Vaccine escape in a heterogeneous population: insights for SARS-CoV-2 from a simple model

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Abstract

As a countermeasure to the SARS-CoV-2 pandemic, there has been swift development and clinical trial assessment of candidate vaccines, with subsequent deployment as part of mass vaccination campaigns. However, the SARS-CoV-2 virus has demonstrated the ability to mutate and develop variants, which can modify epidemiological properties and potentially also the effectiveness of vaccines. The widespread deployment of highly effective vaccines may rapidly exert selection pressure on the SARS-CoV-2 virus directed towards mutations that escape the vaccine-induced immune response. This is particularly concerning while infection is widespread. By developing and analysing a mathematical model of two population groupings with differing vulnerability and contact rates, we explore the impact of the deployment of vaccines among the population on the reproduction ratio, cases, disease abundance and vaccine escape pressure. The results from this model illustrate two insights: (i) vaccination aimed at reducing prevalence could be more effective at reducing disease than directly vaccinating the vulnerable; (ii) the highest risk for vaccine escape can occur at intermediate levels of vaccination. This work demonstrates a key principle: the careful targeting of vaccines towards particular population groups could reduce disease as much as possible while limiting the risk of vaccine escape.

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  1. SciScore for 10.1101/2021.03.14.21253544: (What is this?)

    Please note, not all rigor criteria are appropriate for all manuscripts.

    Table 1: Rigor

    NIH rigor criteria are not applicable to paper type.

    Table 2: Resources

    No key resources detected.


    Results from OddPub: We did not detect open data. We also did not detect open code. Researchers are encouraged to share open data when possible (see Nature blog).


    Results from LimitationRecognizer: We detected the following sentences addressing limitations in the study:
    4.2 Caveats and areas for further development: By the very nature of the model being a simple representation of a complex system, there are numerous associated caveats to our approach. We restricted our main analysis to only two types of heterogeneity (vulnerability and mixing). In reality, there are many different risk factors affecting transmission dynamics and vaccine uptake, such as age-dependent susceptibility and infectivity. However, we explored two types of heterogeneity alone in order to assess their effects in as simple a setting as possible, without the effects of additional factors. Furthermore, we considered the population split into equal halves. This is relaxed somewhat in further work in the Supplementary Information, in which we show that our qualitative results are robust to this assumption. But a more realistic structure will involve more than two population groups - we outlined above how the analytical framework may be extended to more general population structures. Even extrapolating from the insight that vaccinating mixers first may be optimal for both reducing disease and vaccine escape risk leaves the question of who those mixers are in practice. The group most central to transmission might not simply be a function of age. For example occupation could be taken into account, e.g. those whose roles necessitate contact with others. Another important dimension could be household structure, e.g. those who live with several other people. The interplay betwee...

    Results from TrialIdentifier: No clinical trial numbers were referenced.


    Results from Barzooka: We did not find any issues relating to the usage of bar graphs.


    Results from JetFighter: We did not find any issues relating to colormaps.


    Results from rtransparent:
    • Thank you for including a conflict of interest statement. Authors are encouraged to include this statement when submitting to a journal.
    • Thank you for including a funding statement. Authors are encouraged to include this statement when submitting to a journal.
    • No protocol registration statement was detected.

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