Evidence map›Paper›PMID 31959856›Full record

ArticleScientific reports2020

The Adaptive and Innate Immune Cell Landscape of Uterine Leiomyosarcomas.

Marco Manzoni, Maddalena M Bolognesi, Asier Antoranz, Rosanna Mancari, Silvestro Carinelli, Mario Faretta, Francesca M Bosisio, Giorgio Cattoretti

Erratum issuedAbstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

16 citing papers in PubMed.

  1. Review
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  11. Rejuvenated Vintage Tissue Sections Highlight Individual Antigen Fate During Processing and Long-term Storage.The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society · 2021
    Article
  12. Review
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  15. Unidentified Variables May Account for Variability in Multiplexing Results.The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society · 2020
    Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors.

Marco Manzoni *Pathology, Department of Medicine and Surgery, Università di Milano-Bicocca, Via Cadore 48, Monza, (MI), Italy.
Maddalena M Bolognesi *Pathology, Department of Medicine and Surgery, Università di Milano-Bicocca, Via Cadore 48, Monza, (MI), Italy.
Asier AntoranzNational Technical University of Athens, Zografou Campus, 9 Iroon Polytechniou str., 15780, Zografou, Athens, Greece.
Rosanna MancariDivision of Gynecologic Oncology and Pathology, European Institute of Oncology, Via Ripamonti 435, 20141, Milan, Italy.
Silvestro CarinelliDivision of Gynecologic Oncology and Pathology, European Institute of Oncology, Via Ripamonti 435, 20141, Milan, Italy.
Mario FarettaDepartment of Experimental Oncology, European Institute of Oncology, IRCCS, via Adamello 16, 20139, Milan, Italy.
Francesca M BosisioLaboratory of Translational Cell and Tissue Research, KU Leuven, Herestraat 49, 3000, Leuven, Belgium.
Giorgio CattorettiPathology, Department of Medicine and Surgery, Università di Milano-Bicocca, Via Cadore 48, Monza, (MI), Italy. giorgio.cattoretti@unimib.it.ORCID http://orcid.org/0000-0003-3799-3221

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Reactivation of the anti-tumor response has shown substantial progress in aggressive tumors such as melanoma and lung cancer. Data on less common histotypes are scanty. Immune checkpoint inhibitor therapy has been applied to few cases of uterine leiomyosarcomas, of which the immune cell composition was not examined in detail. We analyzed the inflammatory infiltrate of 21 such cases in high-dimensional, single cell phenotyping on routinely processed tissue. T-lymphoid cells displayed a composite phenotype common to all tumors, suggestive of antigen-exposure, acute and chronic exhaustion. To the contrary, myelomonocytic cells had case-specific individual combinations of phenotypes and subsets. We identified five distinct monocyte-macrophage cell types, some not described before, bearing immunosuppressive molecules (TIM3, B7H3, VISTA, PD1, PDL1). Detailed in situ analysis of routinely processed tissue yields comprehensive information about the immune status of sarcomas. The method employed provides equivalent information to extractive single-cell technology, with spatial contexture and a modest investment.

Indexed as

Adaptive ImmunityImmunity, InnateAdultAgedB7 AntigensB7-H1 AntigenBiomarkers, TumorFemaleHepatitis A Virus Cellular Receptor 2HumansLeiomyosarcomaMiddle AgedMonocytesProgrammed Cell Death 1 ReceptorSingle-Cell AnalysisT-LymphocytesB7 AntigensB7-H1 AntigenBiomarkers, TumorCD274 protein, humanCD276 protein, humanHAVCR2 protein, humanHepatitis A Virus Cellular Receptor 2PDCD1 protein, humanProgrammed Cell Death 1 ReceptorVSIR protein, human

Identifiers

PMID31959856
PMCPMC6971074

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.