QR-313, an antisense oligonucleotide, shows therapeutic efficacy for treatment of dominant and recessive dystrophic epidermolysis bullosa: a preclinical study

Abstract: Dystrophic epidermolysis bullosa (DEB) is a blistering skin disease caused by mutations in the gene COL7A1 encoding collagen VII. DEB can be inherited as recessive DEB (RDEB) or dominant DEB (DDEB) and is associated with a high wound burden. Perpetual cycles of wounding and healing drive fibrosis in DDEB and RDEB, as well as the formation of a tumor-permissive microenvironment. Prolonging wound-free episodes by improving the quality of wound healing would therefore confer substantial benefit for individuals with DEB. The collagenous domain of collagen VII is encoded by 82 in-frame exons, which makes splice-modulation therapies attractive for DEB. Indeed, antisense oligonucleotide–based exon skipping has shown promise for RDEB. However, the suitability of antisense oligonucleotides for treatment of DDEB remains unexplored. Here, we developed QR-313, a clinically applicable, potent antisense oligonucleotide specifically targeting exon 73. We show the feasibility of topical delivery of QR-313 in a carbomer-composed gel for treatment of wounds to restore collagen VII abundance in human RDEB skin. Our data reveal that QR-313 also shows direct benefit for DDEB caused by exon 73 mutations. Thus, the same topically applied therapeutic could be used to improve the wound healing quality in RDEB and DDEB

Standort
Deutsche Nationalbibliothek Frankfurt am Main
Umfang
Online-Ressource
Sprache
Englisch
Anmerkungen
The journal of investigative dermatology. - 141, 4 (2021) , 883-893.e6, ISSN: 0022-202X

Ereignis
Veröffentlichung
(wo)
Freiburg
(wer)
Universität
(wann)
2020
Urheber
Bornert, Olivier
Hogervorst, Marieke
Nauroy, Pauline
Bischof, Johannes
Swildens, Jim
Athanasiou, Ioannis
Tufa, Sara F.
Keene, Douglas R.
Kiritsi, Dimitra
Hainzl, Stefan
Murauer, Eva M.
Marinkovich, M. Peter
Platenburg, Gerard
Haußer-Siller, Ingrid
Wally, Verena
Ritsema, Tita
Koller, Ulrich
Haisma, Elisabeth M.
Nyström, Alexander

DOI
10.1016/j.jid.2020.08.018
URN
urn:nbn:de:bsz:25-freidok-1699016
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Letzte Aktualisierung
14.08.2025, 10:48 MESZ

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Beteiligte

Entstanden

  • 2020

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