Evidence map›Paper›PMID 24457989›Full record

Trial reportJAMA ophthalmology2014

Safety and effects of the vector for the Leber hereditary optic neuropathy gene therapy clinical trial.

Rajeshwari D Koilkonda, Hong Yu, Tsung-Han Chou, William J Feuer, Marco Ruggeri, Vittorio Porciatti, David Tse, William W Hauswirth, Vince Chiodo, Sanford L Boye and 4 more

2 registry-linked trialsOpen access · greenAbstract readClinical Trial
In one paragraph

Trial report in JAMA ophthalmology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 62 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
62citing papers in PubMed, 1 pooled it
4.7field-weighted citation impact, top 4% 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.

NCT01267422 nacompletednot on this map

Safety and Efficacy Study of a Single Intravitreal Injection of rAAV2-ND4 Treatment of Leber Hereditary Optic Neuropathy

TypeinterventionalSponsorBin LiRan2011 to 2015Enrolled9ConditionsLeber Hereditary Optic NeuropathyArmsrAAV2-ND4
NCT02161380 phase1completednot on this map

An Open-label Dose Escalation Study of an Adeno-associated Virus Vector (scAAV2-P1ND4v2) for Gene Therapy of Leber's Hereditary Optic Neuropathy (LHON) Caused by the G11778A Mutation in Mitochondrial DNA

TypeinterventionalSponsorByron LamRan2014 to 2025Enrolled28ConditionsLeber's Hereditary Optic NeuropathyArmsinjection of scAAV2-P1ND4v2 1.18x10e9 vg (Low),, injection of scAAV2-P1ND4v2 5.81 X10e9 vg (Med), injection of scAAV2-P1ND4v2 2.4 X10e10vg (High), injection of scAAV2-P1ND4v2 1.0 X10e11vg (Higher)
3 · Its place in the literature

Who cites it

62 citing papers in PubMed, 1 synthesis or guideline pooled it, 103 citations in OpenAlex.

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  12. Targeting Mitochondrial Complex I Deficiency in MPPBiological procedures online · 2024
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2 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

14 authors at 3 institutions in 1 country.

Rajeshwari D KoilkondaBascom Palmer Eye Institute, Miller School of Medicine, University of Miami, Miami, Florida.
Hong YuBascom Palmer Eye Institute, Miller School of Medicine, University of Miami, Miami, Florida.
Tsung-Han ChouBascom Palmer Eye Institute, Miller School of Medicine, University of Miami, Miami, Florida.
William J FeuerBascom Palmer Eye Institute, Miller School of Medicine, University of Miami, Miami, Florida.
Marco RuggeriBascom Palmer Eye Institute, Miller School of Medicine, University of Miami, Miami, Florida.
Vittorio PorciattiBascom Palmer Eye Institute, Miller School of Medicine, University of Miami, Miami, Florida.
David TseBascom Palmer Eye Institute, Miller School of Medicine, University of Miami, Miami, Florida.
William W HauswirthDepartment of Ophthalmology, College of Medicine, University of Florida, Gainesville.
Vince ChiodoDepartment of Ophthalmology, College of Medicine, University of Florida, Gainesville.
Sanford L BoyeDepartment of Ophthalmology, College of Medicine, University of Florida, Gainesville.
Alfred S LewinDepartment of Molecular Genetics and Microbiology, College of Medicine, University of Florida, Gainesville.
Martha NeuringerDivision of Neuroscience, Oregon National Primate Research Center, Oregon Health and Science University, Beaverton, Oregon.
Lauren RennerDivision of Neuroscience, Oregon National Primate Research Center, Oregon Health and Science University, Beaverton, Oregon.
John GuyBascom Palmer Eye Institute, Miller School of Medicine, University of Miami, Miami, Florida.
University of Miami · USUniversity of Florida · USOregon National Primate Research Center · US

