[1]李 瑞 综述 艾文兵 校审.NKT细胞在胶质瘤免疫治疗中的研究进展[J].中国临床神经外科杂志,2020,(11):805-807.[doi:doi:10.13798/j.issn.1009-153X.2020.11.027]
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NKT细胞在胶质瘤免疫治疗中的研究进展()
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《中国临床神经外科杂志》[ISSN:1009-153X/CN:42-1603/TN]

卷:
期数:
2020年11期
页码:
805-807
栏目:
综述
出版日期:
2020-11-25

文章信息/Info

文章编号:
1009-153X(2020)11-0805-03
作者:
李 瑞 综述 艾文兵 校审
443100 湖北宜昌,三峡大学医学院(李 瑞);443100 湖北,宜昌市夷陵医院神经外科(艾文兵)
关键词:
脑胶质瘤细胞免疫治疗NKT细胞肿瘤免疫
分类号:
R 739.41; R 730.51
DOI:
doi:10.13798/j.issn.1009-153X.2020.11.027
文献标志码:
A

参考文献/References:

[1] Cui Y, Wan Q. NKT cells in neurological diseases [J]. Front Cell Neurosci, 2019, 13: 245-251.
[2] Gerth E, Mattner J. The role of adaptor proteins in the biolo-gy of natural killer T (NKT) cells [J]. Front Immunol, 2019,10: 1449-1453.
[3] Cerundolo V, Barral P, Batista FD. Synthetic iNKT cell-agonists as vaccine adjuvants--finding the balance [J]. Curr Opin Immunol, 2010, 22(3): 417-424.
[4] McEwen-Smith RM, Salio M, Cerundolo V. The regulatory role of invariant NKT cells in tumor immunity [J]. Cancer Immunol Res, 2015, 3(5): 425-435.
[5] Dempsey LA. NKT cells aid antiviral responses [J]. NatImmunol, 2018, 19(2): 99-103.
[6] 赵炜熠,初 明. 胶质瘤免疫抑制与治疗的研究进展[J]. 中国临床神经外科杂志,2018,23(3):212-214.
[7] Dashtsoodol N, Shigeura T, Tashiro T, et al. Natural killer T cell-targeted immunotherapy mediating long-term memory responses and strong antitumor activity [J]. Front Immunol,2017, 8: 1206-1211.
[8] Nair S, Dhodapkar MV. Natural killer T cells in cancer im-munotherapy [J]. Front Immunol, 2017, 8: 1178-1181.
[9] Lindau D, Gielen P, Kroesen M, et al. The immunosuppres-sive tumour network: myeloid-derived suppressor cells, regulatory T cells and natural killer T cells [J]. Immunology,2013, 138(2): 105-115.
[10] Marcus A, Gowen BG, Thompson TW, et al. Recognition of tumors by the innate immune system and natural killer cells[J]. Adv Immunol, 2014, 122: 91-128.
[11] Mackay A, Burford A, Molinari V, et al. Molecular, patholo-gical, radiological, and immune profiling of non-brainstem pediatric high-grade glioma from the HERBY phase Ⅱrandomized trial [J]. Cancer Cell, 2018, 33(5): 829-842.
[12] Wolf BJ, Choi JE, Exley MA. Novel approaches to exploiting invariant NKT cells in cancer immunotherapy [J]. Front Immunol, 2018, 9: 384-389.
[13] Liu D, Song L, Brawley VS, et al. Medulloblastomaexpresses CD1d and can be targeted for immunotherapy with NKT cells [J]. Clin Immunol, 2013, 149(1): 55-64.
[14] Chong TW, Goh FY, Sim MY, et al. CD1d expression inrenal cell carcinoma is associated with higher relapse rates, poorer cancer-specific and overall survival [J]. J Clin Pathol, 2015, 68(3): 200-205.
[15] Borg NA, Wun KS, Kjer-Nielsen L, et al. CD1d-lipid-antigen recognition by the semi-invariant NKT T-cell receptor [J]. Nature, 2007, 448(7149): 44-49.
[16] Gebremeskel S, Clattenburg DR, Slauenwhite D, et al. Natu-ral killer T cell activation overcomes immunosuppression to enhance clearance of postsurgical breast cancer metastasis in mice [J]. Onco Immunol, 2015, 4(3): e55-62.
[17] Marsh JC, Goldfarb J, Shafman TD, et al. Current status of immunotherapy and gene therapy for high-grade gliomas [J]. Cancer Control, 2013, 20(1): 43-48.
[18] Ghinnagow R, De Meester J, Cruz LJ, et al. Co-delivery of the NKT agonist alpha-galactosylceramide and tumor anti-gens to cross-priming dendritic cells breaks tolerance to self-antigens and promotes antitumor responses [J]. OncoImmunol, 2017, 6(9): 33-38.
[19] Hunn MK, Hermans IF. Exploiting invariant NKT cells to promote T-cell responses to cancer vaccines [J]. OncoImmunol, 2013, 2(4): 78-89.
[20] Tang B, Wu W, Wei X, et al. Activation of glioma cellsgenerates immune tolerant NKT cells [J]. J Biol Chem, 2014, 289(50): 34595-34600.

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备注/Memo

备注/Memo:
基金项目:湖北省卫生计生西医类重点资助项目(WJ2015MA023)通讯作者:艾文兵,E-mail:1043642574@qq.com
更新日期/Last Update: 2020-11-25