Evidence map›Paper›PMID 30972063›Full record

ReviewFrontiers in immunology2019

Role of Type I Interferon (IFN) in the Respiratory Syncytial Virus (RSV) Immune Response and Disease Severity.

Diego R Hijano, Luan D Vu, Lawrence M Kauvar, Ralph A Tripp, Fernando P Polack, Stephania A Cormier

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 87 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
87citing papers in PubMed, 1 pooled it
10.5field-weighted citation impact, top 1% 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

87 citing papers in PubMed, 1 synthesis or guideline pooled it, 133 citations in OpenAlex.

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27 more citing papers are in PubMed but not listed here.

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 5 institutions in 2 countries.

Diego R HijanoDepartment of Infectious Diseases, St Jude Children's Research Hospital, Memphis, TN, United States.
Luan D VuDepartment of Biological Sciences, Louisiana State University and School of Veterinary Medicine, Baton Rouge, LA, United States.
Lawrence M KauvarTrellis Bioscience, LLC, Redwood City, CA, United States.
Ralph A TrippDepartment of Infectious Disease, University of Georgia, Athens, GA, United States.
Fernando P PolackFundacion INFANT, Buenos Aires, Argentina.
Stephania A CormierDepartment of Biological Sciences, Louisiana State University and School of Veterinary Medicine, Baton Rouge, LA, United States.
Louisiana State University · USInfant Foundation · ARSt. Jude Children's Research Hospital · USTrellis Bioscience (United States) · USUniversity of Georgia · US

Funding

Role of microbiota in increased influenza severity due to particulate matter exposureP42ES013648 · NIEHS · LOUISIANA STATE UNIV A&M COL BATON ROUGE · PI SPRUNGER, PHILLIP · 2009 to 2024
$27.6M
The Role of IL4R Alpha in Neonatal RSV ImmunopathologyR01AI090059 · NIAID · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI CORMIER, STEPHANIA A · 2011 to 2025
$6.7M
Therapeutic Antibody for RSV IIBR44AI122360 · NIAID · TRELLIS BIOSCIENCE, INC. · PI KAUVAR, LAWRENCE MICHAEL · 2016 to 2021
$5.8M
Combustion Generated PM0.1 and Predisposition to AsthmaR01ES015050 · NIEHS · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI CORMIER, STEPHANIA A · 2006 to 2022
$4.6M
NIAID NIH HHS R01 AI090059NIAID NIH HHS R44 AI122360NIEHS NIH HHS P42 ES013648NIEHS NIH HHS R01 ES015050
6 · The paper itself

Abstract

Respiratory syncytial virus (RSV) is the most common cause of lower respiratory tract disease in children <2 years of age. Increased morbidity and mortality have been reported in high-risk patients, such as premature infants, patients with cardiac disease, and severely immune compromised patients. Severe disease is associated with the virulence of the virus as well as host factors specifically including the innate immune response. The role of type I interferons (IFNs) in the response to RSV infection is important in regulating the rate of virus clearance and in directing the character of the immune response, which is normally associated with protection and less severe disease. Two RSV non-structural proteins, NS1 and NS2, as well as the envelope G glycoprotein are known to suppress type I IFN production and a robust type I IFN response to RSV does not occur in human infants or neonatal mouse models of RSV infection. Additionally, presence of type I IFNs are associated with mild symptoms in infants and administration of IFN-α prior to infection of neonatal mice with RSV reduces immunopathology. This evidence has driven RSV prophylaxis and therapeutic efforts to consider strategies for enhancing type I IFN production.

Indexed as

AnimalsHumansInterferon Type IInterleukin-33MiceRespiratory Syncytial Virus InfectionsRespiratory Syncytial Virus VaccinesToll-Like ReceptorsInterferon Type IInterleukin-33Respiratory Syncytial Virus VaccinesToll-Like Receptorshumaninfant immunitymouserespiratory syncytial virustype I interferonsvaccine

Identifiers

PMID30972063
PMCPMC6443902
OpenAlexW2923745023

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.