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用抑制性嵌合抗原受体靶向血液系统恶性肿瘤中的 HLA-DR 缺失。

Targeting HLA-DR loss in hematologic malignancies with an inhibitory chimeric antigen receptor.

机构信息

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.

出版信息

Mol Ther. 2022 Mar 2;30(3):1215-1226. doi: 10.1016/j.ymthe.2021.11.013. Epub 2021 Nov 18.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c134/8899520/93db6def8549/fx1.jpg

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