γδ T cells as a potential therapeutic agent for glioblastoma

被引:8
|
作者
Kang, In [1 ]
Kim, Yumin [2 ]
Lee, Heung Kyu [1 ,2 ]
机构
[1] Korea Adv Inst Sci & Technol KAIST, Grad Sch Med Sci & Engn, Daejeon, South Korea
[2] Korea Adv Inst Sci & Technol, Dept Biol Sci, Daejeon, South Korea
来源
FRONTIERS IN IMMUNOLOGY | 2023年 / 14卷
基金
新加坡国家研究基金会;
关键词
glioblastoma; tumor microenvironment; gamma delta T cells; immunotherapy; engineering; CENTRAL-NERVOUS-SYSTEM; TUMOR-TREATING FIELDS; ADJUVANT TEMOZOLOMIDE; IMMUNE CELLS; BRAIN; RADIATION; RESPONSES; ACTIVATION; RESISTANCE; EXPRESSION;
D O I
10.3389/fimmu.2023.1273986
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Although gamma delta T cells comprise a small population of T cells, they perform important roles in protecting against infection and suppressing tumors. With their distinct tissue-localizing properties, combined with their various target recognition mechanisms, gamma delta T cells have the potential to become an effective solution for tumors that do not respond to current therapeutic procedures. One such tumor, glioblastoma (GBM), is a malignant brain tumor with the highest World Health Organization grade and therefore the worst prognosis. The immune-suppressive tumor microenvironment (TME) and immune-evasive glioma stem cells are major factors in GBM immunotherapy failure. Currently, encouraged by the strong anti-tumoral function of gamma delta T cells revealed at the preclinical and clinical levels, several research groups have shown progression of gamma delta T cell-based GBM treatment. However, several limitations still exist that block effective GBM treatment using gamma delta T cells. Therefore, understanding the distinct roles of gamma delta T cells in anti-tumor immune responses and the suppression mechanism of the GBM TME are critical for successful gamma delta T cell-mediated GBM therapy. In this review, we summarize the effector functions of gamma delta T cells in tumor immunity and discuss current advances and limitations of gamma delta T cell-based GBM immunotherapy. Additionally, we suggest future directions to overcome the limitations of gamma delta T cell-based GBM immunotherapy to achieve successful treatment of GBM.
引用
收藏
页数:14
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