Evidence map›Paper›PMID 28580947›Full record

ArticleNature communications2017

Pyrin-only protein 2 limits inflammation but improves protection against bacteria.

Sivakumar Periasamy, Kristen A Porter, Maninjay K Atianand, Hongnga T Le, Sarah Earley, Ellen B Duffy, Matthew C Haller, Heather Chin, Jonathan A Harton

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
0.9field-weighted citation impact, top 27% 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

17 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. An overview of human inflammasomes: Activation and regulation.Journal of immunology (Baltimore, Md. : 1950) · 2026
    Review
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  13. Article
  14. The NLRP3 Inflammasome and Its Role in T1DM.Frontiers in immunology · 2020
    Review
  15. Review
  16. COPs and POPs Patrol Inflammasome Activation.Journal of molecular biology · 2018
    Review
  17. 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

9 authors at 2 institutions in 2 countries.

Sivakumar PeriasamyDepartment of Immunology and Microbial Disease, Albany Medical College, Albany, New York 12208 USA.
Kristen A PorterDepartment of Immunology and Microbial Disease, Albany Medical College, Albany, New York 12208 USA.
Maninjay K AtianandDepartment of Immunology and Microbial Disease, Albany Medical College, Albany, New York 12208 USA.
Hongnga T LeDepartment of Immunology and Microbial Disease, Albany Medical College, Albany, New York 12208 USA.
Sarah EarleyDepartment of Immunology and Microbial Disease, Albany Medical College, Albany, New York 12208 USA.
Ellen B DuffyDepartment of Immunology and Microbial Disease, Albany Medical College, Albany, New York 12208 USA.
Matthew C HallerDepartment of Immunology and Microbial Disease, Albany Medical College, Albany, New York 12208 USA.
Heather ChinDepartment of Immunology and Microbial Disease, Albany Medical College, Albany, New York 12208 USA.
Jonathan A HartonDepartment of Immunology and Microbial Disease, Albany Medical College, Albany, New York 12208 USA.ORCID 0000-0002-0350-1877
Albany Medical Center Hospital · USVietnam National University Ho Chi Minh City · VN

Funding

TLR2/NLR Signal Regulation of Protective Immunity to F. TularensisP01AI056320 · NIAID · ALBANY MEDICAL COLLEGE · PI METZGER, DENNIS W · 2003 to 2016
$22.9M
Regulation of Innate Immunity by Pyrin ProteinsR01AI072259 · NIAID · ALBANY MEDICAL COLLEGE · PI HARTON, JONATHAN A · 2009 to 2012
$1.4M
NIAID NIH HHS P01 AI056320NIAID NIH HHS R01 AI072259
6 · The paper itself

Abstract

Pyrin domain-only proteins (POPs) are recently evolved, primate-specific proteins demonstrated in vitro as negative regulators of inflammatory responses. However, their in vivo function is not understood. Of the four known POPs, only POP2 is reported to regulate NF-κB-dependent transcription and multiple inflammasomes. Here we use a transgenic mouse-expressing POP2 controlled by its endogenous human promotor to study the immunological functions of POP2. Despite having significantly reduced inflammatory cytokine responses to LPS and bacterial infection, POP2 transgenic mice are more resistant to bacterial infection than wild-type mice. In a pulmonary tularaemia model, POP2 enhances IFN-γ production, modulates neutrophil numbers, improves macrophage functions, increases bacterial control and diminishes lung pathology. Thus, unlike other POPs thought to diminish innate protection, POP2 reduces detrimental inflammation while preserving and enhancing protective immunity. Our findings suggest that POP2 acts as a high-order regulator balancing cellular function and inflammation with broad implications for inflammation-associated diseases and therapeutic intervention.

Indexed as

AnimalsCell LineFemaleFrancisellaGram-Negative Bacterial InfectionsHEK293 CellsHeLa CellsHumansInflammasomesInflammationInterferon-gammaListeria monocytogenesMacrophagesMaleMiceMice, Inbred BALB CInflammasomesInterferon-gammaNLR Family, Pyrin Domain-Containing 3 ProteinNLRP3 protein, humanRELA protein, humanTranscription Factor RelA

Identifiers

PMID28580947
PMCPMC5512670
OpenAlexW2624175370

What OpenQuestion 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 OpenQuestion graph.