Evidence map›Paper›PMID 30883742›Full record

ArticleThe Journal of pathology2019

Morpholino-induced exon skipping stimulates cell-mediated and humoral responses to dystrophin in mdx mice.

Maria C Vila, James S Novak, Margaret Benny Klimek, Ning Li, Melissa Morales, Alexander G Fritz, Katie Edwards, Jessica F Boehler, Marshall W Hogarth, Travis B Kinder and 11 more

Open access · greenAbstract read
In one paragraph

Article in The Journal of pathology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
1.2field-weighted citation impact, top 22% 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

16 citing papers in PubMed, 1 synthesis or guideline pooled it, 19 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. Review
  13. Exon-Skipping in Duchenne Muscular Dystrophy.Journal of neuromuscular diseases · 2021
    Review
  14. Review
  15. Article
  16. Micro-utrophin Therapy for Duchenne Muscular Dystrophy.Molecular therapy : the journal of the American Society of Gene Therapy · 2019
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

21 authors at 3 institutions in 1 country.

Maria C VilaCenter for Genetic Medicine, Children's National Health System, Washington, DC, USA.
James S NovakCenter for Genetic Medicine, Children's National Health System, Washington, DC, USA.ORCID 0000-0002-9989-8724
Margaret Benny KlimekCenter for Genetic Medicine, Children's National Health System, Washington, DC, USA.
Ning LiDepartment of Pharmaceutical Sciences, School of Pharmacy and Pharmaceutical Sciences, Binghamton University, Binghamton, NY, USA.ORCID 0000-0002-5997-7700
Melissa MoralesDepartment of Pharmaceutical Sciences, School of Pharmacy and Pharmaceutical Sciences, Binghamton University, Binghamton, NY, USA.
Alexander G FritzDepartment of Pharmaceutical Sciences, School of Pharmacy and Pharmaceutical Sciences, Binghamton University, Binghamton, NY, USA.
Katie EdwardsDepartment of Pharmaceutical Sciences, School of Pharmacy and Pharmaceutical Sciences, Binghamton University, Binghamton, NY, USA.
Jessica F BoehlerCenter for Genetic Medicine, Children's National Health System, Washington, DC, USA.
Marshall W HogarthCenter for Genetic Medicine, Children's National Health System, Washington, DC, USA.
Travis B KinderCenter for Genetic Medicine, Children's National Health System, Washington, DC, USA.
Aiping ZhangCenter for Genetic Medicine, Children's National Health System, Washington, DC, USA.
Davi MazalaCenter for Genetic Medicine, Children's National Health System, Washington, DC, USA.
Alyson A FiorilloCenter for Genetic Medicine, Children's National Health System, Washington, DC, USA.
Bonnie DouglasCenter for Genetic Medicine, Children's National Health System, Washington, DC, USA.
Yi-Wen ChenCenter for Genetic Medicine, Children's National Health System, Washington, DC, USA.
John van den AnkerCenter for Genetic Medicine, Children's National Health System, Washington, DC, USA.
Qi L LuDepartment of Neurology, McColl-Lockwood Laboratory for Muscular Dystrophy Research, Neuromuscular/ALS Center, Carolinas Medical Center, Charlotte, NC, USA.
Yetrib HathoutCenter for Genetic Medicine, Children's National Health System, Washington, DC, USA.
Eric P HoffmanCenter for Genetic Medicine, Children's National Health System, Washington, DC, USA.
Terence A PartridgeCenter for Genetic Medicine, Children's National Health System, Washington, DC, USA.
Kanneboyina NagarajuCenter for Genetic Medicine, Children's National Health System, Washington, DC, USA.
Children's National · USBinghamton University · USMuscular Dystrophy Association · US

