Evidence map›Paper›PMID 23840879›Full record

ArticlePloS one2013

Examination of MARCO activity on dendritic cell phenotype and function using a gene knockout mouse.

Hiroshi Komine, Lisa Kuhn, Norimasa Matsushita, James J Mulé, Shari Pilon-Thomas

Abstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
–field-weighted citation impact
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

10 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Identification of Novel Genes for Cell Fusion during Osteoclast Formation.International journal of molecular sciences · 2022
    Article
  6. Review
  7. Review
  8. Article
  9. Review
  10. 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

5 authors.

Hiroshi KomineImmunology Program, H Lee Moffitt Cancer Center and Research Institute, Tampa, Florida, United States of America.
Lisa Kuhn
Norimasa Matsushita
James J Mulé
Shari Pilon-Thomas

Funding

TRANSLATIONAL RESEARCHP30CA076292 · NCI · UNIVERSITY OF SOUTH FLORIDA · PI KENNETH Lynn WRIGHT · 1998 to 2026
$93.5M
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
NCI NIH HHS 5 R01 CA071669-10NCI NIH HHS P30 CA076292NCI NIH HHS R01 CA071669
6 · The paper itself

Abstract

We have reported the upregulation of MARCO, a member of the class A scavenger receptor family, on the surface of murine and human dendritic cells (DCs) pulsed with tumor lysates. Exposure of murine tumor lysate-pulsed DCs to an anti-MARCO antibody led to loss of dendritic-like processes and enhanced migratory capacity. In this study, we have further examined the biological and therapeutic implications of MARCO expression by DCs. DCs generated from the bone marrow (bm) of MARCO knockout (MARCO⁻/⁻) mice were phenotypically similar to DCs generated from the bm of wild-type mice and produced normal levels of IL-12 and TNF-α when exposed to LPS. MARCO⁻/⁻ DCs demonstrated enhanced migratory capacity in response to CCL-21 in vitro. After subcutaneous injection into mice, MARCO⁻/⁻ TP-DCs migrated more efficiently to the draining lymph node leading to enhanced generation of tumor-specific IFN-γ producing T cells and improved tumor regression and survival in B16 melanoma-bearing mice. These results support targeting MARCO on the surface of DCs to improve trafficking and induction of anti-tumor immunity.

Indexed as

AnimalsCell MovementCytokinesDendritic CellsFemaleHumansImmunotherapyInterferon-gammaMelanoma, ExperimentalMiceMice, Inbred C57BLMice, KnockoutReceptors, ImmunologicT-LymphocytesCytokinesInterferon-gammaMarco protein, mouseReceptors, Immunologic

Identifiers

PMID23840879
PMCPMC3698187

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.