Evidence map›Paper›PMID 29311385›Full record

ReviewJournal of immunology (Baltimore, Md. : 1950)2018

Immune Cell Infiltration and Tertiary Lymphoid Structures as Determinants of Antitumor Immunity.

Victor H Engelhard, Anthony B Rodriguez, Ileana S Mauldin, Amber N Woods, J David Peske, Craig L Slingluff

Abstract readReview
In one paragraph

Review in Journal of immunology (Baltimore, Md. : 1950), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 153 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
153citing papers in PubMed, 1 pooled it
–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

153 citing papers in PubMed, 1 synthesis or guideline pooled it.

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93 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.

Victor H EngelhardCarter Immunology Center, University of Virginia School of Medicine, Charlottesville, VA 22908; vhe@virginia.edu.ORCID 0000-0002-1741-0925
Anthony B RodriguezCarter Immunology Center, University of Virginia School of Medicine, Charlottesville, VA 22908.
Ileana S MauldinCarter Immunology Center, University of Virginia School of Medicine, Charlottesville, VA 22908.
Amber N WoodsCarter Immunology Center, University of Virginia School of Medicine, Charlottesville, VA 22908.
J David PeskeCarter Immunology Center, University of Virginia School of Medicine, Charlottesville, VA 22908.ORCID 0000-0001-6314-6881
Craig L SlingluffCarter Immunology Center, University of Virginia School of Medicine, Charlottesville, VA 22908.

Funding

Women's Oncology Program - WONP30CA044579 · NCI · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI Thomas P. Loughran · 1987 to 2026
$72.1M
Cancer Research Training Program: From Molecular Mechanisms to Therapeutic StrategiesT32CA009109 · NCI · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI Andrew Carl Dudley, Melanie R Rutkowski · 1985 to 2026
$13.9M
MEDICAL SCIENTIST TRAINING PROGRAMT32GM007267 · NIGMS · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI GARCIA-BLANCO, MARIANO A. · 1985 to 2024
$13.4M
INTERDISCIPLINARY TRAINING PROGRAM IN IMMUNOLOGYT32AI007496 · NIAID · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI Michael G. Brown, Coleen A McNamara · 1995 to 2026
$10.2M
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
Lymph node-like vasculature and naive T cell infiltration into tumorsR21CA181794 · NCI · UNIVERSITY OF VIRGINIA · PI ENGELHARD, VICTOR H · 2015 to 2016
$378k
NCI NIH HHS P30 CA044579NCI NIH HHS R01 CA078400NCI NIH HHS R21 CA181794NCI NIH HHS T32 CA009109NIAID NIH HHS T32 AI007496NIGMS NIH HHS T32 GM007267
6 · The paper itself

Abstract

Limited representation of intratumoral immune cells is a major barrier to tumor control. However, simply enhancing immune responses in tumor-draining lymph nodes or through adoptive transfer may not overcome the limited ability of tumor vasculature to support effector infiltration. An alternative is to promote a sustained immune response intratumorally. This idea has gained traction with the observation that many tumors are associated with tertiary lymphoid structures (TLS), which organizationally resemble lymph nodes. These peri- and intratumoral structures are usually, but not always, associated with positive prognoses in patients. Preclinical and clinical data support a role for TLS in modulating immunity in the tumor microenvironment. However, there appear to be varied functions of TLS, potentially based on their structure or location in relation to the tumor or the origin or location of the tumor itself. Understanding more about TLS development, composition, and function may offer new therapeutic opportunities to modulate antitumor immunity.

Indexed as

ImmunityAnimalsHumansLymphocytes, Tumor-InfiltratingNeoplasmsNeovascularization, PathologicPrognosisTertiary Lymphoid StructuresTumor Microenvironment

Identifiers

PMID29311385
PMCPMC5777336

What OpenQuestion holds

Textmetadata
LicenceTDM
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.