Estimating seroconversion rates accounting for repeated infections by approximate Bayesian computation

Author:

Teunis Peter F. M.1ORCID,Wang Yuke1,Aiemjoy Kristen23ORCID,Kretzschmar Mirjam45,Aerts Marc6

Affiliation:

1. Hubert Department of Global Health, Center for Global Safe WASH, Rollins School of Public Health Emory University Atlanta Georgia USA

2. Department of Public Health Sciences, Division of Epidemiology University of California Davis California USA

3. Department of Microbiology and Immunology Mahidol University Faculty of Tropical Medicine Bangkok Thailand

4. Julius Center for Health Sciences and Primary Care University Medical Center Utrecht, Utrecht University Utrecht The Netherlands

5. Center for Infectious Disease Control National Institute for Public Health and the Environment Bilthoven The Netherlands

6. Center for Statistics (CenStat) University Hasselt Hasselt Belgium

Abstract

This study presents a novel approach for inferring the incidence of infections by employing a quantitative model of the serum antibody response. Current methodologies often overlook the cumulative effect of an individual's infection history, making it challenging to obtain a marginal distribution for antibody concentrations. Our proposed approach leverages approximate Bayesian computation to simulate cross‐sectional antibody responses and compare these to observed data, factoring in the impact of repeated infections. We then assess the empirical distribution functions of the simulated and observed antibody data utilizing Kolmogorov deviance, thereby incorporating a goodness‐of‐fit check. This new method not only matches the computational efficiency of preceding likelihood‐based analyses but also facilitates the joint estimation of antibody noise parameters. The results affirm that the predictions generated by our within‐host model closely align with the observed distributions from cross‐sectional samples of a well‐characterized population. Our findings mirror those of likelihood‐based methodologies in scenarios of low infection pressure, such as the transmission of pertussis in Europe. However, our simulations reveal that in settings of higher infection pressure, likelihood‐based approaches tend to underestimate the force of infection. Thus, our novel methodology presents significant advancements in estimating infection incidence, thereby enhancing our understanding of disease dynamics in the field of epidemiology.

Funder

Fogarty International Center

Publisher

Wiley

Subject

Statistics and Probability,Epidemiology

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