Literature DB >> 26022168

Emerging treatments for pediatric leukodystrophies.

Guy Helman1, Keith Van Haren2, Maria L Escolar3, Adeline Vanderver4.   

Abstract

The leukodystrophies are a heterogeneous group of inherited disorders with broad clinical manifestations and variable pathologic mechanisms. Improved diagnostic methods have allowed identification of the underlying cause of these diseases, facilitating identification of their pathologic mechanisms. Clinicians are now able to prioritize treatment strategies and advance research in therapies for specific disorders. Although only a few of these disorders have well-established treatments or therapies, a number are on the verge of clinical trials. As investigators are able to shift care from symptomatic management of disorders to targeted therapeutics, the unmet therapeutic needs could be reduced for these patients.
Copyright © 2015 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Disease modifying; Gene therapy; Genomics; Leukodystrophy; Stem cell; Symptomatic; Therapy

Mesh:

Year:  2015        PMID: 26022168      PMCID: PMC5712822          DOI: 10.1016/j.pcl.2015.03.006

Source DB:  PubMed          Journal:  Pediatr Clin North Am        ISSN: 0031-3955            Impact factor:   3.278


  76 in total

Review 1.  Aicardi-Goutieres syndrome: from patients to genes and beyond.

Authors:  C Chahwan; R Chahwan
Journal:  Clin Genet       Date:  2012-01-08       Impact factor: 4.438

2.  Recovery of PEX1-Gly843Asp peroxisome dysfunction by small-molecule compounds.

Authors:  Rui Zhang; Li Chen; Sarn Jiralerspong; Ann Snowden; Steven Steinberg; Nancy Braverman
Journal:  Proc Natl Acad Sci U S A       Date:  2010-03-08       Impact factor: 11.205

3.  Lorenzo's oil inhibits ELOVL1 and lowers the level of sphingomyelin with a saturated very long-chain fatty acid.

Authors:  Takayuki Sassa; Takeshi Wakashima; Yusuke Ohno; Akio Kihara
Journal:  J Lipid Res       Date:  2014-01-31       Impact factor: 5.922

4.  Disorders of peroxisome biogenesis due to mutations in PEX1: phenotypes and PEX1 protein levels.

Authors:  C Walter; J Gootjes; P A Mooijer; H Portsteffen; C Klein; H R Waterham; P G Barth; J T Epplen; W H Kunau; R J Wanders; G Dodt
Journal:  Am J Hum Genet       Date:  2001-06-01       Impact factor: 11.025

Review 5.  A clinical approach to the diagnosis of patients with leukodystrophies and genetic leukoencephelopathies.

Authors:  Sumit Parikh; Geneviève Bernard; Marc C Patterson; Ryan J Taft; Adeline Vanderver; Richard J Leventer; Marjo S van der Knaap; Johan van Hove; Amy Pizzino; Nathan H McNeill; Guy Helman; Cas Simons; Johanna L Schmidt; William B Rizzo
Journal:  Mol Genet Metab       Date:  2014-12-29       Impact factor: 4.797

6.  Umbilical cord blood transplantation for juvenile metachromatic leukodystrophy.

Authors:  Tyler Mark Pierson; Carsten G Bonnemann; Richard S Finkel; Nancy Bunin; Gihan I Tennekoon
Journal:  Ann Neurol       Date:  2008-11       Impact factor: 10.422

7.  Trex1 prevents cell-intrinsic initiation of autoimmunity.

Authors:  Daniel B Stetson; Joan S Ko; Thierry Heidmann; Ruslan Medzhitov
Journal:  Cell       Date:  2008-08-22       Impact factor: 41.582

8.  Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1.

