Evidence map›Paper›PMID 36796366›Full record

ArticleCell reports. Medicine2023

OX40 agonism enhances PD-L1 checkpoint blockade by shifting the cytotoxic T cell differentiation spectrum.

Tetje C van der Sluis, Guillaume Beyrend, Esmé T I van der Gracht, Tamim Abdelaal, Simon P Jochems, Robert A Belderbos, Thomas H Wesselink, Suzanne van Duikeren, Floortje J van Haften, Anke Redeker and 13 more

Open access · goldFull text read
In one paragraph

Article in Cell reports. Medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
5.1field-weighted citation impact, top 4% 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

16 citing papers in PubMed, 22 citations in OpenAlex.

  1. Trial
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  3. Cell cycle arrest enhances CD8Nature immunology · 2026
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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

23 authors at 4 institutions in 2 countries.

Tetje C van der SluisDepartment of Immunology, Leiden University Medical Center, 2333ZA Leiden, the Netherlands.
Guillaume BeyrendDepartment of Immunology, Leiden University Medical Center, 2333ZA Leiden, the Netherlands.
Esmé T I van der GrachtDepartment of Immunology, Leiden University Medical Center, 2333ZA Leiden, the Netherlands.
Tamim AbdelaalDepartment of Radiology, Leiden University Medical Center, 2333ZA Leiden, the Netherlands; Systems and Biomedical Engineering Department, Faculty of Engineering, Cairo University, Giza 12613, Egypt; Pattern Recognition and Bioinformatics, Delft University of Technology, 2628XE Delft, the Netherlands.
Simon P JochemsDepartment of Parasitology, Leiden University Center for Infectious Diseases, Leiden University Medical Center, 2333ZA Leiden, the Netherlands.
Robert A BelderbosDepartment of Pulmonary Diseases, Erasmus Medical Center, 3015GD Rotterdam, the Netherlands.
Thomas H WesselinkDepartment of Immunology, Leiden University Medical Center, 2333ZA Leiden, the Netherlands.
Suzanne van DuikerenDepartment of Immunology, Leiden University Medical Center, 2333ZA Leiden, the Netherlands.
Floortje J van HaftenDepartment of Immunology, Leiden University Medical Center, 2333ZA Leiden, the Netherlands.
Anke RedekerDepartment of Immunology, Leiden University Medical Center, 2333ZA Leiden, the Netherlands.
Laura F OuboterDepartment of Immunology, Leiden University Medical Center, 2333ZA Leiden, the Netherlands.
Elham Beyranvand NejadDepartment of Immunology, Leiden University Medical Center, 2333ZA Leiden, the Netherlands.
Marcel CampsDepartment of Immunology, Leiden University Medical Center, 2333ZA Leiden, the Netherlands.
Kees L M C FrankenDepartment of Immunology, Leiden University Medical Center, 2333ZA Leiden, the Netherlands.
Margot M LinssenCentral Animal and Transgenic Facility, Leiden University Medical Center, 2333ZA Leiden, the Netherlands.
Peter HohensteinCentral Animal and Transgenic Facility, Leiden University Medical Center, 2333ZA Leiden, the Netherlands.
Noel F C C de MirandaDepartment of Pathology, Leiden University Medical Center, 2333ZA Leiden, the Netherlands.
Hailiang MeiDepartment of Biomedical Data Sciences, Sequencing Analysis Support Core, Leiden University Medical Center, 2333ZA Leiden, the Netherlands.
Adriaan D BinsDepartment of Internal Medicine, Amsterdam University Medical Center, 1105AZ Amsterdam, the Netherlands.
John B A G HaanenDivision of Molecular Oncology and Immunology, Netherlands Cancer Institute, 1066CX Amsterdam, the Netherlands.
Joachim G AertsDepartment of Pulmonary Diseases, Erasmus Medical Center, 3015GD Rotterdam, the Netherlands.
Ferry OssendorpDepartment of Immunology, Leiden University Medical Center, 2333ZA Leiden, the Netherlands.
Ramon ArensDepartment of Immunology, Leiden University Medical Center, 2333ZA Leiden, the Netherlands. Electronic address: r.arens@lumc.nl.
Leiden University Medical Center · NLAmsterdam University Medical Centers · NLCairo University · EGThe Netherlands Cancer Institute · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Immune checkpoint therapy (ICT) has the power to eradicate cancer, but the mechanisms that determine effective therapy-induced immune responses are not fully understood. Here, using high-dimensional single-cell profiling, we interrogate whether the landscape of T cell states in the peripheral blood predict responses to combinatorial targeting of the OX40 costimulatory and PD-1 inhibitory pathways. Single-cell RNA sequencing and mass cytometry expose systemic and dynamic activation states of therapy-responsive CD4

Indexed as

CD8-Positive T-LymphocytesNeoplasmsAnimalsB7-H1 AntigenCell DifferentiationMiceReceptors, ChemokineReceptors, OX40B7-H1 AntigenReceptors, ChemokineReceptors, OX40Tnfrsf4 protein, mouseimmune checkpoint therapyimmunotherapymass cytometrypredictive biomarkerssingle-cell RNA sequencingsystemic immune activationT cells

Identifiers

PMID36796366
PMCPMC10040386
OpenAlexW4320914687

What OpenQuestion holds

Textfull text, public
LicenceCC BY
measurements read50
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.