Evidence map›Paper›PMID 19363220›Full record

ArticleBlood2009

Lymphoid-tissue-specific homing of bone-marrow-derived dendritic cells.

Rémi J Creusot, Shahriar S Yaghoubi, Pearl Chang, Justine Chia, Christopher H Contag, Sanjiv S Gambhir, C Garrison Fathman

Open access · bronzeAbstract read
In one paragraph

Article in Blood, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed, 1 pooled it
2.0field-weighted citation impact, top 13% 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

42 citing papers in PubMed, 1 synthesis or guideline pooled it, 66 citations in OpenAlex.

  1. Pooled it
  2. Donor-Specific Blood Transfusion Induces a Transfusion-Related Early Protective Effect in Murine Lung Transplantation.Transplant international : official journal of the European Society for Organ Transplantation · 2026
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  3. Review
  4. Therapeutic cancer vaccines: advancements, challenges, and prospects.Signal transduction and targeted therapy · 2023
    Review
  5. Review
  6. Article
  7. Article
  8. Flt3-L enhances trans-epithelial migration and antigen presentation of dendritic cells adoptively transferred to genital mucosa.Journal of controlled release : official journal of the Controlled Release Society · 2021
    Article
  9. Vitamin D as a Potential Therapy for Multiple Sclerosis: Where Are We?International journal of molecular sciences · 2020
    Review
  10. Article
  11. AAV9 Edits Muscle Stem Cells in Normal and Dystrophic Adult Mice.Molecular therapy : the journal of the American Society of Gene Therapy · 2019
    Article
  12. Article
  13. Review
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Kidney international reports · 2016
    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

7 authors at 2 institutions in 1 country.

Rémi J CreusotDepartment of Medicine, Division of Immunology and Rheumatology, Stanford University School of Medicine, 300 Pasteur Drive, Stanford, CA 94305, USA.
Shahriar S Yaghoubi
Pearl Chang
Justine Chia
Christopher H Contag
Sanjiv S Gambhir
C Garrison Fathman
Center for Rheumatology · USStanford University · US

Funding

THE ROLE OF TNF-ALPHA IN LYMPHOCYTE DEVELOPMENT IN NOD MICEP01AI036535 · NIAID · STANFORD UNIVERSITY · PI FATHMAN, CHARLES GARRISON · 1994 to 2008
$6.6M
Spatiotemporal Analysis of Neoplasia in Animal ModelsR24CA092862 · NCI · STANFORD UNIVERSITY · PI CONTAG, CHRISTOPHER H · 2001 to 2006
$4.4M
Immunoregulation of AutoimmunityU01DK078123 · NIDDK · STANFORD UNIVERSITY · PI FATHMAN, CHARLES GARRISON · 2006 to 2011
$1.9M
NCI NIH HHS R24 CA092862NCI NIH HHS R24CA92862NIAID NIH HHS AI36535-13NIAID NIH HHS P01 AI036535NIDDK NIH HHS DK078123-03NIDDK NIH HHS U01 DK078123
6 · The paper itself

Abstract

Because of their potent immunoregulatory capacity, dendritic cells (DCs) have been exploited as therapeutic tools to boost immune responses against tumors or pathogens, or dampen autoimmune or allergic responses. Murine bone marrow-derived DCs (BM-DCs) are the closest known equivalent of the blood monocyte-derived DCs that have been used for human therapy. Current imaging methods have proven unable to properly address the migration of injected DCs to small and deep tissues in mice and humans. This study presents the first extensive analysis of BM-DC homing to lymph nodes (and other selected tissues) after intravenous and intraperitoneal inoculation. After intravenous delivery, DCs accumulated in the spleen, and preferentially in the pancreatic and lung-draining lymph nodes. In contrast, DCs injected intraperitoneally were found predominantly in peritoneal lymph nodes (pancreatic in particular), and in omentum-associated lymphoid tissue. This uneven distribution of BM-DCs, independent of the mouse strain and also observed within pancreatic lymph nodes, resulted in the uneven induction of immune response in different lymphoid tissues. These data have important implications for the design of systemic cellular therapy with DCs, and in particular underlie a previously unsuspected potential for specific treatment of diseases such as autoimmune diabetes and pancreatic cancer.

Indexed as

AnimalsBone Marrow CellsCell MovementDendritic CellsFemaleGenes, ReporterImmunotherapy, AdoptiveInjections, IntraperitonealInjections, IntravenousLuciferases, FireflyLungLymph NodesLymphoid TissueMiceMice, Inbred BALB CMice, Inbred NODLuciferases, Firefly

Identifiers

PMID19363220
PMCPMC2710920
OpenAlexW2014601653

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.