Department of Otorhinolaryngology, Head and Neck Surgery, Graduate School of Medicine, Chiba University, 1-8-1 Inohana, Chuo-ku, Chiba, 260-8670, Japan.
Department of Medical Immunology, Graduate School of Medicine, Chiba University, Chiba, Japan.
BMC Cancer. 2018 Dec 17;18(1):1254. doi: 10.1186/s12885-018-5179-7.
Salivary gland cancers are not sensitive to conventional radiotherapy or chemotherapy regimens. Therefore, the development of a new treatment strategy is of critical importance for improving the prognosis. We examined the expression of mesothelin molecules in salivary gland cancers and the efficacy of adoptive cell therapy based on mesothelin-specific chimeric antigen receptor transduced T cells.
The expression of mesothelin molecule was studied in salivary gland cancer samples obtained from 16 patients as well as a salivary gland cancer cell line (A-253) and five other cell lines. The activation of mesothelin-specific chimeric antigen receptor-expressing CD8 T cells after stimulation with mesothelin and the effects of invariant natural killer T cells on this activation were evaluated.
Mesothelin was detected in the A-253 cells and the surgical specimens except for the case of squamous cell carcinoma to various degrees. Following stimulation with mesothelin expressing cancer cells, chimeric antigen receptor T cells were dose-dependently activated; this activation was enhanced by co-culture with invariant natural killer T cells and subsequently abrogated by treatment with anti-interferon-γ antibodies. Furthermore, the cytotoxicity of chimeric antigen receptor T cells against various cancer cells was further augmented by invariant natural killer T cells.
The use of adoptive transfer with mesothelin-specific chimeric antigen receptor-expressing CD8 T cells against salivary gland cancers is an effective therapy and invariant natural killer T cells are expected to be used in adjuvant treatment for T cell-based immunotherapy.
唾液腺癌对常规放化疗方案不敏感。因此,开发新的治疗策略对于改善预后至关重要。我们研究了间皮素分子在唾液腺癌中的表达以及基于间皮素特异性嵌合抗原受体转导 T 细胞的过继细胞治疗的疗效。
我们研究了 16 名患者的唾液腺癌样本、唾液腺癌细胞系(A-253)和其他 5 种细胞系中间皮素分子的表达。评估了间皮素特异性嵌合抗原受体表达的 CD8 T 细胞在间皮素刺激下的激活情况以及不变自然杀伤 T 细胞对这种激活的影响。
间皮素在 A-253 细胞和手术标本中均有不同程度的表达,除了鳞状细胞癌病例。在表达间皮素的癌细胞刺激后,嵌合抗原受体 T 细胞呈剂量依赖性激活;这种激活通过与不变自然杀伤 T 细胞共培养而增强,随后被抗干扰素-γ抗体阻断。此外,不变自然杀伤 T 细胞进一步增强了嵌合抗原受体 T 细胞对各种癌细胞的细胞毒性。
使用间皮素特异性嵌合抗原受体表达的 CD8 T 细胞过继转移治疗唾液腺癌是一种有效的治疗方法,预计不变自然杀伤 T 细胞将用于 T 细胞为基础的免疫治疗的辅助治疗。