4.8 Article

Durability of mRNA-1273 vaccine-induced antibodies against SARS-CoV-2 variants

期刊

SCIENCE
卷 373, 期 6561, 页码 1372-+

出版社

AMER ASSOC ADVANCEMENT SCIENCE
DOI: 10.1126/science.abj4176

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资金

  1. Emory Executive Vice President for Health Affairs Synergy Fund Award
  2. Pediatric Research Alliance Center for Childhood Infections and Vaccines and Children's Healthcare of Atlanta
  3. Woodruff Health Sciences Center 2020 COVID-19 CURE Award
  4. National Institutes of Health [UM1AI148373, HHSN272201500002C, UM1AI148576, UM1AI148684, P51OD011132]
  5. Intramural Research Program of the Vaccine Research Center, NIAID, NIH
  6. Coalition for Epidemic Preparedness Innovation

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The study assessed the impact of SARS-CoV-2 variants on antibody responses induced by the mRNA vaccine over 7 months, showing that most individuals maintained binding and functional antibodies against variants, with B.1.351 having the lowest antibody recognition.
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) mutations may diminish vaccineinduced protective immune responses, particularly as antibody titers wane over time. Here, we assess the effect of SARS-CoV-2 variants B.1.1.7 (Alpha), B.1.351 (Beta), P.1 (Gamma), B.1.429 (Epsilon), B.1.526 (Iota), and B.1.617.2 (Delta) on binding, neutralizing, and angiotensin-converting enzyme 2 (ACE2)competing antibodies elicited by the messenger RNA (mRNA) vaccine mRNA-1273 over 7 months. Cross-reactive neutralizing responses were rare after a single dose. At the peak of response to the second vaccine dose, all individuals had responses to all variants. Binding and functional antibodies against variants persisted in most subjects, albeit at low levels, for 6 months after the primary series of the mRNA-1273 vaccine. Across all assays, B.1.351 had the lowest antibody recognition. These data complement ongoing studies to inform the potential need for additional boost vaccinations.

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