Funding

Upgrade of confocal microscopy at the Oregon National Primate Research CenterP51OD011092 · OD · OREGON HEALTH & SCIENCE UNIVERSITY · PI Bonnie J. Nagel · 2012 to 2026
$203.9M
Shared Equipment ModuleP30EY014801 · NEI · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI Victor L Perez · 2004 to 2026
$12.2M
Leber Hereditary Optic Neuropathy: Gene Therapy TrialR24EY018600 · NEI · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI GUY, JOHN · 2008 to 2012
$5.1M
Transgenic Mitomice Models for Treatment of Blinding DiseasesR01EY012355 · NEI · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI GUY, JOHN · 1999 to 2016
$3.4M
RETINAL GANGLION CELL PLASTICITY IN GLAUCOMAR01EY019077 · NEI · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI PORCIATTI, VITTORIO · 2009 to 2015
$2.1M
NEI NIH HHS P30 EY014801NEI NIH HHS P30EY014801NEI NIH HHS R01 EY012355NEI NIH HHS R01EY012355NEI NIH HHS R01EY01714NEI NIH HHS R01 EY019077NEI NIH HHS R24 EY018600NEI NIH HHS R24EY018600NIH HHS P51 OD011092NIH HHS P51OD011092
6 · The paper itself

Abstract

IMPORTANCE We developed a novel strategy for treatment of Leber hereditary optic neuropathy (LHON) caused by a mutation in the nicotinamide adenine dinucleotide dehydrogenase subunit IV (ND4) mitochondrial gene. OBJECTIVE To demonstrate the safety and effects of the gene therapy vector to be used in a proposed gene therapy clinical trial. DESIGN AND SETTING In a series of laboratory experiments, we modified the mitochondrial ND4 subunit of complex I in the nuclear genetic code for import into mitochondria. The protein was targeted into the organelle by agency of a targeting sequence (allotopic expression). The gene was packaged into adeno-associated viral vectors and then vitreally injected into rodent, nonhuman primate, and ex vivo human eyes that underwent testing for expression and integration by immunohistochemical analysis and blue native polyacrylamide gel electrophoresis. During serial follow-up, the animal eyes underwent fundus photography, optical coherence tomography, and multifocal or pattern electroretinography. We tested for rescue of visual loss in rodent eyes also injected with a mutant G11778A ND4 homologue responsible for most cases of LHON. EXPOSURE Ocular infection with recombinant adeno-associated viral vectors containing a wild-type allotopic human ND4 gene. MAIN OUTCOMES AND MEASURES Expression of human ND4 and rescue of optic neuropathy induced by mutant human ND4. RESULTS We found human ND4 expressed in almost all mouse retinal ganglion cells by 1 week after injection and ND4 integrated into the mouse complex I. In rodent eyes also injected with a mutant allotopic ND4, wild-type allotopic ND4 prevented defective adenosine triphosphate synthesis, suppressed visual loss, reduced apoptosis of retinal ganglion cells, and prevented demise of axons in the optic nerve. Injection of ND4 in the ex vivo human eye resulted in expression in most retinal ganglion cells. Primates undergoing vitreal injection with the ND4 test article and followed up for 3 months had no serious adverse reactions. CONCLUSIONS AND RELEVANCE Expression of our allotopic ND4 vector in the ex vivo human eye, safety of the test article, rescue of the LHON mouse model, and the severe irreversible loss of visual function in LHON support clinical testing with mutated G11778A mitochondrial DNA in our patients.

Indexed as

AnimalsClinical Trials as TopicDependovirusDisease Models, AnimalDNA, MitochondrialElectroretinographyFemaleGene Expression RegulationGenetic TherapyGenetic VectorsGreen Fluorescent ProteinsHumansIntravitreal InjectionsMacaca mulattaMaleMiceDNA, MitochondrialGreen Fluorescent ProteinsNADH DehydrogenaseNADH dehydrogenase subunit 4

Identifiers

PMID24457989
PMCPMC4266107
OpenAlexW2155161284

What OpenQuestion holds

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Registered trials

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.