Evidence map›Paper›PMID 40832312›Full record

ArticlebioRxiv : the preprint server for biology2025

Predicting viral sensitivity to antibodies using genetic sequences and antibody similarities.

Kai S Shimagaki, Gargi Kher, Rebecca M Lynch, John P Barton

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors.

Kai S ShimagakiDepartment of Computational and Systems Biology, University of Pittsburgh School of Medicine, USA.ORCID 0000-0001-7580-4781
Gargi KherDepartment of Computational and Systems Biology, University of Pittsburgh School of Medicine, USA.
Rebecca M LynchDepartment of Microbiology, Immunology and Tropical Medicine, School of Medicine and Health Sciences, George Washington University, USA.ORCID 0000-0002-7188-8073
John P BartonDepartment of Computational and Systems Biology, University of Pittsburgh School of Medicine, USA.ORCID 0000-0003-1467-421X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

For genetically variable pathogens such as human immunodeficiency virus (HIV)-1, individual viral isolates can differ dramatically in their sensitivity to antibodies. The ability to predict which viruses will be sensitive and which will be resistant to a specific antibody could aid in the design of antibody therapies and help illuminate resistance evolution. Due to the enormous number of possible combinations, it is not possible to experimentally measure neutralization values for all pairs of viruses and antibodies. Here, we developed a simple and interpretable method called grouped neutralization learning (GNL) to predict neutralization values by leveraging viral genetic sequences and similarities in neutralization profiles between antibodies. Our method compares favorably to state-of-the-art approaches and is robust to model parameter assumptions. GNL can predict neutralization values for viruses with no observed data, an essential capability for evaluating novel viral strains. We also demonstrate that GNL can successfully transfer knowledge between independent data sets, allowing rapid estimates of viral sensitivity based on prior knowledge.

Identifiers

PMID40832312
PMCPMC12363850

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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.