Evidence map›Paper›PMID 20538915›Full record

ArticleScience (New York, N.Y.)2010

Reprogramming of T cells to natural killer-like cells upon Bcl11b deletion.

Peng Li, Shannon Burke, Juexuan Wang, Xiongfeng Chen, Mariaestela Ortiz, Song-Choon Lee, Dong Lu, Lia Campos, David Goulding, Bee Ling Ng and 7 more

Registry-linked trialAbstract read
In one paragraph

Article in Science (New York, N.Y.), 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03882840 (Induced-T Cell Like NK Cellular Immunotherapy for Cancers That Are Lack of MHC-I Expression), which is not on this map. Cited by 220 papers.

0numbers the graph read from it
0cells of the map it votes in
220citing 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.

NCT03882840 phase1 / phase2recruitingnot on this mapstarted 2019, after this paper: background citation

Induced-T Cell Like NK Cellular Immunotherapy for Cancers That Are Lack of MHC-I Expression

TypeinterventionalSponsorSecond Affiliated Hospital of Guangzhou Medical UniversityRan2019 to 2035Enrolled60ConditionsAnti-cancer Cell Immunotherapy, T Cell and NK CellArmsITNK cell therapy
3 · Its place in the literature

Who cites it

220 citing papers in PubMed.

  1. Trial
  2. Review
  3. Article
  4. Article
  5. Animals have expanded the evolutionary legacy of unicellular ancestors in blood cells.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  6. Article
  7. Review
  8. The double-positive cells in the tumor microenvironment.Journal of translational internal medicine · 2026
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Frontiers in immunology · 2025
    Article

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors.

Peng LiWellcome Trust Sanger Institute, Hinxton, Cambridge CB10 1HH, UK.
Shannon Burke
Juexuan Wang
Xiongfeng Chen
Mariaestela Ortiz
Song-Choon Lee
Dong Lu
Lia Campos
David Goulding
Bee Ling Ng
Gordon Dougan
Brian Huntly
Bertie Gottgens
Nancy A Jenkins
Neal G Copeland
Francesco Colucci
Pentao Liu

Funding

Biotechnology and Biological Sciences Research CouncilMedical Research Council G0501150Medical Research Council G0800784Medical Research Council G116/187National Centre for the Replacement, Refinement and Reduction of Animals in Research G0900729/1Wellcome Trust 076962Wellcome Trust 077186
6 · The paper itself

Abstract

T cells develop in the thymus and are critical for adaptive immunity. Natural killer (NK) lymphocytes constitute an essential component of the innate immune system in tumor surveillance, reproduction, and defense against microbes and viruses. Here, we show that the transcription factor Bcl11b was expressed in all T cell compartments and was indispensable for T lineage development. When Bcl11b was deleted, T cells from all developmental stages acquired NK cell properties and concomitantly lost or decreased T cell-associated gene expression. These induced T-to-natural killer (ITNK) cells, which were morphologically and genetically similar to conventional NK cells, killed tumor cells in vitro, and effectively prevented tumor metastasis in vivo. Therefore, ITNKs may represent a new cell source for cell-based therapies.

Indexed as

Cell LineageLymphopoiesisAnimalsCell Line, TumorCells, CulturedCoculture TechniquesCytotoxicity, ImmunologicGene DeletionGene Expression ProfilingGene Expression Regulation, DevelopmentalGene Knock-In TechniquesGenes, T-Cell Receptor betaKiller Cells, NaturalMelanoma, ExperimentalMiceMice, Inbred C57BLafimoxifeneBcl11b protein, mouseReceptors, Antigen, T-Cell, alpha-betaRepressor ProteinsTamoxifenTumor Suppressor Proteins

Identifiers

PMID20538915
PMCPMC3628452

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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.