Cereblon modulator iberdomide induces degradation of the transcription factors Ikaros and Aiolos: immunomodulation in healthy volunteers and relevance to systemic lupus erythematosus.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 29945920.
- Also identified by DOI 10.1136/annrheumdis-2017-212916 and PMC identifier 6161670.
- Licence recorded as CC BY-NC.
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Abstract
<i>IKZF1</i> and <i>IKZF3 (</i>encoding transcription factors Ikaros and Aiolos) are susceptibility loci for systemic lupus erythematosus (SLE). The pharmacology of iberdomide (CC-220), a cereblon (<i>CRBN</i>) modulator targeting Ikaros and Aiolos, was studied in SLE patient cells and in a phase 1 healthy volunteer study. <i>CRBN</i>, <i>IKZF1</i> and <i>IKZF3</i> gene expression was measured in peripheral blood mononuclear cells (PBMC) from patients with SLE and healthy volunteers. Ikaros and Aiolos protein levels were measured by Western blot and flow cytometry. Anti-dsDNA and anti-phospholipid autoantibodies were measured in SLE PBMC cultures treated for 7 days with iberdomide. Fifty-six healthy volunteers were randomised to a single dose of iberdomide (0.03-6 mg, n=6 across seven cohorts) or placebo (n=2/cohort). CD19+ B cells, CD3+ T cells and intracellular Aiolos were measured by flow cytometry. Interleukin (IL)-2 and IL-1β production was stimulated with anti-CD3 and lipopolysaccharide, respectively, in an ex vivo whole blood assay. SLE patient PBMCs expressed significantly higher <i>CRBN</i> (1.5-fold), <i>IKZF1</i> (2.1-fold) and <i>IKZF3</i> (4.1-fold) mRNA levels compared with healthy volunteers. Iberdomide significantly reduced Ikaros and Aiolos protein levels in B cells, T cells and monocytes. In SLE PBMC cultures, iberdomide inhibited anti-dsDNA and anti-phospholipid autoantibody production (IC<sub>50</sub> ≈10 nM). Single doses of iberdomide (0.3-6 mg) in healthy volunteers decreased intracellular Aiolos (minimum mean per cent of baseline: ≈12%-28% (B cells); ≈0%-33% (T cells)), decreased absolute CD19+ B cells, increased IL-2 and decreased IL-1β production ex vivo. These findings demonstrate pharmacodynamic activity of iberdomide and support its further clinical development for the treatment of SLE. NCT01733875; Results.
Medical subject headings
- Heterocyclic Compounds, 4 or More Rings
- Ikaros Transcription Factor
- Lupus Erythematosus, Systemic
- Peptide Hydrolases