral Fellowship

向作者/读者索取更多资源

Despite challenges posed by COVID-19 variants, convalescent individuals receiving mRNA vaccines exhibit robust and long-lasting immune responses against circulating SARS-CoV-2 variants, providing hope for effective control of the pandemic.
More than one year after its inception, the coronavirus disease 2019 (COVID-19) pandemic caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) remains difficult to control despite the availability of several working vaccines. Progress in controlling the pandemic is slowed by the emergence of variants that appear to be more transmissible and more resistant to antibodies(1,2). Here we report on a cohort of 63 individuals who have recovered from COVID-19 assessed at 1.3, 6.2 and 12 months after SARS-CoV-2 infection, 41% of whom also received mRNA vaccines(3,4). In the absence of vaccination, antibody reactivity to the receptor binding domain (RBD) of SARS-CoV-2, neutralizing activity and the number of RBD-specific memory B cells remain relatively stable between 6 and 12 months after infection. Vaccination increases all components of the humoral response and, as expected, results in serum neutralizing activities against variants of concern similar to or greater than the neutralizing activity against the original Wuhan Hu-1 strain achieved by vaccination of naive individuals(2,5-8). The mechanism underlying these broad-based responses involves ongoing antibody somatic mutation, memory B cell clonal turnover and development of monoclonal antibodies that are exceptionally resistant to SARS-CoV-2 RBD mutations, including those found in the variants of concern(4,9). In addition, B cell clones expressing broad and potent antibodies are selectively retained in the repertoire over time and expand markedly after vaccination. The data suggest that immunity in convalescent individuals will be very long lasting and that convalescent individuals who receive available mRNA vaccines will produce antibodies and memory B cells that should be protective against circulating SARS-CoV-2 variants.

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