Evidence map›Paper›PMID 27207606›Full record

ArticleCancer immunology, immunotherapy : CII2016

CTLA-4 in mesothelioma patients: tissue expression, body fluid levels and possible relevance as a prognostic factor.

Silvio Roncella, Stefania Laurent, Vincenzo Fontana, Paola Ferro, Maria Cristiana Franceschini, Sandra Salvi, Serena Varesano, Simona Boccardo, Antonella Vigani, Anna Morabito and 12 more

Open access · greenAbstract read
In one paragraph

Article in Cancer immunology, immunotherapy : CII, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed, 1 pooled it
3.3field-weighted citation impact, top 8% 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

34 citing papers in PubMed, 1 synthesis or guideline pooled it, 49 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. CTLA-4-two pathways to anti-tumour immunity?Immunotherapy advances · 2025
    Review
  4. Article
  5. Observational
  6. Soluble CTLA-4 attenuates T cell activation and modulates anti-tumor immunity.Molecular therapy : the journal of the American Society of Gene Therapy · 2024
    Article
  7. Review
  8. Review
  9. Article
  10. Article
  11. Review
  12. Review
  13. Review
  14. [Research Progress of Immune Checkpoint Inhibitors 
in Malignant Pleural Mesothelioma].Zhongguo fei ai za zhi = Chinese journal of lung cancer · 2021
    Review
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Review
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

22 authors at 2 institutions in 1 country.

Silvio RoncellaDivision of Histopathology and Cytopathology, ASL5, La Spezia, Italy.
Stefania LaurentDepartment of Internal Medicine (DIMI), University of Genoa, Genoa, Italy.
Vincenzo FontanaUnit of Clinical Epidemiology, IRCCS AOU San Martino-IST, Genoa, Italy.
Paola FerroDivision of Histopathology and Cytopathology, ASL5, La Spezia, Italy.
Maria Cristiana FranceschiniDivision of Histopathology and Cytopathology, ASL5, La Spezia, Italy.
Sandra SalviDivision of Histopathology and Cytopathology, IRCCS AOU San Martino-IST, Genoa, Italy.
Serena VaresanoDivision of Histopathology and Cytopathology, IRCCS AOU San Martino-IST, Genoa, Italy.
Simona BoccardoDivision of Histopathology and Cytopathology, IRCCS AOU San Martino-IST, Genoa, Italy.
Antonella ViganiUnit of Clinical Oncology, ASL5, La Spezia, Italy.
Anna MorabitoUnit of Tumor Epigenetics, IRCCS AOU San Martino-IST, Genoa, Italy.
Pier Aldo CanessaDivision of Pneumology, ASL5, La Spezia, Italy.
Ugo GiannoniUnit of Radiodiagnostic, ASL5, La Spezia, Italy.
Ilan RosenbergUnit of Radiodiagnostic, ASL5, La Spezia, Italy.
Alessandro ValentinoDivision of Histopathology and Cytopathology, ASL5, La Spezia, Italy.
Franco FedeliDivision of Histopathology and Cytopathology, ASL5, La Spezia, Italy.
Domenico Franco MerloUnit of Clinical Epidemiology, IRCCS AOU San Martino-IST, Genoa, Italy.
Marcello CeppiUnit of Clinical Epidemiology, IRCCS AOU San Martino-IST, Genoa, Italy.
Salvatore RiggioBlood Transfusion Centre, IRCCS AOU-San Martino-IST, Genoa, Italy.
Massimo RomaniUnit of Tumor Epigenetics, IRCCS AOU San Martino-IST, Genoa, Italy.
Daniele SaverinoDepartment of Experimental Medicine, University of Genoa, Genoa, Italy.
Alessandro PoggiUnit of Molecular Oncology and Angiogenesis, IRCCS AOU San Martino-IST, Genoa, Italy.
Maria Pia PistilloUnit of Tumor Epigenetics, IRCCS AOU San Martino-IST, Genoa, Italy. mariapia.pistillo@hsanmartino.it.
Ospedale Policlinico San Martino · ITUniversity of Genoa · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

CTLA-4 function as a negative regulator of T cell-mediated immune response is well established, whereas much less is known about the immunoregulatory role of its soluble isoform (sCTLA-4). No data are available on CTLA-4 expression and prognostic impact in malignant pleural mesothelioma (MPM). We investigated, by immunohistochemistry, CTLA-4 expression in tumor tissues and, by ELISA, sCTLA-4 levels in sera and matched pleural effusions from 45 MPM patients. Prognostic effect of CTLA-4 expression on overall survival (OS) was assessed through Cox regression and prognostic significance expressed as death rate ratio (HR). We found that 56.0 % of MPM tissues expressed CTLA-4 with variable intensity and percentage of positive cells estimated by the immunoreactive score. sCTLA-4 levels were significantly higher in sera (S-sCTLA-4) than in pleural effusions (PE-sCTLA-4) (geometric mean ratio = 2.70, P value = 0.020). CTLA-4 expression at the tissue level was higher in the epithelioid histological subtype than in the sarcomatoid, whereas at the serum level, it was higher in the sarcomatoid subtype. A homogeneous favorable prognostic effect was found for CTLA-4 overexpression in tissue, serum and pleural effusion. Interestingly, only the PE-sCTLA-4 was found to be a statistically significant positive prognostic factor (HR = 0.37, 95 % CI = 0.18-0.77, P value = 0.007). Indeed, PE-sCTLA-4 correlated with CTLA-4 expression in tissues, whereas this latter expression showed a weak association with OS. To confirm our findings, further experimental evidences obtained from a larger cohort of MPM patients are required. However, our results would indicate a positive correlation of PE-sCTLA-4 levels and OS in MPM patients.

Indexed as

AgedAged, 80 and overCTLA-4 AntigenFemaleHumansMaleMesotheliomaMiddle AgedPrognosisSurvival AnalysisCTLA-4 AntigenCTLA4 protein, humanCTLA-4MesotheliomaOverall survivalPleural effusionPrognostic factor

Identifiers

PMID27207606
PMCPMC11029598
OpenAlexW2398861322

What OpenQuestion holds

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Registered trials

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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.