Evidence map›Paper›PMID 30875727›Full record

ArticleMicroorganisms2019

Multi-Level Model to Predict Antibody Response to Influenza Vaccine Using Gene Expression Interaction Network Feature Selection.

Saeid Parvandeh, Greg A Poland, Richard B Kennedy, Brett A McKinney

Abstract read
In one paragraph

Article in Microorganisms, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed.

  1. Article
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  7. Review
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  9. Consensus features nested cross-validation.Bioinformatics (Oxford, England) · 2020
    Article
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  11. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Saeid ParvandehTandy School of Computer Science, University of Tulsa, Tulsa, OK 74104, USA. parvandehsaied@gmail.com.ORCID 0000-0003-0917-2784
Greg A PolandMayo Vaccine Group, Mayo Clinic, Rochester, MN 55905, USA. poland.gregory@mayo.edu.
Richard B KennedyMayo Vaccine Group, Mayo Clinic, Rochester, MN 55905, USA. kennedy.rick@mayo.edu.
Brett A McKinneyTandy School of Computer Science, University of Tulsa, Tulsa, OK 74104, USA. brett-mckinney@utulsa.edu.

Funding

National Institutes of Health GM10345
6 · The paper itself

Abstract

Vaccination is an effective prevention of influenza infection. However, certain individuals develop a lower antibody response after vaccination, which may lead to susceptibility to subsequent infection. An important challenge in human health is to find baseline gene signatures to help identify individuals who are at higher risk for infection despite influenza vaccination. We developed a multi-level machine learning strategy to build a predictive model of vaccine response using pre-vaccination antibody titers and network interactions between pre-vaccination gene expression levels. The first-level baseline-antibody model explains a significant amount of variation in post-vaccination response, especially for subjects with large pre-existing antibody titers. In the second level, we clustered individuals based on pre-vaccination antibody titers to focus gene-based modeling on individuals with lower baseline HAI where additional response variation may be predicted by baseline gene expression levels. In the third level, we used a gene-association interaction network (GAIN) feature selection algorithm to find the best pairs of genes that interact to influence antibody response within each baseline titer cluster. We used ratios of the top interacting genes as predictors to stabilize machine learning model generalizability. We trained and tested the multi-level approach on data with young and older individuals immunized against influenza vaccine in multiple cohorts. Our results indicate that the GAIN feature selection approach improves model generalizability and identifies genes enriched for immunologically relevant pathways, including B Cell Receptor signaling and antigen processing. Using a multi-level approach, starting with a baseline HAI model and stratifying on baseline HAI, allows for more targeted gene-based modeling. We provide an interactive tool that may be extended to other vaccine studies.

Indexed as

gene interactionnested cross-validationvaccine immune response

Identifiers

PMID30875727
PMCPMC6462975

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.