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. 2025 Aug 26:S0092-8674(25)00908-0.
doi: 10.1016/j.cell.2025.07.045. Online ahead of print.

Molecular impact of antisense oligonucleotide therapy in C9orf72-associated ALS

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Free article

Molecular impact of antisense oligonucleotide therapy in C9orf72-associated ALS

Zachary T McEachin et al. Cell. .
Free article

Abstract

C9orf72-associated amyotrophic lateral sclerosis (c9ALS) is caused by an intronic G4C2 repeat expansion that leads to toxic RNA transcripts and dipeptide repeat proteins (DPRs). A clinical trial using the antisense oligonucleotide (ASO) BIIB078 to target these transcripts was discontinued after failing to provide clinical benefit. Here, we determine the extent of target engagement in the central nervous system (CNS) and elucidate pharmacodynamic cerebrospinal fluid (CSF) biomarkers following treatment. CSF from BIIB078-treated cases showed reduced DPRs and sustained increases in inflammatory biomarkers, including C-C motif chemokine ligand 26 (CCL26). BIIB078 was widely distributed in postmortem CNS tissue; however, DPRs and phosphorylated TDP-43 remained abundant. Proteomic signatures in c9ALS spinal cord were not altered with treatment, although a distinct increase in RNase T2 abundance that correlated with BIIB078 concentration was observed. Thus, despite widespread distribution, BIIB078 did not significantly impact key CNS pathologies, emphasizing the need to identify pharmacodynamic biomarkers that reflect disease-relevant neuropathological changes in response to ASO therapies.

Keywords: BIIB078; C9orf72; NULISA; TDP-43; amyotrophic lateral sclerosis; antisense oligonucleotides; dipeptide repeat proteins; proteomics.

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Conflict of interest statement

Declaration of interests N.T.S., Z.T.M., and J.D.G. are co-founders of StitchRx. N.T.S. and D.M.D. are co-founders and consultants of Emtherapro and Arc Proteomics.

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