Evidence map›Paper›PMID 31191534›Full record

ArticleFrontiers in immunology2019

Peritoneal Cells Mediate Immune Responses and Cross-Protection Against Influenza A Virus.

Avishekh Gautam, Byoung Kwon Park, Te Ha Kim, Madhav Akauliya, Dongbum Kim, Sony Maharjan, Joongwon Park, Jinsoo Kim, Hanseul Lee, Man-Seong Park and 2 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 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

13 citing papers in PubMed, 25 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

12 authors at 3 institutions in 1 country.

Avishekh GautamDepartment of Microbiology, College of Medicine, Hallym University, Chuncheon, South Korea.
Byoung Kwon ParkCenter for Medical Science Research, College of Medicine, Hallym University, Chuncheon, South Korea.
Te Ha KimDepartment of Microbiology, College of Medicine, Hallym University, Chuncheon, South Korea.
Madhav AkauliyaDepartment of Microbiology, College of Medicine, Hallym University, Chuncheon, South Korea.
Dongbum KimCenter for Medical Science Research, College of Medicine, Hallym University, Chuncheon, South Korea.
Sony MaharjanCenter for Medical Science Research, College of Medicine, Hallym University, Chuncheon, South Korea.
Joongwon ParkDepartment of Microbiology, College of Medicine, Hallym University, Chuncheon, South Korea.
Jinsoo KimDepartment of Microbiology, College of Medicine, Hallym University, Chuncheon, South Korea.
Hanseul LeeDepartment of Microbiology, College of Medicine, Hallym University, Chuncheon, South Korea.
Man-Seong ParkDepartment of Microbiology, College of Medicine, and the Institute for Viral Diseases, Korea University, Seoul, South Korea.
Younghee LeeDepartment of Biochemistry, College of Natural Sciences, Chungbuk National University, Cheongju, South Korea.
Hyung-Joo KwonDepartment of Microbiology, College of Medicine, Hallym University, Chuncheon, South Korea.
Hallym University · KRChungbuk National University · KRKorea University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Intraperitoneal inoculation with live influenza A virus confers protection against intranasal infections in mice and ferrets. However, the responses of peritoneal cells to influenza A virus have not been investigated. Here we show that intraperitoneal inoculation with A/WSN/1933 (H1N1) virus induced virus-reactive IgG production in the peritoneal cavity in mice. The infection resulted in substantial but transient B cell and macrophage depletion along with massive neutrophil infiltration, but virus growth was not detected. Influenza A viruses bound to α-2,6-linked sialic acids of B cells and macrophages and induced apoptotic death of peritoneal cavity cells. However, re-infection with A/WSN/1933 virus did not have adverse effects on immune cells most likely because of the neutralizing antibodies produced in response to the first exposure. Infection of BALB/c mice with A/WSN/1933 induced cross-protection against an otherwise lethal intraperitoneal dose of A/Hongkong/4801/2014 (H3N2) virus. This information suggests that immunological responses in the peritoneal cavity can induce effective defense against future virus infection. Considering the unexpected potent immunoregulatory activity of the peritoneal cells against influenza viruses, we suggest that comparative studies on various immune reactions after infection through different routes may contribute to better selection of vaccination routes in development of efficacious influenza vaccines.

Indexed as

Administration, IntranasalAnimalsAntibodies, NeutralizingAntibodies, ViralCross ProtectionDogsInfluenza A virusInfluenza A Virus, H1N1 SubtypeInfluenza A Virus, H3N2 SubtypeInfluenza VaccinesInjections, IntraperitonealMadin Darby Canine Kidney CellsMiceMice, Inbred BALB COrthomyxoviridae InfectionsPeritoneal CavityAntibodies, NeutralizingAntibodies, ViralInfluenza Vaccinesapoptosiscross protectioninfluenza A virusneutralizing antibodyperitoneal cells

Identifiers

PMID31191534
PMCPMC6546726
OpenAlexW2946957023

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.