Bishani Ali, Makarova Darya M, Shmendel Elena V, Maslov Mikhail A, Sen'kova Aleksandra V, Savin Innokenty A, Gladkikh Daniil V, Zenkova Marina A, Chernolovskaya Elena L
Institute of Chemical Biology and Fundamental Medicine SB RAS, Lavrentieva Ave. 8, 630090 Novosibirsk, Russia.
Lomonosov Institute of Fine Chemical Technologies, MIREA-Russian Technological University, Vernadsky Ave. 86, 119571 Moscow, Russia.
Pharmaceutics. 2023 Aug 23;15(9):2184. doi: 10.3390/pharmaceutics15092184.
In this study, the impact of different delivery systems on the cytokine-inducing, antiproliferative, and antitumor activities of short immunostimulatory double-stranded RNA (isRNA) was investigated. The delivery systems, consisting of the polycationic amphiphile 1,26-bis(cholest-5-en-3-yloxycarbonylamino)-7,11,16,20 tetraazahexacosan tetrahydrochloride (2X3), and the lipid-helper dioleoylphosphatidylethanolamine (DOPE), were equipped with polyethylene glycol lipoconjugates differing in molecular weight and structure. The main findings of this work are as follows: (i) significant activation of MCP-1 and INF-α, β, and γ production in CBA mice occurs under the action of isRNA complexes with liposomes containing lipoconjugates with long PEG chains, while activation of MCP-1 and INF-γ, but not INF-α or β, was observed under the action of isRNA lipoplexes containing lipoconjugates with short PEG chains; (ii) a pronounced antiproliferative effect on B16 melanoma cells in vitro, as well as an antitumor and hepatoprotective effect in vivo, was induced by isRNA pre-complexes with non-pegylated liposomes, while complexes containing lipoconjugates with long-chain liposomes were inactive; (iii) the antitumor activity of isRNA correlated with the efficiency of its accumulation in the cells and did not explicitly depend on the activation of cytokine and interferon production. Thus, the structure of the delivery system plays a vital role in determining the response to isRNA and allows for the choice of a delivery system depending on the desired effect.
在本研究中,研究了不同递送系统对短免疫刺激双链RNA(isRNA)的细胞因子诱导、抗增殖和抗肿瘤活性的影响。递送系统由聚阳离子两亲物1,26-双(胆甾-5-烯-3-基氧基羰基氨基)-7,11,16,20-四氮杂二十六烷四盐酸盐(2X3)和脂质辅助剂二油酰磷脂酰乙醇胺(DOPE)组成,并配备了分子量和结构不同的聚乙二醇脂质缀合物。这项工作的主要发现如下:(i)在含有长PEG链脂质缀合物的脂质体与isRNA形成的复合物作用下,CBA小鼠体内MCP-1以及INF-α、β和γ的产生显著激活,而在含有短PEG链脂质缀合物的isRNA脂质复合物作用下,观察到MCP-1和INF-γ的激活,但未观察到INF-α或β的激活;(ii)非聚乙二醇化脂质体与isRNA的预复合物在体外对B16黑色素瘤细胞具有显著的抗增殖作用,在体内具有抗肿瘤和肝保护作用,而含有长链脂质体脂质缀合物的复合物则无活性;(iii)isRNA的抗肿瘤活性与其在细胞中的积累效率相关,且并未明确依赖于细胞因子和干扰素产生的激活。因此,递送系统的结构在决定对isRNA的反应中起着至关重要的作用,并允许根据所需效果选择递送系统。