Why the study?
Does systemic delivery of IL-2/15Rβ siRNA reduce disease progression in a rat model of adjuvant-induced arthritis?
Does systemic delivery of IL-2/15Rβ siRNA reduce disease progression in a rat model of adjuvant-induced arthritis?
Systemic delivery of siRNA targeting the IL-2/15 receptor beta chain effectively reduces inflammation and joint destruction in a rat model of rheumatoid arthritis.
IL-2/15Rβ siRNA shows preclinical efficacy in rat arthritis; leaves open translation to human rheumatoid arthritis.
The role of interleukin (IL)-15 in the pathogenesis of rheumatoid arthritis (RA) is well established; however, systemic knockdown of IL-15 receptor (IL-15R) for reduction in inflammation at local sites has not been demonstrated. In this study, the therapeutic effect of intravenously administered siRNA targeting the β chain of IL-15R which is shared by the receptor for IL-2 was examined in rats with adjuvant-induced arthritis (AA). Polyethylenimine (PEI)-complexed siRNA nanoparticles could easily accumulate in arthritic paws of AA rats. In the paws, the nanoparticles were avidly taken up by macrophages and to a lesser extent by T cells. Weekly administered IL-2/15Rβ siRNA polyplexes were capable of decreasing disease progression in AA rats, with striking inhibition of clinical, radiologic, and histologic features of RA. The observed therapeutic effect was associated with reduced expression of proinflammatory mediators in the inflamed joints. Thus, this study provides evidence that IL-2/15Rβ could be targeted for the treatment of RA.
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Zhang et al. (2013) studied this question.
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