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CD19 靶向免疫治疗后出现的改变导致错误折叠的蛋白质滞留在内质网中。

CD19 Alterations Emerging after CD19-Directed Immunotherapy Cause Retention of the Misfolded Protein in the Endoplasmic Reticulum.

机构信息

Division of Experimental Pathology, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.

Immunology, Microenvironment and Metastasis Program, The Wistar Institute, Philadelphia, Pennsylvania, USA.

出版信息

Mol Cell Biol. 2018 Oct 15;38(21). doi: 10.1128/MCB.00383-18. Print 2018 Nov 1.

Abstract

We previously described a mechanism of acquired resistance of B-cell acute lymphoblastic leukemia to CD19-directed chimeric antigen receptor T-cell (CART) immunotherapy. It was based on in-frame insertions in or skipping of CD19 exon 2. To distinguish between epitope loss and defects in surface localization, we used retroviral transduction and genome editing to generate cell lines expressing CD19 exon 2 variants (CD19ex2vs) bearing vesicular stomatitis virus G protein (VSVg) tags. These lines were negative by live-cell flow cytometry with an anti-VSVg antibody and resistant to killing by VSVg-directed antibody-drug conjugates (ADCs), suggestive of a defect in surface localization. Indeed, pulse-chase and α-mannosidase inhibitor assays showed that all CD19ex2vs acquired endoplasmic reticulum (ER)-specific high-mannose-type sugars but not complex-type glycans synthesized in the Golgi apparatus. When fused with green fluorescent protein (GFP), CD19ex2vs (including a mutant lacking the relevant disulfide bond) showed colocalization with ER markers, implying protein misfolding. Mass spectrometric profiling of CD19-interacting proteins demonstrated that CD19ex2vs fail to bind to the key tetraspanin CD81 and instead interact with ER-resident chaperones, such as calnexin, and ER transporters involved in antigen presentation. Thus, even the intact domains of CD19ex2vs cannot be easily targeted with ADCs or current CD19 CARTs but could serve as sources of peptides for major histocompatibility complex (MHC)-restricted presentation and T-cell receptor (TCR)-mediated killing.

摘要

我们之前描述了 B 细胞急性淋巴细胞白血病对 CD19 导向嵌合抗原受体 T 细胞(CART)免疫疗法产生获得性耐药的机制。该机制基于 CD19 外显子 2 的框内插入或跳过。为了区分表位丢失和表面定位缺陷,我们使用逆转录病毒转导和基因组编辑生成表达 CD19 外显子 2 变体(CD19ex2vs)的细胞系,这些变体带有水疱性口炎病毒 G 蛋白(VSVg)标签。这些细胞系通过抗 VSVg 抗体的活细胞流式细胞术呈阴性,并且对 VSVg 导向的抗体药物偶联物(ADC)的杀伤具有抗性,提示表面定位缺陷。事实上,脉冲追踪和α-甘露糖苷酶抑制剂测定表明,所有 CD19ex2vs 均获得内质网(ER)特异性高甘露糖型糖,但不能获得在高尔基体中合成的复杂型聚糖。当与绿色荧光蛋白(GFP)融合时,CD19ex2vs(包括缺乏相关二硫键的突变体)与 ER 标志物共定位,暗示蛋白质错误折叠。CD19 相互作用蛋白的质谱分析表明,CD19ex2vs 不能与关键的四跨膜蛋白 CD81 结合,而是与内质网驻留伴侣蛋白(如钙联蛋白)以及参与抗原呈递的 ER 转运蛋白相互作用。因此,即使是 CD19ex2vs 的完整结构域也不能轻易被 ADC 或当前的 CD19 CART 靶向,但可以作为主要组织相容性复合物(MHC)受限呈递和 TCR 介导杀伤的肽源。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5861/6189457/c7750b61560c/zmb9991018510001.jpg

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