癌症研究
嵌合抗原受体
抗原
受体
自然杀伤细胞
免疫疗法
免疫学
癌症
生物
免疫系统
抗体
单克隆抗体
头颈部癌
细胞毒性T细胞
遗传学
体外
作者
Miriam T. Jacobs,Pamela Wong,Alice Y. Zhou,Michelle Becker‐Hapak,Nancy D. Marín,Lynne Marsala,Mark Foster,Jennifer A. Foltz,Celia C. Cubitt,Jennifer Tran,David A. Russler‐Germain,Carly Neal,Samantha Kersting-Schadek,Lily Chang,Timothy Schappe,Patrick Pence,Ethan McClain,Jose P. Zevallos,Jason T. Rich,Randal C. Paniello
标识
DOI:10.1158/1078-0432.ccr-23-0156
摘要
Head and neck squamous cell carcinoma (HNSCC) is an aggressive tumor with low response rates to frontline PD-1 blockade. Natural killer (NK) cells are a promising cellular therapy for T cell therapy-refractory cancers, but are frequently dysfunctional in patients with HNSCC. Strategies are needed to enhance NK cell responses against HNSCC. We hypothesized that memory-like (ML) NK cell differentiation, tumor targeting with cetuximab, and engineering with an anti-EphA2 (Erythropoietin-producing hepatocellular receptor A2) chimeric antigen receptor (CAR) enhance NK cell responses against HNSCC.
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