RNF43 p.G659fs 通过 PI3K/AKT/mTOR 信号通路和 HLA-E 上调导致 MSI-high 结直肠癌中 NK 细胞功能障碍
RNF43 p.G659fs leads to natural killer cell dysfunction in MSI-high colorectal cancer through PI3K/AKT/mTOR signaling and HLA-E up-regulation.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Immunomodulatory drugs: a promising clinical ally for cancer immunotherapy.
Immunomodulatory drugs: a promising clinical ally for cancer immunotherapy.
分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。
免疫调节酰亚胺类药物(IMiD)获批用于治疗血液系统癌症已超过 20 年,但人们近来才逐渐认识到其能够刺激抗肿瘤 T 细胞和自然杀伤(NK)细胞反应。临床试验数据日益表明,抗体、T 细胞和疫苗等靶向免疫疗法与 IMiD 衍生物来那度胺或泊马度胺联合使用,可改善治疗结局。本文回顾这些临床数据,强调 IMiD 对血液系统肿瘤和实体瘤联合免疫疗法的意义。进一步研究 IMiD 分子机制并加深对其免疫调节作用的理解,可能有助于优化 IMiD 的特定应用,并改进未来临床试验设计,使 IMiD 在联合癌症免疫治疗中发挥更重要作用。
While immunomodulatory imide drugs (IMiDs) have been authorised for treatment of haematological cancers for over two decades, the appreciation of their ability to stimulate antitumour T cell and natural killer (NK) cell responses is relatively recent. Clinical trial data increasingly show that targeted immunotherapies, such as antibodies, T cells, and vaccines, improve outcomes when delivered in combination with the IMiD derivatives lenalidomide or pomalidomide.
Here, we review these clinical data to highlight the relevance of IMiDs in combinatorial immunotherapy for both haematological and solid tumours.
Further research into the molecular mechanisms of IMiDs and an increased understanding of their immunomodulatory effects may refine the specific applications of IMiDs and improve the design of future clinical trials, moving IMiDs to the forefront of combinatorial cancer immunotherapy.
MEMBER ACCOUNT
登录成功会直接打开下一页。