Evidence map›Paper›PMID 35961978›Full record

ReviewCell death & disease2022

Chromatin-Associated Molecular Patterns (CAMPs) in sepsis.

Colleen P Nofi, Ping Wang, Monowar Aziz

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 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.8field-weighted citation impact, top 8% 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

23 citing papers in PubMed, 34 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Review
  5. Anti-DAMP therapies for acute inflammation.Frontiers in immunology · 2025
    Review
  6. Review
  7. Review
  8. An anti-eCIRP strategy for necrotizing enterocolitis.Molecular medicine (Cambridge, Mass.) · 2024
    Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. A novel opsonic eCIRP inhibitor for lethal sepsis.Journal of leukocyte biology · 2024
    Article
  15. Review
  16. Review
  17. Article
  18. DAMPs and radiation injury.Frontiers in immunology · 2024
    Review
  19. Review
  20. Article
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

3 authors at 2 institutions in 1 country.

Colleen P NofiCenter for Immunology and Inflammation, The Feinstein Institutes for Medical Research, Manhasset, NY, USA.
Ping Wang *Center for Immunology and Inflammation, The Feinstein Institutes for Medical Research, Manhasset, NY, USA. Pwang@northwell.edu.ORCID 0000-0002-1557-0394
Monowar Aziz *Center for Immunology and Inflammation, The Feinstein Institutes for Medical Research, Manhasset, NY, USA. Maziz1@northwell.edu.
Northwell Health · USFeinstein Institute for Medical Research · US

Funding

IMPROVEMENT OF ORGAN FUNCTION AFTER SEVERE HYPOVOLEMIAR01HL076179 · NHLBI · FEINSTEIN INSTITUTE FOR MEDICAL RESEARCH · PI PING WANG · 2004 to 2026
$7.6M
Novel Approaches to Maintaining Organ Function in SepsisR35GM118337 · NIGMS · FEINSTEIN INSTITUTE FOR MEDICAL RESEARCH · PI PING WANG · 2016 to 2026
$5.2M
Mechanisms of Radiation-Induced Innate Immune Dysfunction and Its CountermeasuresU01AI170018 · NIAID · FEINSTEIN INSTITUTE FOR MEDICAL RESEARCH · PI Monowar Aziz, Max Brenner · 2022 to 2026
$4.2M
The Role of Ionizing Radiation in Alzheimer’s DiseaseU01AI133655 · NIAID · FEINSTEIN INSTITUTE FOR MEDICAL RESEARCH · PI BRENNER, MAX, WANG, PING · 2017 to 2022
$3.4M
Promotion of Alzheimers Disease by Alcohol - Role of eCIRPR01AA028947 · NIAAA · FEINSTEIN INSTITUTE FOR MEDICAL RESEARCH · PI MARAMBAUD, PHILIPPE, WANG, PING · 2020 to 2024
$2.1M
Neutrophils in Sepsis: Role of CIRPR01GM129633 · NIGMS · FEINSTEIN INSTITUTE FOR MEDICAL RESEARCH · PI AZIZ, MONOWAR · 2018 to 2022
$1.6M
NHLBI NIH HHS R01 HL076179NIAAA NIH HHS R01 AA028947NIAID NIH HHS U01 AI133655NIAID NIH HHS U01 AI170018NIGMS NIH HHS R01 GM129633NIGMS NIH HHS R35 GM118337U.S. Department of Health & Human Services | National Institutes of Health (NIH) R01GM129633U.S. Department of Health & Human Services | National Institutes of Health (NIH) R01HL076179U.S. Department of Health & Human Services | National Institutes of Health (NIH) R35GM118337U.S. Department of Health & Human Services | National Institutes of Health (NIH) U01AI133655U.S. Department of Health & Human Services | National Institutes of Health (NIH) U01AI170018U.S. Department of Health & Human Services | NIH | Office of Extramural Research, National Institutes of Health (OER) R01AA028947
6 · The paper itself

Abstract

Several molecular patterns have been identified that recognize pattern recognition receptors. Pathogen-associated molecular patterns (PAMPs) and damage-associated molecular patterns (DAMPs) are commonly used terminologies to classify molecules originating from pathogen and endogenous molecules, respectively, to heighten the immune response in sepsis. Herein, we focus on a subgroup of endogenous molecules that may be detected as foreign and similarly trigger immune signaling pathways. These chromatin-associated molecules, i.e., chromatin containing nuclear DNA and histones, extracellular RNA, mitochondrial DNA, telomeric repeat-containing RNA, DNA- or RNA-binding proteins, and extracellular traps, may be newly classified as chromatin-associated molecular patterns (CAMPs). Herein, we review the release of CAMPs from cells, their mechanism of action and downstream immune signaling pathways, and targeted therapeutic approaches to mitigate inflammation and tissue injury in inflammation and sepsis.

Indexed as

ChromatinSepsisDNA, MitochondrialHumansInflammationPathogen-Associated Molecular Pattern MoleculesReceptors, Pattern RecognitionChromatinDNA, MitochondrialPathogen-Associated Molecular Pattern MoleculesReceptors, Pattern Recognition

Identifiers

PMID35961978
PMCPMC9372964
OpenAlexW4291633830

What OpenQuestion holds

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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 OpenQuestion graph.