Evidence map›Paper›PMID 37898752›Full record

ArticleJournal of experimental & clinical cancer research : CR2023

CD28/PD1 co-expression: dual impact on CD8

Belinda Palermo, Ornella Franzese, Giuseppe Frisullo, Lorenzo D'Ambrosio, Mariangela Panetta, Giulia Campo, Daniel D'Andrea, Isabella Sperduti, Francesca De Nicola, Frauke Goeman and 4 more

Open access · goldAbstract read
In one paragraph

Article in Journal of experimental & clinical cancer research : CR, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
7.8field-weighted citation impact, top 2% 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

37 citing papers in PubMed, 34 citations in OpenAlex.

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  3. Sequential Immune Activation of Effector T Cells as Biomarkers of Response to Durvalumab in Patients with Locally Advanced NSCLC.Clinical cancer research : an official journal of the American Association for Cancer Research · 2026
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  4. Viscoelastic Niches Shape γδ T-Cell Phenotype and Effector Function.bioRxiv : the preprint server for biology · 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

14 authors at 4 institutions in 3 countries.

Belinda Palermo *Tumor Immunology and Immunotherapy Unit, IRCCS-Regina Elena National Cancer Institute, Rome, Italy.
Ornella Franzese *Department of Systems Medicine, University of Rome "Tor Vergata", Rome, Italy.
Giuseppe FrisulloTumor Immunology and Immunotherapy Unit, IRCCS-Regina Elena National Cancer Institute, Rome, Italy.
Lorenzo D'AmbrosioTumor Immunology and Immunotherapy Unit, IRCCS-Regina Elena National Cancer Institute, Rome, Italy.
Mariangela PanettaTumor Immunology and Immunotherapy Unit, IRCCS-Regina Elena National Cancer Institute, Rome, Italy.
Giulia CampoTumor Immunology and Immunotherapy Unit, IRCCS-Regina Elena National Cancer Institute, Rome, Italy.
Daniel D'AndreaDepartment of Biosciences, School of Science and Technology, Nottingham Trent University, Nottingham, UK.
Isabella SperdutiBiostatistics and Scientific Direction, IRCCS-Regina Elena National Cancer Institute, Rome, Italy.
Francesca De NicolaSAFU Unit, IRCCS-Regina Elena National Cancer Institute, Rome, Italy.
Frauke GoemanSAFU Unit, IRCCS-Regina Elena National Cancer Institute, Rome, Italy.
Filippo GallinaThoracic-Surgery Unit, IRCCS-Regina Elena National Cancer Institute, Rome, Italy.
Paolo ViscaPathology Unit, IRCCS-Regina Elena National Cancer Institute, Rome, Italy.
Francesco FaccioloThoracic-Surgery Unit, IRCCS-Regina Elena National Cancer Institute, Rome, Italy.
Paola NisticòTumor Immunology and Immunotherapy Unit, IRCCS-Regina Elena National Cancer Institute, Rome, Italy. paola.nistico@ifo.it.ORCID http://orcid.org/0000-0003-4409-2261
Istituti di Ricovero e Cura a Carattere Scientifico · ITNational Cancer Institute · MYNottingham Trent University · GBUniversity of Rome Tor Vergata · IT

Funding

Associazione Italiana per la Ricerca sul Cancro IG 19822Ministero della Salute Ricerca corrente 2023
6 · The paper itself

Abstract

backgroundImmune checkpoint blockade (ICB) has significantly prolonged survival of non-small cell lung cancer (NSCLC) patients, although most patients develop mechanisms of resistance. Recently single-cell RNA-sequencing (scRNA-Seq) revealed a huge T-cell phenotypic and (dys)functional state variability. Accordingly, T-cell exhaustion is recognized as a functional adaptation, with a dynamic progression from a long-lived "pre-exhausted stem-like progenitor" to a "terminally exhausted" state. In this scenario it is crucial to understand the complex interplay between co-stimulatory and inhibitory molecules in CD8

methodsTo gain a baseline landscape of the composition, functional states, and transcriptomic signatures predictive of prognosis, we analyzed CD8

resultsDespite the increased PD1 levels, an improved PD1

conclusionsOur findings identify signatures able to stratify survival of LUAD patients and predict ICB response in advanced NSCLC. CD28 is advocated as a key determinant in the signatures identified, in both periphery and tumor site, thus likely providing feasible biomarkers of ICB response.

Indexed as

Adenocarcinoma of LungCarcinoma, Non-Small-Cell LungLung NeoplasmsCD28 AntigensCD8-Positive T-LymphocytesHepatitis A Virus Cellular Receptor 2HumansImmune Checkpoint InhibitorsCD28 AntigensHepatitis A Virus Cellular Receptor 2Immune Checkpoint InhibitorsCD28CD8+ T cellsImmune Checkpoint BlockadeNon-small cell lung cancerPD-1Single-cell RNA-SeqT-cell functionality

Identifiers

PMID37898752
PMCPMC10612243
OpenAlexW4388034464

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.