Evidence map›Paper›PMID 39126041›Full record

ArticleInternational journal of molecular sciences2024

Neutrophil-like Monocytes Increase in Patients with Colon Cancer and Induce Dysfunctional TIGIT+ NK Cells.

Alessia Calabrò, Fabiana Drommi, Giacomo Sidoti Migliore, Gaetana Pezzino, Grazia Vento, José Freni, Gregorio Costa, Riccardo Cavaliere, Irene Bonaccorsi, Mariagrazia Sionne and 5 more

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
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

7 citing papers in PubMed.

  1. Article
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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

15 authors.

Alessia CalabròLaboratory of Immunology and Biotherapy, Department Human Pathology "G. Barresi", University of Messina, Via Consolare Valeria 1, 98125 Messina, Italy.
Fabiana DrommiLaboratory of Immunology and Biotherapy, Department Human Pathology "G. Barresi", University of Messina, Via Consolare Valeria 1, 98125 Messina, Italy.
Giacomo Sidoti MiglioreTranslational Immunobiology Unit, Laboratory of Infectious Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, BLDG 50, RM 6308, Bethesda, MD 20892, USA.ORCID 0000-0001-5406-6863
Gaetana PezzinoLaboratory of Immunology and Biotherapy, Department Human Pathology "G. Barresi", University of Messina, Via Consolare Valeria 1, 98125 Messina, Italy.
Grazia VentoDepartment of Experimental Medicine (DIMES), University of Genoa, Via Leon Battista Alberti 2, 16132 Genova, Italy.
José FreniLaboratory of Histology, Department of Biomedical, Dental, Morphological and Functional Imaging Sciences, University of Messina, Via Consolare Valeria 1, 98125 Messina, Italy.
Gregorio CostaLaboratory of Immunology and Biotherapy, Department Human Pathology "G. Barresi", University of Messina, Via Consolare Valeria 1, 98125 Messina, Italy.
Riccardo CavaliereClinical Pathology Unit, University Hospital Policlinico G. Martino, 98125 Messina, Italy.
Irene BonaccorsiLaboratory of Immunology and Biotherapy, Department Human Pathology "G. Barresi", University of Messina, Via Consolare Valeria 1, 98125 Messina, Italy.
Mariagrazia SionneOncologic Surgery, Department of Human Pathology of Adult and Evolutive Age, University of Messina, Via Consolare Valeria 1, 98125 Messina, Italy.
Stefania NigroOncologic Surgery, Department of Human Pathology of Adult and Evolutive Age, University of Messina, Via Consolare Valeria 1, 98125 Messina, Italy.
Giuseppe NavarraOncologic Surgery, Department of Human Pathology of Adult and Evolutive Age, University of Messina, Via Consolare Valeria 1, 98125 Messina, Italy.
Guido FerlazzoDepartment of Experimental Medicine (DIMES), University of Genoa, Via Leon Battista Alberti 2, 16132 Genova, Italy.
Claudia De PasqualeLaboratory of Immunology and Biotherapy, Department Human Pathology "G. Barresi", University of Messina, Via Consolare Valeria 1, 98125 Messina, Italy.
Stefania CampanaLaboratory of Immunology and Biotherapy, Department Human Pathology "G. Barresi", University of Messina, Via Consolare Valeria 1, 98125 Messina, Italy.

Funding

Finanziamento Annuale Individuale Attività Base di Ricerca, FFABR FFABR 2023Ministero della Salute PNRR-MAD-2022-12375909Ministero della Salute PNRR-MCNT2-2023-12378122Ministero della Salute PNRR-TR1-2023-12378316Ministero della Salute Ricerca Finalizzata 2018Ministero dell'Istruzione e del Merito PRIN 2017Ministero dell'Istruzione e del Merito PRIN 2022Ministero dell'Istruzione e del Merito PRIN 2022 PNRR
6 · The paper itself

Abstract

Myeloid-derived suppressor cells (MDSCs) are a heterogeneous family of immune cells including granulocytic (CD14neg/CD15+/HLA-DRneg) and monocytic subtypes (CD14+/CD15neg/HLA-DRneg). In the present study, we found a population of monocytes expressing the granulocyte marker CD15 that significantly increased in both peripheral blood (PB) and tumoral tissues of patients with colorectal cancer (CRC). Further phenotypical analysis confirmed the granulocytic-like features of this monocyte subpopulation that is associated with an increase in granulocyte-monocyte precursors (GMPs) in the PB of these patients (pts). Mechanistically, this granulocyte-like monocyte population suppressed NK cell activity by inducing TIGIT and engaging NKp30. Accordingly, an increased frequency of TIGIT+ NK cells with impaired functions was found in both the PB and tumoral tissue of CRC pts. Collectively, we provided new mechanistic explanations for tumor immune escape occurring in CRC by showing the increase in this new kind of MDSC, in both PB and CRC tissue, which is able to significantly impair the effector functions of NK cells, thereby representing a potential therapeutic target for cancer immunotherapy.

Indexed as

Colonic NeoplasmsKiller Cells, NaturalMonocytesReceptors, ImmunologicAgedFemaleHumansMaleMiddle AgedMyeloid-Derived Suppressor CellsNeutrophilsReceptors, ImmunologicTIGIT protein, humanCRChumanMDSCsmonocytesneutrophil-like cellsNK cellsTIGIT

Identifiers

PMID39126041
PMCPMC11313383

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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.