Department of Pharmacology and Pharmaceutical Sciences, School of Pharmacy, University of Southern California, Los Angeles, CA 90089, USA.
Cancer and Blood Disease Institute, Division of Hematology-Oncology, Children's Hospital Los Angeles, Los Angeles, CA 90027, USA; Norris Comprehensive Cancer Center, Keck School of Medicine, University of Southern California, Los Angeles, CA 90089, USA.
Mol Ther. 2022 Mar 2;30(3):1215-1226. doi: 10.1016/j.ymthe.2021.11.013. Epub 2021 Nov 18.
Chimeric antigen receptor natural killer (CAR-NK) cells have remarkable cytotoxicity against hematologic malignancies; however, they may also attack normal cells sharing the target antigen. Since human leukocyte antigen DR (HLA-DR) is reportedly lost or downregulated in a substantial proportion of hematologic malignancies, presumably a mechanism to escape immune surveillance, we hypothesize that the anti-cancer specificity of CAR-NK cells can be enhanced by activating them against cancer antigens while inhibiting them against HLA-DR. Here, we report the development of an anti-HLA-DR inhibitory CAR (iCAR) that can effectively suppress NK cell activation against HLA-DR-expressing cells. We show that dual CAR-NK cells, which co-express the anti-CD19 or CD33 activating CAR and the anti-HLA-DR iCAR, can preferentially target HLA-DR-negative cells over HLA-DR-positive cells in vitro. We find that the HLA-DR-mediated inhibition is positively correlated with both iCAR and HLA-DR densities. We also find that HLA-DR-expressing surrounding cells do not affect the target selectivity of dual CAR-NK cells. Finally, we confirm that HLA-DR-positive cells are resistant to dual CAR-NK cell-mediated killing in a xenograft mouse model. Our approach holds great promise for enhancing CAR-NK and CAR-T cell specificity against malignancies with HLA-DR loss.
嵌合抗原受体自然杀伤 (CAR-NK) 细胞对血液系统恶性肿瘤具有显著的细胞毒性;然而,它们也可能攻击具有相同靶抗原的正常细胞。由于人白细胞抗原 DR (HLA-DR) 在相当一部分血液系统恶性肿瘤中据报道丢失或下调,推测是一种逃避免疫监视的机制,我们假设通过激活它们针对癌症抗原,同时抑制它们针对 HLA-DR,可以增强 CAR-NK 细胞的抗癌特异性。在这里,我们报告了一种抗 HLA-DR 抑制性 CAR(iCAR)的开发,该 CAR 可以有效抑制 NK 细胞对 HLA-DR 表达细胞的激活。我们表明,共表达抗 CD19 或 CD33 激活 CAR 和抗 HLA-DR iCAR 的双 CAR-NK 细胞可以在体外优先靶向 HLA-DR 阴性细胞而不是 HLA-DR 阳性细胞。我们发现 HLA-DR 介导的抑制与 iCAR 和 HLA-DR 密度呈正相关。我们还发现 HLA-DR 表达的周围细胞不影响双 CAR-NK 细胞的靶选择性。最后,我们在异种移植小鼠模型中证实,HLA-DR 阳性细胞对双 CAR-NK 细胞介导的杀伤具有抗性。我们的方法为增强针对 HLA-DR 缺失的恶性肿瘤的 CAR-NK 和 CAR-T 细胞特异性提供了很大的希望。