Evidence map›Paper›PMID 40739437›Full record

ArticleCommunications biology2025

HLAIIPred: cross-attention mechanism for modeling the interaction of HLA class II molecules with peptides.

Mojtaba Haghighatlari, Nicholas Marze, Robert Seward, Andrew Ciarla, Rachel Hindin, Jennifer Calderini, Benjamin Keenan, Santosh Dhule, Sarah Hall-Swan, Timothy P Hickling and 3 more

Abstract read
In one paragraph

Article in Communications biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Review
  3. 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

13 authors.

Mojtaba HaghighatlariMachine Learning and Computational Sciences, Pfizer Research and Development, Cambridge, MA, USA. mojtaba.haghighatlari@pfizer.com.ORCID http://orcid.org/0000-0002-3779-2246
Nicholas MarzeBiomedicine Design, Pfizer Research and Development, Cambridge, MA, USA.
Robert SewardPharmacokinetics, Dynamics and Metabolism, Pfizer Research and Development, Andover, MA, USA.
Andrew CiarlaPharmacokinetics, Dynamics and Metabolism, Pfizer Research and Development, Andover, MA, USA.
Rachel HindinPharmacokinetics, Dynamics and Metabolism, Pfizer Research and Development, Andover, MA, USA.
Jennifer CalderiniPharmacokinetics, Dynamics and Metabolism, Pfizer Research and Development, Andover, MA, USA.
Benjamin KeenanPharmacokinetics, Dynamics and Metabolism, Pfizer Research and Development, Andover, MA, USA.
Santosh DhulePharmacokinetics, Dynamics and Metabolism, Pfizer Research and Development, Andover, MA, USA.
Sarah Hall-SwanMachine Learning and Computational Sciences, Pfizer Research and Development, Cambridge, MA, USA.
Timothy P HicklingBiomedicine Design, Pfizer Research and Development, Cambridge, MA, USA.ORCID http://orcid.org/0000-0002-8918-2140
Eric BennettBiomedicine Design, Pfizer Research and Development, Cambridge, MA, USA.ORCID http://orcid.org/0000-0001-5784-0797
Brajesh RaiMachine Learning and Computational Sciences, Pfizer Research and Development, Cambridge, MA, USA.ORCID http://orcid.org/0000-0001-6399-4813
Sophie TourdotPharmacokinetics, Dynamics and Metabolism, Pfizer Research and Development, Andover, MA, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We introduce HLAIIPred, a deep learning model to predict peptides presented by class II human leukocyte antigens (HLAII) on the surface of antigen presenting cells. HLAIIPred is trained using a Transformer-based neural network and a dataset comprising of HLAII-presented peptides identified by mass spectrometry. In addition to predicting peptide presentation, the model can also provide important insights into peptide-HLAII interactions by identifying core peptide residues that form such interactions. We evaluate the performance of HLAIIPred on three different tasks, peptide presentation in monoallelic samples, immunogenicity prediction of therapeutic antibodies, and neoantigen prioritization for cancer immunotherapy. Additionally, we created a dataset of biotherapeutics HLAII peptides presented by human dendritic cells. This data is used to develop screening strategies to predict the unwanted immunogenic segments of therapeutic antibodies by HLAII presentation models. HLAIIPred demonstrates superior or equivalent performance when compared to the latest models across all evaluated benchmark datasets. We achieve a 16% increase in prediction of presented peptides compared to the second-best model on a set of unseen peptides presented by less frequent alleles. The model improves clinical immunogenicity prediction, identifies epitopes in therapeutic antibodies and prioritize neoantigens with high accuracy.

Indexed as

Deep LearningHistocompatibility Antigens Class IIPeptidesAntigen PresentationHumansHistocompatibility Antigens Class IIPeptides

Identifiers

PMID40739437
PMCPMC12310933

What OpenQuestion holds

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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.