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Application and prospect of chimeric antigen receptor-modified T cell therapy for glioblastoma
Online published: 2021-08-03
Supported by
The 13th Innovation Project of Shanghai Jiao Tong University School of Medicine(1319003)
Glioblastoma is one of the most common and deadly neoplasms in adults. The rapid progress and strong invasiveness of glioblastoma and the presence of the blood-brain barrier make the treatment of glioblastoma different from other solid tumors and these are the reasons for the poor prognosis of conventional treatment. The exploration of immunotherapy in the treatment of glioblastoma has lasted for decades, but the outcome is not good yet. However, with the research progress of glioblastoma-specific antigen, the development of various related technologies and the success of early clinical trials, it has come back to people's attention. Chimeric antigen receptor-modified T cell(CAR-T) is a new kind of tumor immunotherapy. Reviewing the previous literatures, this article summarizes some related antigens that can be used to CAR-T therapy to treat glioblastoma, the problems and challenges faced by CAR-T therapy in the treatment of glioblastoma and other solid tumors, including T cell depletion in tumor microenvironment, heterogeneity of tumor and low homing rate, and some potential improvements in CAR-T therapy.
Paerhati NADINA , Yan YAN , Qian-ji CHE , Jing LUO , Xin-nan LIU , Bin LI . Application and prospect of chimeric antigen receptor-modified T cell therapy for glioblastoma[J]. Journal of Shanghai Jiao Tong University (Medical Science), 2021 , 41(7) : 982 -986 . DOI: 10.3969/j.issn.1674-8115.2021.07.023
1 | Wirsching HG, Galanis E, Weller M. Glioblastoma[J]. Handb Clin Neurol, 2016, 134: 381. |
2 | Stepanenko AA, Chekhonin VP. Recent advances in oncolytic virotherapy and immunotherapy for glioblastoma: a glimmer of hope in the search for an effective therapy?[J]. Cancers (Basel), 2018, 10(12): E492. |
3 | Xie ZQ, Janczyk P?, Zhang Y, et al. A cytoskeleton regulator AVIL drives tumorigenesis in glioblastoma[J]. Nat Commun, 2020, 11(1): 3457. |
4 | Wang DR, Starr R, Chang WC, et al. Chlorotoxin-directed CAR T cells for specific and effective targeting of glioblastoma[J]. Sci Transl Med, 2020, 12(533): eaaw2672. |
5 | Felsberg J, Hentschel B, Kaulich K, et al. Epidermal growth factor receptor variant Ⅲ (EGFRvⅢ) positivity in EGFR-amplified glioblastomas: prognostic role and comparison between primary and recurrent tumors[J]. Clin Cancer Res, 2017, 23(22): 6846-6855. |
6 | Bielamowicz K, Fousek K, Byrd TT, et al. Trivalent CAR T cells overcome interpatient antigenic variability in glioblastoma[J]. Neuro Oncol, 2018, 20(4): 506-518. |
7 | Eskilsson E, R?sland GV, Solecki G, et al. EGFR heterogeneity and implications for therapeutic intervention in glioblastoma[J]. Neuro Oncol, 2018, 20(6): 743-752. |
8 | Milner JJ, Toma C, Yu BF, et al. Runx3 programs CD8+ T cell residency in non-lymphoid tissues and tumours[J]. Nature, 2017, 552(7684): 253-257. |
9 | Caruana I, Savoldo B, Hoyos V, et al. Heparanase promotes tumor infiltration and antitumor activity of CAR-redirected T lymphocytes[J]. Nat Med, 2015, 21(5): 524-529. |
10 | Hao CH, Parney IF, Roa WH, et al. Cytokine and cytokine receptor mRNA expression in human glioblastomas: evidence of Th1, Th2 and Th3 cytokine dysregulation[J]. Acta Neuropathol, 2002, 103(2): 171-178. |
11 | Martinez M, Moon EK. CAR T cells for solid tumors: new strategies for finding, infiltrating, and surviving in the tumor microenvironment[J]. Front Immunol, 2019, 10: 128. |
12 | Jacobs JF, Idema AJ, Bol KF, et al. Regulatory T cells and the PD-L1/PD-1 pathway mediate immune suppression in malignant human brain tumors[J]. Neuro Oncol, 2009, 11(4): 394-402. |
13 | Mirzaei R, Sarkar S, Yong VW. T cell exhaustion in glioblastoma: intricacies of immune checkpoints[J]. Trends Immunol, 2017, 38(2): 104-115. |
