Evidence map›Paper›PMID 41118427›Full record

ArticlePLoS computational biology2025

Scalable, trustworthy generative model for virtual multi-staining from H&E whole slide images.

Mehdi Ounissi, Ilias Sarbout, Jean-Pierre Hugot, Christine Martinez-Vinson, Dominique Berrebi, Daniel Racoceanu

Abstract read
In one paragraph

Article in PLoS computational 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. Article
  2. Article
  3. Machine learning methods for histopathological image analysis: Updates in 2024.Computational and structural biotechnology journal · 2025
    Review
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

6 authors.

Mehdi OunissiSorbonne Université; CNRS; Inserm; Inria; Paris Brain Institute - ICM; AP-HP, Paris, France.ORCID 0000-0003-0655-8112
Ilias SarboutSorbonne Université; CNRS; Inserm; Inria; Paris Brain Institute - ICM; AP-HP, Paris, France.ORCID 0009-0003-4437-7897
Jean-Pierre HugotParis Cité University; AP-HP; Centre de Recherche sur l'inflammation, Paris, France.
Christine Martinez-VinsonAP-HP; Robert Debré University Hospitals; Centre de Recherche sur l'inflammation, Paris, France.
Dominique BerrebiParis Cité University; Inserm; AP-HP; Necker-Enfants Malades University Hospitals; Anatomopathology Department; Centre de recherche sur l'inflammation, Paris, France.
Daniel RacoceanuSorbonne Université; CNRS; Inserm; Inria; Paris Brain Institute - ICM; AP-HP, Paris, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chemical staining methods, while reliable, are time consuming and can be resource-intensive, involving costly chemical reagents and raising environmental concerns. This underscores the compelling need for alternative solutions such as virtual staining, which not only accelerates the diagnostic process but also enhances the flexibility of stain applications without the associated physical and chemical costs. Generative artificial intelligence technologies prove to be immensely useful in addressing these challenges. However, in healthcare, particularly within computational pathology, the high-stakes nature of decisions complicates the adoption of these tools due to their often opaque processes. Our work introduces an innovative approach that harnesses generative models for virtual stain transformations, improving performance, trustworthiness, scalability, and adaptability within computational pathology. The core of the proposed methodology involves a singular Hematoxylin and Eosin (H&E) encoder that supports multiple stain decoders. This design prioritizes critical regions in the latent space of H&E tissues, leading to a richer representation that enables precise synthetic stain generation by the decoders. Tested to simultaneously generate eight different stains from a single H&E slide, our method also offers significant scalability benefits for routine use by loading only necessary model components during production. We integrate label-free knowledge during training, using loss functions and regularization to minimize artifacts, thereby enhancing the accuracy of virtual staining in both paired and unpaired settings. To build trust in these synthetic stains, we employ a real-time self-inspection methodology using trained discriminators for each stain type, providing pathologists with confidence heatmaps to aid in their evaluations. In addition, we perform automatic quality checks on new H&E slides to ensure that they conform to the trained H&E distribution, guaranteeing the generation of high-quality synthetic stained slides. Recognizing the challenges pathologists face in adopting new technologies, we have encapsulated our method in an open-source, cloud-based proof-of-concept system. This system enables users to easily and virtually stain their H&E slides through a browser, eliminating the need for specialized technical knowledge and addressing common hardware and software challenges. It also facilitates real-time user feedback integration. Lastly, we have curated a novel dataset comprising eight different paired H&E/stains related to pediatric Crohn's disease at diagnosis, providing 30 whole slide images (WSIs) for each stain set (total of 480 WSIs) to stimulate further research in computational pathology.

Indexed as

Image Processing, Computer-AssistedStaining and LabelingAlgorithmsArtificial IntelligenceComputational BiologyEosine Yellowish-(YS)HematoxylinHumansEosine Yellowish-(YS)Hematoxylin

Identifiers

PMID41118427
PMCPMC12578341

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.