Evidence map›Paper›PMID 35501340›Full record

ReviewCell death & disease2022

Types of necroinflammation, the effect of cell death modalities on sterile inflammation.

Anett Mázló, Viktória Jenei, Sára Burai, Tamás Molnár, Attila Bácsi, Gábor Koncz

Open access · goldAbstract readReview
In one paragraph

Review in Cell death & disease, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed, 1 pooled it
5.8field-weighted citation impact, top 3% 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

38 citing papers in PubMed, 1 synthesis or guideline pooled it, 66 citations in OpenAlex.

  1. Pooled it
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  5. Regulated cell death programs shaping cancer therapy.Cellular oncology (Dordrecht, Netherlands) · 2026
    Review
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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

6 authors at 1 institution in 1 country.

Anett Mázló *Department of Immunology, Faculty of Medicine, University of Debrecen, Egyetem square 1, Debrecen, 4032, Hungary. mazlo.anett@med.unideb.hu.ORCID 0000-0001-7012-7101
Viktória Jenei *Department of Immunology, Faculty of Medicine, University of Debrecen, Egyetem square 1, Debrecen, 4032, Hungary.
Sára BuraiDepartment of Immunology, Faculty of Medicine, University of Debrecen, Egyetem square 1, Debrecen, 4032, Hungary.
Tamás MolnárDepartment of Immunology, Faculty of Medicine, University of Debrecen, Egyetem square 1, Debrecen, 4032, Hungary.ORCID 0000-0002-5720-0447
Attila BácsiDepartment of Immunology, Faculty of Medicine, University of Debrecen, Egyetem square 1, Debrecen, 4032, Hungary.
Gábor KonczDepartment of Immunology, Faculty of Medicine, University of Debrecen, Egyetem square 1, Debrecen, 4032, Hungary. konczgb@gmail.com.ORCID 0000-0002-4888-6838
University of Debrecen · HU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Distinct types of immune responses are activated by infections, which cause the development of type I, II, or III inflammation, regulated by Th1, Th2, Th17 helper T cells and ILC1, ILC2 and ILC3 cells, respectively. While the classification of immune responses to different groups of pathogens is widely accepted, subtypes of the immune response elicited by sterile inflammation have not yet been detailed. Necroinflammation is associated with the release of damage-associated molecular patterns (DAMP) from dying cells. In this review, we present that the distinct molecular mechanisms activated during apoptosis, necroptosis, pyroptosis, and ferroptosis lead to the release of different patterns of DAMPs and their suppressors, SAMPs. We summarize the currently available data on how regulated cell death pathways and released DAMPs and SAMPs direct the differentiation of T helper and ILC cells. Understanding the subtypes of necroinflammation can be crucial in developing strategies for the treatment of sterile inflammatory diseases caused by cell death processes.

Indexed as

Immunity, InnateLymphocytesAlarminsCell DeathHumansInflammationAlarmins

Identifiers

PMID35501340
PMCPMC9061831
OpenAlexW4225275235

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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 Socratic graph.