IP20-003, Data driven transmission models to optimize influenza vaccination and pandemic mitigation strategies - COVID-19 Supplement
- Funded by National Institutes of Health (NIH)
- Total publications:0 publications
Grant number: 5U01IP001138-05
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Key facts
Disease
UnspecifiedStart & end year
20202025Known Financial Commitments (USD)
$360,803Funder
National Institutes of Health (NIH)Principal Investigator
ASSISTANT PROFESSOR Jonathan ZelnerResearch Location
United States of AmericaLead Research Institution
UNIVERSITY OF MICHIGAN AT ANN ARBORResearch Priority Alignment
N/A
Research Category
Infection prevention and control
Research Subcategory
N/A
Special Interest Tags
N/A
Study Type
Unspecified
Clinical Trial Details
N/A
Broad Policy Alignment
Pending
Age Group
Unspecified
Vulnerable Population
Unspecified
Occupations of Interest
Unspecified
Abstract
Project Summary/Abstract Because influenza pandemics occur with little warning, vaccine development and distribution take place at a slower timescale than transmission of the emergent strain. Similarly, although seasonal influenza epidemics occur annually, they are also notoriously difficult to predict, and necessitate rapid response to changing circumstances. While vaccination, antivirals and non-pharmaceutical interventions (NPIs) are available to mitigate these challenges, imperfect protection and coverage mean that their direct and indirect protective benefits are conditional on the state of immunity in the population. Therefore, the overall objective of this application is to develop a sustainable, scalable pipeline of analytic, predictive, and visualization tools to translate detailed clinical and cohort data to into timely population-level guidance on vaccination, antiviral use, and NPIs. We will accomplish these goals through the following specific aims: Aim 1) We will use the extensive clinical and cohort data resources generated by the Michigan Influenza Center to identify and address key questions in influenza prevention and control; Aim 2) We will integrate these multiple sources of data using statistical and simulation based models of infectious disease transmission. Specifically, we will Aim 2A) use robust models of longitudinal serologic data to characterize response to natural infection and vaccination, and then in Aim 2B) integrate this information into household-based transmission models to understand the impact of these immune responses on susceptibility to influenza infection. Using the predictions of these individual- level models parameterized using longitudinal cohort data, in Aim 2C) we will construct synthetic cohorts representative of the age-specific distribution of immunity in different populations, e.g. the State of Michigan, and use these data to develop targeted population-level strategies for influenza vaccination. In Aim 2D) we will then apply the insights of these models to the layered application of antivirals and NPIs in an influenza pandemic using a network-based simulation platform we have developed. All of these models will be designed, implemented and analyzed in collaboration with CDC and other partners to ensure clearly-articulated guidelines for modeling assumptions and inputs (Aim 3). This will be augmented by tools for automated model verification, validation and synthesis which will ensure adherence to these standards and integrate the findings of multiple modeling groups (Aims 4 & 5). All of these tools will be released publicly as open-source software and interactive tools. All of these products will be implemented with the goal of communicating key findings as well as uncertainty in model inputs, structure, and outcomes as clearly as possible to a wide array of scientific and policy-focused stakeholders using state-of-the-art tools for data visualization (Aims 6,7 & 8). The outcome of this project will be the development of a validated, systematic and collaborative modeling approach tailored for rapid evaluation of both pandemic and seasonal influenza mitigation strategies.