Evidence map›Paper›PMID 21158979›Full record

ReviewJournal of internal medicine2011

Dendritic cells and immunity against cancer.

K Palucka, H Ueno, J Fay, J Banchereau

Open access · bronzeAbstract readReview
In one paragraph

Review in Journal of internal medicine, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 75 papers.

0numbers the graph read from it
0cells of the map it votes in
75citing papers in PubMed
7.7field-weighted citation impact, top 2% 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

75 citing papers in PubMed, 161 citations in OpenAlex.

  1. Trial
  2. Review
  3. Review
  4. Review
  5. Review
  6. Article
  7. Review
  8. Article
  9. Therapeutic applications of nanobiotechnology.Journal of nanobiotechnology · 2023
    Review
  10. Immunotherapy for advanced or recurrent hepatocellular carcinoma.World journal of gastrointestinal oncology · 2023
    Review
  11. Review
  12. Review
  13. Combination therapy for pancreatic cancer: anti-PD-(L)1-based strategy.Journal of experimental & clinical cancer research : CR · 2022
    Review
  14. Article
  15. Review
  16. Systemic Interleukins' Profile in Early and Advanced Colorectal Cancer.International journal of molecular sciences · 2021
    Review
  17. Article
  18. Article
  19. Review
  20. Review

15 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

4 authors at 3 institutions in 1 country.

K PaluckaBaylor Institute for Immunology Research, Baylor University Medical Center, Dallas, TX, USA. karolinp@baylorhealth.edu
H Ueno
J Fay
J Banchereau
Icahn School of Medicine at Mount Sinai · USBaylor Institute for Rehabilitation · USBaylor University · US

Funding

Targeting Dendritic Cells for Enhanced Musocal ImmunityU19AI057234 · NIAID · BAYLOR RESEARCH INSTITUTE · PI ZURAWSKI, GERARD · 2003 to 2013
$49.2M
Induction of melanoma immunity by dendritic cell subsetsP01CA084512 · NCI · ROCKEFELLER UNIVERSITY · PI BANCHEREAU, JACQUES F · 2000 to 2010
$12.1M
SUBPOPULATIONS OF HUMAN DENDRITIC CELLSR01CA078846 · NCI · BAYLOR RESEARCH INSTITUTE · PI BANCHEREAU, JACQUES F · 1999 to 2008
$2.5M
Altered CD8+ T cell Compartment in SLE PatientsR01AI068842 · NIAID · BAYLOR RESEARCH INSTITUTE · PI BANCHEREAU, JACQUES F · 2006 to 2010
$1.8M
Vaccination with IL-15 DC to Generate Melanoma-specific Protective Memory T CellsR01CA140602 · NCI · BAYLOR RESEARCH INSTITUTE · PI PALUCKA, ANNA KAROLINA · 2010 to 2013
$1.4M
Dendritic Cells and Breast Cancer ImmunityR01CA089440 · NCI · BAYLOR RESEARCH INSTITUTE · PI PALUCKA, ANNA KAROLINA · 2001 to 2004
$930k
NCI NIH HHS CA078846NCI NIH HHS P01 CA084512NCI NIH HHS P01 CA084514NCI NIH HHS R01 CA078846NCI NIH HHS R01 CA089440NCI NIH HHS R01 CA140602NIAID NIH HHS R01 AI068842NIAID NIH HHS U19 AI057234PHS HHS U19 AIO57234
6 · The paper itself

Abstract

T cells can reject established tumours when adoptively transferred into patients, thereby demonstrating the power of the immune system for cancer therapy. However, it has proven difficult to maintain adoptively transferred T cells in the long term. Vaccines have the potential to induce tumour-specific effector and memory T cells. However, clinical efficacy of current vaccines is limited, possibly because tumours skew the immune system by means of myeloid-derived suppressor cells, inflammatory type 2 T cells and regulatory T cells (Tregs), all of which prevent the generation of effector cells. To improve the clinical efficacy of cancer vaccines in patients with metastatic disease, we need to design novel and improved strategies that can boost adaptive immunity to cancer, help overcome Tregs and allow the breakdown of the immunosuppressive tumour microenvironment. This can be achieved by exploiting the fast increasing knowledge about the dendritic cell (DC) system, including the existence of distinct DC subsets that respond differentially to distinct activation signals, (functional plasticity), both contributing to the generation of unique adaptive immune responses. We foresee that these novel cancer vaccines will be used as monotherapy in patients with resected disease and in combination with drugs targeting regulatory/suppressor pathways in patients with metastatic disease.

Indexed as

Cancer VaccinesDendritic CellsHumansImmunity, CellularImmunotherapy, AdoptiveNeoplasmsT-Lymphocyte SubsetsTumor MicroenvironmentCancer Vaccines

Identifiers

PMID21158979
PMCPMC3023888
OpenAlexW2152865079

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.