共 50 条
Immunology Meets Bioengineering: Improving the Effectiveness of Glioblastoma Immunotherapy
被引:8
|作者:
Fekrirad, Zahra
[1
]
Barzegar Behrooz, Amir
[2
]
Ghaemi, Shokoofeh
[3
]
Khosrojerdi, Arezou
[4
,5
]
Zarepour, Atefeh
[6
]
Zarrabi, Ali
[6
]
Arefian, Ehsan
[3
,7
]
Ghavami, Saeid
[8
,9
,10
,11
]
机构:
[1] Shahed Univ, Fac Basic Sci, Dept Biol, Tehran 18735136, Iran
[2] Asu Vanda Gene Ind Res Co, Dept Canc, Brain Canc Res Grp, Tehran 1533666398, Iran
[3] Univ Tehran, Sch Biol, Dept Microbiol, Coll Sci, Tehran 141556619, Iran
[4] Birjand Univ Med Sci, Cellular & Mol Res Ctr, Birjand 9717853577, Iran
[5] Tarbiat Modares Univ, Dept Immunol, Fac Med Sci, Tehran 14115111, Iran
[6] Istinye Univ, Fac Engn & Nat Sci, Dept Biomed Engn, TR-34396 Istanbul, Turkey
[7] Univ Tehran Med Sci, Gene Cell & Tissue Res Inst, Pediat Cell & Gene Therapy Res Ctr, Tehran 141556559, Iran
[8] Univ Technol Katowice, Fac Med Zabrze, Acad Silesia, PL-41800 Zabrze, Poland
[9] Res Inst Oncol & Hematol, Canc Care Manitoba Univ Manitoba, Winnipeg, MB R3E 3P5, Canada
[10] Univ Manitoba, Children Hosp Res Inst Manitoba, Biol Breathing Theme, Winnipeg, MB R3E 3P5, Canada
[11] Univ Manitoba, Dept Human Anat & Cell Sci, Coll Med, Winnipeg, MB R3E 3P5, Canada
来源:
关键词:
glioblastoma;
immunotherapy;
oncolytic virotherapy;
nanomedicine;
nanoparticles;
autophagy;
REGULATORY T-CELLS;
GROWTH-FACTOR RECEPTOR;
VESICULAR STOMATITIS-VIRUS;
NEWCASTLE-DISEASE VIRUS;
DRUG-DELIVERY SYSTEM;
SENECA VALLEY VIRUS;
ONCOLYTIC ADENOVIRUS;
TARGETED DELIVERY;
MACROPHAGE POLARIZATION;
POLYMERIC NANOPARTICLES;
D O I:
10.3390/cancers14153698
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
Simple Summary Glioblastoma (GBM) is the main malignant brain tumor in adults. It has a poor survival rate and a short disease-free life in spite of all available treatments. The science of cancer immunotherapy is constantly adapting to address the particular needs and problems of a wide range of cancers, including GBM. As of yet, most immunotherapeutic approaches have been unsuccessful, and conventional treatments have been of little effect. Genetically engineered oncolytic viruses (OV) with immunomodulatory transgene expression are now a research focus in the treatment of GBM. There are various challenges that must be addressed in order for immunotherapies to be effective, including physical limitations to medication delivery (e.g., BBB). The present research suggests that nanomedicine and immunotherapy may be a step toward personalized medicine for GBM. Glioblastoma (GBM) therapy has seen little change over the past two decades. Surgical excision followed by radiation and chemotherapy is the current gold standard treatment. Immunotherapy techniques have recently transformed many cancer treatments, and GBM is now at the forefront of immunotherapy research. GBM immunotherapy prospects are reviewed here, with an emphasis on immune checkpoint inhibitors and oncolytic viruses. Various forms of nanomaterials to enhance immunotherapy effectiveness are also discussed. For GBM treatment and immunotherapy, we outline the specific properties of nanomaterials. In addition, we provide a short overview of several 3D (bio)printing techniques and their applications in stimulating the GBM microenvironment. Lastly, the susceptibility of GBM cancer cells to the various immunotherapy methods will be addressed.
引用
收藏
页数:40
相关论文