Evidence map›Paper›PMID 34514023›Full record

ArticleMolecular therapy. Methods & clinical development2021

Efficacious, safe, and stable inhibition of corneal neovascularization by AAV-vectored anti-VEGF therapeutics.

Wenqi Su, Shuo Sun, Bo Tian, Phillip W L Tai, Yongwen Luo, Jihye Ko, Wei Zhan, Xiao Ke, Qiang Zheng, Xiaorong Li and 3 more

Open access · goldAbstract read
In one paragraph

Article in Molecular therapy. Methods & clinical development, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.7field-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

10 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Review
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  6. Article
  7. Article
  8. Corneal stromal repair and regeneration.Progress in retinal and eye research · 2022
    Review
  9. Review
  10. 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

13 authors at 4 institutions in 2 countries.

Wenqi SuDepartment of Ophthalmology, Tianjin Medical University General Hospital, Tianjin 300052, China.
Shuo SunDepartment of Ophthalmology and Visual Sciences, University of Massachusetts Medical School, Worcester, MA 01655, USA.
Bo TianDepartment of Ophthalmology and Visual Sciences, University of Massachusetts Medical School, Worcester, MA 01655, USA.
Phillip W L TaiHorae Gene Therapy Center, University of Massachusetts Medical School, Worcester, MA 01605, USA.
Yongwen LuoCollege of Veterinary Medicine, South China Agricultural University, No. 483, Wushan Road, Guangzhou 510642, China.
Jihye KoViral Vector Core, University of Massachusetts Medical School, Worcester, MA 01605, USA.
Wei ZhanHorae Gene Therapy Center, University of Massachusetts Medical School, Worcester, MA 01605, USA.
Xiao KeChengdu Kanghong Pharmaceutical Group, 36 Shuxi Rd., Jinniu District, Chengdu, Sichuan 610036, China.
Qiang ZhengChengdu Kanghong Pharmaceutical Group, 36 Shuxi Rd., Jinniu District, Chengdu, Sichuan 610036, China.
Xiaorong LiTianjin Key Laboratory of Retinal Functions and Diseases, Tianjin International Joint Research and Development Centre of Ophthalmology and Vision Science, Eye Institute and School of Optometry, Tianjin Medical University Eye Hospital, Tianjin 300384, China.
Hua YanDepartment of Ophthalmology, Tianjin Medical University General Hospital, Tianjin 300052, China.
Guangping GaoHorae Gene Therapy Center, University of Massachusetts Medical School, Worcester, MA 01605, USA.
Haijiang LinDepartment of Ophthalmology and Visual Sciences, University of Massachusetts Medical School, Worcester, MA 01655, USA.
University of Massachusetts Chan Medical School · USTianjin Medical University · CNTianjin Medical University General Hospital · CNSouth China Agricultural University · CN

Funding

Oligodendrocyte-focused rAAV gene therapy strategies for Canavan disease and LeukodystrophiesR01NS076991 · NINDS · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI Guangping Gao · 2012 to 2026
$5.7M
NINDS NIH HHS R01 NS076991
6 · The paper itself

Abstract

Corneal neovascularization (CoNV) leads to visual impairment, affecting over 1.4 million people in the United States per year. It is caused by a variety of pathologies, such as inflammation, hypoxia, and limbal barrier dysfunction. Injection of the anti-vascular endothelial growth factor (VEGF) drug KH902 (conbercept) can inhibit CoNV but requires repeated dosing that produces associated side effects, such as cornea scar. To explore more efficacious and long-lasting treatment of CoNV, we employed recombinant adeno-associated virus (rAAV)2 and rAAV8 vectors to mediate KH902 expression via a single intrastromal injection and investigated its anti-angiogenic effects and safety in both alkali-burn- and suture-induced CoNV mouse models. Our results showed that rAAV-mediated

Indexed as

anti-VEGFcorneal neovascularizationgene therapyrecombinant adeno-associated virus

Identifiers

PMID34514023
PMCPMC8413663
OpenAlexW3174282158

What Socratic holds

Textmetadata
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 Socratic graph.