Modulation of Pro-Inflammatory IL-6 Trans-Signaling Axis by Splice Switching Oligonucleotides as a Therapeutic Modality in Inflammation

被引:5
作者
Gupta, Dhanu [1 ,2 ]
Orehek, Sara [2 ,4 ]
Turunen, Janne [2 ,5 ]
O'Donovan, Liz [3 ]
Gait, Michael J. [3 ]
El-Andaloussi, Samir [2 ]
Wood, Matthew J. A. [1 ]
机构
[1] Univ Oxford, Dept Paediat, Oxford OX3 7TY, England
[2] Karolinska Inst, Dept Lab Med, Div Biomol & Cellular Med, Biomol Med, S-14151 Huddinge, Sweden
[3] Med Res Council Lab Mol Biol, Cambridge CB2 0QH, England
[4] Natl Inst Chem, Dept Synthet Biol & Immunol, Ljubljana 1000, Slovenia
[5] ProQR Therapeut, NL-2333 CK Leiden, Netherlands
关键词
inflammation; nucleic acid therapies; IL-6; trans-signaling; oligonucleotides; SOLUBLE GP130; INTERLEUKIN-6; CYTOKINE; RECEPTORS; BLOCKADE;
D O I
10.3390/cells12182285
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Interleukin-6 (IL-6) is a pleiotropic cytokine that plays a crucial role in maintaining normal homeostatic processes under the pathogenesis of various inflammatory and autoimmune diseases. This context-dependent effect from a cytokine is due to two distinctive forms of signaling: cis-signaling and trans-signaling. IL-6 cis-signaling involves binding IL-6 to the membrane-bound IL-6 receptor and Glycoprotein 130 (GP130) signal-transducing subunit. By contrast, in IL-6 trans-signaling, complexes of IL-6 and the soluble form of the IL-6 receptor (sIL-6R) signal via membrane-bound GP130. Various strategies have been employed in the past decade to target the pro-inflammatory effect of IL-6 in numerous inflammatory disorders. However, their development has been hindered since these approaches generally target global IL-6 signaling, also affecting the anti-inflammatory effects of IL-6 signaling too. Therefore, novel strategies explicitly targeting the pro-inflammatory IL-6 trans-signaling without affecting the IL-6 cis-signaling are required and carry immense therapeutic potential. Here, we have developed a novel approach to specifically decoy IL-6-mediated trans-signaling by modulating alternative splicing in GP130, an IL-6 signal transducer, by employing splice switching oligonucleotides (SSO), to induce the expression of truncated soluble isoforms of the protein GP130. This isoform is devoid of signaling domains but allows for specifically sequestering the IL-6/sIL-6R receptor complex with high affinity in serum and thereby suppressing inflammation. Using the state-of-the-art Pip6a cell-penetrating peptide conjugated to PMO-based SSO targeting GP130 for efficient in vivo delivery, reduced disease phenotypes in two different inflammatory mouse models of systemic and intestinal inflammation were observed. Overall, this novel gene therapy platform holds great potential as a refined therapeutic intervention for chronic inflammatory diseases.
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页数:16
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