Evidence map›Paper›PMID 32001504›Full record

ArticleJournal for immunotherapy of cancer2020

Increased antitumor efficacy of PD-1-deficient melanoma-specific human lymphocytes.

Lucine Marotte, Sylvain Simon, Virginie Vignard, Emilie Dupre, Malika Gantier, Jonathan Cruard, Jean-Baptiste Alberge, Melanie Hussong, Cecile Deleine, Jean-Marie Heslan and 8 more

Open access · goldAbstract read
In one paragraph

Article in Journal for immunotherapy of cancer, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.7field-weighted citation impact, top 14% 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

21 citing papers in PubMed, 29 citations in OpenAlex.

  1. Review
  2. Review
  3. Armored human CAR TScience advances · 2025
    Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Review
  11. CRISPR/Cas9 revitalizes adoptive T-cell therapy for cancer immunotherapy.Journal of experimental & clinical cancer research : CR · 2021
    Review
  12. Review
  13. Review
  14. Review
  15. Article
  16. Article
  17. Engineering better chimeric antigen receptor T cells.Experimental hematology & oncology · 2020
    Review
  18. Ready for Repair? Gene Editing Enters the Clinic for the Treatment of Human Disease.Molecular therapy. Methods & clinical development · 2020
    Review
  19. Review
  20. 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

18 authors at 2 institutions in 2 countries.

Lucine MarotteUniversité de Nantes, Inserm, CRCINA, F-44000 Nantes, France.
Sylvain SimonUniversité de Nantes, Inserm, CRCINA, F-44000 Nantes, France.
Virginie VignardUniversité de Nantes, Inserm, CRCINA, F-44000 Nantes, France.
Emilie DupreUniversité de Nantes, Inserm, CRCINA, F-44000 Nantes, France.
Malika GantierLabEx IGO, Université de Nantes, Nantes, France.
Jonathan CruardUniversité de Nantes, Inserm, CRCINA, F-44000 Nantes, France.
Jean-Baptiste AlbergeUniversité de Nantes, Inserm, CRCINA, F-44000 Nantes, France.
Melanie HussongNGS Assay Research & Development, Qiagen Sciences, Frederick, Maryland, United States.
Cecile DeleineUniversité de Nantes, Inserm, CRCINA, F-44000 Nantes, France.
Jean-Marie HeslanLabEx IGO, Université de Nantes, Nantes, France.
Jonathan ShafferNGS Assay Research & Development, Qiagen Sciences, Frederick, Maryland, United States.
Tiffany BeauvaisUniversité de Nantes, Inserm, CRCINA, F-44000 Nantes, France.
Joelle GaschetUniversité de Nantes, Inserm, CRCINA, F-44000 Nantes, France.
Emmanuel ScotetUniversité de Nantes, Inserm, CRCINA, F-44000 Nantes, France.
Delphine FradinUniversité de Nantes, Inserm, CRCINA, F-44000 Nantes, France.
Anne JarryUniversité de Nantes, Inserm, CRCINA, F-44000 Nantes, France.
Tuan NguyenUniversité de Nantes, Inserm, CRTI, F-44000 Nantes, France.
Nathalie LabarriereUniversité de Nantes, Inserm, CRCINA, F-44000 Nantes, France Nathalie.Labarriere@univ-nantes.fr.ORCID 0000-0002-1407-6546
Inserm · FRQiagen (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGenome editing offers unique perspectives for optimizing the functional properties of T cells for adoptive cell transfer purposes. So far,

methodsHere we used the transfection of CAS9/sgRNA ribonucleoproteic complexes to edit

resultsHere we demonstrated the feasibility to edit

conclusionThe use of such lymphocytes for adoptive cell transfer purposes, associated with other approaches modulating the tumor microenvironment, would be a promising alternative to improve immunotherapy efficacy in solid tumors.

Indexed as

AnimalsCell Line, TumorFemaleGene EditingHumansImmunotherapy, AdoptiveMelanomaMiceMice, Inbred NODMice, SCIDProgrammed Cell Death 1 ReceptorRandom AllocationT-Lymphocytes, CytotoxicTransfectionXenograft Model Antitumor AssaysPDCD1 protein, humanProgrammed Cell Death 1 ReceptorCD8-Positive T-Lymphocytescell engineeringcostimulatory and inhibitory T-cell receptorsimmunotherapy, adoptivemelanoma

Identifiers

PMID32001504
PMCPMC7057432
OpenAlexW3003355855

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.