Evidence map›Paper›PMID 35983035›Full record

ArticleFrontiers in immunology2022

Neutrophil heterogeneity in complement C1q expression associated with sepsis mortality.

Alissa Trzeciak, Raj Kumar Mongre, Ma Rie Kim, Kihong Lim, Rafael A Madero, Christopher N Parkhurst, Anthony P Pietropaoli, Minsoo Kim

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

10 citing papers in PubMed, 9 citations in OpenAlex.

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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

8 authors at 3 institutions in 1 country.

Alissa TrzeciakDepartment of Microbiology and Immunology, David H. Smith Center for Vaccine Biology and Immunology, University of Rochester, Rochester, NY, United States.
Raj Kumar MongreDepartment of Microbiology and Immunology, David H. Smith Center for Vaccine Biology and Immunology, University of Rochester, Rochester, NY, United States.
Ma Rie KimDepartment of Biomedical Engineering, University of Rochester Medical Center, Rochester, NY, United States.
Kihong LimDepartment of Microbiology and Immunology, David H. Smith Center for Vaccine Biology and Immunology, University of Rochester, Rochester, NY, United States.
Rafael A MaderoDepartment of Microbiology and Immunology, David H. Smith Center for Vaccine Biology and Immunology, University of Rochester, Rochester, NY, United States.
Christopher N ParkhurstDivision of Pulmonary and Critical Care Medicine, Weill-Cornell Medicine, New York, NY, United States.
Anthony P PietropaoliPulmonary and Critical Care Medicine Division, University of Rochester, Rochester, NY, United States.
Minsoo KimDepartment of Microbiology and Immunology, David H. Smith Center for Vaccine Biology and Immunology, University of Rochester, Rochester, NY, United States.
University of Rochester · USUniversity of Rochester Medical Center · USCornell University · US

Funding

Tissue regulation of T cell function - Reagents CoreP01AI102851 · NIAID · UNIVERSITY OF ROCHESTER · PI Deborah J Fowell · 2014 to 2026
$26.0M
Complement C1q and sepsis associated fatalitiesR01HL160723 · NHLBI · UNIVERSITY OF ROCHESTER · PI KIM, MINSOO, PIETROPAOLI, ANTHONY P · 2022 to 2025
$2.7M
Infection and Immunity: The Pathogenesis of Host-Microbe InteractionsT32AI118689 · NIAID · UNIVERSITY OF ROCHESTER · PI Paul M. Dunman, BRIAN M WARD · 2015 to 2026
$2.5M
Identification of a Damaging Subset of Neutrophils that Arises in Septic PatientsR01HL147525 · NHLBI · RHODE ISLAND HOSPITAL · PI KIM, MINSOO, REICHNER, JONATHAN S · 2019 to 2022
$2.0M
Visualizing the resolution of innate immune responses during influenza infectionR21AI149775 · NIAID · UNIVERSITY OF ROCHESTER · PI KIM, MINSOO · 2020 to 2021
$424k
NHLBI NIH HHS R01 HL147525NHLBI NIH HHS R01 HL160723NIAID NIH HHS P01 AI102851NIAID NIH HHS R21 AI149775NIAID NIH HHS T32 AI118689
6 · The paper itself

Abstract

Sepsis is a life-threatening systemic inflammatory condition causing approximately 11 million annual deaths worldwide. Although key hyperinflammation-based organ dysfunctions that drive disease pathology have been recognized, our understanding of the factors that predispose patients to septic mortality is limited. Due to the lack of reliable prognostic measures, the development of appropriate clinical management that improves patient survival remains challenging. Here, we discovered that a subpopulation of CD49c

Indexed as

NeutrophilsSepsisAnimalsComplement C1qDisease Models, AnimalHumansMiceUp-RegulationComplement C1qC1qefferocytosisinflammationneutrophilsepsis

Identifiers

PMID35983035
PMCPMC9380571
OpenAlexW4289545528

What OpenQuestion holds

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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.