Will vaccine-derived protective immunity curtail COVID-19 variants in the US?

Show simple item record

dc.contributor.author Mancuso, Marina
dc.contributor.author Eikenberry, Steffen E.
dc.contributor.author Gumel, Abba B.
dc.date.accessioned 2022-04-01T11:59:03Z
dc.date.available 2022-04-01T11:59:03Z
dc.date.issued 2021-09-09
dc.description.abstract Multiple effective vaccines are currently being deployed to combat the COVID-19 pandemic, and are viewed as the major factor in marked reductions of disease burden in regions with moderate to high vaccination coverage. The effectiveness of COVID-19 vaccination programs is, however, significantly threatened by the emergence of new SARS-COV-2 variants that, in addition to being more transmissible than the wild-type (original) strain, may at least partially evade existing vaccines. A two-strain (one wildtype, one variant) and two-group (vaccinated or otherwise) mechanistic mathematical model is designed and used to assess the impact of the vaccine-induced cross-protective efficacy on the spread the COVID-19 pandemic in the United States. Rigorous analysis of the model shows that, in the absence of any co-circulating SARS-CoV-2 variant, the vaccine-derived herd immunity threshold needed to eliminate the wild-type strain can be achieved if 59% of the US population is fully-vaccinated with either the Pfizer or Moderna vaccine. This threshold increases to 76% if the wild-type strain is co-circulating with the Alpha variant (a SARS-CoV-2 variant that is 56% more transmissible than the wild-type strain). If the wild-type strain is co-circulating with the Delta variant (which is estimated to be 100% more transmissible than the wild-type strain), up to 82% of the US population needs to be vaccinated with either of the aforementioned vaccines to achieve the vaccine-derived herd immunity. Global sensitivity analysis of the model reveal the following four parameters as the most influential in driving the value of the reproduction number of the variant strain (hence, COVID-19 dynamics) in the US: (a) the infectiousness of the co-circulating SARS-CoV-2 variant, (b) the proportion of individuals fully vaccinated (using Pfizer or Moderna vaccine) against the wild-type strain, (c) the cross-protective efficacy the vaccines offer against the variant strain and (d) the modification parameter accounting for the reduced infectiousness of fully-vaccinated individuals experiencing breakthrough infection. Specifically, numerical simulations of the model show that future waves or surges of the COVID-19 pandemic can be prevented in the US if the two vaccines offer moderate level of cross-protection against the variant (at least 67%). This study further suggests that a new SARS-CoV-2 variant can cause a significant disease surge in the US if (i) the vaccine coverage against the wild-type strain is low (roughly <66%) (ii) the variant is much more transmissible (e.g., 100% more transmissible), than the wild-type strain, or (iii) the level of cross-protection offered by the vaccine is relatively low (e.g., less than 50%). A new SARS-CoV-2 variant will not cause such surge in the US if it is only moderately more transmissible (e.g., the Alpha variant, which is 56% more transmissible) than the wild-type strain, at least 66% of the population of the US is fully vaccinated, and the three vaccines being deployed in the US (Pfizer, Moderna, and Johnson & Johnson) offer a moderate level of cross-protection against the variant. en_ZA
dc.description.department Mathematics and Applied Mathematics en_ZA
dc.description.librarian am2022 en_ZA
dc.description.sponsorship The Simons Foundation and the National Science Foundation. en_ZA
dc.description.uri http://www.keaipublishing.com/idm en_ZA
dc.identifier.citation Mancuso, M., Eikenberry, S.E., Gumel, A.B. 2021, 'Will vaccine-derived protective immunity curtail COVID-19 variants in the US?', Infectious Disease Modelling, vol. 6, pp. 1110-1134. en_ZA
dc.identifier.issn 2468-0427
dc.identifier.other 10.1016/j.idm.2021.08.008
dc.identifier.uri http://hdl.handle.net/2263/84766
dc.language.iso en en_ZA
dc.publisher KeAi Communications en_ZA
dc.rights © 2021 The Authors. Production and hosting by Elsevier B.V. on behalf of KeAi Communications Co., Ltd. This is an open access article under the CC BY-NC-ND license. en_ZA
dc.subject Vaccine en_ZA
dc.subject Wild-type en_ZA
dc.subject Variant en_ZA
dc.subject Reproduction number en_ZA
dc.subject Herd immunity en_ZA
dc.subject Coronavirus disease 2019 (COVID-19) en_ZA
dc.subject COVID-19 pandemic en_ZA
dc.subject Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) en_ZA
dc.title Will vaccine-derived protective immunity curtail COVID-19 variants in the US? en_ZA
dc.type Article en_ZA


Files in this item

This item appears in the following Collection(s)

Show simple item record