用nfat诱导的膜系留IL-15/IL-21工程化的gpc2靶向CAR - T细胞对神经母细胞瘤表现出增强的活性。

IF 8.2 1区 医学 Q1 IMMUNOLOGY
Reona Okada, Jeyshka M Reyes-González, Constanza Rodriguez, Taisuke Kondo, Jangsuk Oh, Ming Sun, Michael C Kelly, Ling Zhang, James Gulley, Jack F Shern, Mitchell Ho, Christian S Hinrichs, Naomi N Taylor, Xiyuan Zhang, Rosa Nguyen
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引用次数: 0

摘要

神经母细胞瘤(NB)是一种高度侵袭性的儿童实体肿瘤,预后较差。嵌合抗原受体(CAR) T细胞在NB中显示出有限的疗效,在低肿瘤负荷患者中报道的最佳结果,突出了进一步CAR优化的必要性。解决高肿瘤负荷的一种方法是工程CAR - T细胞释放或表达转基因细胞因子。然而,它的全身毒性仍然是一个重要的治疗挑战。在这里,我们评估了白细胞介素(IL)-15-和IL-21增强的glypican-2 (GPC2)靶向CAR - T细胞(GPC2-CAR - T细胞)靶向高负荷NB的疗效。评估了三种表达细胞因子的策略:组成性分泌(GPC2-CAR+sol.IL15.IL21)、组成性膜系表达(GPC2-CAR+ th. il15 . il21)和nfat诱导的膜系表达(GPC2-CAR+NFAT.IL15.IL21)。利用高nb负荷异种移植模型对工程GPC2-CAR - T细胞进行了体外和体内测试。此外,单细胞RNA测序用于分析肿瘤微环境中的效应细胞。与对照GPC2-CAR - T细胞相比,所有三种版本的GPC2-CAR - T细胞在体外和体内均显著增强了对高NB负荷的杀伤能力。GPC2-CAR+NFAT.IL15治疗小鼠。il - 21表现出明显较低的厌食症相关发病率/死亡率。肿瘤浸润性GPC2-CAR+NFAT.IL15支持这些数据。il - 21在肿瘤消退时产生免疫抑制转录谱,导致治疗小鼠的存活时间延长。相比之下,GPC2-CAR+teth.IL15。尽管接近肿瘤清除,il - 21仍保持促炎转录特征,导致高细胞分裂血症和死亡。nfat诱导的系留IL-15/IL-21的共表达增强了GPC2-CAR - t细胞对小鼠高NB负荷的功能,并具有可接受的耐受性。需要进一步的研究来验证这些发现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
GPC2-Targeted CAR T Cells Engineered with NFAT-Inducible Membrane-Tethered IL15/IL21 Exhibit Enhanced Activity against Neuroblastoma.

Neuroblastoma is a highly aggressive childhood solid tumor with poor outcomes. Chimeric antigen receptor (CAR) T cells have shown limited efficacy in neuroblastoma, with the best outcomes reported in patients with a low tumor burden, highlighting the need for further CAR optimization. One approach to addressing the high tumor burden involves engineering CAR T cells to release or express transgenic cytokines. However, its systemic toxicity remains an important therapeutic challenge. In this study, we evaluated the efficacy of IL15- and IL21-enhanced glypican 2 (GPC2)-targeted CAR T cells (GPC2-CAR T cells) in targeting high-burden neuroblastoma. Three strategies for expressing the cytokines were evaluated: constitutive secretion (GPC2-CAR + sol.IL15.IL21), constitutive membrane-tethered expression (GPC2-CAR + teth.IL15.IL21), and NFAT-inducible membrane-tethered expression (GPC2-CAR + NFAT.IL15.IL21). Engineered GPC2-CAR T cells were tested in vitro and in vivo using high neuroblastoma burden xenograft models. Additionally, single-cell RNA sequencing was used to profile the effector cells in the tumor microenvironment. All three versions of GPC2-CAR T cells significantly enhanced killing against a high neuroblastoma burden, both in vitro and in vivo, relative to control GPC2-CAR T cells. Mice treated with GPC2-CAR + NFAT.IL15.IL21 exhibited significantly lower anorexia-associated morbidity/mortality. Supporting these data, tumor-infiltrating GPC2-CAR + NFAT.IL15.IL21 developed an immunosuppressive transcriptional profile upon tumor regression, leading to prolonged survival in treated mice. In contrast, GPC2-CAR + teth.IL15.IL21 maintained a proinflammatory transcriptional signature despite near tumor clearance, resulting in hypercytokinemia and death. NFAT-inducible co-expression of tethered IL15/IL21 enhanced GPC2-CAR T-cell function against a high neuroblastoma burden with acceptable tolerability in mice. Further studies are required to validate these findings.

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来源期刊
Cancer immunology research
Cancer immunology research ONCOLOGY-IMMUNOLOGY
CiteScore
15.60
自引率
1.00%
发文量
260
期刊介绍: Cancer Immunology Research publishes exceptional original articles showcasing significant breakthroughs across the spectrum of cancer immunology. From fundamental inquiries into host-tumor interactions to developmental therapeutics, early translational studies, and comprehensive analyses of late-stage clinical trials, the journal provides a comprehensive view of the discipline. In addition to original research, the journal features reviews and opinion pieces of broad significance, fostering cross-disciplinary collaboration within the cancer research community. Serving as a premier resource for immunology knowledge in cancer research, the journal drives deeper insights into the host-tumor relationship, potent cancer treatments, and enhanced clinical outcomes. Key areas of interest include endogenous antitumor immunity, tumor-promoting inflammation, cancer antigens, vaccines, antibodies, cellular therapy, cytokines, immune regulation, immune suppression, immunomodulatory effects of cancer treatment, emerging technologies, and insightful clinical investigations with immunological implications.
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