14 | Zhu CB, Mustafa D, Zheng PP, et al. Activation of CECR1 in M2-like TAMs promotes paracrine stimulation-mediated glial tumor progression[J]. Neuro Oncol, 2017, 19(5): 648-659. |
15 | Shi Y, Ping YF, Zhou WC, et al. Tumour-associated macrophages secrete pleiotrophin to promote PTPRZ1 signalling in glioblastoma stem cells for tumour growth[J]. Nat Commun, 2017, 8: 15080. |
16 | Fitzgerald JC, Weiss SL, Maude SL, et al. Cytokine release syndrome after chimeric antigen receptor T cell therapy for acute lymphoblastic leukemia[J]. Crit Care Med, 2017, 45(2): e124-e131. |
17 | Teachey DT, Lacey SF, Shaw PA, et al. Identification of predictive biomarkers for cytokine release syndrome after chimeric antigen receptor T-cell therapy for acute lymphoblastic leukemia[J]. Cancer Discov, 2016, 6(6): 664-679. |
18 | O′Rourke DM, Nasrallah MP, Desai A, et al. A single dose of peripherally infused EGFRvⅢ-directed CAR T cells mediates antigen loss and induces adaptive resistance in patients with recurrent glioblastoma[J]. Sci Transl Med, 2017, 9(399): eaaa0984. |
19 | Howard SC, Trifilio S, Gregory TK, et al. Tumor lysis syndrome in the era of novel and targeted agents in patients with hematologic malignancies: a systematic review[J]. Ann Hematol, 2016, 95(4): 563-573. |
20 | Maude SL, Frey N, Shaw PA, et al. Chimeric antigen receptor T cells for sustained remissions in leukemia[J]. N Engl J Med, 2014, 371(16): 1507-1517. |
21 | Hay KA. Cytokine release syndrome and neurotoxicity after CD19 chimeric antigen receptor-modified (CAR-) T cell therapy[J]. Br J Haematol, 2018, 183(3): 364-374. |
22 | Hamieh M, Dobrin A, Cabriolu A, et al. CAR T cell trogocytosis and cooperative killing regulate tumour antigen escape[J]. Nature, 2019, 568(7750): 112-116. |
23 | Chen J, López-Moyado IF, Seo H, et al. NR4A transcription factors limit CAR T cell function in solid tumours[J]. Nature, 2019, 567(7749): 530-534. |
24 | Santoro SP, Kim S, Motz GT, et al. T cells bearing a chimeric antigen receptor against prostate-specific membrane antigen mediate vascular disruption and result in tumor regression[J]. Cancer Immunol Res, 2015, 3(1): 68-84. |
25 | Deng CW, Zhao JJ, Zhou SX, et al. The vascular disrupting agent CA4P improves the antitumor efficacy of CAR-T cells in preclinical models of solid human tumors[J]. Mol Ther, 2020, 28(1): 75-88. |
26 | Schmidts A, Maus MV. Making CAR T cells a solid option for solid tumors[J]. Front Immunol, 2018, 9: 2593. |
27 | Hegde M, Mukherjee M, Grada Z, et al. Tandem CAR T cells targeting HER2 and IL13Rα2 mitigate tumor antigen escape[J]. J Clin Invest, 2019, 129(8): 3464. |
28 | Borriello L, Nakata R, Sheard MA, et al. Cancer-associated fibroblasts share characteristics and protumorigenic activity with mesenchymal stromal cells[J]. Cancer Res, 2017, 77(18): 5142-5157. |
29 | Kloss CC, Lee J, Zhang A, et al. Dominant-negative TGF?β receptor enhances PSMA-targeted human CAR T cell proliferation and augments prostate cancer eradication[J]. Mol Ther, 2018, 26(7): 1855-1866. |
30 | Liu XJ, Ranganathan R, Jiang SG, et al. A chimeric switch-receptor targeting PD1 augments the efficacy of second-generation CAR T cells in advanced solid tumors[J]. Cancer Res, 2016, 76(6): 1578-1590. |
31 | Li YX, Xiao FJ, Zhang AM, et al. Oncolytic adenovirus targeting TGF?β enhances anti-tumor responses of mesothelin-targeted chimeric antigen receptor T cell therapy against breast cancer[J]. Cell Immunol, 2020, 348: 104041. |
32 | Jin L, Tao H, Karachi A, et al. CXCR1- or CXCR2-modified CAR T cells co-opt IL-8 for maximal antitumor efficacy in solid tumors[J]. Nat Commun, 2019, 10(1): 4016. |
33 | Craddock JA, Lu A, Bear A, et al. Enhanced tumor trafficking of GD2 chimeric antigen receptor T cells by expression of the chemokine receptor CCR2b[J]. J Immunother, 2010, 33(8): 780-788. |
34 | Giordano-Attianese G, Gainza P, Gray-Gaillard E, et al. A computationally designed chimeric antigen receptor provides a small-molecule safety switch for T-cell therapy[J]. Nat Biotechnol, 2020, 38(4): 426-432. |
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