Univ. Lille, CHU Lille, Laboratoire de Virologie URL3610, Lille, France.
Vaxinano SAS, Loos, France.
Intervirology. 2024;67(1):99-105. doi: 10.1159/000539601. Epub 2024 Jul 26.
The effect of maltodextrin-based nanoparticles with an anionic phospholipid core (lipid-based nanoparticles [NPLs]) on the infection of a human tumoral cell line with poliovirus (PV) has been studied.
NPLs were synthesized and associated with the PV type 1 Sabin strain, and the formulations were characterized. PV and PV/NPL formulations were inoculated to HEp-2 cells.
The surface charge and the diameter of PV/NPL formulation suggest that viral particles were adsorbed onto NPLs. When HEp-2 cells were inoculated with 1 tissue culture 50% infectious dose/mL PV associated with NPLs, the cytopathic effect appeared obvious; the levels of the infectious titer of culture supernatants and the proportion of VP1-positive cells were higher. The level of intracellular viral RNA extracted from HEp-2 cells inoculated with PV/NPL formulation was higher as well.
These results show that NPLs can enhance the infection with a virus and suggest that they might be used in virotherapy to increase the virus-mediated lysis of tumor cells.
本研究探讨了基于麦芽糊精的带阴离子磷脂核心(脂基纳米粒[NPLs])对人肿瘤细胞系感染脊髓灰质炎病毒(PV)的影响。
合成 NPLs 并使其与 PV 1 型 Sabin 株结合,对制剂进行了表征。将 PV 和 PV/NPL 制剂接种到 HEp-2 细胞中。
PV/NPL 制剂的表面电荷和直径表明病毒颗粒被吸附到 NPLs 上。当用 1 组织培养 50%感染剂量/mL 的与 NPLs 结合的 PV 接种 HEp-2 细胞时,细胞病变效应明显;培养上清液的感染滴度和 VP1 阳性细胞的比例更高。从接种 PV/NPL 制剂的 HEp-2 细胞中提取的细胞内病毒 RNA 水平也更高。
这些结果表明 NPLs 可以增强病毒感染,并提示它们可用于病毒治疗以增加病毒介导的肿瘤细胞裂解。