Evidence map›Paper›PMID 31191522›Full record

ReviewFrontiers in immunology2019

Notch Signaling Regulates Immune Responses in Atherosclerosis.

Francesco Vieceli Dalla Sega, Francesca Fortini, Giorgio Aquila, Gianluca Campo, Mauro Vaccarezza, Paola Rizzo

Abstract readReview
In one paragraph

Review 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 61 papers.

0numbers the graph read from it
0cells of the map it votes in
61citing 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

61 citing papers in PubMed.

  1. Ticagrelor IncreasesInternational journal of molecular sciences · 2020
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  13. Research progress on macrophages in cardiovascular diseases.Journal of cardiothoracic surgery · 2025
    Review
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  15. Article
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  17. Article
  18. Article
  19. Review
  20. Aging · 2024
    Article

1 more citing papers are in PubMed but not listed here.

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

6 authors.

Francesco Vieceli Dalla SegaTranslational Research Center, Maria Cecilia Hospital GVM Care & Research, Cotignola, Italy.
Francesca FortiniTranslational Research Center, Maria Cecilia Hospital GVM Care & Research, Cotignola, Italy.
Giorgio AquilaDepartment of Medical Sciences, University of Ferrara, Ferrara, Italy.
Gianluca CampoTranslational Research Center, Maria Cecilia Hospital GVM Care & Research, Cotignola, Italy.
Mauro VaccarezzaFaculty of Health Sciences, School of Pharmacy and Biomedical Sciences, Curtin University, Perth, WA, Australia.
Paola RizzoTranslational Research Center, Maria Cecilia Hospital GVM Care & Research, Cotignola, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Atherosclerosis is a chronic autoimmune inflammatory disease that can cause coronary artery disease, stroke, peripheral artery disease, depending on which arteries are affected. At the beginning of atherosclerosis plasma lipoproteins accumulate in the sub-endothelial space. In response, monocytes migrate from the circulation through the endothelium into the intima where they differentiate into macrophages. These early events trigger a complex immune response that eventually involves many cellular subtypes of both innate and adaptive immunity. The Notch signaling pathway is an evolutionary conserved cell signaling system that mediates cell-to-cell communication. Recent studies have revealed that Notch modulate atherosclerosis by controlling macrophages polarization into M1 or M2 subtypes. Furthermore, it is known that Notch signaling controls differentiation and activity of T-helper and cytotoxic T-cells in inflammatory diseases. In this review, we will discuss the role of Notch in modulating immunity in the context of atherosclerosis and whether targeting Notch may represent a therapeutic strategy.

Indexed as

AnimalsAtherosclerosisDisease ProgressionHumansMacrophagesMyocardial IschemiaReceptors, NotchSignal TransductionT-LymphocytesReceptors, NotchatherosclerosisDll4endothelial dysfunctionGSIimmunityM1 macrophagesNotchT cells

Identifiers

PMID31191522
PMCPMC6540611

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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.