Interleukin gene delivery for cancer gene therapy: In vitro and in vivo studies

被引:1
|
作者
Azimifar, Mohammad Amin [1 ]
Hashemi, Maryam [2 ,3 ]
Babaei, Nahid [1 ]
Salmasi, Zahra [2 ]
Doosti, Abbas [4 ]
机构
[1] Islamic Azad Univ, Dept Cell Mol Biol, Bushehr Branch, Bushehr, Iran
[2] Mashhad Univ Med Sci, Pharmaceut Technol Inst, Nanotechnol Res Ctr, Mashhad, Iran
[3] Mashhad Univ Med Sci, Sch Pharm, Dept Pharmaceut Biotechnol, Mashhad, Iran
[4] Islamic Azad Univ, Biotechnol Res Ctr, Shahrekord Branch, Shahrekord, Iran
关键词
Cancer; Gene delivery vector; Immunotherapy; Interleukin; Mesenchymal stem cells; MESENCHYMAL STEM-CELLS; MARROW STROMAL CELLS; CYTOKINE; TUMOR; GLIOMA; IMMUNOTHERAPY; VEHICLES; IMMUNITY; GROWTH; IL-21;
D O I
10.22038/IJBMS.2022.66890.14668
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Cytokine-mediated cancer therapy has the potential to enhance immunotherapeutic approaches and cancer elimination plans through the endowing of the immune system by providing improved anticancer immunity. Despite the encouraging pioneer studies on interleukins (ILs), the influence of ILs-originated therapeutics is still restricted by a class of potent immunoregulatory cytokines, systemic dose-limiting toxicities, ILs pleiotropy, and administration issues. During previous years, the area of transferring genes encoding immunostimulatory ILs was fundamentally widened to overcome these challenges and expedite ILs-based tumor regression. Numerous viral and non-viral delivery systems are currently available to act as crucial elements of the gene therapy toolbox. Moreover, cell -based cancer therapies are recruiting MSCs in the role of versatile gene delivery platforms to design one of the promising therapeutic approaches. These formulated gene carrier systems can provide possible alternatives to diminish dose-limiting adverse effects, promote administration, and enhance the therapeutic activity of ILs-derived treatment modalities in cancer treatment. This review provides a discussion on the advances of ILs gene delivery systems while focusing on the developing platforms in preclinical cancer immunogene therapy studies.
引用
收藏
页码:128 / 138
页数:11
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