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抗 CEA 嵌合抗原受体 T 细胞与抗 CEA-IL2 免疫细胞因子联合治疗的肿瘤消退和免疫。

Tumor regression and immunity in combination therapy with anti-CEA chimeric antigen receptor T cells and anti-CEA-IL2 immunocytokine.

机构信息

Department of Immunology and Theranostics, City of Hope, Duarte, USA.

Irell & Manella Graduate School of Biological Sciences, City of Hope, Duarte, USA.

出版信息

Oncoimmunology. 2021 Mar 18;10(1):1899469. doi: 10.1080/2162402X.2021.1899469.

Abstract

Targeted immunotherapy of solid cancers with chimeric antigen receptor (CAR) T cells and immunocytokines are attractive options in that they both rely on the specificity of tumor-targeted antibodies. Since carcinoembryonic antigen (CEA) expression in both colon and breast cancers is correlated with poor prognosis, it was chosen as a model tumor target in immunocompetent CEA transgenic (CEATg) mice. A second-generation anti-CEA CAR derived from CEA-specific antibody T84.66 was used to treat murine MC38 colon or E0771 breast carcinomas transfected with CEA. Anti-CEA CAR vs. mock transduced T cells exhibited a CEA-specific cytotoxic and IFN dose response to both CEA transfected cell lines vs. their CEA-negative controls. Anti-CEA CAR vs. mock transduced T cells delayed the median survival of CEA transfected s.c. MC38 or orthotopic E0771 tumor-bearing CEATg mice by 2 days. With the addition of one-day prior cyclophosphamide (CY) lymphodepletion, anti-CEA CAR T cell treatment delayed the median survival of MC38/CEA and E0771/CEA tumor-bearing CEATg mice by ten and 3 days, respectively. Since CAR T cells require IL2 for survival and expansion, anti-CEA-IL2 immunocytokine (ICK) treatment was performed post CAR T cell therapy. Single ICK treatment 1 day after CY plus anti-CEA CAR T cell therapy in the MC38/CEA model, and two ICK treatments every 3 days after CY plus anti-CEA CAR T cell therapy in the E0771/CEA model were ineffective, while four ICK treatments every 3 days after CY plus anti-CEA CAR T cell therapy completely eradicated MC38/CEA tumor growth and induced tumor immunity when the mice were re-challenged with tumor. These studies show the therapeutic potential of anti-CEA CAR T cells combined with ICK to treat CEA-positive tumors. CAR: Chimeric antigen receptor, CEA: Carcinoembryonic antigen, CEACAM5, ICK: Immunocytokine, CY: Cyclophosphamide, CEATg mouse: transgenic CEA mouse, TDLN: Tumor-draining lymph node.

摘要

用嵌合抗原受体 (CAR) T 细胞和免疫细胞因子对实体瘤进行靶向免疫治疗是一种很有吸引力的选择,因为它们都依赖于肿瘤靶向抗体的特异性。由于癌胚抗原 (CEA) 在结肠癌和乳腺癌中的表达与预后不良相关,因此它被选为免疫功能正常的 CEA 转基因 (CEATg) 小鼠中的模型肿瘤靶标。一种源自 CEA 特异性抗体 T84.66 的第二代抗 CEA CAR 被用于治疗转染 CEA 的小鼠 MC38 结肠或 E0771 乳腺癌。与 mock 转导 T 细胞相比,抗 CEA CAR 对两种转染 CEA 的细胞系及其 CEA 阴性对照均表现出 CEA 特异性细胞毒性和 IFN-γ 剂量反应。与 mock 转导 T 细胞相比,抗 CEA CAR 延迟了皮下 MC38/CEA 和原位 E0771/CEA 肿瘤携带 CEATg 小鼠的中位生存期 2 天。用环磷酰胺 (CY) 一天前进行淋巴细胞耗竭 (TDLN),抗 CEA CAR T 细胞治疗将 MC38/CEA 和 E0771/CEA 肿瘤携带 CEATg 小鼠的中位生存期分别延长了 10 天和 3 天。由于 CAR T 细胞的存活和扩增需要 IL2,因此在 CAR T 细胞治疗后进行了抗 CEA-IL2 免疫细胞因子 (ICK) 治疗。在 MC38/CEA 模型中,在 CY 加抗 CEA CAR T 细胞治疗后 1 天进行单次 ICK 治疗,在 E0771/CEA 模型中,在 CY 加抗 CEA CAR T 细胞治疗后每 3 天进行两次 ICK 治疗均无效,而在 CY 加抗 CEA CAR T 细胞治疗后每 3 天进行四次 ICK 治疗则完全消除了 MC38/CEA 肿瘤的生长,并在小鼠重新接受肿瘤挑战时诱导了肿瘤免疫。这些研究表明,抗 CEA CAR T 细胞联合 ICK 治疗 CEA 阳性肿瘤具有治疗潜力。CAR:嵌合抗原受体,CEA:癌胚抗原,CEACAM5,ICK:免疫细胞因子,CY:环磷酰胺,CEATg 小鼠:转 CEA 基因小鼠,TDLN:肿瘤引流淋巴结。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f9f/7993151/83298b6841bf/KONI_A_1899469_F0001_OC.jpg

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