Literature DB >> 32179957

[Gene-selective treatment approaches for Huntington's disease].

A Mühlbäck1,2, K S Lindenberg1, C Saft3, J Priller4, G B Landwehrmeyer5.   

Abstract

In Germany at least 8000 and probably up to ca. 14,000 people currently suffer from clinically manifest Huntington's disease (HD). In addition, an estimated 24,000 Germans carry the HD mutation in the huntingtin (HTT) gene and will develop HD during their lifetime. Although HD is a rare neurodegenerative disease, it is currently in the focus of general medical interest: clinical trials have begun that provide a rational basis for hope to slow down the so far relentless progression of the disease, ultimately resulting in patients becoming entirely dependent on nursing care. If treatment is started early enough it may be possible to mitigate the clinical manifestation of HD. These innovative therapeutic approaches aim at inhibiting the de novo production of mutant HTT gene products. A first clinical drug trial to demonstrate the efficacy (phase III) of intrathecal antisense oligonucleotides (ASO, active substance RG6042) was started in 2019. Additional clinical studies on alternative treatment approaches with allele-selective ASOs as well as gene therapeutic approaches using RNA molecules and zinc finger repressor complexes are imminent. This article gives an overview of the current gene-selective therapeutic approaches in HD under discussion.

Entities:  

Keywords:  Adeno-associated viruses; Antisense oligonucleotide; Gene therapy; Huntingtin; Zinc finger repressor complexes

Mesh:

Substances:

Year:  2020        PMID: 32179957     DOI: 10.1007/s00115-020-00882-4

Source DB:  PubMed          Journal:  Nervenarzt        ISSN: 0028-2804            Impact factor:   1.214


  42 in total

Review 1.  [Antisense therapies for neurological diseases].

Authors:  Stefan-M Pulst
Journal:  Nervenarzt       Date:  2019-08       Impact factor: 1.214

2.  Epidemiology of Huntington disease: first post-HTT gene analysis of prevalence in Italy.

Authors:  F Squitieri; A Griguoli; G Capelli; A Porcellini; B D'Alessio
Journal:  Clin Genet       Date:  2015-03-15       Impact factor: 4.438

Review 3.  Protein aggregates in Huntington's disease.

Authors:  Montserrat Arrasate; Steven Finkbeiner
Journal:  Exp Neurol       Date:  2011-12-19       Impact factor: 5.330

Review 4.  Repeat instability as the basis for human diseases and as a potential target for therapy.

Authors:  Arturo López Castel; John D Cleary; Christopher E Pearson
Journal:  Nat Rev Mol Cell Biol       Date:  2010-03       Impact factor: 94.444

Review 5.  Huntington's disease: from molecular pathogenesis to clinical treatment.

Authors:  Christopher A Ross; Sarah J Tabrizi
Journal:  Lancet Neurol       Date:  2011-01       Impact factor: 44.182

Review 6.  Antisense oligonucleotide therapeutics in neurodegenerative diseases: the case of polyglutamine disorders.

Authors:  Ana C Silva; Diana D Lobo; Inês M Martins; Sara M Lopes; Carina Henriques; Sónia P Duarte; Jean-Cosme Dodart; Rui Jorge Nobre; Luis Pereira de Almeida
Journal:  Brain       Date:  2020-02-01       Impact factor: 13.501

7.  A programmable dual-RNA-guided DNA endonuclease in adaptive bacterial immunity.

Authors:  Martin Jinek; Krzysztof Chylinski; Ines Fonfara; Michael Hauer; Jennifer A Doudna; Emmanuelle Charpentier
Journal:  Science       Date:  2012-06-28       Impact factor: 47.728

8.  Efficient gene transfer into nondividing cells by adeno-associated virus-based vectors.

Authors:  G Podsakoff; K K Wong; S Chatterjee
Journal:  J Virol       Date:  1994-09       Impact factor: 5.103

Review 9.  What is CRISPR/Cas9?

Authors:  Melody Redman; Andrew King; Caroline Watson; David King
Journal:  Arch Dis Child Educ Pract Ed       Date:  2016-04-08       Impact factor: 1.309

Review 10.  The Prevalence of Huntington's Disease.

Authors:  Michael D Rawlins; Nancy S Wexler; Alice R Wexler; Sarah J Tabrizi; Ian Douglas; Stephen J W Evans; Liam Smeeth
Journal:  Neuroepidemiology       Date:  2016-01-30       Impact factor: 3.282

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