Authors:  Yanick J Crow; Diana S Chase; Johanna Lowenstein Schmidt; Marcin Szynkiewicz; Gabriella M A Forte; Hannah L Gornall; Anthony Oojageer; Beverley Anderson; Amy Pizzino; Guy Helman; Mohamed S Abdel-Hamid; Ghada M Abdel-Salam; Sam Ackroyd; Alec Aeby; Guillermo Agosta; Catherine Albin; Stavit Allon-Shalev; Montse Arellano; Giada Ariaudo; Vijay Aswani; Riyana Babul-Hirji; Eileen M Baildam; Nadia Bahi-Buisson; Kathryn M Bailey; Christine Barnerias; Magalie Barth; Roberta Battini; Michael W Beresford; Geneviève Bernard; Marika Bianchi; Thierry Billette de Villemeur; Edward M Blair; Miriam Bloom; Alberto B Burlina; Maria Luisa Carpanelli; Daniel R Carvalho; Manuel Castro-Gago; Anna Cavallini; Cristina Cereda; Kate E Chandler; David A Chitayat; Abigail E Collins; Concepcion Sierra Corcoles; Nuno J V Cordeiro; Giovanni Crichiutti; Lyvia Dabydeen; Russell C Dale; Stefano D'Arrigo; Christian G E L De Goede; Corinne De Laet; Liesbeth M H De Waele; Ines Denzler; Isabelle Desguerre; Koenraad Devriendt; Maja Di Rocco; Michael C Fahey; Elisa Fazzi; Colin D Ferrie; António Figueiredo; Blanca Gener; Cyril Goizet; Nirmala R Gowrinathan; Kalpana Gowrishankar; Donncha Hanrahan; Bertrand Isidor; Bülent Kara; Nasaim Khan; Mary D King; Edwin P Kirk; Ram Kumar; Lieven Lagae; Pierre Landrieu; Heinz Lauffer; Vincent Laugel; Roberta La Piana; Ming J Lim; Jean-Pierre S-M Lin; Tarja Linnankivi; Mark T Mackay; Daphna R Marom; Charles Marques Lourenço; Shane A McKee; Isabella Moroni; Jenny E V Morton; Marie-Laure Moutard; Kevin Murray; Rima Nabbout; Sheela Nampoothiri; Noemi Nunez-Enamorado; Patrick J Oades; Ivana Olivieri; John R Ostergaard; Belén Pérez-Dueñas; Julie S Prendiville; Venkateswaran Ramesh; Magnhild Rasmussen; Luc Régal; Federica Ricci; Marlène Rio; Diana Rodriguez; Agathe Roubertie; Elisabetta Salvatici; Karin A Segers; Gyanranjan P Sinha; Doriette Soler; Ronen Spiegel; Tommy I Stödberg; Rachel Straussberg; Kathryn J Swoboda; Mohnish Suri; Uta Tacke; Tiong Y Tan; Johann te Water Naude; Keng Wee Teik; Maya Mary Thomas; Marianne Till; Davide Tonduti; Enza Maria Valente; Rudy Noel Van Coster; Marjo S van der Knaap; Grace Vassallo; Raymon Vijzelaar; Julie Vogt; Geoffrey B Wallace; Evangeline Wassmer; Hannah J Webb; William P Whitehouse; Robyn N Whitney; Maha S Zaki; Sameer M Zuberi; John H Livingston; Flore Rozenberg; Pierre Lebon; Adeline Vanderver; Simona Orcesi; Gillian I Rice
Journal:  Am J Med Genet A       Date:  2015-01-16       Impact factor: 2.802

Review 9.  Enzyme, cell and gene-based therapies for metachromatic leukodystrophy.

Authors:  C Sevin; P Aubourg; N Cartier
Journal:  J Inherit Metab Dis       Date:  2007-03-08       Impact factor: 4.750

Review 10.  Hypomyelinating leukodystrophies: translational research progress and prospects.

