Evidence map›Paper›PMID 26481100›Full record

ArticleScientific reports2015

Genome editing of CXCR4 by CRISPR/cas9 confers cells resistant to HIV-1 infection.

Panpan Hou, Shuliang Chen, Shilei Wang, Xiao Yu, Yu Chen, Meng Jiang, Ke Zhuang, Wenzhe Ho, Wei Hou, Jian Huang and 1 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 124 papers.

0numbers the graph read from it
0cells of the map it votes in
124citing papers in PubMed
13.7field-weighted citation impact, top 1% 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

124 citing papers in PubMed, 213 citations in OpenAlex.

  1. Review
  2. Review
  3. Searching for a HIV-1 Cure.Theranostics · 2026
    Review
  4. Review
  5. Review
  6. Review
  7. Review
  8. Review
  9. Article
  10. Review
  11. Review
  12. Article
  13. Article
  14. A mitochondrial surveillance mechanism activated bybioRxiv : the preprint server for biology · 2024
    Article
  15. Review
  16. Article
  17. Efficient Editing of the CXCR4 Locus Using Cas9 Ribonucleoprotein Complexes Stabilized with Polyglutamic Acid.Doklady biological sciences : proceedings of the Academy of Sciences of the USSR, Biological sciences sections · 2023
    Article
  18. CRISPR/Cas9 Landscape: Current State and Future Perspectives.International journal of molecular sciences · 2023
    Review
  19. Article
  20. Review

64 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 3 institutions in 2 countries.

Panpan HouSchool of Basic Medical Sciences, Wuhan University, Wuhan, 430071, PR China.
Shuliang ChenSchool of Basic Medical Sciences, Wuhan University, Wuhan, 430071, PR China.
Shilei WangCollege of Life Sciences, Wuhan University, Wuhan, 430072, PR China.
Xiao YuCollege of Life Sciences, Wuhan University, Wuhan, 430072, PR China.
Yu ChenCollege of Life Sciences, Wuhan University, Wuhan, 430072, PR China.
Meng JiangRenmin Hospital of Wuhan University, Wuhan 430060, PR China.
Ke ZhuangThe Center for Animal Experiment and ABSL-3 Laboratory, Wuhan University School of Medicine, Wuhan, 430071, PR China.
Wenzhe HoThe Center for Animal Experiment and ABSL-3 Laboratory, Wuhan University School of Medicine, Wuhan, 430071, PR China.
Wei HouSchool of Basic Medical Sciences, Wuhan University, Wuhan, 430071, PR China.
Jian HuangDepartment of Pathology and Laboratory Medicine, School of Medicine, Temple University, Philadelphia, PA 19103.
Deyin GuoSchool of Basic Medical Sciences, Wuhan University, Wuhan, 430071, PR China.
Wuhan University · CNRenmin Hospital of Wuhan University · CNTemple University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Genome editing via CRISPR/Cas9 has become an efficient and reliable way to make precise, targeted changes to the genome of living cells. CXCR4 is a co-receptor for the human immunodeficiency virus type 1 (HIV-1) infection and has been considered as an important therapeutic target for AIDS. CXCR4 mediates viral entry into human CD4(+) cells by binding to envelope protein, gp120. Here, we show that human CXCR4 gene is efficiently disrupted by CRISPR/Cas9-mediated genome editing, leading to HIV-1 resistance of human primary CD4(+) T cells. We also show that the Cas9-mediated ablation of CXCR4 demonstrated high specificity and negligible off-target effects without affecting cell division and propagation. The precise and efficient genome editing of CXCR4 will provide a new strategy for therapeutic application against HIV-1 infection.

Indexed as

CRISPR-Cas SystemsGene TargetingHIV-1RNA EditingAllelesAnimalsBase SequenceCD4-Positive T-LymphocytesCell LineCell MembraneCells, CulturedDisease ResistanceGene DeletionGene ExpressionGenetic LociHIV InfectionsReceptors, CXCR4

Identifiers

PMID26481100
PMCPMC4612538
OpenAlexW2416043666

What OpenQuestion holds

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LicenceCC BY
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.