Evidence map›Paper›PMID 29109732›Full record

ArticleFrontiers in immunology2017

CCL3 Enhances Antitumor Immune Priming in the Lymph Node

Frederick Allen, Peter Rauhe, David Askew, Alexander A Tong, Joseph Nthale, Saada Eid, Jay T Myers, Caryn Tong, Alex Y Huang

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 1 pooled it
1.1field-weighted citation impact, top 23% 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

28 citing papers in PubMed, 1 synthesis or guideline pooled it, 46 citations in OpenAlex.

  1. Pooled it
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  9. Establishment of a CD8+ T cells-related prognostic risk model for acral melanoma based on single-cell and bulk RNA sequencing.Skin research and technology : official journal of International Society for Bioengineering and the Skin (ISBS) [and] International Society for Digital Imaging of Skin (ISDIS) [and] International Society for Skin Imaging (ISSI) · 2024
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  15. Cell Trafficking at the Intersection of the Tumor-Immune Compartments.Annual review of biomedical engineering · 2022
    Review
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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

9 authors at 3 institutions in 1 country.

Frederick AllenDepartment of Pathology, Case Western Reserve University School of Medicine, Cleveland, OH, United States.
Peter RauheDepartment of Pediatrics, Case Western Reserve University School of Medicine, Cleveland, OH, United States.
David AskewDepartment of Pediatrics, Case Western Reserve University School of Medicine, Cleveland, OH, United States.
Alexander A TongDepartment of Pathology, Case Western Reserve University School of Medicine, Cleveland, OH, United States.
Joseph NthaleDepartment of Pediatrics, Case Western Reserve University School of Medicine, Cleveland, OH, United States.
Saada EidDepartment of Pediatrics, Case Western Reserve University School of Medicine, Cleveland, OH, United States.
Jay T MyersDepartment of Pediatrics, Case Western Reserve University School of Medicine, Cleveland, OH, United States.
Caryn TongDepartment of Pediatrics, Case Western Reserve University School of Medicine, Cleveland, OH, United States.
Alex Y HuangDepartment of Pathology, Case Western Reserve University School of Medicine, Cleveland, OH, United States.
Case Western Reserve University · USUniversity School · USRainbow Babies & Children's Hospital · US

Funding

Mechanistic Dynamic Study of Intranodal Chemokine-aided Antitumor Immune PrimingR01CA154656 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI HUANG, ALEX YEE-CHEN · 2011 to 2015
$1.7M
Cdk5 signaling in ICN1-induced T Cell LeukemogenesisR21CA181875 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI HUANG, ALEX YEE-CHEN, LETTERIO, JOHN JAMES · 2015 to 2016
$379k
INFLAMMATORY CHEMOKINE CCL3 IN THE TUMOR MICROENVIRONMENT LEADS TO ENHANCED ANTITUMOR IMMUNE DEVELOPMENT IN THE DRAINING LYMPH NODEF31CA192874 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI ALLEN, FREDERICK · 2014 to 2016
$96k
NCI NIH HHS F31 CA192874NCI NIH HHS R01 CA154656NCI NIH HHS R21 CA181875
6 · The paper itself

Abstract

Lymph node (LN) plays a critical role in tumor cell survival outside of the primary tumor sites and dictates overall clinical response in many tumor types (1, 2). Previously, we and others have demonstrated that CCL3 plays an essential role in orchestrating T cell-antigen-presenting cell (APC) encounters in the draining LN following vaccination, and such interactions enhance the magnitude of the memory T cell pool (3-5). In the current study, we investigate the cellular responses in the tumor-draining lymph nodes (TDLNs) of a CCL3-secreting CT26 colon tumor (L3TU) as compared to wild-type tumor (WTTU) during the priming phase of an antitumor response (≤10 days). In comparison to WTTU, inoculation of L3TU resulted in suppressed tumor growth, a phenomenon that is accompanied by altered

Indexed as

CCL3CD103+ dendritic cellsinterferon-gammalymph nodelymphocytesnatural killer cells

Identifiers

PMID29109732
PMCPMC5660298
OpenAlexW2766732330

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.