Evidence map›Paper›PMID 14530375›Full record

ArticleThe Journal of experimental medicine2003

Route of immunization with peptide-pulsed dendritic cells controls the distribution of memory and effector T cells in lymphoid tissues and determines the pattern of regional tumor control.

David W Mullins, Stacey L Sheasley, Rebecca M Ream, Timothy N J Bullock, Yang-Xin Fu, Victor H Engelhard

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 92 papers.

0numbers the graph read from it
0cells of the map it votes in
92citing papers in PubMed
4.9field-weighted citation impact, top 4% 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

92 citing papers in PubMed, 225 citations in OpenAlex.

  1. Immunotherapy by autologous dendritic cell vaccine in patients with advanced HCC.Journal of cancer research and clinical oncology · 2013
    Trial
  2. Trial
  3. Trial
  4. Dendritic cell-based cancer immunotherapy targeting MUC-1.Cancer immunology, immunotherapy : CII · 2006
    Trial
  5. Biodistribution of radiolabelled human dendritic cells injected by various routes.European journal of nuclear medicine and molecular imaging · 2005
    Trial
  6. Lymphoid-Tissue-on-Chip Recapitulates Human Antibody Responses In Vitro.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. An iPSC-derived exosome-pulsed dendritic cell vaccine boosts antitumor immunity in melanoma.Molecular therapy : the journal of the American Society of Gene Therapy · 2023
    Article
  14. Article
  15. Review
  16. Resident memory CD8Immunity · 2021
    Article
  17. Article
  18. Robust induction of TMolecular therapy. Methods & clinical development · 2021
    Article
  19. Article
  20. Review

32 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

6 authors at 2 institutions in 1 country.

David W MullinsCarter Immunology Center, University of Virginia, Box 801386, Charlottesville, VA 22908, USA.
Stacey L Sheasley
Rebecca M Ream
Timothy N J Bullock
Yang-Xin Fu
Victor H Engelhard
University of Virginia · USUniversity of Chicago · US

Funding

Quality and location of presented Ag as determinants of tumor-specific immunityR01CA078400 · NCI · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI ENGELHARD, VICTOR H · 1998 to 2012
$4.4M
CO-FACILITATORS: NOVEL REGULATORS OF HORMONE METABOLISMR01DK058891 · NIDDK · CEDARS-SINAI MEDICAL CENTER · PI ADAMS, JOHN S. · 2001 to 2004
$1.3M
DEVELOPMENT AND FUNCTION OF LYMPHOID TISSUESR01HD037104 · NICHD · UNIVERSITY OF CHICAGO · PI FU, YANG-XIN · 1999 to 2003
$491k
NCI NIH HHS CA 78400NCI NIH HHS R01 CA078400NICHD NIH HHS HD 37104NICHD NIH HHS R01 HD037104NIDDK NIH HHS DK 58891NIDDK NIH HHS R01 DK058891NIGMS NIH HHS GM 07627
6 · The paper itself

Abstract

We have established that the route of immunization with peptide-pulsed, activated DC leads to memory CD8+ T cells with distinct distributions in lymphoid tissues, which determines the ability to control tumors growing in different body sites. Both intravenous (i.v.) and subcutaneous (s.c.) immunization induced memory T cells in spleen and control of metastatic-like lung tumors. s.c. immunization also induced memory T cells in lymph nodes (LNs), imparting protection against subcutaneously growing tumors. In contrast, i.v. immunization-induced memory was restricted to spleen and failed to impart protective immunity against subcutaneously growing tumors. Memory cell distribution and tumor control were both linked to injection route-dependent localization of DCs in lymphoid compartments. Using peripheral LN-ablated mice, these LNs were shown to be essential for control of subcutaneously growing tumors but not lung metastases; in contrast, using immunized asplenic mice, we found that the spleen is necessary and sufficient for control of lung tumors, but unnecessary for control of subcutaneously growing tumors. These data demonstrate the existence of a previously undescribed population of splenic-resident memory CD8 T cells that are essential for the control of lung metastases. Thus, regional immunity based on memory T cell residence patterns is an important factor in DC-based tumor immunotherapy.

Indexed as

Immunologic MemoryAnimalsDendritic CellsInjections, IntravenousInjections, SubcutaneousLung NeoplasmsLymph NodesMelanoma, ExperimentalMiceNeoplasms, ExperimentalSkin NeoplasmsT-LymphocytesVaccination

Identifiers

PMID14530375
PMCPMC2194213
OpenAlexW2097829667

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.