Evidence map›Paper›PMID 31001479›Full record

ReviewFrontiers in oncology2019

Radiotherapy Both Promotes and Inhibits Myeloid-Derived Suppressor Cell Function: Novel Strategies for Preventing the Tumor-Protective Effects of Radiotherapy.

Suzanne Ostrand-Rosenberg, Lucas A Horn, Nicholas G Ciavattone

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in oncology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed, 1 pooled it
3.3field-weighted citation impact, top 7% 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

51 citing papers in PubMed, 1 synthesis or guideline pooled it, 69 citations in OpenAlex.

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  15. Radiation Therapy and Myeloid-Derived Suppressor Cells: Breaking Down Their Cancerous Partnership.International journal of radiation oncology, biology, physics · 2024
    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

3 authors at 3 institutions in 1 country.

Suzanne Ostrand-RosenbergDepartment of Pathology and Huntsman Cancer Institute, University of Utah, Salt Lake City, UT, United States.
Lucas A HornDepartment of Biological Sciences, University of Maryland Baltimore County, Baltimore, MD, United States.
Nicholas G CiavattoneMarlene and Stewart Greenebaum Comprehensive Cancer Center, University of Maryland, Baltimore, MD, United States.
Huntsman Cancer Institute · USUniversity of Maryland, Baltimore · USUniversity of Maryland, Baltimore County · US

Funding

Ubiquitinated Proteins in Exosomes of Immune Suppressive Myeloid CellsR01GM021248 · NIGMS · UNIV OF MARYLAND, COLLEGE PARK · PI FENSELAU, CATHERINE C, FUSHMAN, DAVID · 1985 to 2017
$4.6M
Cell-based tumor vaccines targeting CD4+ T lymphocytesR01CA084232 · NCI · UNIVERSITY OF MARYLAND BALTIMORE COUNTY · PI OSTRAND-ROSENBERG, SUZANNE · 2000 to 2011
$2.6M
Tumor-Induced immune suppressionR01CA115880 · NCI · UNIVERSITY OF MARYLAND BALTIMORE COUNTY · PI OSTRAND-ROSENBERG, SUZANNE · 2006 to 2010
$1.3M
NCI NIH HHS R01 CA084232NCI NIH HHS R01 CA115880NIGMS NIH HHS R01 GM021248
6 · The paper itself

Abstract

Cancer immunotherapies aimed at neutralizing the programmed death-1 (PD-1) immune suppressive pathway have yielded significant therapeutic efficacy in a subset of cancer patients. However, only a subset of patients responds to antibody therapy with either anti-PD-1 or anti-PD-L1 antibodies. These patients appear to have so-called "hot" tumors containing tumor-reactive T cells. Therefore, checkpoint blockade therapy may be effective in a larger percentage of cancer patients if combined with therapeutics that also activate tumor-reactive T cells. Radiotherapy (RT) is a prime candidate for combination therapy because it facilitates activation of both local antitumor immunity and antitumor immunity at non-radiated, distant sites (abscopal response). However, RT also promotes tumor cell expression of PD-L1 and facilitates the development of myeloid-derived suppressor cells (MDSC), a population of immune suppressive cells that also suppress through PD-L1. This article will review how RT induces MDSC, and then describe two novel therapeutics that are designed to simultaneously activate tumor-reactive T cells and neutralize PD-1-mediated immune suppression. One therapeutic, a CD3xPD-L1 bispecific T cell engager (BiTE), activates and targets cytotoxic T and NKT cells to kill PD-L1

Indexed as

bi-specific T cell engager (BiTE)myeloid-derived suppressor cells (MDSC)programmed death ligand 1 (PD-L1)radiotherapy-induced immune suppressionsolubilized CD80

Identifiers

PMID31001479
PMCPMC6454107
OpenAlexW2925479072

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.