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Quantifying and mitigating motor phenotypes induced by antisense oligonucleotides in the central nervous system.

Authors :
Moazami MP
Rembetsy-Brown JM
Sarli SL
McEachern HR
Wang F
Ohara M
Wagh A
Kelly K
Krishnamurthy PM
Weiss A
Marosfoi M
King RM
Motwani M
Gray-Edwards H
Fitzgerald KA
Brown RH
Watts JK
Source :
Molecular therapy : the journal of the American Society of Gene Therapy [Mol Ther] 2024 Dec 04; Vol. 32 (12), pp. 4401-4417. Date of Electronic Publication: 2024 Oct 28.
Publication Year :
2024

Abstract

Antisense oligonucleotides (ASOs) are emerging as a promising class of therapeutics for neurological diseases. When injected directly into cerebrospinal fluid, ASOs distribute broadly across brain regions and exert long-lasting therapeutic effects. However, many phosphorothioate (PS)-modified gapmer ASOs show transient motor phenotypes when injected into the cerebrospinal fluid, ranging from reduced motor activity to ataxia or acute seizure-like phenotypes. Using a behavioral scoring assay customized to reflect the timing and nature of these effects, we show that both sugar and phosphate modifications influence acute motor phenotypes. Among sugar analogs, DNA induces the strongest motor phenotypes while 2'-substituted RNA modifications improve the tolerability of PS ASOs. Reducing the PS content of gapmer ASOs, which contain a stretch of PS-DNA, improves their toxicity profile, but in some cases also reduces efficacy or duration of effect. We show that this acute toxicity is not mediated by major nucleic acid sensing immune pathways. Formulating ASOs with divalent ions before injection and avoiding phosphate-based buffers modestly improved tolerability through mechanisms at least partially distinct from reduced PS content. Overall, our work identifies and quantifies an understudied aspect of oligonucleotide toxicology in the CNS, explores its mechanism, and presents platform-level medicinal chemistry and formulation approaches that improve tolerability of this class of compounds.<br />Competing Interests: Declaration of interests F.W., R.H.B., and J.K.W. are co-founders of Nucyrna Therapeutics. J.K.W. is advisory board member of EnPlusOne, PepGen, and Sixfold. R.H.B. is co-founder and Scientific Advisory Board member of ApicBio. The authors have filed patent applications on oligonucleotides and designs intended for use in the CNS.<br /> (Copyright © 2024 The Author(s). Published by Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
1525-0024
Volume :
32
Issue :
12
Database :
MEDLINE
Journal :
Molecular therapy : the journal of the American Society of Gene Therapy
Publication Type :
Academic Journal
Accession number :
39460376
Full Text :
https://doi.org/10.1016/j.ymthe.2024.10.024