Evidence map›Paper›PMID 31497016›Full record

ArticleFrontiers in immunology2019

Different Features of Tumor-Associated NK Cells in Patients With Low-Grade or High-Grade Peritoneal Carcinomatosis.

Silvia Pesce, Valerio Belgrano, Marco Greppi, Simona Carlomagno, Margherita Squillario, Annalisa Barla, Mariella Della Chiesa, Stefano Di Domenico, Domenico Mavilio, Lorenzo Moretta and 4 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

20 citing papers in PubMed, 26 citations in OpenAlex.

  1. Review
  2. Intraperitoneal infusion of NKG2D CAR-NK cells induces endogenous CD8Molecular therapy : the journal of the American Society of Gene Therapy · 2025
    Article
  3. PD-1Journal of experimental & clinical cancer research : CR · 2025
    Article
  4. Article
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  6. Review
  7. Article
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  13. Review
  14. Review
  15. Article
  16. Article
  17. Review
  18. Review
  19. Review
  20. miRNAs in NK Cell-Based Immune Responses and Cancer Immunotherapy.Frontiers in cell and developmental biology · 2020
    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

14 authors at 4 institutions in 2 countries.

Silvia PesceDepartment of Experimental Medicine, University of Genoa, Genoa, Italy.
Valerio BelgranoDepartment of Surgical Sciences and Integrated Diagnostics, IRCCS Policlinico San Martino, University General Hospital, University of Genoa, Genoa, Italy.
Marco GreppiDepartment of Experimental Medicine, University of Genoa, Genoa, Italy.
Simona CarlomagnoDepartment of Experimental Medicine, University of Genoa, Genoa, Italy.
Margherita SquillarioDepartment of Informatic Bioengineering, Robotic and System Engineering, University of Genoa, Genoa, Italy.
Annalisa BarlaDepartment of Informatic Bioengineering, Robotic and System Engineering, University of Genoa, Genoa, Italy.
Mariella Della ChiesaDepartment of Experimental Medicine, University of Genoa, Genoa, Italy.
Stefano Di DomenicoDepartment of Surgical Sciences and Integrated Diagnostics, IRCCS Policlinico San Martino, University General Hospital, University of Genoa, Genoa, Italy.
Domenico MavilioUnit of Clinical and Experimental Immunology, Humanitas Clinical and Research Center, Rozzano, Milan, Italy.
Lorenzo MorettaDepartment of Immunology, IRCCS Bambino Gesù Children's Hospital, Rome, Italy.
Simona CandianiDepartment of Earth Science, Environment and Life, University of Genoa, Genoa, Italy.
Simona SivoriDepartment of Experimental Medicine, University of Genoa, Genoa, Italy.
Franco De CianDepartment of Surgical Sciences and Integrated Diagnostics, IRCCS Policlinico San Martino, University General Hospital, University of Genoa, Genoa, Italy.
Emanuela MarcenaroDepartment of Experimental Medicine, University of Genoa, Genoa, Italy.
University of Genoa · ITOspedale Policlinico San Martino · ITIstituti di Ricovero e Cura a Carattere Scientifico · ITUniversity of Milan · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Peritoneal carcinomatosis (PC) is a rare disease defined as diffused implantation of neoplastic cells in the peritoneal cavity. This clinical picture occurs during the evolution of peritoneal tumors, and it is the main cause of morbidity and mortality of patients affected by these pathologies, though cytoreductive surgery with heated intra-peritoneal chemotherapy (CRS/HIPEC) is yielding promising results. In the present study, we evaluated whether the tumor microenvironment of low-grade and high-grade PC could affect the phenotypic and functional features and thus the anti-tumor potential of NK cells. We show that while in the peritoneal fluid (PF) of low-grade PC most CD56dim NK cells show a relatively immature phenotype (NKG2A+KIR-CD57-CD16dim), in the PF of high-grade PC NK cells are, in large majority, mature (CD56dimKIR+CD57+CD16bright). Furthermore, in low-grade PC, PF-NK cells are characterized by a sharp down-regulation of some activating receptors, primarily NKp30 and DNAM-1, while, in high-grade PC, PF-NK cells display a higher expression of the PD-1 inhibitory checkpoint. The compromised phenotype observed in low-grade PC patients corresponds to a functional impairment. On the other hand, in the high-grade PC patients PF-NK cells show much more important defects that only partially reflect the compromised phenotype detected. These data suggest that the PC microenvironment may contribute to tumor escape from immune surveillance by inducing different NK cell impaired features leading to altered anti-tumor activity. Notably, after CRS/HIPEC treatment, the altered NK cell phenotype of a patient with a low-grade disease and favorable prognosis was reverted to a normal one. Our present data offer a clue for the development of new immunotherapeutic strategies capable of restoring the NK-mediated anti-tumor responses in association with the CRS/HIPEC treatment to increase the effectiveness of the current therapy.

Indexed as

Cell Line, TumorHumansKiller Cells, NaturalPeritoneal NeoplasmsPhenotypeSeverity of Illness IndexTumor EscapeTumor Microenvironmenthuman NK cellsimmune checkpointimmune escapeNK cell receptorsNKp30PD-1/PD-Lperitoneal carcinomatosispseudomyxoma peritonei

Identifiers

PMID31497016
PMCPMC6712073
OpenAlexW2964791181

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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.