Evidence map›Paper›PMID 27170155›Full record

ReviewHuman genetics2016

TALEN gene editing takes aim on HIV.

Ronald Benjamin, Bradford K Berges, Antonio Solis-Leal, Omoyemwen Igbinedion, Christy L Strong, Martin R Schiller

Abstract readReview
In one paragraph

Review in Human genetics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing 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

40 citing papers in PubMed.

  1. Review
  2. Searching for a HIV-1 Cure.Theranostics · 2026
    Review
  3. Review
  4. Article
  5. Article
  6. Review
  7. Advanced Therapies for Human Immunodeficiency Virus.Medical sciences (Basel, Switzerland) · 2024
    Review
  8. Review
  9. Review
  10. Review
  11. Review
  12. Review
  13. Review
  14. Review
  15. Pulsed Electric Fields Alter Expression of NF-κB Promoter-Controlled Gene.International journal of molecular sciences · 2021
    Article
  16. Review
  17. Review
  18. Cell and Gene Therapy for Anemia: Hematopoietic Stem Cells and Gene Editing.International journal of molecular sciences · 2021
    Review
  19. Article
  20. Review
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

6 authors.

Ronald BenjaminNevada Institute of Personalized Medicine and School of Life Sciences, University of Nevada, Las Vegas, NV, USA.
Bradford K BergesDepartment of Microbiology and Molecular Biology, Brigham Young University, Provo, UT, USA.
Antonio Solis-LealDepartment of Microbiology and Molecular Biology, Brigham Young University, Provo, UT, USA.
Omoyemwen IgbinedionNevada Institute of Personalized Medicine and School of Life Sciences, University of Nevada, Las Vegas, NV, USA.
Christy L StrongNevada Institute of Personalized Medicine and School of Life Sciences, University of Nevada, Las Vegas, NV, USA.
Martin R SchillerNevada Institute of Personalized Medicine and School of Life Sciences, University of Nevada, Las Vegas, NV, USA. martin.schiller@unlv.edu.

Funding

A novel high-throughput functional screen based upon chimeric minimotif decoysR21AI116411 · NIAID · UNIVERSITY OF NEVADA LAS VEGAS · PI SCHILLER, MARTIN R · 2015 to 2016
$407k
HIV Toolbox, an interactive, visual, and customizable HIV Protein OntologyR56AI109156 · NIAID · UNIVERSITY OF NEVADA LAS VEGAS · PI SCHILLER, MARTIN R · 2014 to 2014
$332k
NIAID NIH HHS R21 AI116411NIAID NIH HHS R56 AI109156
6 · The paper itself

Abstract

Transcription activator-like effector nucleases (TALENs) are one of several types of programmable, engineered nucleases that bind and cleave specific DNA sequences. Cellular machinery repairs the cleaved DNA by introducing indels. In this review, we emphasize the potential, explore progress, and identify challenges in using TALENs as a therapeutic tool to treat HIV infection. TALENs have less off-target editing and can be more effective at tolerating HIV escape mutations than CRISPR/Cas-9. Scientists have explored TALEN-mediated editing of host genes such as viral entry receptors (CCR5 and CXCR4) and a protein involved in proviral integration (LEDGF/p75). Viral targets include the proviral DNA, particularly focused on the long terminal repeats. Major challenges with translating gene therapy from bench to bedside are improving cleavage efficiency and delivery, while minimizing off-target editing, cytotoxicity, and immunogenicity. However, rapid improvements in TALEN technology are enhancing cleavage efficiency and specificity. Therapeutic testing in animal models of HIV infection will help determine whether TALENs are a viable HIV treatment therapy. TALENs or other engineered nucleases could shift the therapeutic paradigm from life-long antiretroviral therapy toward eradication of HIV infection.

Indexed as

Gene EditingTranscription Activator-Like Effector NucleasesBase SequenceHIV InfectionsHumansSequence Homology, Nucleic AcidTranscription Activator-Like Effector Nucleases

Identifiers

PMID27170155
PMCPMC5002248

What OpenQuestion holds

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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.