Evidence map›Paper›PMID 32295911›Full record

ArticleJournal of virology2020

gp96 Is Critical for both Human Herpesvirus 6A (HHV-6A) and HHV-6B Infections.

Jingjing Ma, Junli Jia, Xuefeng Jiang, Mengyuan Xu, Jinfeng Guo, Tian Tang, Xianyi Xu, Zhisheng Wu, Benshun Hu, Kun Yao and 2 more

Open access · greenAbstract read
In one paragraph

Article in Journal of virology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.3field-weighted citation impact, top 19% 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

11 citing papers in PubMed, 18 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Article
  6. Review
  7. Review
  8. Review
  9. Article
  10. Article
  11. Article
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 2 institutions in 1 country.

Jingjing Ma *Department of Immunology, Nanjing Medical University, Nanjing, People's Republic of China.
Junli Jia *Department of Immunology, Nanjing Medical University, Nanjing, People's Republic of China.
Xuefeng JiangDepartment of Immunology, Nanjing Medical University, Nanjing, People's Republic of China.
Mengyuan XuDepartment of Immunology, Nanjing Medical University, Nanjing, People's Republic of China.
Jinfeng GuoDepartment of Immunology, Nanjing Medical University, Nanjing, People's Republic of China.
Tian TangDepartment of Immunology, Nanjing Medical University, Nanjing, People's Republic of China.
Xianyi XuDepartment of Immunology, Nanjing Medical University, Nanjing, People's Republic of China.
Zhisheng WuDepartment of Immunology, Nanjing Medical University, Nanjing, People's Republic of China.
Benshun HuDepartment of Immunology, Nanjing Medical University, Nanjing, People's Republic of China.
Kun YaoDepartment of Immunology, Nanjing Medical University, Nanjing, People's Republic of China.
Lingyun LiDepartment of Medical Genetics, Nanjing Medical University, Nanjing, People's Republic of China.
Huamin TangDepartment of Immunology, Nanjing Medical University, Nanjing, People's Republic of China htang@njmu.edu.cn.
Nanjing Medical University · CNNational Health and Family Planning Commission · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Human herpesviruses 6A and 6B (HHV-6A and HHV-6B, respectively) are two virus species in the betaherpesvirus subfamily that exhibit T cell tropism. CD46 and CD134 are the cellular receptors for HHV-6A and HHV-6B, respectively. Interestingly, the efficiency of HHV-6A/6B entry is different among different types of target cells despite similar receptor expression levels on these cells. Here, we found that the cellular factor gp96 (also known as glucose-regulated protein 94 [GRP94]) is expressed on the cell surface and interacts with viral glycoprotein Q1 (gQ1) during virus entry. gp96 cell surface expression levels are associated with the efficiency of HHV-6A and HHV-6B entry into target cells. Both loss-of-function and gain-of-function experiments indicated that gp96 plays an important role in HHV-6 infection. Our findings provide new insight into the HHV-6 entry process and might suggest novel therapeutic targets for HHV-6 infection.

Indexed as

Cell LineFetal BloodHerpesvirus 6, HumanHumansMembrane GlycoproteinsPrimary Cell CultureProtein BindingRoseolovirus InfectionsT-LymphocytesViral Envelope ProteinsVirus InternalizationendoplasminMembrane GlycoproteinsViral Envelope Proteinsentrygp96HHV-6

Identifiers

PMID32295911
PMCPMC7307172
OpenAlexW3016804741

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.