Literature DB >> 35213027

In Vivo Models for the Evaluation of Antisense Oligonucleotides in Skin.

Jeroen Bremer1,2, Peter C van den Akker3,4,5.   

Abstract

Here, we describe an in vivo model in which antisense oligonucleotides were preclinically evaluated in reconstituted patient and healthy control skin. The aim was to investigate the effect of antisense oligonucleotides upon local or systemic administration. This allows for clinically relevant evaluation of antisense oligonucleotides in an in vivo setting. In this model, primary human keratinocytes and fibroblasts were placed into silicone grafting chambers, implanted onto the back of athymic nude mice. After sufficient cells were expanded, within a few weeks, human skin grafts were generated with a high success rate. These mice bearing grafts were subsequently treated with antisense oligonucleotides targeting exon 105 of the COL7A1 gene which encodes type VII collagen. Patients completely lacking expression of type VII collagen develop severe blistering of skin and mucosa, i.e., recessive dystrophic epidermolysis bullosa. In this chapter, we describe the in vivo model used for the preclinical evaluation of antisense oligonucleotides as therapeutic approach for recessive dystrophic epidermolysis bullosa.
© 2022. The Author(s).

Entities:  

Keywords:  Antisense RNA; Epidermolysis bullosa; Exon skipping; Skin equivalent mouse model; Splice modulating; Therapy

Mesh:

Substances:

Year:  2022        PMID: 35213027     DOI: 10.1007/978-1-0716-2010-6_21

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  5 in total

1.  Spontaneous cell sorting of fibroblasts and keratinocytes creates an organotypic human skin equivalent.

Authors:  C K Wang; C F Nelson; A M Brinkman; A C Miller; W K Hoeffler
Journal:  J Invest Dermatol       Date:  2000-04       Impact factor: 8.551

2.  Analysis of the functional consequences of targeted exon deletion in COL7A1 reveals prospects for dystrophic epidermolysis bullosa therapy.

Authors:  Olivier Bornert; Tobias Kühl; Jeroen Bremer; Peter C van den Akker; Anna Mg Pasmooij; Alexander Nyström
Journal:  Mol Ther       Date:  2016-05-09       Impact factor: 11.454

Review 3.  Consensus reclassification of inherited epidermolysis bullosa and other disorders with skin fragility.

Authors:  C Has; J W Bauer; C Bodemer; M C Bolling; L Bruckner-Tuderman; A Diem; J-D Fine; A Heagerty; A Hovnanian; M P Marinkovich; A E Martinez; J A McGrath; C Moss; D F Murrell; F Palisson; A Schwieger-Briel; E Sprecher; K Tamai; J Uitto; D T Woodley; G Zambruno; J E Mellerio
Journal:  Br J Dermatol       Date:  2020-03-11       Impact factor: 9.302

4.  Antisense Oligonucleotide-mediated Exon Skipping as a Systemic Therapeutic Approach for Recessive Dystrophic Epidermolysis Bullosa.

Authors:  Jeroen Bremer; Olivier Bornert; Alexander Nyström; Antoni Gostynski; Marcel F Jonkman; Annemieke Aartsma-Rus; Peter C van den Akker; Anna Mg Pasmooij
Journal:  Mol Ther Nucleic Acids       Date:  2016-10-18       Impact factor: 10.183

5.  Natural Exon Skipping Sets the Stage for Exon Skipping as Therapy for Dystrophic Epidermolysis Bullosa.

Authors:  Jeroen Bremer; Elisabeth H van der Heijden; Daryll S Eichhorn; Rowdy Meijer; Henny H Lemmink; Hans Scheffer; Richard J Sinke; Marcel F Jonkman; Anna M G Pasmooij; Peter C Van den Akker
Journal:  Mol Ther Nucleic Acids       Date:  2019-09-19       Impact factor: 8.886

  5 in total

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