ArticleAmerican journal of epidemiology2026
Statistical methods for estimating the protective effects of immune markers using test-negative designs.
Article in American journal of epidemiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
2 citing papers in PubMed.
- Use of the test-negative design to estimate the protective effect of a scalar immune measure: a simulation analysis.American journal of epidemiology · 2026Article
- Influenza Antibody Levels Associated with Laboratory-Confirmed Influenza in a Test-Negative Study Design, US Flu VE Network, November 2018-May 2019.medRxiv : the preprint server for health sciences · 2026Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
2 authors.
Funding
Abstract
While widely used to study vaccine effectiveness, test-negative designs (TNDs) also provide a platform for identifying and quantifying immunological correlates of protection against disease. A key component of such studies is the protection function, the mathematical relationship between the value of an immunological assay and the relative risk of disease. This function is often estimated using logistic regression, comparing the odds of disease at a given assay value to the odds at assay value zero. Here, we show through mathematical analysis and simulation experiments that logistic regression, while common, fundamentally constrains the functional forms of protection that can be inferred from data in TNDs, potentially leading to overly simplistic estimates of the protection function. To address this limitation, we adapt and analyze a scaled logit model, originally developed for case-control data, as a flexible alternative that allows for greater flexibility in estimating protection functions from TND data. We demonstrate that this approach improves accuracy across a range of biologically plausible protection functions, highlight conditions under which it may fail, and provide practical guidance for researchers to adopt it as a new standard for TND studies evaluating correlates of protection.
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Registered trials
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