Yasinska Inna M, Calzolai Luigi, Raap Ulrike, Hussain Rohanah, Siligardi Giuliano, Sumbayev Vadim V, Gibbs Bernhard F
Medway School of Pharmacy, Universities of Kent and Greenwich, Chatham Maritime, United Kingdom.
European Commission, Joint Research Centre, Ispra, Italy.
Front Pharmacol. 2019 Mar 29;10:333. doi: 10.3389/fphar.2019.00333. eCollection 2019.
Calcineurin inhibitors potentially prevent pro-allergic mediator release from basophils and mast cells but are rarely used systemically due to ubiquitous expressions of target signaling proteins. However, specific targeting of allergic effector cells with these inhibitors could circumvent unwanted side effects. We recently demonstrated the biocompatibility of gold nanoparticles (AuNPs) as a platform for non-toxic delivery of signaling inhibitors due to unique physicochemical properties of these nanomaterials. Since AuNPs can be conjugated with both anti-allergic drugs and antibodies or other proteins that specifically recognize basophils and mast cells, our aims were to assess specific targeting of allergic effector cell function using AuNPs conjugated with the calcineurin inhibitor ascomycin. Purified human basophils and LAD2 human mast cells were used for investigations with AuNPs conjugated either to CD203c antibodies or containing stem cell factor (SCF), respectively, which were amine-coupled to acidic groups of reduced glutathione (GSH). GSH was also used as a spacer for immobilization of ascomycin on the gold surface. AuNPs conjugated with anti-CD203c and ascomycin strikingly blocked IgE-dependent degranulation of both purified basophils and those present in mixed leukocyte preparations, suggesting specific targeting of these cells. In contrast, LAD2 mast cell responses were not inhibited using anti-CD203c-containing nanoconjugates but were when the conjugates contained SCF. Successful targeting of allergic effector cells using gold nanoconjugates indicates that this technology may have therapeutic potential for the treatment of allergies by specifically delivering highly effective signaling inhibitors with reduced side effects.
钙调神经磷酸酶抑制剂有可能阻止嗜碱性粒细胞和肥大细胞释放促过敏介质,但由于靶信号蛋白的广泛表达,很少全身使用。然而,用这些抑制剂特异性靶向过敏效应细胞可以规避不必要的副作用。我们最近证明了金纳米颗粒(AuNPs)作为信号抑制剂无毒递送平台的生物相容性,这归因于这些纳米材料独特的物理化学性质。由于AuNPs可以与抗过敏药物以及特异性识别嗜碱性粒细胞和肥大细胞的抗体或其他蛋白质偶联,我们的目的是评估使用与钙调神经磷酸酶抑制剂子囊霉素偶联的AuNPs对过敏效应细胞功能的特异性靶向作用。分别使用纯化的人嗜碱性粒细胞和LAD2人肥大细胞进行研究,AuNPs分别与CD203c抗体偶联或含有干细胞因子(SCF),它们通过胺偶联到还原型谷胱甘肽(GSH)的酸性基团上。GSH也用作将子囊霉素固定在金表面的间隔物。与抗CD203c和子囊霉素偶联的AuNPs显著阻断了纯化嗜碱性粒细胞以及混合白细胞制剂中嗜碱性粒细胞的IgE依赖性脱颗粒,表明对这些细胞的特异性靶向作用。相比之下,使用含抗CD203c的纳米偶联物时,LAD2肥大细胞反应未受抑制,但当偶联物含有SCF时则受到抑制。使用金纳米偶联物成功靶向过敏效应细胞表明,该技术可能具有通过特异性递送高效信号抑制剂并减少副作用来治疗过敏的治疗潜力。