Evidence map›Paper›PMID 30315349›Full record

ArticleCancer immunology, immunotherapy : CII2019

Histamine targets myeloid-derived suppressor cells and improves the anti-tumor efficacy of PD-1/PD-L1 checkpoint blockade.

Hanna Grauers Wiktorin, Malin S Nilsson, Roberta Kiffin, Frida Ewald Sander, Brianna Lenox, Anna Rydström, Kristoffer Hellstrand, Anna Martner

Open access · hybridAbstract read
In one paragraph

Article in Cancer immunology, immunotherapy : CII, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 62 papers.

0numbers the graph read from it
0cells of the map it votes in
62citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

62 citing papers in PubMed, 82 citations in OpenAlex.

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2 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

8 authors at 2 institutions in 1 country.

Hanna Grauers WiktorinTIMM Laboratory, Sahlgrenska Cancer Center, University of Gothenburg, Medicinaregatan 1F, Box 425, 413 90, Göteborg, Sweden.ORCID http://orcid.org/0000-0002-4412-5695
Malin S NilssonTIMM Laboratory, Sahlgrenska Cancer Center, University of Gothenburg, Medicinaregatan 1F, Box 425, 413 90, Göteborg, Sweden.ORCID http://orcid.org/0000-0002-0981-2617
Roberta KiffinTIMM Laboratory, Sahlgrenska Cancer Center, University of Gothenburg, Medicinaregatan 1F, Box 425, 413 90, Göteborg, Sweden.ORCID http://orcid.org/0000-0002-4058-1327
Frida Ewald SanderTIMM Laboratory, Sahlgrenska Cancer Center, University of Gothenburg, Medicinaregatan 1F, Box 425, 413 90, Göteborg, Sweden.ORCID http://orcid.org/0000-0002-9726-6344
Brianna LenoxTIMM Laboratory, Sahlgrenska Cancer Center, University of Gothenburg, Medicinaregatan 1F, Box 425, 413 90, Göteborg, Sweden.ORCID http://orcid.org/0000-0001-8681-9153
Anna RydströmTIMM Laboratory, Sahlgrenska Cancer Center, University of Gothenburg, Medicinaregatan 1F, Box 425, 413 90, Göteborg, Sweden.ORCID http://orcid.org/0000-0002-0429-3889
Kristoffer HellstrandTIMM Laboratory, Sahlgrenska Cancer Center, University of Gothenburg, Medicinaregatan 1F, Box 425, 413 90, Göteborg, Sweden.ORCID http://orcid.org/0000-0002-6617-5976
Anna MartnerTIMM Laboratory, Sahlgrenska Cancer Center, University of Gothenburg, Medicinaregatan 1F, Box 425, 413 90, Göteborg, Sweden. anna.martner@gu.se.ORCID http://orcid.org/0000-0002-6598-5221
University of Gothenburg · SESahlgrenska University Hospital · SE

Funding

Cancerfonden CAN 2016/351The Swedish state via the ALF agreement ALFGBG-724881Vetenskapsrådet 2016-01928
6 · The paper itself

Abstract

Myeloid-derived suppressor cells (MDSCs) are immature monocytes and granulocytes that impede immune-mediated clearance of malignant cells by multiple mechanisms, including the formation of immunosuppressive reactive oxygen species (ROS) via the myeloid cell NADPH oxidase (NOX2). Histamine dihydrochloride (HDC), a NOX2 inhibitor, exerts anti-cancer efficacy in experimental tumor models but the detailed mechanisms are insufficiently understood. To determine effects of HDC on the MDSC compartment we utilized three murine cancer models known to entail accumulation of MDSC, i.e. EL-4 lymphoma, MC-38 colorectal carcinoma, and 4T1 mammary carcinoma. In vivo treatment with HDC delayed EL-4 and 4T1 tumor growth and reduced the ROS formation by intratumoral MDSCs. HDC treatment of EL-4 bearing mice also reduced the accumulation of intratumoral MDSCs and reduced MDSC-induced suppression of T cells ex vivo. Experiments using GR1-depleted and Nox2 knock out mice supported that the anti-tumor efficacy of HDC required presence of NOX2

Indexed as

AdultAnimalsAntibodiesB7-H1 AntigenCell Line, TumorClinical Trials, Phase IV as TopicDisease-Free SurvivalDrug SynergismFemaleHistamineHistamine AgonistsHumansMice, Inbred BALB CMice, Inbred C57BLMice, KnockoutMyeloid-Derived Suppressor CellsAntibodiesB7-H1 AntigenHistamineHistamine AgonistsProgrammed Cell Death 1 ReceptorCheckpoint inhibitionHistamine dihydrochlorideMyeloid-derived suppressor cellsNOX2PD-1Reactive oxygen species

Identifiers

PMID30315349
PMCPMC6394491
OpenAlexW2897145425

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.