Evidence map›Paper›PMID 28541315›Full record

ReviewNature2017

Therapeutic T cell engineering.

Michel Sadelain, Isabelle Rivière, Stanley Riddell

3 registry-linked trialsAbstract readReview
In one paragraph

Review in Nature, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 3 registered trials, which are not on this map. Cited by 499 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
499citing papers in PubMed, 4 pooled it
38.3field-weighted citation impact, top 1% 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.

NCT04969354 phase1recruitingnot on this mapstarted 2021, after this paper: background citation

Clinical Study of CAIX-targeted CAR-T Cells in the Treatment of Advanced Renal Cell Carcinoma

TypeinterventionalSponsorThe Affiliated Hospital of Xuzhou Medical UniversityRan2021 to 2026Enrolled20ConditionsImmunotherapyArmsCAR-T cell immunotherapy
NCT05354375 phase1recruitingnot on this mapstarted 2022, after this paper: background citation

Clinical Study of PSMA-targeted CAR-T Cells in the Treatment of Castration-resistant Prostate Cancer

TypeinterventionalSponsorThe Affiliated Hospital of Xuzhou Medical UniversityRan2022 to 2026Enrolled20ConditionsImmunotherapyArmsCAR-T cell immunotherapy
NCT06720324 phase1 / phase2recruitingnot on this mapstarted 2024, after this paper: background citation

An Open-label Clinical Study on the Efficacy and Safety of CD7-specific CAR-T Cell Injection in the Treatment of CD7-positive Relapsed/Refractory Hematologic Tumors

TypeinterventionalSponsorUnion Hospital, Tongji Medical College, Huazhong University of Science and TechnologyRan2024 to 2027Enrolled80ConditionsHematologic MalignancyArmsFludarabine + Cyclophosphamide + CD7-specific CAR-T Cells
3 · Its place in the literature

Who cites it

499 citing papers in PubMed, 4 syntheses or guidelines pooled it, 853 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Pooled it
  5. Trial
  6. Trial
  7. A Gene-Program Architecture of Mouse T cells.bioRxiv : the preprint server for biology · 2026
    Article
  8. Article
  9. Article
  10. Review
  11. Review
  12. Article
  13. Article
  14. Review
  15. Review
  16. Article
  17. CDK4/6 inhibition enhances CAR-T cell therapy in solid tumors.Molecular therapy : the journal of the American Society of Gene Therapy · 2026
    Article
  18. Article
  19. Article
  20. Target identification and assessment in the era of AI.Nature reviews. Drug discovery · 2026
    Review

439 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

3 authors at 2 institutions in 1 country.

Michel SadelainMemorial Sloan Kettering Cancer Center, New York, New York 10065, USA.
Isabelle RivièreMemorial Sloan Kettering Cancer Center, New York, New York 10065, USA.
Stanley RiddellFred Hutchinson Cancer Research Center, Seattle, Washington 98109, USA.
Memorial Sloan Kettering Cancer Center · USFred Hutch Cancer Center · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
TUMORICIDAL FUNCTIONS OF T LYMPHOCYTES IN PSMA TUMORSP01CA059350 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI O'REILLY, RICHARD JOHN · 1992 to 2012
$21.4M
TARGETING ROR1 WITH CHIMERIC ANTIGEN RECEPTOR MODIFIED T CELLSR01CA114536 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Sylvain Simon · 2005 to 2026
$8.4M
Targeted therapy of B cell malignances with CAR-T cells of defined compositionR01CA136551 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI JENSEN, MICHAEL C, RIDDELL, STANLEY R. · 2009 to 2018
$5.5M
NCI NIH HHS P01 CA059350NCI NIH HHS P30 CA008748NCI NIH HHS R01 CA114536NCI NIH HHS R01 CA136551
6 · The paper itself

Abstract

Genetically engineered T cells are powerful new medicines, offering hope for curative responses in patients with cancer. Chimaeric antigen receptors (CARs) are a class of synthetic receptors that reprogram lymphocyte specificity and function. CARs targeting CD19 have demonstrated remarkable potency in B cell malignancies. Engineered T cells are applicable in principle to many cancers, pending further progress to identify suitable target antigens, overcome immunosuppressive tumour microenvironments, reduce toxicities, and prevent antigen escape. Advances in the selection of optimal T cells, genetic engineering, and cell manufacturing are poised to broaden T-cell-based therapies and foster new applications in infectious diseases and autoimmunity.

Indexed as

AnimalsAntigens, CD19Autoimmune DiseasesCell EngineeringHumansInfectionsNeoplasmsReceptors, Antigen, T-CellRecombinant Fusion ProteinsT-LymphocytesTumor MicroenvironmentAntigens, CD19Receptors, Antigen, T-CellRecombinant Fusion Proteins

Identifiers

PMID28541315
PMCPMC5632949
OpenAlexW2619886251

What OpenQuestion holds

Textmetadata
LicenceTDM
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.