Funding

RNA fidelity and protein function of Becker-like in-frame deletionsP50AR060836 · NIAMS · CHILDREN'S RESEARCH INSTITUTE · PI CLEMENS, PAULA R · 2011 to 2015
$7.8M
Preclinical dosing optimization: Dosing schedule, tissueU54HD071601 · NICHD · CHILDREN'S RESEARCH INSTITUTE · PI VAN DEN ANKER, JOHN NICOLAAS · 2011 to 2015
$4.0M
Genetics and Genomics of Muscle Postdoctoral Training ProgramT32AR056993 · NIAMS · CHILDREN'S RESEARCH INSTITUTE · PI JAISWAL, JYOTI K, PARTRIDGE, TERENCE A · 2010 to 2019
$2.2M
Dystrophin turnover after exon-skippingR56NS097229 · NINDS · STATE UNIVERSITY OF NY,BINGHAMTON · PI NAGARAJU, KANNEBOYINA, PARTRIDGE, TERENCE A · 2016 to 2016
$390k
Preclinical drug trial in mouse models of inflammationK26RR032082 · NCRR · CHILDREN'S RESEARCH INSTITUTE · PI NAGARAJU, KANNEBOYINA · 2011 to 2011
$106k
NCRR NIH HHS K26 RR032082NIAMS NIH HHS P50 AR060836NIAMS NIH HHS T32 AR056993NICHD NIH HHS U54 HD071601NINDS NIH HHS R56 NS097229
6 · The paper itself

Abstract

Exon skipping is a promising genetic therapeutic strategy for restoring dystrophin expression in the treatment of Duchenne muscular dystrophy (DMD). The potential for newly synthesized dystrophin to trigger an immune response in DMD patients, however, is not well established. We have evaluated the effect of chronic phosphorodiamidate morpholino oligomer (PMO) treatment on skeletal muscle pathology and asked whether sustained dystrophin expression elicits a dystrophin-specific autoimmune response. Here, two independent cohorts of dystrophic mdx mice were treated chronically with either 800 mg/kg/month PMO for 6 months (n = 8) or 100 mg/kg/week PMO for 12 weeks (n = 11). We found that significant muscle inflammation persisted after exon skipping in skeletal muscle. Evaluation of humoral responses showed serum-circulating antibodies directed against de novo dystrophin in a subset of mice, as assessed both by Western blotting and immunofluorescent staining; however, no dystrophin-specific antibodies were observed in the control saline-treated mdx cohorts (n = 8) or in aged (12-month-old) mdx mice with expanded 'revertant' dystrophin-expressing fibers. Reactive antibodies recognized both full-length and truncated exon-skipped dystrophin isoforms in mouse skeletal muscle. We found more antigen-specific T-cell cytokine responses (e.g. IFN-g, IL-2) in dystrophin antibody-positive mice than in dystrophin antibody-negative mice. We also found expression of major histocompatibility complex class I on some of the dystrophin-expressing fibers along with CD8+ and perforin-positive T cells in the vicinity, suggesting an activation of cell-mediated damage had occurred in the muscle. Evaluation of complement membrane attack complex (MAC) deposition on the muscle fibers further revealed lower MAC deposition on muscle fibers of dystrophin antibody-negative mice than on those of dystrophin antibody-positive mice. Our results indicate that de novo dystrophin expression after exon skipping can trigger both cell-mediated and humoral immune responses in mdx mice. Our data highlights the need to further investigate the autoimmune response and its long-term consequences after exon-skipping therapy. Copyright © 2019 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.

Indexed as

AnimalsDisease Models, AnimalDystrophinExonsGenetic TherapyMaleMice, Inbred C57BLMice, Inbred mdxMice, TransgenicMorpholinosMuscle Fibers, SkeletalMuscle, SkeletalMuscular Dystrophy, DuchenneDystrophinMorpholinosanti-dystrophin antibodiesantisense oligonucleotidescellular and humoral immune responsede novo dystrophinDuchenne muscular dystrophymdx micemorpholinoT-cell

Identifiers

PMID30883742
PMCPMC6579705
OpenAlexW2920801323

What OpenQuestion holds

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Registered trials

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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.