Evidence map›Paper›PMID 30195798›Full record

ArticleMolecular therapy. Nucleic acids2018

Zinc-Finger Nucleases Induced by HIV-1 Tat Excise HIV-1 from the Host Genome in Infected and Latently Infected Cells.

Haiyan Ji, Panpan Lu, Baochi Liu, Xiying Qu, Yanan Wang, Zhengtao Jiang, Xinyi Yang, Yangcheng Zhong, He Yang, Hanyu Pan and 4 more

Open access · goldAbstract read
In one paragraph

Article in Molecular therapy. Nucleic acids, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.9field-weighted citation impact, top 16% 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

14 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Review
  6. Article
  7. Therapeutic Application of Genome Editing Technologies in Viral Diseases.International journal of molecular sciences · 2022
    Review
  8. Review
  9. Review
  10. Review
  11. Review
  12. Block and Lock HIV Cure Strategies to Control the Latent Reservoir.Frontiers in cellular and infection microbiology · 2020
    Review
  13. Targeting HIV-1 proviral transcription.Current opinion in virology · 2019
    Review
  14. 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

14 authors at 3 institutions in 1 country.

Haiyan JiState Key Laboratory of Genetic Engineering and Key Laboratory of Medical Molecular Virology of the Ministry of Education/Health, Gene & Cell Therapy Research Center, School of Life Sciences, Fudan University, Shanghai 200438, China.
Panpan LuState Key Laboratory of Genetic Engineering and Key Laboratory of Medical Molecular Virology of the Ministry of Education/Health, Gene & Cell Therapy Research Center, School of Life Sciences, Fudan University, Shanghai 200438, China.
Baochi LiuShanghai Public Health Clinical Center, Fudan University, Shanghai 200433, China.
Xiying QuState Key Laboratory of Genetic Engineering and Key Laboratory of Medical Molecular Virology of the Ministry of Education/Health, Gene & Cell Therapy Research Center, School of Life Sciences, Fudan University, Shanghai 200438, China.
Yanan WangState Key Laboratory of Genetic Engineering and Key Laboratory of Medical Molecular Virology of the Ministry of Education/Health, Gene & Cell Therapy Research Center, School of Life Sciences, Fudan University, Shanghai 200438, China.
Zhengtao JiangState Key Laboratory of Genetic Engineering and Key Laboratory of Medical Molecular Virology of the Ministry of Education/Health, Gene & Cell Therapy Research Center, School of Life Sciences, Fudan University, Shanghai 200438, China.
Xinyi YangState Key Laboratory of Genetic Engineering and Key Laboratory of Medical Molecular Virology of the Ministry of Education/Health, Gene & Cell Therapy Research Center, School of Life Sciences, Fudan University, Shanghai 200438, China.
Yangcheng ZhongState Key Laboratory of Genetic Engineering and Key Laboratory of Medical Molecular Virology of the Ministry of Education/Health, Gene & Cell Therapy Research Center, School of Life Sciences, Fudan University, Shanghai 200438, China.
He YangState Key Laboratory of Genetic Engineering and Key Laboratory of Medical Molecular Virology of the Ministry of Education/Health, Gene & Cell Therapy Research Center, School of Life Sciences, Fudan University, Shanghai 200438, China.
Hanyu PanState Key Laboratory of Genetic Engineering and Key Laboratory of Medical Molecular Virology of the Ministry of Education/Health, Gene & Cell Therapy Research Center, School of Life Sciences, Fudan University, Shanghai 200438, China.
Lin ZhaoState Key Laboratory of Genetic Engineering and Key Laboratory of Medical Molecular Virology of the Ministry of Education/Health, Gene & Cell Therapy Research Center, School of Life Sciences, Fudan University, Shanghai 200438, China.
Jianqing XuShanghai Public Health Clinical Center, Fudan University, Shanghai 200433, China.
Hongzhou LuShanghai Public Health Clinical Center, Fudan University, Shanghai 200433, China.
Huanzhang ZhuState Key Laboratory of Genetic Engineering and Key Laboratory of Medical Molecular Virology of the Ministry of Education/Health, Gene & Cell Therapy Research Center, School of Life Sciences, Fudan University, Shanghai 200438, China. Electronic address: hzzhu@fudan.edu.cn.
Fudan University · CNState Key Laboratory of Genetic EngineeringShanghai Public Health Clinical Center · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Highly active anti-retroviral therapy (HAART) cannot clear infected cells harboring HIV-1 proviral DNA from HIV-1-infected patients. We previously demonstrated that zinc-finger nucleases (ZFNs) can specifically and efficiently excise HIV-1 proviral DNA from latently infected human T cells by targeting long terminal repeats (LTRs), a novel and alternative antiretroviral strategy for eradicating HIV-1 infection. To prevent unwanted off-target effects from constantly expressed ZFNs, in this study, we engineered the expression of ZFNs under the control of HIV-1 LTR, by which ZFN expression can be activated by the HIV-1 (Trans-Activator of Transcription) Tat protein. Our results show that functional expression of ZFNs induced by Tat excise the integrated proviral DNA of HIV-NL4-3-eGFP in approximately 30% of the population of HIV-1-infected cells. The results from HIV-1-infected human primary T cells and latently infected T cells treated with the inducible ZFNs further validated that proviral DNA can be excised. Taken together, positively regulated expression of ZFNs in the presence of HIV-1 Tat may provide a safer and novel implementation of genome-editing technology for eradicating HIV-1 proviral DNA from infected host cells.

Indexed as

gene therapygenome editinggenomic excisionHIV-1inducibleTatzinc-finger nuclease

Identifiers

PMID30195798
PMCPMC6023959
OpenAlexW2801579480

What OpenQuestion holds

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LicenceCC BY-NC-ND
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.