Evidence map›Paper›PMID 24795361›Full record

ArticleCancer immunology research2014

Reprogramming tumor-infiltrating dendritic cells for CD103+ CD8+ mucosal T-cell differentiation and breast cancer rejection.

Te-Chia Wu, Kangling Xu, Romain Banchereau, Florentina Marches, Chun I Yu, Jan Martinek, Esperanza Anguiano, Alexander Pedroza-Gonzalez, G Jackson Snipes, Joyce O'Shaughnessy and 6 more

Open access · bronzeAbstract read
In one paragraph

Article in Cancer immunology research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed, 1 pooled it
2.4field-weighted citation impact, top 11% 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

51 citing papers in PubMed, 1 synthesis or guideline pooled it, 74 citations in OpenAlex.

  1. Pooled it
  2. CD8MedComm · 2026
    Review
  3. Article
  4. Article
  5. Review
  6. Review
  7. Review
  8. Review
  9. Review
  10. Article
  11. Review
  12. Review
  13. Human T lymphocytes at tumor sites.Seminars in immunopathology · 2022
    Review
  14. Review
  15. Article
  16. Review
  17. Article
  18. Integrin-αNature communications · 2021
    Article
  19. Article
  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

16 authors at 5 institutions in 1 country.

Te-Chia WuAuthors' Affiliations: Department of Oncological Sciences, Mount Sinai School of Medicine, New York, New York.
Kangling Xu
Romain Banchereau
Florentina Marches
Chun I Yu
Jan Martinek
Esperanza Anguiano
Alexander Pedroza-Gonzalez
G Jackson Snipes
Joyce O'Shaughnessy
Stephen Nishimura
Yong-Jun Liu
Virginia Pascual
Jacques Banchereau
Sangkon Oh
Karolina Palucka
Baylor University · USBaylor University Medical Center · USIcahn School of Medicine at Mount Sinai · USTexas Oncology · USUniversity of California, San Francisco · US

Funding

Dendritic Cells and Breast Cancer ImmunityR01CA089440 · NCI · BAYLOR RESEARCH INSTITUTE · PI PALUCKA, ANNA KAROLINA · 2001 to 2004
$930k
NCI NIH HHS R01 CA089440
6 · The paper itself

Abstract

Our studies showed that tumor-infiltrating dendritic cells (DC) in breast cancer drive inflammatory Th2 (iTh2) cells and protumor inflammation. Here, we show that intratumoral delivery of the β-glucan curdlan, a ligand of dectin-1, blocks the generation of iTh2 cells and prevents breast cancer progression in vivo. Curdlan reprograms tumor-infiltrating DCs via the ligation of dectin-1, enabling the DCs to become resistant to cancer-derived thymic stromal lymphopoietin (TSLP), to produce IL-12p70, and to favor the generation of Th1 cells. DCs activated via dectin-1, but not those activated with TLR-7/8 ligand or poly I:C, induce CD8+ T cells to express CD103 (αE integrin), a ligand for cancer cells, E-cadherin. Generation of these mucosal CD8+ T cells is regulated by DC-derived integrin αvβ8 and TGF-β activation in a dectin-1-dependent fashion. These CD103+ CD8+ mucosal T cells accumulate in the tumors, thereby increasing cancer necrosis and inhibiting cancer progression in vivo in a humanized mouse model of breast cancer. Importantly, CD103+ CD8+ mucosal T cells elicited by reprogrammed DCs can reject established cancer. Thus, reprogramming tumor-infiltrating DCs represents a new strategy for cancer rejection.

Indexed as

Animalsbeta-GlucansBreast NeoplasmsCD8-Positive T-LymphocytesCell DifferentiationCell Line, TumorCell Transformation, NeoplasticDectin-1Dendritic CellsDisease Models, AnimalFemaleHumansLectins, C-TypeMiceMucous MembraneSignal Transductionbeta-GlucanscurdlanDectin-1Lectins, C-TypeTransforming Growth Factor beta

Identifiers

PMID24795361
PMCPMC4014008
OpenAlexW2129045181

What OpenQuestion holds

Textmetadata
LicenceTDM
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.