Evidence map›Paper›PMID 30833387›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2019

AAV

Wenjun Xiong, David M Wu, Yunlu Xue, Sean K Wang, Michelle J Chung, Xuke Ji, Parimal Rana, Sophia R Zhao, Shuyi Mai, Constance L Cepko

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 169 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
169citing papers in PubMed, 3 pooled it
11.7field-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

169 citing papers in PubMed, 3 syntheses or guidelines pooled it, 267 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Immune function in X-linked retinoschisis subjects in an AAV8-RS1 phase I/IIa gene therapy trial.Molecular therapy : the journal of the American Society of Gene Therapy · 2021
    Trial
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  16. AAV NRF2 gene therapy preserves retinal structure and function in rodent models of oxidative damage.Molecular therapy : the journal of the American Society of Gene Therapy · 2026
    Article
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  19. Article
  20. Article

109 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

10 authors at 5 institutions in 3 countries.

Wenjun XiongDepartment of Biomedical Sciences, City University of Hong Kong, Kowloon, Hong Kong SAR, China; wenjun.xiong@cityu.edu.hk cepko@genetics.med.harvard.edu.
David M WuDepartment of Genetics, Harvard Medical School, Boston, MA 02115.
Yunlu XueDepartment of Genetics, Harvard Medical School, Boston, MA 02115.
Sean K WangDepartment of Genetics, Harvard Medical School, Boston, MA 02115.
Michelle J ChungDepartment of Genetics, Harvard Medical School, Boston, MA 02115.
Xuke JiDepartment of Genetics, Harvard Medical School, Boston, MA 02115.
Parimal RanaDepartment of Genetics, Harvard Medical School, Boston, MA 02115.
Sophia R ZhaoDepartment of Genetics, Harvard Medical School, Boston, MA 02115.
Shuyi MaiDepartment of Biomedical Sciences, City University of Hong Kong, Kowloon, Hong Kong SAR, China.
Constance L CepkoDepartment of Genetics, Harvard Medical School, Boston, MA 02115; wenjun.xiong@cityu.edu.hk cepko@genetics.med.harvard.edu.
Harvard University · USMassachusetts Eye and Ear Infirmary · USHoward Hughes Medical Institute · USCity University of Hong Kong · HKCity University of Hong Kong, Shenzhen Research Institute · CN

Funding

Accelerating vision restoration with in-vivo cellular imaging of retinal functionU01EY025497 · NEI · UNIVERSITY OF ROCHESTER · PI WILLIAMS, DAVID R · 2015 to 2019
$4.1M
Molecular Profiling of Rods to Identify New Therapies for Retinal DegenerationsK08EY023993 · NEI · MASSACHUSETTS EYE AND EAR INFIRMARY · PI WU, DAVID · 2014 to 2018
$1.1M
Howard Hughes Medical InstituteNEI NIH HHS K08 EY023993NEI NIH HHS U01 EY025497
6 · The paper itself

Abstract

Adeno-associated viral vectors (AAVs) have become popular for gene therapy, given their many advantages, including their reduced inflammatory profile compared with that of other viruses. However, even in areas of immune privilege such as the eye, AAV vectors are capable of eliciting host-cell responses. To investigate the effects of such responses on several ocular cell types, we tested multiple AAV genome structures and capsid types using subretinal injections in mice. Assays of morphology, inflammation, and physiology were performed. Pathological effects on photoreceptors and the retinal pigment epithelium (RPE) were observed. Müller glia and microglia were activated, and the proinflammatory cytokines TNF-α and IL-1β were up-regulated. There was a strong correlation between

Indexed as

AnimalsDependovirusGenetic TherapyGenetic VectorsGene Transfer TechniquesMiceMice, Inbred C57BLPhotoreceptor CellsPromoter Regions, GeneticRetinaRetinal Pigment EpitheliumTransduction, GeneticTransgenesVision, OcularAAVgene therapyretinaretinal pigment epitheliumtoxicity

Identifiers

PMID30833387
PMCPMC6431174
OpenAlexW2920682232

What Socratic holds

Textmetadata
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 Socratic graph.