Evidence map›Paper›PMID 42453687›Full record

ArticlePatterns (New York, N.Y.)2026

H3BERTa: A CDR-H3-specific language model for antibody repertoire analysis.

Chiara Rodella, Thomas Lemmin

Abstract read
In one paragraph

Article in Patterns (New York, N.Y.), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

2 authors.

Chiara RodellaInstitute of Biochemistry and Molecular Medicine (IBMM), University of Bern, Bühlstrasse 28, 3012 Bern, Switzerland.
Thomas LemminInstitute of Biochemistry and Molecular Medicine (IBMM), University of Bern, Bühlstrasse 28, 3012 Bern, Switzerland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Antibodies are central to immune defense and therapeutic design, yet predicting functional sequences remains challenging. Deep learning models trained on full variable regions often struggle due to sparse experimental data, signal dilution from conserved framework residues, and extreme diversity of hypervariable loops. The heavy-chain complementarity-determining region 3 (CDR-H3) is the most variable segment, shaping antigen specificity and immune diversity. Here, we present H3BERTa, a language model trained solely on CDR-H3 sequences to assess the extent of biological information encoded by this region. H3BERTa embeddings recapitulate immunologically relevant features, including J-gene usage, inferred B cell maturation state, and antigen binding. Pseudo-perplexity profiles enable repertoire analysis, distinguishing healthy from human immunodeficiency virus type 1 (HIV-1)-derived sequences and suggesting measurable immune response signatures. These embeddings support classifiers for broadly neutralizing antibodies using limited labeled data, highlighting utility for antibody discovery. CDR-H3 alone encodes a rich immunological signal, which H3BERTa captures, offering a focused tool for repertoire analysis and antibody engineering.

Indexed as

AbLMantibodyantibody language modelB cell repertoire analysisbnAbsbroadly neutralizing antibodiesCDR-H3low-resource learningmachine learningprotein language modelrepertoire analysis

Identifiers

PMID42453687
PMCPMC13366522

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.