CVB3 multi-mechanism antiviral methods and base-specific termination model (defensive publication)

Defensive publication placing in the public domain: (i) a CVB3 lifecycle ODE model with an interferon/ISG arm, a viperin-to-ddhCTP chain-termination arm, a base-specific termination model weighted by the CVB3 genome base composition, mitophagy and immune-effector arms; (ii) a base-set redundancy method for selecting non-redundant RdRp-directed agents; (iii) a titration-to-undetectable (UND) treatment method; and (iv) a diagnostic-gated four-mechanism treatment method with IFN-beta defect-site stratification. Purpose: prior art, to prevent enclosure. Model outputs are illustrative and direction-anchored, not clinical predictions. v1.1 adds an addendum relating this disclosure to the published complete-kinetics model of CVB3 (Lopacinski et al., Cell Systems 2021, doi:10.1016/j.cels.2021.02.004) and clarifying the distinct subject matter: the base-specific termination model, the viperin/ddhCTP arm, the base-set redundancy method, and the titration-to-UND and diagnostic-gated treatment methods.

Authors

Publication Details

Journal
Zenodo (CERN European Organization for Nuclear Research)
Published
2026-10-17
DOI
https://doi.org/10.5281/zenodo.23435117
Primary Topic
interferon and immune responses
Type
article
Field-Weighted Citation Impact
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article

CVB3 multi-mechanism antiviral methods and base-specific termination model (defensive publication)

Precision Insight Network (PIN) contributors
Zenodo (CERN European Organization for Nuclear Research)
interferon and immune responses
article

CVB3 multi-mechanism antiviral methods and base-specific termination model (defensive publication)

Precision Insight Network (PIN) contributors
article en

Abstract

Defensive publication placing in the public domain: (i) a CVB3 lifecycle ODE model with an interferon/ISG arm, a viperin-to-ddhCTP chain-termination arm, a base-specific termination model weighted by the CVB3 genome base composition, mitophagy and immune-effector arms; (ii) a base-set redundancy method for selecting non-redundant RdRp-directed agents; (iii) a titration-to-undetectable (UND) treatment method; and (iv) a diagnostic-gated four-mechanism treatment method with IFN-beta defect-site stratification. Purpose: prior art, to prevent enclosure. Model outputs are illustrative and direction-anchored, not clinical predictions. v1.1 adds an addendum relating this disclosure to the published complete-kinetics model of CVB3 (Lopacinski et al., Cell Systems 2021, doi:10.1016/j.cels.2021.02.004) and clarifying the distinct subject matter: the base-specific termination model, the viperin/ddhCTP arm, the base-set redundancy method, and the titration-to-UND and diagnostic-gated treatment methods.

Zenodo (CERN European Organization for Nuclear Research)
Good health and well-being
Openalex Percentile: Top 20%
interferon and immune responses
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