Niemeyer-van der Kolk Tessa, Assil Salma, Buters Thomas P, Rijsbergen Melanie, Klaassen Erica S, Feiss Gary, Florencia Edwin, Prens Errol P, Burggraaf Jacobus, van Doorn Martijn B A, Rissmann Robert, Moerland Matthijs
Centre for Human Drug Research, Leiden, The Netherlands.
Cutanea Life Science, Wayne, Pennsylvania, USA.
Clin Transl Sci. 2020 May;13(3):573-579. doi: 10.1111/cts.12741. Epub 2020 Feb 13.
Omiganan (OMN; a synthetic cationic peptide) and imiquimod (IMQ; a TLR7 agonist) have synergistic effects on interferon responses in vitro. The objective of this study was to translate this to a human model for proof-of-concept, and to explore the potential of OMN add-on treatment for viral skin diseases. Sixteen healthy volunteers received topical IMQ, OMN, or a combination of both for up to 4 days on tape-stripped skin. Skin inflammation was quantified by laser speckle contrast imaging and 2D photography, and molecular and cellular responses were analyzed in biopsies. IMQ treatment induced an inflammatory response of the skin. Co-treatment with OMN enhanced this inflammatory response to IMQ, with increases in perfusion (+17.1%; 95% confidence interval (CI) 5.6%-30%; P < 0.01) and erythema (+1.5; 95% CI 0.25%-2.83; P = 0.02). Interferon regulatory factor-driven and NFκB-driven responses following TLR7 stimulation were enhanced by OMN (increases in IL-6, IL-10, MXA, and IFNɣ), and more immune cell infiltration was observed (in particular CD4+, CD8+, and CD14+ cells). These findings are in line with the earlier mechanistic in vitro data, and support evaluation of imiquimod/OMN combination therapy in human papillomavirus-induced skin diseases.
奥米加南(OMN;一种合成阳离子肽)和咪喹莫特(IMQ;一种Toll样受体7激动剂)在体外对干扰素反应具有协同作用。本研究的目的是将此转化为人体模型以进行概念验证,并探索奥米加南附加治疗病毒性皮肤病的潜力。16名健康志愿者在胶带剥离的皮肤上接受局部咪喹莫特、奥米加南或两者联合治疗,持续长达4天。通过激光散斑对比成像和二维摄影对皮肤炎症进行量化,并在活检组织中分析分子和细胞反应。咪喹莫特治疗可诱导皮肤炎症反应。与奥米加南联合治疗增强了对咪喹莫特的这种炎症反应,灌注增加(+17.1%;95%置信区间(CI)5.6%-30%;P<0.01)和红斑增加(+1.5;95%CI 0.25%-2.83;P=0.02)。奥米加南增强了Toll样受体7刺激后干扰素调节因子驱动和核因子κB驱动的反应(白细胞介素-6、白细胞介素-10、MX蛋白A和干扰素γ增加),并观察到更多免疫细胞浸润(特别是CD4+、CD8+和CD14+细胞)。这些发现与早期的体外机制数据一致,并支持在人乳头瘤病毒引起的皮肤病中评估咪喹莫特/奥米加南联合治疗。