Evidence map›Paper›PMID 30984173›Full record

ArticleFrontiers in immunology2019

Sublingual Immunization With an RSV G Glycoprotein Fragment Primes IL-17-Mediated Immunopathology Upon Respiratory Syncytial Virus Infection.

In Su Cheon, Joo Young Kim, Youngjoo Choi, Byoung-Shik Shim, Jung-Ah Choi, Dae-Im Jung, Jae-Ouk Kim, Thomas J Braciale, Hyewon Youn, Man Ki Song and 1 more

Open access · goldAbstract read
In one paragraph

Article 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 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.6field-weighted citation impact, top 30% 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, 10 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

11 authors at 4 institutions in 2 countries.

In Su CheonLaboratory Science Division, International Vaccine Institute, Seoul, South Korea.
Joo Young KimGraduate School of Pharmaceutical Sciences, Ewha Womans University, Seoul, South Korea.
Youngjoo ChoiLaboratory Science Division, International Vaccine Institute, Seoul, South Korea.
Byoung-Shik ShimLaboratory Science Division, International Vaccine Institute, Seoul, South Korea.
Jung-Ah ChoiLaboratory Science Division, International Vaccine Institute, Seoul, South Korea.
Dae-Im JungLaboratory Science Division, International Vaccine Institute, Seoul, South Korea.
Jae-Ouk KimLaboratory Science Division, International Vaccine Institute, Seoul, South Korea.
Thomas J BracialeThe Beirne B. Carter Center for Immunology Research and Department of Pathology, The University of Virginia, Charlottesville, VA, United States.
Hyewon YounDepartment of Nuclear Medicine, Cancer Research Institute, Seoul National University College of Medicine, Seoul, South Korea.
Man Ki SongLaboratory Science Division, International Vaccine Institute, Seoul, South Korea.
Jun ChangGraduate School of Pharmaceutical Sciences, Ewha Womans University, Seoul, South Korea.
International Vaccine Institute · KREwha Womans University · KRCarter Center · USSeoul National University Hospital · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Respiratory syncytial virus (RSV) is the leading cause of serious respiratory tract disease but there is no licensed RSV vaccine. Immunopathological mechanisms have long been suspected as operating in the development of severe RSV disease and have hampered the development of safe and effective vaccines. Here, we show that unlike intranasal immunization, sublingual immunization with RSV glycoprotein fragment containing the central conserved region (Gcf) primes the host for severe disease upon RSV challenge. This increased pathology does not require replication by the challenge virus and is associated with massive infiltration of inflammatory cells, extensive cell death, and excessive mucus production in the airway and lungs. This exacerbated RSV disease primed by sublingual Gcf immunization is distinct from the immunopathology by G-expressing vaccinia virus or formalin-inactivated RSV, and preceded by prominent IL-17 production. IL-17 deficiency abolished the enhanced disease. Our results suggest a novel mechanism of RSV vaccine-induced immunopathology by IL-17, and highlights the importance of vaccination site.

Indexed as

Administration, SublingualAnimalsBronchoalveolar Lavage FluidCD4-Positive T-LymphocytesCytokinesEosinophilsFemaleLungMice, Inbred BALB CNeutrophilsRespiratory Syncytial Virus InfectionsRespiratory Syncytial Virus VaccinesViral Fusion ProteinsCytokinesG glycoprotein, Respiratory syncytial virusRespiratory Syncytial Virus VaccinesViral Fusion ProteinsglycoproteinIL-17immunopathologyRSVsublingual

Identifiers

PMID30984173
PMCPMC6447673
OpenAlexW2920793883

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.