Literature DB >> 28541820

Assessment of the Effects of 2'-Methoxyethyl Antisense Oligonucleotides on Platelet Count in Cynomolgus Nonhuman Primates.

Scott P Henry1, Padmakumar Narayanan1, Lijiang Shen1, Sanjay Bhanot1, Husam S Younis1, Sebastien A Burel1.   

Abstract

Decreases in platelet (PLT) counts observed in nonhuman primates (NHPs) given 2'-O-methoxyethyl modified antisense inhibitors (2'-MOE ASOs) have been reported, but the incidence and severity of the change vary considerably between sequences, studies, and animals. This article will broadly illustrate the spectrum of effects on PLT count in NHPs. From queries of an NHP safety database representing over 102 independent 2'-MOE ASOs, from 61 studies and >2200 NHPs, two patterns of PLT changes emerged. The first is a consistent and reproducible decrease in group mean values, observed with about 30% of the compounds, in which PLT count typically remains ≥150K cells/μL. The second is a sporadic decrease in PLTs to <50K cells/μL (2%-4% incidence at doses >5 mg/kg) that is often not reproducible. In both cases, the reduction in PLT count is dose dependent and reversible. The human relevance of PLT change observed in NHPs was investigated using ISIS 404173. In a chronic NHP study (20 mg/kg/wk for 26 weeks), a gradual decrease in group mean PLT count was observed at ≥10 mg/kg/wk, which plateaued by 13 weeks generally within the normal range and was maintained through 26 weeks of treatment. However, PLT counts <50K cells/μL occurred in 1 of 16 NHP at 10 mg/kg/wk and 3 of 16 NHP at 20 mg/kg/wk. In a 26-week double-blind, placebo-controlled Phase 2 trial, 62 patients were treated with 200 mg/wk ISIS 404173 (∼3.3 mg/kg/wk) there was an increased incidence of PLT count >30% decreased compared to baseline but no incidence of PLT <75K cells/μL. Based on these data, the consistent, self-limiting PLT reduction seen in NHP may translate to humans, but these changes appear to be of limited clinical significance. However, NHPs appear to overpredict the incidence of sporadic PLT <50K cells/μL compared to humans.

Entities:  

Keywords:  antisense; nonhuman primate; oligonucleotide; platelet

Mesh:

Substances:

Year:  2017        PMID: 28541820     DOI: 10.1089/nat.2017.0666

Source DB:  PubMed          Journal:  Nucleic Acid Ther        ISSN: 2159-3337            Impact factor:   5.486


  6 in total

Review 1.  Cholesterol Lowering Biotechnological Strategies: From Monoclonal Antibodies to Antisense Therapies. A Pre-Clinical Perspective Review.

Authors:  S Bellosta; C Rossi; A S Alieva; A L Catapano; A Corsini; A Baragetti
Journal:  Cardiovasc Drugs Ther       Date:  2022-01-13       Impact factor: 3.727

Review 2.  The Nonclinical Safety Profile of GalNAc-conjugated RNAi Therapeutics in Subacute Studies.

Authors:  Maja M Janas; Carole E Harbison; Victoria K Perry; Brenda Carito; Jessica E Sutherland; Akshay K Vaishnaw; Natalie D Keirstead; Garvin Warner
Journal:  Toxicol Pathol       Date:  2018-08-23       Impact factor: 1.902

3.  IONIS-PKKRx a Novel Antisense Inhibitor of Prekallikrein and Bradykinin Production.

Authors:  Jason D Ferrone; Gourab Bhattacharjee; Alexey S Revenko; Thomas A Zanardi; Marshelle S Warren; Frederick J Derosier; Nicholas J Viney; Nguyen C Pham; Gwendolyn E Kaeser; Brenda F Baker; Eugene Schneider; Steven G Hughes; Brett P Monia; A Robert MacLeod
Journal:  Nucleic Acid Ther       Date:  2019-02-28       Impact factor: 5.486

4.  An Integrated Safety Analysis of Infants and Children with Symptomatic Spinal Muscular Atrophy (SMA) Treated with Nusinersen in Seven Clinical Trials.

Authors:  Basil T Darras; Michelle A Farrar; Eugenio Mercuri; Richard S Finkel; Richard Foster; Steven G Hughes; Ishir Bhan; Wildon Farwell; Sarah Gheuens
Journal:  CNS Drugs       Date:  2019-09       Impact factor: 5.749

Review 5.  The Progression of Treatment for Refractory Hypercholesterolemia: Focus on the Prospect of Gene Therapy.

Authors:  Zhi-Fan Li; Na-Qiong Wu
Journal:  Front Genet       Date:  2022-06-09       Impact factor: 4.772

6.  Sequence-specific 2'-O-methoxyethyl antisense oligonucleotides activate human platelets through glycoprotein VI, triggering formation of platelet-leukocyte aggregates.

Authors:  Martina H Lundberg Slingsby; Prakrith Vijey; I-Ting Tsai; Harvey Roweth; Genevieve Couldwell; Adrian R Wilkie; Hans Gaus; Jazana M Goolsby; Ross Okazaki; Brooke E Terkovich; John W Semple; Jonathan N Thon; Scott P Henry; Padmakumar Narayanan; Joseph E Italiano
Journal:  Haematologica       Date:  2022-02-01       Impact factor: 9.941

  6 in total

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