Evidence map›Paper›PMID 35396219›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2022

Mice Expressing Cosegregating Single Nucleotide Polymorphisms (D298G and N397I) in TLR4 Have Enhanced Responses to House Dust Mite Allergen.

Marc Y Fink, Xiulan Qi, Kari Ann Shirey, Rachel Fanaroff, Svetlana Chapoval, Rose M Viscardi, Stefanie N Vogel, Achsah D Keegan

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.7field-weighted citation impact, top 32% 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

7 citing papers in PubMed, 6 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 1 institution in 1 country.

Marc Y FinkCenter for Vascular and Inflammatory Diseases, University of Maryland School of Medicine, Baltimore, MD.ORCID 0000-0002-3550-3455
Xiulan QiCenter for Vascular and Inflammatory Diseases, University of Maryland School of Medicine, Baltimore, MD.
Kari Ann ShireyDepartment of Microbiology and Immunology, University of Maryland School of Medicine, Baltimore, MD.
Rachel FanaroffDepartment of Anatomical Pathology, University of Maryland Medical Center, Baltimore, MD.ORCID 0000-0002-7564-5597
Svetlana ChapovalCenter for Vascular and Inflammatory Diseases, University of Maryland School of Medicine, Baltimore, MD.ORCID 0000-0002-7590-4421
Rose M ViscardiDepartment of Pediatrics, University of Maryland School of Medicine, Baltimore, MD; and.
Stefanie N VogelDepartment of Microbiology and Immunology, University of Maryland School of Medicine, Baltimore, MD.ORCID 0000-0001-8244-2555
Achsah D KeeganCenter for Vascular and Inflammatory Diseases, University of Maryland School of Medicine, Baltimore, MD; akeegan@som.umaryland.edu.ORCID 0000-0002-7029-4417
University of Maryland, Baltimore · US

Funding

Signaling Pathways in Innate ImmunityT32AI095190 · NIAID · UNIVERSITY OF MARYLAND BALTIMORE · PI Stefanie N. Vogel · 2012 to 2026
$4.7M
IL-4-activated macrophages: Contribution to allergic lung inflammation linked to viral infectionR01AI143845 · NIAID · UNIVERSITY OF MARYLAND BALTIMORE · PI KEEGAN, ACHSAH D., VISCARDI, ROSE MARIE · 2019 to 2023
$3.1M
Macrophage differentiation and disease outcome in influenza infectionR01AI123371 · NIAID · UNIVERSITY OF MARYLAND BALTIMORE · PI VOGEL, STEFANIE N. · 2017 to 2021
$2.7M
Role of Semaphorin 4A in Allergic InflammationR01AI122631 · NIAID · UNIVERSITY OF MARYLAND BALTIMORE · PI KEEGAN, ACHSAH D. · 2018 to 2022
$1.9M
Role of Semaphorin 4A in Allergic InflammationR56AI122631 · NIAID · UNIVERSITY OF MARYLAND BALTIMORE · PI KEEGAN, ACHSAH D. · 2016 to 2016
$385k
Regulation of Macrophage Activation by House Dust MiteI01BX001850 · VA · BALTIMORE VA MEDICAL CENTER · PI KEEGAN, ACHSAH D. · 2013 to 2022
–
BLRD VA I01 BX001850NIAID NIH HHS R01 AI122631NIAID NIH HHS R01 AI123371NIAID NIH HHS R01 AI143845NIAID NIH HHS R56 AI122631NIAID NIH HHS T32 AI095190
6 · The paper itself

Abstract

Asthma is a common and ubiquitous chronic respiratory disease that is associated with airway inflammation and hyperreactivity resulting in airway obstruction. It is now accepted that asthma is controlled by a combination of host genetics and environment in a rather complex fashion; however, the link between sensing of the environment and development and exacerbation of allergic lung inflammation is unclear. Human populations expressing cosegregating D299G and T399I polymorphisms in the

Indexed as

Antigens, DermatophagoidesAsthmaPulmonary EosinophiliaToll-Like Receptor 4AllergensAnimalsInflammationLipopolysaccharidesMicePolymorphism, Single NucleotidePyroglyphidaeAllergensAntigens, DermatophagoidesLipopolysaccharidesTlr4 protein, mouseToll-Like Receptor 4

Identifiers

PMID35396219
PMCPMC9176710
OpenAlexW4223605071

What OpenQuestion holds

Textmetadata
LicenceTDM
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.