Evidence map›Paper›PMID 26957202›Full record

ReviewCurrent HIV research2016

Inhibition of HIV Entry by Targeting the Envelope Transmembrane Subunit gp41.

Hyun A Yi, Brian C Fochtman, Robert C Rizzo, Amy Jacobs

Abstract readReview
In one paragraph

Review in Current HIV research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
–field-weighted citation impact
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

28 citing papers in PubMed.

  1. Article
  2. Review
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  11. Review
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  18. Optimization of peptidic HIV-1 fusion inhibitor T20 by phage display.Protein science : a publication of the Protein Society · 2019
    Article
  19. Article
  20. 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

4 authors.

Hyun A Yi
Brian C Fochtman
Robert C Rizzo
Amy JacobsDepartment of Microbiology and Immunology, School of Medicine and Biomedical Sciences, State University of New York at Buffalo, Buffalo, New York, USA. jacobs2@buffalo.edu.

Funding

Computational Design of Fusion Inhibitors Targeting Drug-resistant HIVgp41R01GM083669 · NIGMS · STATE UNIVERSITY NEW YORK STONY BROOK · PI RIZZO, ROBERT C. · 2008 to 2016
$2.6M
Molecular details of HIV fusion revealed using novel gp41 labelingR21AI102796 · NIAID · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI JACOBS, AMY LYNN · 2013 to 2014
$379k
NIAID NIH HHS R21 AI102796NIAID NIH HHS R21AI102796NIGMS NIH HHS R01 GM083669NIGMS NIH HHS R01GM083669
6 · The paper itself

Abstract

backgroundThe transmembrane subunit of the HIV envelope protein, gp41 is a vulnerable target to inhibit HIV entry. There is one fusion inhibitor T20 (brand name: Fuzeon, generic name: enfuvirtide) available by prescription. However, it has several drawbacks such as a high level of development of drug resistance, a short-half life in vivo, rapid renal clearance, low oral bioavailability, and it is only used as a salvage therapy. Therefore, investigators have been studying a variety of different modalities to attempt to overcome these limitations.

methodsComprehensive literature searches were performed on HIV gp41, inhibition mechanisms, and inhibitors. The latest structural information was collected, and multiple inhibition strategies targeting gp41 were reviewed.

resultsMany of the recent advances in inhibitors were peptide-based. Several creative modification strategies have also been performed to improve inhibitory efficacy of peptides and to overcome the drawbacks of T20 treatment. Small compounds have also been an area of intense research. There is a wide variety in development from those identified by virtual screens targeting specific regions of the protein to natural products. Finally, broadly neutralizing antibodies have also been important area of research. The inaccessible nature of the target regions for antibodies is a challenge, however, extensive efforts to develop better neutralizing antibodies are ongoing.

conclusionThe fusogenic protein, gp41 has been extensively studied as a promising target to inhibit membrane fusion between the virus and target cells. At the same time, it is a challenging target because the vulnerable conformations of the protein are exposed only transiently. However, advances in biochemical, biophysical, structural, and immunological studies are coming together to move the field closer to an understanding of gp41 structure and function that will lead to the development of novel drugs and vaccines.

Indexed as

AnimalsAntibodies, NeutralizingDrug DiscoveryHIV-1HIV AntibodiesHIV Envelope Protein gp41HIV Fusion InhibitorsHIV InfectionsHumansMolecular StructurePeptidesProtein Interaction Domains and MotifsProtein SubunitsVirus InternalizationAntibodies, Neutralizinggp41 protein, Human immunodeficiency virus 1HIV AntibodiesHIV Envelope Protein gp41HIV Fusion InhibitorsPeptidesProtein Subunits

Identifiers

PMID26957202
PMCPMC4909398

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Registered trials

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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.