Bartz Holger, Mendoza Yuri, Gebker Miriam, Fischborn Till, Heeg Klaus, Dalpke Alexander
Institute of Medical Microbiology and Hygiene, Philipps-University, Pilgrimstein 2, D-35037 Marburg, Germany.
Vaccine. 2004 Nov 25;23(2):148-55. doi: 10.1016/j.vaccine.2004.05.020.
CpG-oligonucleotides (CpG-ODN) have been shown to exert strong immuno-stimulatory effects through activation of Toll-like receptor 9 (TLR-9). However, TLR-9 triggering takes place in endosomal compartments and thus CpG-ODN have to be taken up prior to signal transduction. We here report that 3'-poly-guanosine strings can improve cellular internalisation of phosphodiester but not of phosphorothioate CpG-ODN. Improved cellular uptake correlated with enhanced IL-6 secretion and proliferation of PBMC. Also, TLR-9 transfected HEK293 cells were activated more efficiently by poly-guanosine modified CpG-ODN. The results indicate that the synthesis of stimulatory CpG-ODN based on a phosphodiester backbone is feasible via such poly-guanosine substitutions. In addition we observed that phosphorothioate ODN were able to exert immunostimulatory effects independent of the presence of CpG motifs.
CpG寡核苷酸(CpG-ODN)已被证明可通过激活Toll样受体9(TLR-9)发挥强大的免疫刺激作用。然而,TLR-9的触发发生在内体区室中,因此CpG-ODN必须在信号转导之前被摄取。我们在此报告,3'-聚鸟苷链可改善磷酸二酯型而非硫代磷酸酯型CpG-ODN的细胞内化。细胞摄取的改善与PBMC中IL-6分泌和增殖的增强相关。此外,转染了TLR-9的HEK293细胞被聚鸟苷修饰的CpG-ODN更有效地激活。结果表明,基于磷酸二酯骨架的刺激性CpG-ODN通过这种聚鸟苷取代合成是可行的。此外,我们观察到硫代磷酸酯ODN能够发挥免疫刺激作用,而与CpG基序的存在无关。