Delivery is key: lessons learnt from developing splice‐switching antisense therapies

نویسندگان

  • Caroline Godfrey
  • Lourdes R Desviat
  • Bård Smedsrød
  • France Piétri-Rouxel
  • Michela A Denti
  • Petra Disterer
  • Stéphanie Lorain
  • Gisela Nogales-Gadea
  • Valentina Sardone
  • Rayan Anwar
  • Samir El Andaloussi
  • Taavi Lehto
  • Bernard Khoo
  • Camilla Brolin
  • Willeke Mc van Roon-Mom
  • Aurélie Goyenvalle
  • Annemieke Aartsma-Rus
  • Virginia Arechavala-Gomeza
چکیده

The use of splice-switching antisense therapy is highly promising, with a wealth of pre-clinical data and numerous clinical trials ongoing. Nevertheless, its potential to treat a variety of disorders has yet to be realized. The main obstacle impeding the clinical translation of this approach is the relatively poor delivery of antisense oligonucleotides to target tissues after systemic delivery. We are a group of researchers closely involved in the development of these therapies and would like to communicate our discussions concerning the validity of standard methodologies currently used in their pre-clinical development, the gaps in current knowledge and the pertinent challenges facing the field. We therefore make recommendations in order to focus future research efforts and facilitate a wider application of therapeutic antisense oligonucleotides.

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عنوان ژورنال:

دوره 9  شماره 

صفحات  -

تاریخ انتشار 2017