Literature DB >> 35271811

Leber Hereditary Optic Neuropathy Gene Therapy: Adverse Events and Visual Acuity Results of All Patient Groups.

Byron L Lam1, William J Feuer2, Janet L Davis2, Vittorio Porciatti2, Hong Yu2, Robert B Levy2, Elizabeth Vanner2, John Guy2.   

Abstract

PURPOSE: To assess safety of gene therapy in G11778A Leber hereditary optic neuropathy (LHON).
DESIGN: Phase 1 clinical trial.
METHODS: Setting: single institution. PARTICIPANTS: Patients with G11778A LHON and chronic bilateral visual loss >12 months (group 1, n = 11), acute bilateral visual loss <12 months (group 2, n = 9), or unilateral visual loss (group 3, n = 8). INTERVENTION: unilateral intravitreal AAV2(Y444,500,730F)-P1ND4v2 injection with low, medium, high, and higher doses to worse eye for groups 1 and 2 and better eye for group 3. OUTCOME MEASURES: Best-corrected visual acuity (BCVA), adverse events, and vector antibody responses. Mean follow-up was 24 months (range, 12-36 months); BCVAs were compared with a published prospective natural history cohort with designated surrogate study and fellow eyes.
RESULTS: Incident uveitis (8 of 28, 29%), the only vector-related adverse event, resulted in no attributable vision sequelae and was related to vector dose: 5 of 7 (71%) higher-dose eyes vs 3 of 21 (14%) low-, medium-, or high-dose eyes (P < .001). Incident uveitis requiring treatment was associated with increased serum AAV2 neutralizing antibody titers (p=0.007) but not serum AAV2 polymerase chain reaction. Improvements of ≥15-letter BCVA occurred in some treated and fellow eyes of groups 1 and 2 and some surrogate study and fellow eyes of natural history subjects. All study eyes (BCVA ≥20/40) in group 3 lost ≥15 letters within the first year despite treatment.
CONCLUSIONS: G11778A LHON gene therapy has a favorable safety profile. Our results suggest that if there is an efficacy effect, it is likely small and not dose related. Demonstration of efficacy requires randomization of patients to a group not receiving vector in either eye.
Copyright © 2022 Elsevier Inc. All rights reserved.

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Year:  2022        PMID: 35271811      PMCID: PMC9444871          DOI: 10.1016/j.ajo.2022.02.023

Source DB:  PubMed          Journal:  Am J Ophthalmol        ISSN: 0002-9394            Impact factor:   5.488


  13 in total

1.  Efficacy and Safety of Intravitreal Gene Therapy for Leber Hereditary Optic Neuropathy Treated within 6 Months of Disease Onset.

Authors:  Nancy J Newman; Patrick Yu-Wai-Man; Valerio Carelli; Mark L Moster; Valerie Biousse; Catherine Vignal-Clermont; Robert C Sergott; Thomas Klopstock; Alfredo A Sadun; Piero Barboni; Adam A DeBusk; Jean François Girmens; Günther Rudolph; Rustum Karanjia; Magali Taiel; Laure Blouin; Gerard Smits; Barrett Katz; José-Alain Sahel
Journal:  Ophthalmology       Date:  2021-01-12       Impact factor: 12.079

Review 2.  Protein import into mitochondria.

Authors:  W Neupert
Journal:  Annu Rev Biochem       Date:  1997       Impact factor: 23.643

3.  Safety of rAAV2/2-ND4 Gene Therapy for Leber Hereditary Optic Neuropathy.

Authors:  Catherine Vignal; Scott Uretsky; Serge Fitoussi; Anne Galy; Laure Blouin; Jean-François Girmens; Samuel Bidot; Nitza Thomasson; Céline Bouquet; Sonia Valero; Sandrine Meunier; Jean-Philippe Combal; Bernard Gilly; Barrett Katz; José-Alain Sahel
Journal:  Ophthalmology       Date:  2018-02-14       Impact factor: 12.079

4.  Rescue of a deficiency in ATP synthesis by transfer of MTATP6, a mitochondrial DNA-encoded gene, to the nucleus.

Authors:  Giovanni Manfredi; Jin Fu; Joseline Ojaimi; James E Sadlock; Jennifer Q Kwong; John Guy; Eric A Schon
Journal:  Nat Genet       Date:  2002-02-25       Impact factor: 38.330

5.  Leber's Hereditary Optic Neuropathy.

Authors:  Alfredo A Sadun; Chiara La Morgia; Valerio Carelli
Journal:  Curr Treat Options Neurol       Date:  2011-02       Impact factor: 3.598

6.  Trial end points and natural history in patients with G11778A Leber hereditary optic neuropathy : preparation for gene therapy clinical trial.

Authors:  Byron L Lam; William J Feuer; Joyce C Schiffman; Vittorio Porciatti; Ruth Vandenbroucke; Potyra R Rosa; Giovanni Gregori; John Guy
Journal:  JAMA Ophthalmol       Date:  2014-04-01       Impact factor: 7.389

7.  Pedigree analysis in Leber hereditary optic neuropathy families with a pathogenic mtDNA mutation.

Authors:  A E Harding; M G Sweeney; G G Govan; P Riordan-Eva
Journal:  Am J Hum Genet       Date:  1995-07       Impact factor: 11.025

8.  The clinical features of Leber's hereditary optic neuropathy defined by the presence of a pathogenic mitochondrial DNA mutation.

Authors:  P Riordan-Eva; M D Sanders; G G Govan; M G Sweeney; J Da Costa; A E Harding
Journal:  Brain       Date:  1995-04       Impact factor: 13.501

9.  Gene Therapy for Leber Hereditary Optic Neuropathy: Initial Results.

Authors:  William J Feuer; Joyce C Schiffman; Janet L Davis; Vittorio Porciatti; Phillip Gonzalez; Rajeshwari D Koilkonda; Huijun Yuan; Anil Lalwani; Byron L Lam; John Guy
Journal:  Ophthalmology       Date:  2015-11-19       Impact factor: 12.079

10.  Intravitreal Gene Therapy vs. Natural History in Patients With Leber Hereditary Optic Neuropathy Carrying the m.11778G>A ND4 Mutation: Systematic Review and Indirect Comparison.

Authors:  Nancy J Newman; Patrick Yu-Wai-Man; Valerio Carelli; Valerie Biousse; Mark L Moster; Catherine Vignal-Clermont; Robert C Sergott; Thomas Klopstock; Alfredo A Sadun; Jean-François Girmens; Chiara La Morgia; Adam A DeBusk; Neringa Jurkute; Claudia Priglinger; Rustum Karanjia; Constant Josse; Julie Salzmann; François Montestruc; Michel Roux; Magali Taiel; José-Alain Sahel
Journal:  Front Neurol       Date:  2021-05-24       Impact factor: 4.003

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  1 in total

1.  Using Noninvasive Electrophysiology to Determine Time Windows of Neuroprotection in Optic Neuropathies.

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Journal:  Int J Mol Sci       Date:  2022-05-20       Impact factor: 6.208

  1 in total

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