Evidence map›Paper›PMID 26387945›Full record

ArticleCell reports2015

IFITM Proteins Restrict HIV-1 Infection by Antagonizing the Envelope Glycoprotein.

Jingyou Yu, Minghua Li, Jordan Wilkins, Shilei Ding, Talia H Swartz, Anthony M Esposito, Yi-Min Zheng, Eric O Freed, Chen Liang, Benjamin K Chen and 1 more

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 125 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
125citing papers in PubMed, 1 pooled it
8.3field-weighted citation impact, top 2% 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

125 citing papers in PubMed, 1 synthesis or guideline pooled it, 161 citations in OpenAlex.

  1. Pooled it
  2. Mechanisms of HIV-1 assembly, release and maturation.Nature reviews. Microbiology · 2026
    Review
  3. Review
  4. Article
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  6. Review
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  9. Autophagy-mediated downregulation of AXL and TIM-1 promotes sustained Zika virus infection.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
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  12. Review
  13. Review
  14. Article
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  20. Review

65 more citing papers are in PubMed but not listed here.

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.

Jingyou YuDepartment of Molecular Microbiology and Immunology, Bond Life Sciences Center, University of Missouri, Columbia, MO 65211, USA.
Minghua LiDepartment of Molecular Microbiology and Immunology, Bond Life Sciences Center, University of Missouri, Columbia, MO 65211, USA.
Jordan WilkinsDepartment of Molecular Microbiology and Immunology, Bond Life Sciences Center, University of Missouri, Columbia, MO 65211, USA.
Shilei DingMcGill AIDS Centre, Lady Davis Institute, Montreal, QC H3T 1E2, Canada; Department of Microbiology and Immunology, McGill University, Montreal, QC H3A 2B4, Canada.
Talia H SwartzDivision of Infectious Diseases, Department of Medicine, Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, New York 10029, USA.
Anthony M EspositoDivision of Infectious Diseases, Department of Medicine, Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, New York 10029, USA.
Yi-Min ZhengDepartment of Molecular Microbiology and Immunology, Bond Life Sciences Center, University of Missouri, Columbia, MO 65211, USA.
Eric O FreedVirus-Cell Interaction Section, HIV Dynamics and Replication Program, National Cancer Institute-Frederick, Frederick, MD 21702, USA.
Chen LiangMcGill AIDS Centre, Lady Davis Institute, Montreal, QC H3T 1E2, Canada; Department of Microbiology and Immunology, McGill University, Montreal, QC H3A 2B4, Canada.
Benjamin K ChenDivision of Infectious Diseases, Department of Medicine, Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, New York 10029, USA.
Shan-Lu LiuDepartment of Molecular Microbiology and Immunology, Bond Life Sciences Center, University of Missouri, Columbia, MO 65211, USA. Electronic address: liushan@missouri.edu.
University of Missouri · USIcahn School of Medicine at Mount Sinai · USMcGill University · CANational Cancer Institute · US

Funding

Imaging Virological Synapses During Parenteral HIV TransmissionDP1DA028866 · NIDA · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI CHEN, BENJAMIN K · 2009 to 2013
$4.1M
IFITM-mediated Inhibition of HIV Infection and Viral CountermeasuresR01AI112381 · NIAID · UNIVERSITY OF MISSOURI-COLUMBIA · PI LIU, SHAN-LU · 2014 to 2018
$1.7M
Mechanisms of efficient HIV infection through T cell virological synapsesR01GM113885 · NIGMS · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI CHEN, BENJAMIN K · 2014 to 2017
$1.7M
Novel Cellular Factors Restricting Viral Membrane FusionR21AI105584 · NIAID · UNIVERSITY OF MISSOURI-COLUMBIA · PI LIU, SHAN-LU · 2013 to 2014
$421k
Inhibition of Ebolavirus Entry by IFITM2 ProteinR21AI109464 · NIAID · UNIVERSITY OF MISSOURI-COLUMBIA · PI LIU, SHAN-LU · 2014 to 2015
$400k
Restriction of Viral Membrane Fusion and Entry by IFITM ProteinsR56AI107095 · NIAID · UNIVERSITY OF MISSOURI-COLUMBIA · PI LIU, SHAN-LU · 2014 to 2014
$393k
Canadian Institutes of Health ResearchIntramural NIH HHSNIAID NIH HHS AI105584NIAID NIH HHS AI107095NIAID NIH HHS AI109464NIAID NIH HHS AI112381NIAID NIH HHS R01 AI112381NIAID NIH HHS R21 AI105584NIAID NIH HHS R21 AI109464NIAID NIH HHS R56 AI107095NIDA NIH HHS DA028866NIDA NIH HHS DP1 DA028866NIGMS NIH HHS GM113885NIGMS NIH HHS R01 GM113885
6 · The paper itself

Abstract

The interferon-induced transmembrane (IFITM) proteins have been recently shown to restrict HIV-1 and other viruses. Here, we provide evidence that IFITM proteins, particularly IFITM2 and IFITM3, specifically antagonize the HIV-1 envelope glycoprotein (Env), thereby inhibiting viral infection. IFITM proteins interact with HIV-1 Env in viral producer cells, leading to impaired Env processing and virion incorporation. Notably, the level of IFITM incorporation into HIV-1 virions does not strictly correlate with the extent of inhibition. Prolonged passage of HIV-1 in IFITM-expressing T lymphocytes leads to emergence of Env mutants that overcome IFITM restriction. The ability of IFITMs to inhibit cell-to-cell infection can be extended to HIV-1 primary isolates, HIV-2 and SIVs; however, the extent of inhibition appears to be virus-strain dependent. Overall, our study uncovers a mechanism by which IFITM proteins specifically antagonize HIV-1 Env to restrict HIV-1 infection and provides insight into the specialized role of IFITMs in HIV infection.

Indexed as

Cell CommunicationGene Expression RegulationHEK293 CellsHeLa CellsHIV-1HIV-2HIV Envelope Protein gp120HIV Envelope Protein gp160HIV Envelope Protein gp41Host-Pathogen InteractionsHumansJurkat CellsLeukocytes, MononuclearMembrane ProteinsPrimary Cell CultureRNA-Binding ProteinsHIV Envelope Protein gp120HIV Envelope Protein gp160HIV Envelope Protein gp41IFITM2 protein, humanIFITM3 protein, humanMembrane ProteinsRNA-Binding Proteins

Identifiers

PMID26387945
PMCPMC4602366
OpenAlexW2141199943

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.