Evidence map›Paper›PMID 30674630›Full record

ArticleJournal of virology2019

CD4-Dependent Modulation of HIV-1 Entry by LY6E.

Jingyou Yu, Chen Liang, Shan-Lu Liu

Open access · bronzeAbstract read
In one paragraph

Article in Journal of virology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

22 citing papers in PubMed, 31 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

3 authors at 2 institutions in 2 countries.

Jingyou YuCenter for Retrovirus Research, The Ohio State University, Columbus, Ohio, USA.
Chen LiangMcGill AIDS Centre, Lady Davis Institute, Montreal, Quebec, Canada.
Shan-Lu LiuCenter for Retrovirus Research, The Ohio State University, Columbus, Ohio, USA liu.6244@osu.edu.
The Ohio State University · USMcGill University · CA

Funding

IFITM-mediated Inhibition of HIV Infection and Viral CountermeasuresR01AI112381 · NIAID · UNIVERSITY OF MISSOURI-COLUMBIA · PI LIU, SHAN-LU · 2014 to 2018
$1.7M
TIM-mediated Inhibition of HIV Release: Cooperation with SERINC and Antagonism by NefR01AI150473 · NIAID · OHIO STATE UNIVERSITY · PI LIU, SHAN-LU · 2019 to 2021
$995k
TIM-mediated Inhibition of HIV Release: Cooperation with SERINC and Antagonism by NefR01GM132069 · NIGMS · OHIO STATE UNIVERSITY · PI LIU, SHAN-LU · 2018 to 2018
$332k
NIAID NIH HHS R01 AI112381NIAID NIH HHS R01 AI150473NIGMS NIH HHS R01 GM132069
6 · The paper itself

Abstract

Lymphocyte antigen 6E (LY6E) is a GPI-anchored, interferon-inducible protein that has been shown to modulate viral infection in a cell type-dependent manner. Our recent work showed that LY6E promotes HIV-1 infection in some high-CD4-expressing cells, including human peripheral blood mononuclear cells (PBMCs) and the SupT1 cell line. In this work, we provide evidence that LY6E inhibits HIV-1 entry and spread in low-CD4-expressing Jurkat cells and human monocyte-derived macrophages (MDMs) through downregulation of the viral receptor CD4. We found that knockdown of LY6E in Jurkat cells and MDMs increases HIV-1 infection, yet overexpression of LY6E in Jurkat cells inhibits HIV-1 entry and replication. LY6E was found to be colocalized with CD4 on the plasma membrane of Jurkat cells and MDMs and enhances CD4 internalization. We artificially manipulated the CD4 level in Jurkat and SupT1 cells and found that overexpression of CD4 in Jurkat cells overcomes the inhibitory effect of LY6E; conversely, blocking the function of CD4 in SupT1 with a neutralizing antibody eliminates the enhancement of LY6E on HIV-1 entry. The CD4-dependent inhibitory phenotype of LY6E in low-CD4-expressing human MDMs can be recapitulated for a panel of transmitted founder viruses and laboratory-adapted HIV-1 strains. Given that HIV-1 can target low-CD4-expressing cells during acute infection yet replicates efficiently in high-CD4-expressing T cells at the late stage of disease, our observation that LY6E differentially modulates HIV-1 replication in a CD4-dependent manner has implications for understanding the complex roles of interferon (IFN)-induced proteins in AIDS pathogenesis.

Indexed as

Antibodies, NeutralizingAntigens, SurfaceCD4 AntigensCD4-Positive T-LymphocytesCell LineCell Line, TumorCell MembraneGPI-Linked ProteinsHEK293 CellsHeLa CellsHIV-1HIV InfectionsHumansInterferonsJurkat CellsLeukocytes, MononuclearAntibodies, NeutralizingAntigens, SurfaceCD4 AntigensGPI-Linked ProteinsInterferonsLY6E protein, humanCD4entryhuman immunodeficiency virusLY6E

Identifiers

PMID30674630
PMCPMC6430548
OpenAlexW2912903776

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.