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Cytokine-induced Killer Cells/natural Killer Cells Combined with Anti-GD2 Monoclonal Antibody Increase Cell Death Rate in Neuroblastoma SK-N-SH Cells

Overview
Journal Oncol Lett
Specialty Oncology
Date 2019 Dec 7
PMID 31807172
Citations 4
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Abstract

Neuroblastoma (NB) is one of the most common extracranial, solid, pediatric malignancies. Despite improvements in conventional therapies, including surgery, chemotherapy and radiation therapy, the prognosis of stage IV NB remains poor, indicating that novel treatment strategies are required. Immunotherapies, such as anti-GD2 monoclonal antibodies, used alone or in combination with cytokines, and peripheral blood mononuclear cells or cord blood mononuclear cells (CBMNCs), have been indicated to cause NB cell death and to prolong patient survival in high-risk NB; however, they remain limited by severe cytotoxicity and side effects. In the present study, it was determined that anti-GD2 monoclonal antibody alone or CBMNC-isolated cytokine-induced killer (CIK)/natural killer (NK) cells alone significantly induced cell death of NB SK-N-SH cells, and the combination of anti-GD2 antibody and CIK/NK cells could significantly increase the cell death rate compared with either treatment alone. In addition, based on a method referred to our previous study, it was identified that a two-cytokine culture system, using interleukin IL-2 and IL-7, effectively stimulated the proliferation of CIK/NK cells. These results serve to suggest a novel treatment strategy for relapsed/refractory NB with high efficiency and few side effects.

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References
1.
Ladenstein R, Potschger U, Valteau-Couanet D, Luksch R, Castel V, Yaniv I . Interleukin 2 with anti-GD2 antibody ch14.18/CHO (dinutuximab beta) in patients with high-risk neuroblastoma (HR-NBL1/SIOPEN): a multicentre, randomised, phase 3 trial. Lancet Oncol. 2018; 19(12):1617-1629. DOI: 10.1016/S1470-2045(18)30578-3. View

2.
Tran H, Wan Z, Sheard M, Sun J, Jackson J, Malvar J . TGFβR1 Blockade with Galunisertib (LY2157299) Enhances Anti-Neuroblastoma Activity of the Anti-GD2 Antibody Dinutuximab (ch14.18) with Natural Killer Cells. Clin Cancer Res. 2016; 23(3):804-813. PMC: 5361893. DOI: 10.1158/1078-0432.CCR-16-1743. View

3.
Cheung I, Kushner B, Modak S, Basu E, Roberts S, Cheung N . Phase I trial of anti-GD2 monoclonal antibody hu3F8 plus GM-CSF: Impact of body weight, immunogenicity and anti-GD2 response on pharmacokinetics and survival. Oncoimmunology. 2017; 6(11):e1358331. PMC: 5674972. DOI: 10.1080/2162402X.2017.1358331. View

4.
Gao D, Cai Y, Chen Y, Li W, Wei C, Luo X . Novel TLR7 agonist stimulates activity of CIK/NK immunological effector cells to enhance antitumor cytotoxicity. Oncol Lett. 2018; 15(4):5105-5110. PMC: 5840738. DOI: 10.3892/ol.2018.7954. View

5.
Burga R, Yvon E, Chorvinsky E, Fernandes R, Cruz C, Bollard C . Engineering the TGFβ Receptor to Enhance the Therapeutic Potential of Natural Killer Cells as an Immunotherapy for Neuroblastoma. Clin Cancer Res. 2019; 25(14):4400-4412. PMC: 6635028. DOI: 10.1158/1078-0432.CCR-18-3183. View