Evidence map›Paper›PMID 29163508›Full record

ArticleFrontiers in immunology2017

Interferon-α-Enhanced CD100/Plexin-B1/B2 Interactions Promote Natural Killer Cell Functions in Patients with Chronic Hepatitis C Virus Infection.

Yu He, Yonghong Guo, Chao Fan, Yingfeng Lei, Yun Zhou, Mingjie Zhang, Chuantao Ye, Guangxi Ji, Li Ma, Jianqi Lian and 6 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.6field-weighted citation impact, top 35% 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

9 citing papers in PubMed, 15 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. The Role of Semaphorins in Metabolic Disorders.International journal of molecular sciences · 2020
    Review
  9. Observational
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

16 authors at 3 institutions in 2 countries.

Yu HeDepartment of Infectious Diseases, Tangdu Hospital, Fourth Military Medical University, Xi'an, China.
Yonghong GuoDepartment of Infectious Diseases, Tangdu Hospital, Fourth Military Medical University, Xi'an, China.
Chao FanDepartment of Infectious Diseases, Tangdu Hospital, Fourth Military Medical University, Xi'an, China.
Yingfeng LeiDepartment of Microbiology, The Fourth Military Medical University, Xi'an, China.
Yun ZhouDepartment of Infectious Diseases, Tangdu Hospital, Fourth Military Medical University, Xi'an, China.
Mingjie ZhangHANK Biological Engineering Research Institute, Shenzhen, China.
Chuantao YeDepartment of Infectious Diseases, Tangdu Hospital, Fourth Military Medical University, Xi'an, China.
Guangxi JiDepartment of Infectious Diseases, Tangdu Hospital, Fourth Military Medical University, Xi'an, China.
Li MaDepartment of Infectious Diseases, Tangdu Hospital, Fourth Military Medical University, Xi'an, China.
Jianqi LianDepartment of Infectious Diseases, Tangdu Hospital, Fourth Military Medical University, Xi'an, China.
Jonathan P MoormanDepartment of Internal Medicine, Division of Infectious Diseases, James H. Quillen College of Medicine, Center of Excellence in Inflammation, Infectious Diseases, and Immunity, East Tennessee State University, Johnson City, TN, United States.
Zhi Q YaoDepartment of Internal Medicine, Division of Infectious Diseases, James H. Quillen College of Medicine, Center of Excellence in Inflammation, Infectious Diseases, and Immunity, East Tennessee State University, Johnson City, TN, United States.
Jiuping WangDepartment of Infectious Diseases, Tangdu Hospital, Fourth Military Medical University, Xi'an, China.
Chunqiu HaoDepartment of Infectious Diseases, Tangdu Hospital, Fourth Military Medical University, Xi'an, China.
Ying ZhangDepartment of Infectious Diseases, Tangdu Hospital, Fourth Military Medical University, Xi'an, China.
Zhansheng JiaDepartment of Infectious Diseases, Tangdu Hospital, Fourth Military Medical University, Xi'an, China.
Air Force Medical University · CNEast Tennessee State University · USShenzhen Hanke Bioengineering (China) · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCD100, also known as Sema4D, is an immune semaphorin constitutively expressed on natural killer (NK) cells and T cells. As an immune activation molecule, CD100 has important immunoregulatory effects on NK functions by enhancing the interactions between NK cells and target cells. The aim of this study was to investigate whether hepatitis C virus (HCV) infection affects CD100 expression, and whether interferon-α treatment enhances NK killing activity to facilitate HCV clearance

methodsExpression of CD100 on NK cells was evaluated by flow cytometry in patients with chronic HCV infection, with or without pegylated interferon-α-based therapy. NK cell cytotoxicity and interferon (IFN)-γ production were measured by flow cytometry upon culturing the NK cells with K562 and Huh7.5 or HCV JFH-1-infected Huh7.5 cells.

resultsThe frequency of CD100

conclusionThese results implied a novel mechanism by which IFN-α enhanced CD100/Plexin-B1/B2 interaction plays an important role in promoting NK functions in patients with chronic hepatitis C.

Indexed as

CD100hepatitis C virusinterferon-αnatural killer cellsplexin-B1/B2

Identifiers

PMID29163508
PMCPMC5676449
OpenAlexW2766210419

What OpenQuestion holds

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LicenceCC BY
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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.