Evidence map›Paper›PMID 37899130›Full record

ArticleJournal for immunotherapy of cancer2023

Patient-derived lymphoma spheroids integrating immune tumor microenvironment as preclinical follicular lymphoma models for personalized medicine.

Carla Faria, Fabien Gava, Pauline Gravelle, Juan Garcia Valero, Celia Dobaño-López, Nathalie Van Acker, Cathy Quelen, Gael Jalowicki, Renaud Morin, Cédric Rossi and 6 more

Open access · goldAbstract read
In one paragraph

Article in Journal for immunotherapy of cancer, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
3.7field-weighted citation impact, top 6% of its field
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

15 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Review
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  4. Article
  5. Review
  6. Goodbye flat lymphoma biology.FEBS letters · 2025
    Review
  7. Review
  8. Review
  9. Review
  10. Ex Vivo Model of Breast Cancer Cell Invasion in Live Lymph Node Tissue.ACS pharmacology & translational science · 2025
    Article
  11. Review
  12. Article
  13. Review
  14. Ex vivo model of breast cancer cell invasion in live lymph node tissue.bioRxiv : the preprint server for biology · 2024
    Article
  15. 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

16 authors at 5 institutions in 2 countries.

Carla FariaUniversité de Toulouse, Inserm, CNRS, Université Toulouse III-Paul Sabatier, Centre de Recherches en Cancérologie de Toulouse, Toulouse, France.ORCID 0000-0001-9537-4758
Fabien GavaUniversité de Toulouse, Inserm, CNRS, Université Toulouse III-Paul Sabatier, Centre de Recherches en Cancérologie de Toulouse, Toulouse, France.ORCID 0000-0003-1255-6121
Pauline GravelleUniversité de Toulouse, Inserm, CNRS, Université Toulouse III-Paul Sabatier, Centre de Recherches en Cancérologie de Toulouse, Toulouse, France.ORCID 0000-0002-0462-5652
Juan Garcia ValeroDepartment of Hemato-Oncology, IDIBAPS, Barcelona, Spain.ORCID 0000-0003-3193-9099
Celia Dobaño-LópezDepartment of Hemato-Oncology, IDIBAPS, Barcelona, Spain.ORCID 0000-0001-9248-9883
Nathalie Van AckerDepartment of Pathology, Institut Universitaire du Cancer de Toulouse, CHU Toulouse, Toulouse, France.ORCID 0000-0003-0420-5081
Cathy QuelenUniversité de Toulouse, Inserm, CNRS, Université Toulouse III-Paul Sabatier, Centre de Recherches en Cancérologie de Toulouse, Toulouse, France.ORCID 0000-0003-0576-2234
Gael JalowickiIUCT-Oncopole, Toulouse, France.
Renaud MorinIMACTIV3D, Toulouse, France.ORCID 0000-0003-4365-279X
Cédric RossiDepartment of Hematology, Hôpital François Mitterrand and U1231 INSERM, Dijon, France.ORCID 0000-0003-3717-7961
Jean-Michel LagardeIMACTIV3D, Toulouse, France.
Jean-Jacques FourniéUniversité de Toulouse, Inserm, CNRS, Université Toulouse III-Paul Sabatier, Centre de Recherches en Cancérologie de Toulouse, Toulouse, France.ORCID 0000-0001-6542-6908
Loïc YsebaertUniversité de Toulouse, Inserm, CNRS, Université Toulouse III-Paul Sabatier, Centre de Recherches en Cancérologie de Toulouse, Toulouse, France.ORCID 0000-0003-4102-7261
Camille LaurentUniversité de Toulouse, Inserm, CNRS, Université Toulouse III-Paul Sabatier, Centre de Recherches en Cancérologie de Toulouse, Toulouse, France.ORCID 0000-0002-5375-7512
Patricia Pérez-GalánDepartment of Hemato-Oncology, IDIBAPS, Barcelona, Spain christine.bezombes@inserm.fr PPEREZ@recerca.clinic.cat.ORCID 0000-0003-3895-5024
Christine BezombesUniversité de Toulouse, Inserm, CNRS, Université Toulouse III-Paul Sabatier, Centre de Recherches en Cancérologie de Toulouse, Toulouse, France christine.bezombes@inserm.fr PPEREZ@recerca.clinic.cat.ORCID 0000-0003-4079-4872
Centre National de la Recherche Scientifique · FRCentro de Investigación Biomédica en Red de Cáncer · ESCentre Hospitalier Universitaire de Toulouse · FRVision Objects (France) · FRInserm · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundFollicular lymphoma (FL), the most common indolent non-Hodgkin's Lymphoma, is a heterogeneous disease and a paradigm of the contribution of immune tumor microenvironment to disease onset, progression, and therapy resistance. Patient-derived models are scarce and fail to reproduce immune phenotypes and therapeutic responses.

methodsTo capture disease heterogeneity and microenvironment cues, we developed a patient-derived lymphoma spheroid (FL-PDLS) model culturing FL cells from lymph nodes (LN) with an optimized cytokine cocktail that mimics LN stimuli and maintains tumor cell viability.

resultsFL-PDLS, mainly composed of tumor B cells (60% on average) and autologous T cells (13% CD4 and 3% CD8 on average, respectively), rapidly organizes into patient-specific three-dimensional (3D) structures of three different morphotypes according to 3D imaging analysis. RNAseq analysis indicates that FL-PDLS reproduces FL hallmarks with the overexpression of cell cycle, BCR, or mTOR signaling related gene sets. FL-PDLS also recapitulates the exhausted immune phenotype typical of FL-LN, including expression of BTLA, TIGIT, PD-1, TIM-3, CD39 and CD73 on CD3

conclusionsIn summary, FL-PDLS is a robust patient-derived 3D system that can be used as a tool to mimic FL pathology and to test novel immunotherapeutic approaches in a context of personalized medicine.

Indexed as

Lymphoma, FollicularHepatitis A Virus Cellular Receptor 2HumansPrecision MedicineProgrammed Cell Death 1 ReceptorTumor MicroenvironmentHepatitis A Virus Cellular Receptor 2Programmed Cell Death 1 ReceptorHematologic NeoplasmsImmune Checkpoint InhibitorsImmunotherapyTumor Microenvironment

Identifiers

PMID37899130
PMCPMC10619028
OpenAlexW4388033625

What OpenQuestion holds

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LicenceCC BY-NC
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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.