Cellular immune changes during severe antisense oligonucleotide-associated thrombocytopenia in a nonhuman primate model.

Abstract

Antisense oligonucleotides (ASOs) are a new class of single-stranded DNA-based drugs that hold great therapeutic potential. A low incidence of severe, dose-dependent, and reversible thrombocytopenia (TCP) (platelets < 50 K/μl) has been reported in nonhuman primate (NHP) populations, following treatment of monkeys with 2'-O-methoxy ethyl ASOs (2% to 4% at doses > 8 to 10 mg/kg/week). The potential mechanisms for this effect were studied using the Mauritian-sourced NHPs, which were shown to be more susceptible to ASO-induced TCP than Asian-sourced animals. In this pilot study, we used a mass cytometry-based intracellular cytokine staining assay, to evaluate the immune-phenotypic and functional changes in cryopreserved PBMCs, collected over 8 time points of ASO therapy (ISIS 405879) from 12 Cambodian and 12 Mauritian monkeys (9 treated and 3 controls). Unsupervised clustering was performed across markers used for cell type identification in the pooled dataset, followed by unsupervised comparison at each time point and then longitudinal analysis. Major immune cell types showed differential abundance between the 2 groups prior to start of ASO therapy. These included IFNg- and TNF-producing polyfunctional effector T cells (CD4+ and CD8+), which were lower, and MIP1b-producing monocytes and DCs, which were higher, in the Mauritian monkeys. Immune populations also changed over the course of this treatment, wherein IL-17- and GM-CSF-producing T cells and IgM-producing B cells increased markedly in Mauritians. Identification of these differentially abundant immune cell subsets in treatment sensitive NHPs could help decipher potential immune mechanisms contributing to severe TCP observed during administration of specific ASO sequences in humans.