The atlas of RNase H antisense oligonucleotide distribution and activity in the CNS of rodents and non-human primates following central administration

Author:

Jafar-nejad Paymaan1,Powers Berit1,Soriano Armand1,Zhao Hien1,Norris Daniel A1,Matson John1,DeBrosse-Serra Beatrice1,Watson Jamie1,Narayanan Padmakumar1,Chun Seung J1,Mazur Curt1,Kordasiewicz Holly1,Swayze Eric E1,Rigo Frank1ORCID

Affiliation:

1. Ionis Pharmaceuticals Inc. Carlsbad, CA 92010, USA

Abstract

AbstractAntisense oligonucleotides (ASOs) have emerged as a new class of drugs to treat a wide range of diseases, including neurological indications. Spinraza, an ASO that modulates splicing of SMN2 RNA, has shown profound disease modifying effects in Spinal Muscular Atrophy (SMA) patients, energizing efforts to develop ASOs for other neurological diseases. While SMA specifically affects spinal motor neurons, other neurological diseases affect different central nervous system (CNS) regions, neuronal and non-neuronal cells. Therefore, it is important to characterize ASO distribution and activity in all major CNS structures and cell types to have a better understanding of which neurological diseases are amenable to ASO therapy. Here we present for the first time the atlas of ASO distribution and activity in the CNS of mice, rats, and non-human primates (NHP), species commonly used in preclinical therapeutic development. Following central administration of an ASO to rodents, we observe widespread distribution and target RNA reduction throughout the CNS in neurons, oligodendrocytes, astrocytes and microglia. This is also the case in NHP, despite a larger CNS volume and more complex neuroarchitecture. Our results demonstrate that ASO drugs are well suited for treating a wide range of neurological diseases for which no effective treatments are available.

Publisher

Oxford University Press (OUP)

Subject

Genetics

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