Hefei National Laboratory for Physical Sciences at Microscale, The CAS Key Laboratory of Innate Immunity and Chronic Disease, School of Basic Medical Sciences, Division of Life Sciences and Medicine, Institute of Immunology, University of Science and Technology of China, Hefei 230027, China.
Research Unit of NK Cell Study, Chinese Academy of Medical Sciences, Beijing 100864, China.
Cancer Biol Med. 2020 Nov 15;17(4):1026-1038. doi: 10.20892/j.issn.2095-3941.2020.0399. Epub 2020 Dec 15.
Natural killer (NK) cells have gained considerable attention due to their potential in treating "cold tumors," and are therefore considered as one of the new strategies for curing cancer, by using worldwide development of their new possibilities and interventions with NK cell-related therapeutic products.
We constructed a trispecific killer engager (TriKE) consisting of anti-CD16, IL-15, and anti-CD19. This TriKE was designed to attract CD19 tumor cells to CD16 NK cells, whereas IL-15 sustained the proliferation, development, and survival of NK cells.
Treatment with 161519 TriKE in the presence of CD19 targets upregulated expression of CD69, CD107a, TRAIL, IFN-γ, and TNF-α in NK cells, and significantly improved the proliferation and cytotoxicity of NK cells. NK cells "armed" with 161519 TriKE showed stronger cytolysis against CD19 targets compared with that of "unarmed" NK cells. A preclinical model of B-cell lymphoma in human peripheral blood mononuclear cell-reconstituted xenograft mice showed significant inhibition of tumor growth and prolonged overall survival after treatment with 161519 TriKE, when compared with that in control mice or mice treated with 1619 BiKE. Combined use of IL-2 was a more effective treatment with 1619 BiKE, when compared with that using 161519 TriKE.
The newly generated 161519 TriKE enhanced the proliferation, activation, cytokine secretion, and cytotoxicity of NK cells in the presence of CD19 tumor cells. The 161519 TriKE aided inhibition of tumor growth and prolonged the overall survival of murine xenografts, and could be used to treat CD19-positive cancers.
自然杀伤 (NK) 细胞因其在治疗“冷肿瘤”方面的潜力而备受关注,因此被认为是治愈癌症的新策略之一,利用 NK 细胞相关治疗产品的新可能性和干预措施在全球范围内得到了发展。
我们构建了一种由抗 CD16、IL-15 和抗 CD19 组成的三特异性杀伤嵌合分子 (TriKE)。这种 TriKE 旨在吸引 CD19 肿瘤细胞到 CD16 NK 细胞,而 IL-15 则维持 NK 细胞的增殖、发育和存活。
在存在 CD19 靶标的情况下,用 161519 TriKE 处理可上调 NK 细胞中 CD69、CD107a、TRAIL、IFN-γ 和 TNF-α 的表达,并显著改善 NK 细胞的增殖和细胞毒性。与未“武装”的 NK 细胞相比,“武装”有 161519 TriKE 的 NK 细胞对 CD19 靶标的细胞溶解作用更强。在用人外周血单核细胞重建的异种移植小鼠的 B 细胞淋巴瘤临床前模型中,与对照小鼠或用 1619 BiKE 治疗的小鼠相比,用 161519 TriKE 治疗可显著抑制肿瘤生长并延长总生存期。与使用 161519 TriKE 相比,联合使用 IL-2 是一种更有效的治疗方法,用 1619 BiKE 治疗。
新生成的 161519 TriKE 在存在 CD19 肿瘤细胞的情况下增强了 NK 细胞的增殖、激活、细胞因子分泌和细胞毒性。161519 TriKE 有助于抑制肿瘤生长并延长小鼠异种移植的总生存期,可用于治疗 CD19 阳性癌症。