4.8 Article

Epidemiological and evolutionary considerations of SARS-CoV-2 vaccine dosing regimes

期刊

SCIENCE
卷 372, 期 6540, 页码 363-370

出版社

AMER ASSOC ADVANCEMENT SCIENCE
DOI: 10.1126/science.abg8663

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资金

  1. Open Philanthropy
  2. Natural Sciences and Engineering Research Council of Canada
  3. Cooperative Institute for Modeling the Earth System (CIMES)
  4. James S. McDonnell Foundation 21st Century Science Initiative Collaborative Award in Understanding Dynamic and Multiscale Systems
  5. C3.ai Digital Transformation Institute and Microsoft Corporation
  6. Google, LLC
  7. National Science Foundation [CNS-2027908, CCF1917819]
  8. U.S. CDC
  9. Flu Lab

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Given vaccine dose shortages and logistical challenges, various deployment strategies are being proposed to increase population immunity levels to SARS-CoV-2. While focusing on one dose may decrease infections in the short term, the long-term outcomes depend on the relative immune robustness of this approach. Under conditions of partial population immunity, a one-dose policy may increase the potential for antigenic evolution.
Given vaccine dose shortages and logistical challenges, various deployment strategies are being proposed to increase population immunity levels to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Two critical issues arise: How timing of delivery of the second dose will affect infection dynamics and how it will affect prospects for the evolution of viral immune escape via a buildup of partially immune individuals. Both hinge on the robustness of the immune response elicited by a single dose as compared with natural and two-dose immunity. Building on an existing immuno-epidemiological model, we find that in the short term, focusing on one dose generally decreases infections, but that longer-term outcomes depend on this relative immune robustness. We then explore three scenarios of selection and find that a one-dose policy may increase the potential for antigenic evolution under certain conditions of partial population immunity. We highlight the critical need to test viral loads and quantify immune responses after one vaccine dose and to ramp up vaccination efforts globally.

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