Evidence map›Paper›PMID 29554301›Full record

ArticleThe Journal of infectious diseases2018

NKG2D Regulation of Lung Pathology and Dendritic Cell Function Following Respiratory Syncytial Virus Infection.

Huan Liu, Andrew R Osterburg, Jennifer Flury, Shuo Huang, Francis X McCormack, Stephania A Cormier, Michael T Borchers

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of infectious diseases, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
0.3field-weighted citation impact, top 45% 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

6 citing papers in PubMed, 1 synthesis or guideline pooled it, 10 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Review
  5. Observational
  6. Natural Killer Cell Dysfunction and Its Role in COVID-19.International journal of molecular sciences · 2020
    Review
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

7 authors at 3 institutions in 1 country.

Huan LiuDepartment of Internal Medicine, Division of Pulmonary, Critical Care and Sleep Medicine, University of Cincinnati, Ohio.
Andrew R OsterburgDepartment of Internal Medicine, Division of Pulmonary, Critical Care and Sleep Medicine, University of Cincinnati, Ohio.
Jennifer FluryDepartment of Internal Medicine, Division of Pulmonary, Critical Care and Sleep Medicine, University of Cincinnati, Ohio.
Shuo HuangDepartment of Internal Medicine, Division of Pulmonary, Critical Care and Sleep Medicine, University of Cincinnati, Ohio.
Francis X McCormackDepartment of Internal Medicine, Division of Pulmonary, Critical Care and Sleep Medicine, University of Cincinnati, Ohio.
Stephania A CormierDepartments of Pediatrics, Memphis.
Michael T BorchersDepartment of Internal Medicine, Division of Pulmonary, Critical Care and Sleep Medicine, University of Cincinnati, Ohio.
University of Cincinnati · USUniversity of Tennessee at Knoxville · USVeterans Health Administration · US

Funding

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
Combustion Generated PM0.1 and Predisposition to AsthmaR01ES015050 · NIEHS · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI CORMIER, STEPHANIA A · 2006 to 2022
$4.6M
RLDC: Molecular Pathway-Driven Diagnostics & Therapeutics for Rare Lung DiseasesU54HL127672 · NHLBI · CINCINNATI CHILDRENS HOSP MED CTR · PI TRAPNELL, BRUCE C · 2014 to 2018
$3.7M
BLRD VA I01 BX002347NHLBI NIH HHS U54 HL127672NIAID NIH HHS R01 AI090059NIEHS NIH HHS R01 ES015050
6 · The paper itself

Abstract

Background: Respiratory syncytial virus (RSV) is a common cause of respiratory tract infection in vulnerable populations. Natural killer (NK) cells and dendritic cells (DC) are important for the effector functions of both cell types following infection. Methods: Wild-type and NKG2D-deficient mice were infected with RSV. Lung pathology was assessed by histology. Dendritic cell function and phenotype were evaluated by enzyme-linked immunosorbent assay and flow cytometry. The expression of NKG2D ligands on lung and lymph node DCs was measured by immunostaining and flow cytometry. Adoptive transfer experiments were performed to assess the importance of NKG2D-dependent DC function in RSV infection. Results: NKG2D-deficient mice exhibited greater lung pathology, marked by the accumulation of DCs following RSV infection. Dendritic cells isolated from NKG2D-deficient mice had impaired responses toward Toll-like receptor ligands. Dendritic cells expressed NKG2D ligands on their surface, which was further increased in NKG2D-deficient mice and during RSV infection. Adoptive transfer of DCs isolated from wild-type mice into the airways of NKG2D-deficient mice ameliorated the enhanced inflammation in NKG2D-deficient mice after RSV infection. Conclusion: NKG2D-dependent interactions with DCs control the phenotype and function of DCs and play a critical role in pulmonary host defenses against RSV infection.

Indexed as

Respiratory Syncytial Virus InfectionsAnimalsDendritic CellsFemaleInterleukin-12LungLymph NodesMiceMice, Inbred C57BLMice, KnockoutNK Cell Lectin-Like Receptor Subfamily KInterleukin-12Klrk1 protein, mouseNK Cell Lectin-Like Receptor Subfamily K

Identifiers

PMID29554301
PMCPMC6195658
OpenAlexW2793227299

What OpenQuestion holds

Textmetadata
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.