Authors:  Petra J W Pouwels; Adeline Vanderver; Genevieve Bernard; Nicole I Wolf; Steffi F Dreha-Kulczewksi; Sean C L Deoni; Enrico Bertini; Alfried Kohlschütter; William Richardson; Charles Ffrench-Constant; Wolfgang Köhler; David Rowitch; A James Barkovich
Journal:  Ann Neurol       Date:  2014-06-24       Impact factor: 10.422

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  7 in total

1.  Modeling the Mutational and Phenotypic Landscapes of Pelizaeus-Merzbacher Disease with Human iPSC-Derived Oligodendrocytes.

Authors:  Zachary S Nevin; Daniel C Factor; Robert T Karl; Panagiotis Douvaras; Jeremy Laukka; Martha S Windrem; Steven A Goldman; Valentina Fossati; Grace M Hobson; Paul J Tesar
Journal:  Am J Hum Genet       Date:  2017-03-30       Impact factor: 11.025

2.  Gene therapy targeting oligodendrocytes provides therapeutic benefit in a leukodystrophy model.

Authors:  Elena Georgiou; Kyriaki Sidiropoulou; Jan Richter; Christos Papaneophytou; Irene Sargiannidou; Alexia Kagiava; Georg von Jonquieres; Christina Christodoulou; Matthias Klugmann; Kleopas A Kleopa
Journal:  Brain       Date:  2017-03-01       Impact factor: 13.501

3.  Geographic and Specialty Access Disparities in US Pediatric Leukodystrophy Diagnosis.

Authors:  Sara Grineski; Danielle X Morales; Timothy Collins; Jacob Wilkes; Joshua L Bonkowsky
Journal:  J Pediatr       Date:  2020-03-03       Impact factor: 4.406

4.  Defined and Scalable Differentiation of Human Oligodendrocyte Precursors from Pluripotent Stem Cells in a 3D Culture System.

Authors:  Gonçalo M C Rodrigues; Thomas Gaj; Maroof M Adil; Joyce Wahba; Antara T Rao; Franziska K Lorbeer; Rishi U Kulkarni; Maria Margarida Diogo; Joaquim M S Cabral; Evan W Miller; Dirk Hockemeyer; David V Schaffer
Journal:  Stem Cell Reports       Date:  2017-05-25       Impact factor: 7.765

5.  Chemical Screening Identifies Enhancers of Mutant Oligodendrocyte Survival and Unmasks a Distinct Pathological Phase in Pelizaeus-Merzbacher Disease.

Authors:  Matthew S Elitt; H Elizabeth Shick; Mayur Madhavan; Kevin C Allan; Benjamin L L Clayton; Chen Weng; Tyler E Miller; Daniel C Factor; Lilianne Barbar; Baraa S Nawash; Zachary S Nevin; Angela M Lager; Yan Li; Fulai Jin; Drew J Adams; Paul J Tesar
Journal:  Stem Cell Reports       Date:  2018-08-23       Impact factor: 7.765

6.  Natural History of Vanishing White Matter.

Authors:  Eline M C Hamilton; Hannemieke D W van der Lei; Gerre Vermeulen; Jan A M Gerver; Charles M Lourenço; Sakkubai Naidu; Hanna Mierzewska; Reinoud J B J Gemke; Henrica C W de Vet; Bernard M J Uitdehaag; Birgit I Lissenberg-Witte; Marjo S van der Knaap
Journal:  Ann Neurol       Date:  2018-09-06       Impact factor: 11.274

7.  Practical Approaches and Knowledge Gaps in the Care for Children With Leukodystrophies.

Authors:  Stephanie R Keller; Eric J Mallack; Jennifer P Rubin; Jennifer A Accardo; Jennifer A Brault; Camille S Corre; Camila Elizondo; Jennifer Garafola; April C Jackson-Garcia; Jullie Rhee; Elisa Seeger; Kaprice C Shullanberger; Amanda Tourjee; Melissa K Trovato; Amy T Waldman; Jenna L Wallace; Michael R Wallace; Klaus Werner; Angela White; Kevin C Ess; Catherine Becker; Florian S Eichler
Journal:  J Child Neurol       Date:  2020-09-02       Impact factor: 1.987

  7 in total

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