Evidence map›Paper›PMID 16315029›Full record

ArticleCancer immunology, immunotherapy : CII2006

Induction of anti-tumor immunity by vaccination with dendritic cells pulsed with anti-CD44 IgG opsonized tumor cells.

Shari Pilon-Thomas, Monique Verhaegen, Lisa Kuhn, Adam Riker, James J Mulé

Open access · greenAbstract read
In one paragraph

Article in Cancer immunology, immunotherapy : CII, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.6field-weighted citation impact, top 34% 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

13 citing papers in PubMed, 19 citations in OpenAlex.

  1. Review
  2. Extracellular vesicle-based drug delivery in cancer immunotherapy.Drug delivery and translational research · 2023
    Review
  3. Article
  4. Cancer Cell Glycocalyx and Its Significance in Cancer Progression.International journal of molecular sciences · 2018
    Review
  5. Article
  6. Review
  7. Review
  8. Article
  9. Review
  10. Article
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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

5 authors at 2 institutions in 1 country.

Shari Pilon-ThomasH. Lee Moffitt Cancer Center and Research Institute, 12902 Magnolia Dr., SRB-3 Room 23244, Tampa, FL 33612, USA. pilontsa@moffitt.usf.edu
Monique Verhaegen
Lisa Kuhn
Adam Riker
James J Mulé
Moffitt Cancer Center · USUniversity of Michigan–Ann Arbor · US

Funding

SLC and dendritic cells in antitumor immunity &therapyP01CA059327 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI CHANG, ALFRED E · 1992 to 2005
$8.2M
The Significance of MARCO Expression by Tumor-Pulsed Dendritic CellsR01CA071669 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MULE, JAMES J. · 1996 to 2010
$3.2M
DIRECT INTRATUMORAL ADMINISTRATION OF DENDRITIC CELLSR01CA087019 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MULE, JAMES J · 2000 to 2003
$1.6M
NCI NIH HHS 1R01 CA71669NCI NIH HHS 1R01 CA87019NCI NIH HHS 5P01 CA59327NCI NIH HHS P01 CA059327NCI NIH HHS R01 CA071669NCI NIH HHS R01 CA087019
6 · The paper itself

Abstract

Due to the pivotal role that dendritic cells (DC) play in eliciting and maintaining functional anti-tumor T cell responses, these APC have been exploited against tumors. DC express several receptors for the Fc portion of IgG (Fcgamma receptors) that mediate the internalization of antigen-IgG complexes and promote efficient MHC class I and II restricted antigen presentation. In this study, the efficacy of vaccination with DC pulsed with apoptotic B16 melanoma cells opsonized with an anti-CD44 IgG (B16-CD44) was explored. Immature bone marrow derived DC grown in vitro with IL-4 and GM-CSF were pulsed with B16-CD44. After 48 h of pulsing, maturation of DC was demonstrated by production of IL-12 and upregulation of CD80 and CD40 expression. To test the efficacy of vaccination with DC+B16-CD44, mice were vaccinated subcutaneously Lymphocytes from mice vaccinated with DC+B16-CD44 produced IFN-gamma in response to B16 melanoma lysates as well as an MHC class I restricted B16 melanoma-associated peptide, indicating B16 specific CD8 T cell activation. Upon challenge with viable B16 cells, all mice vaccinated with DC alone developed tumor compared to 40% of mice vaccinated with DC+B16-CD44; 60% of the latter mice remained tumor free for at least 8 months. In addition, established lung tumors and distant metastases were significantly reduced in mice treated with DC+B16-CD44. Lastly, delayed growth of established subcutaneous tumors was induced by combination therapy with anti-CD44 antibodies followed by DC injection. This study demonstrates the efficacy of targeting tumor antigens to DC via Fcgamma receptors.

Indexed as

AnimalsAntibodies, MonoclonalCancer VaccinesCombined Modality TherapyDendritic CellsFemaleHyaluronan ReceptorsImmunoglobulin GImmunotherapyLung NeoplasmsMelanoma, ExperimentalMiceMice, Inbred C57BLAntibodies, MonoclonalCancer VaccinesHyaluronan ReceptorsImmunoglobulin G

Identifiers

PMID16315029
PMCPMC11030143
OpenAlexW2020167285

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.