Evidence map›Paper›PMID 29329282›Full record

ArticlePediatric research2018

Induction of high-mobility group Box-1 in vitro and in vivo by respiratory syncytial virus.

Sara Manti, Terri J Harford, Carmelo Salpietro, Fariba Rezaee, Giovanni Piedimonte

Open access · bronzeAbstract read
In one paragraph

Article in Pediatric research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.6field-weighted citation impact, top 11% 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

16 citing papers in PubMed, 27 citations in OpenAlex.

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  16. Baicalin InhibitsInternational journal of molecular sciences · 2018
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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

5 authors at 2 institutions in 2 countries.

Sara MantiCenter for Pediatric Research, Pediatric Institute and Children's Hospital, Cleveland Clinic Foundation, Cleveland, Ohio.
Terri J HarfordCenter for Pediatric Research, Pediatric Institute and Children's Hospital, Cleveland Clinic Foundation, Cleveland, Ohio.
Carmelo SalpietroDepartment of Human Pathology of Adult and Developmental Age "Gaetano Barresi", Unit of Paediatric Genetics and Immunology, University Hospital of Messina, Messina, Sicily, Italy.
Fariba RezaeeCenter for Pediatric Research, Pediatric Institute and Children's Hospital, Cleveland Clinic Foundation, Cleveland, Ohio.
Giovanni PiedimonteCenter for Pediatric Research, Pediatric Institute and Children's Hospital, Cleveland Clinic Foundation, Cleveland, Ohio.
Cleveland Clinic · USIstituto Ortopedico Gaetano Pini · IT

Funding

NEUROGENIC INFLAMMATORY RESPONSE TO RSVR01HL061007 · NHLBI · WEST VIRGINIA UNIVERSITY · PI PIEDIMONTE, GIOVANNI · 1999 to 2022
$7.2M
Airway Epithelial Barrier Dysfunction In Response to Respiratory Syncytial VirusK08AI112781 · NIAID · UNIVERSITY OF ROCHESTER · PI REZAEE, FARIBA · 2015 to 2018
$734k
NHLBI NIH HHS R01 HL061007NIAID NIH HHS K08 AI112781
6 · The paper itself

Abstract

BackgroundDespite decades that have passed since its discovery, accurate biomarkers of respiratory syncytial virus (RSV) disease activity and effective therapeutic strategies are still lacking. The high-mobility group box type 1 (HMGB1) protein has been proposed as a possible link between RSV and immune system, but only limited information is currently available to support this hypothesis.MethodsExpression of HMGB1 gene and protein was analyzed by quantitative PCR, enzyme-linked immunosorbent assay (ELISA), western blot, immunocytochemistry, and confocal microscopy in immortalized and primary human bronchial epithelial cells, as well as in rat pup lungs. The role of HMGB1 in RSV infection was explored using glycyrrhizin, a selective HMGB1 inhibitor.ResultsRSV infection strongly induced HMGB1 expression both in vitro and in vivo. Glycyrrhizin dose-dependently inhibited HMGB1 upregulation in both RSV-infected immortalized and primary human bronchial epithelial cells, and this effect was associated with significant reduction of viral replication.ConclusionOur data suggest that HMGB1 expression increases during RSV replication. This seems to have a critical pathogenic role as its selective inhibition virtually modified the infection. These observations provide further insight into the pathophysiology of RSV infection and uncover a potential biomarker and therapeutic target for the most common respiratory infection of infancy.

Indexed as

AnimalsBiomarkersBronchiBronchiolitisCell LineEpithelial CellsGene Expression ProfilingHMGB1 ProteinHumansImmune SystemLungRatsRats, Inbred F344Respiratory Syncytial VirusesRespiratory Syncytial Virus InfectionsRespiratory Tract InfectionsBiomarkersHbp1 protein, ratHMGB1 ProteinHMGB1 protein, human

Identifiers

PMID29329282
PMCPMC5959750
OpenAlexW2782772946

What OpenQuestion holds

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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.