Evidence map›Paper›PMID 16380819›Full record

ReviewJournal of clinical immunology2005

Human dendritic cell subsets for vaccination.

Peter Dubsky, Hideki Ueno, Bernard Piqueras, John Connolly, Jacques Banchereau, A Karolina Palucka

Open access · bronzeAbstract readReview
PubMed Publisher
In one paragraph

Review in Journal of clinical immunology, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

34 citing papers in PubMed, 94 citations in OpenAlex.

  1. Trial
  2. Review
  3. Review
  4. Review
  5. Review
  6. Article
  7. Article
  8. Review
  9. Effects of combined thymosin and hydrocortisone on immune response in septic mice.International journal of clinical and experimental medicine · 2015
    Article
  10. Article
  11. Dendritic cells: a spot on sialic Acid.Frontiers in immunology · 2013
    Review
  12. Review
  13. Article
  14. Article
  15. Regulation of Na+/H+ exchanger in dendritic cells by Akt2.Pflugers Archiv : European journal of physiology · 2012
    Article
  16. Article
  17. Review
  18. Current advances in understanding of immunopathology of atherosclerosis.Virchows Archiv : an international journal of pathology · 2011
    Review
  19. Article
  20. Article
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

6 authors at 1 institution in 1 country.

Peter DubskyBaylor Institute for Immunology Research, 3434 Live Oak, Dallas, TX 75204, USA.
Hideki Ueno
Bernard Piqueras
John Connolly
Jacques Banchereau
A Karolina Palucka
Baylor University · US

Funding

Targeting Dendritic Cells for Enhanced Musocal ImmunityU19AI057234 · NIAID · BAYLOR RESEARCH INSTITUTE · PI BANCHEREAU, JACQUES F · 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
Dendritic Cells, Heat Shock Proteins and Tumor ImmunityR01CA085540 · NCI · BAYLOR RESEARCH INSTITUTE · PI BANCHEREAU, JACQUES F · 2001 to 2004
$1.0M
Dendritic Cells and Breast Cancer ImmunityR01CA089440 · NCI · BAYLOR RESEARCH INSTITUTE · PI PALUCKA, ANNA KAROLINA · 2001 to 2004
$930k
NCI NIH HHS CA 085540NCI NIH HHS CA 78846NCI NIH HHS CA 89440NCI NIH HHS P01 CA 84512NIAID NIH HHS U19 AI 057234
6 · The paper itself

Abstract

Protective immunity results from the interplay of antigen (Ag)-nonspecific innate immunity and Ag-specific adaptive immunity. The cells and molecules of the innate system employ non-clonal recognition pathways such as lectins and TLRs. B and T lymphocytes of the adaptive immune system employ clonal receptors recognizing Ag or peptides in a highly specific manner. An essential link between innate and adaptive immunity is provided by dendritic cells (DCs). As a component of the innate immune system, DC organize and transfer information from the outside world to the cells of the adaptive immune system. DC can induce such contrasting states as active immune responsiveness or immunological tolerance. Recent years have brought a wealth of information regarding DC biology and pathophysiology that shows the complexity of this cell system. Thus, presentation of antigen by immature (non-activated) DCs leads to tolerance, whereas mature, antigen-loaded DCs are geared towards the launching of antigen-specific immunity. Furthermore, DCs are composed of multiple subsets with distinct functions at the interface of the innate and adaptive immunity. Our increased understanding of DC pathophysiology will permit their rational manipulation for therapy such as vaccination to improve immunity.

Indexed as

Antigen PresentationCancer VaccinesChemotaxis, LeukocyteDendritic CellsHumansImmunotherapy, AdoptiveCancer Vaccines

Identifiers

PMID16380819
OpenAlexW1983365509

What OpenQuestion holds

Textmetadata
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.