Evidence map›Paper›PMID 31900462›Full record

ReviewNature reviews. Drug discovery2020

'Off-the-shelf' allogeneic CAR T cells: development and challenges.

S Depil, P Duchateau, S A Grupp, G Mufti, L Poirot

Registry-linked trialAbstract readReview
PubMed Publisher
In one paragraph

Review in Nature reviews. Drug discovery, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07727668 (Feasibility Study of Iberdomide), which is not on this map. Cited by 770 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
770citing papers in PubMed, 2 pooled it
–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.

NCT07727668 early_phase1not yet recruitingnot on this mapstarted 2026, after this paper: background citation

Feasibility Study of Iberdomide (CC-220) Priming to Improve T Cell Fitness Prior to Leukapheresis for Chimeric Antigen Receptor T Cell (CAR-T) Therapy for Relapsed/Refractory Multiple Myeloma (RRMM)

TypeinterventionalSponsorShambavi RichardRan2026 to 2031Enrolled22ConditionsMultiple Myeloma, Relapsed/Refractory Multiple MyelomaArmsIberdomide, CAR-T Leukapheresis, CAR-T Infusion
3 · Its place in the literature

Who cites it

770 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Recent advances in CAR T and CAR NK cell therapy for AML.International journal of hematology · 2026
    Review
  10. Article
  11. Review
  12. Review
  13. Review
  14. Article
  15. Beyond Oncology: Exploring the Expanding Role of CAR T Cell Therapy in Autoimmune and Infectious Diseases-A Systematic Review.Pathophysiology : the official journal of the International Society for Pathophysiology · 2026
    Review
  16. Article
  17. Pediatric AML CAR T cell therapy.Molecular therapy. Oncology · 2026
    Review
  18. Article
  19. Review
  20. Review

710 more citing papers are in PubMed but not listed here.

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

5 authors.

S DepilCentre Léon Bérard and Centre de Recherche en Cancérologie de Lyon, Lyon, France. stephane.depil@lyon.unicancer.fr.ORCID http://orcid.org/0000-0001-6011-3945
P DuchateauCellectis, Paris, France.
S A GruppChildren's Hospital of Philadelphia and Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
G MuftiKing's College London and King's College Hospital, London, UK.
L PoirotCellectis, Paris, France.ORCID http://orcid.org/0000-0002-5028-2267

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Autologous chimeric antigen receptor (CAR) T cells have changed the therapeutic landscape in haematological malignancies. Nevertheless, the use of allogeneic CAR T cells from donors has many potential advantages over autologous approaches, such as the immediate availability of cryopreserved batches for patient treatment, possible standardization of the CAR-T cell product, time for multiple cell modifications, redosing or combination of CAR T cells directed against different targets, and decreased cost using an industrialized process. However, allogeneic CAR T cells may cause life-threatening graft-versus-host disease and may be rapidly eliminated by the host immune system. The development of next-generation allogeneic CAR T cells to address these issues is an active area of research. In this Review, we analyse the different sources of T cells for optimal allogeneic CAR-T cell therapy and describe the different technological approaches, mainly based on gene editing, to produce allogeneic CAR T cells with limited potential for graft-versus-host disease. These improved allogeneic CAR-T cell products will pave the way for further breakthroughs in the treatment of cancer.

Indexed as

Graft vs Host DiseaseHumansImmunotherapyNeoplasmsReceptors, Antigen, T-CellT-LymphocytesTransplantation, HomologousReceptors, Antigen, T-Cell

Identifiers

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.