再分化使能的 TSHRCART 细胞克服侵袭性甲状腺癌中的抗原丢失
Redifferentiation-enabled TSHRCART cells overcome antigen loss in aggressive thyroid cancers.
这些发现确立了肿瘤再分化作为一种可推广的策略,用于克服抗原丢失并增强 CAR-T 细胞疗法在甲状腺癌以及可能其他实体瘤中的疗效。
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Research progress of immunotherapy against anaplastic thyroid cancer.
Research progress of immunotherapy against anaplastic thyroid cancer.
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甲状腺未分化癌(ATC)是侵袭性最强的甲状腺癌类型。虽然 ATC 较为罕见,但其死亡率很高。手术、放疗和化疗等标准治疗在 ATC 管理中的疗效有限。然而,免疫治疗的出现显著改善了 ATC 患者的预后。免疫治疗通过利用机体免疫细胞的力量,有效靶向并清除肿瘤细胞。新抗原是由体细胞突变产生的一种非典型蛋白,仅见于肿瘤细胞中,且缺乏中枢耐受。新抗原对肿瘤细胞具有增强的特异性,并表现出强大的免疫原性。目前,新抗原治疗主要应用于免疫检查点抑制剂和细胞免疫治疗,包括过继性免疫治疗和肿瘤疫苗。本研究讨论了与 ATC 免疫治疗相关的机制、肿瘤微环境、临床试验、不良事件、局限性及未来方向。
Anaplastic thyroid cancer (ATC) is the most aggressive type of thyroid cancer. While ATC is rare, its mortality is high. Standard treatments, such as surgery, radiotherapy, and chemotherapy, have demonstrated limited efficacy in managing ATC.
However, the advent of immunotherapy has significantly improved the prognosis for patients with ATC. Immunotherapy effectively targets and eliminates tumor cells by using the power of the body's immune cells. The neoantigen is an atypical protein generated by somatic mutation, is exclusively observed in neoplastic cells, and is devoid of central tolerance.
Neoantigens exhibit enhanced specificity towards tumor cells and display robust immunogenic properties. Currently, neoantigen therapy is primarily applied in immune checkpoint inhibitors and cellular immunotherapy, encompassing adoptive immunotherapy and tumor vaccines.
This study discusses the mechanism, tumor microenvironment, clinical trials, adverse events, limitations and future directions associated with ATC immunotherapy.
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