b细胞淋巴瘤对CAR - t细胞治疗的耐药性与可导致转分化的基因组肿瘤变化有关。

Camille Laurent, Charlotte Syrykh, Maxime Hamon, José Adélaïde, Arnaud Guille, Frederic Escudié, Gael Jalowicki, Frederic Fina, Alexandre Bardet, Lenaïg Mescam, Thierry J Molina, Peggy Dartigues, Marie Parrens, Pierre Sujobert, Caroline Besson, Daniel Birnbaum, Luc Xerri
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引用次数: 6

摘要

尽管嵌合抗原受体(CAR) t细胞疗法(CART)治疗b细胞非霍奇金淋巴瘤的疗效令人印象深刻,但持久的反应并不常见。与治疗失败相关的组织病理学和分子特征在很大程度上仍然未知。因此,我们使用免疫组织化学、荧光原位杂交、阵列比较基因组杂交、下一代DNA和RNA测序以及基因组尺度的DNA甲基化分析了来自9例患者的19个序列肿瘤样本,包括先前的抗cd19 CART (CART前)和复发(CART后)。最初诊断为弥漫性大b细胞淋巴瘤(n=6),双恶性b细胞淋巴瘤(n=1), Burkitt淋巴瘤(n=2)。在7/9的患者中,复发时组织病理学特征大多保留,除了经常丢失1个或几个b细胞标记物。其余2例(1例弥漫性大b细胞淋巴瘤和1例Burkitt淋巴瘤)在cart后肿瘤中表现出显著的表型变化,尽管相同克隆免疫球蛋白基因重排持续存在,但b细胞标记物急剧下降,t细胞或组织细胞标记物出现。具有异常t细胞表型的cart后肿瘤显示大多数b细胞基因mRNA表达减少,其启动子甲基化增加。荧光原位杂交和比较基因组杂交显示,所有配对样本的染色体改变都具有全局稳定性,包括17p/TP53缺失。cart后样本中获得的新致病变异包括触发PI3K通路的突变(PIK3R1、PIK3R2、PIK3C2G)或与肿瘤侵袭性相关的突变(KRAS、INPP4B、SF3B1、SYNE1、TBL1XR1)。这些结果表明,cart抵抗性b细胞非霍奇金淋巴瘤表现出基因重塑,这可能导致b细胞分化的严重失调。PI3K和KRAS通路的获得性突变表明,一些靶向治疗可能有助于克服CART耐药性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Resistance of B-Cell Lymphomas to CAR T-Cell Therapy Is Associated With Genomic Tumor Changes Which Can Result in Transdifferentiation.

Despite the impressive efficacy of chimeric antigen receptor (CAR) T-cell therapy (CART) in B-cell non-Hodgkin lymphomas, durable responses are uncommon. The histopathologic and molecular features associated with treatment failure are still largely unknown. Therefore, we have analyzed 19 sequential tumor samples from 9 patients, prior anti-CD19 CART (pre-CART) and at relapse (post-CART), using immunohistochemistry, fluorescence in situ hybridization, array comparative genomic hybridization, next-generation DNA and RNA sequencing, and genome-scale DNA methylation. The initial diagnosis was diffuse large B-cell lymphoma (n=6), double-hit high-grade B-cell lymphoma (n=1), and Burkitt lymphoma (n=2). Histopathologic features were mostly retained at relapse in 7/9 patients, except the frequent loss of 1 or several B-cell markers. The remaining 2 cases (1 diffuse large B-cell lymphoma and 1 Burkitt lymphoma) displayed a dramatic phenotypic shift in post-CART tumors, with the drastic downfall of B-cell markers and emergence of T-cell or histiocytic markers, despite the persistence of identical clonal immunoglobulin gene rearrangements. The post-CART tumor with aberrant T-cell phenotype showed reduced mRNA expression of most B-cell genes with increased methylation of their promoter. Fluorescence in situ hybridization and comparative genomic hybridization showed global stability of chromosomal alterations in all paired samples, including 17p/TP53 deletions. New pathogenic variants acquired in post-CART samples included mutations triggering the PI3K pathway (PIK3R1, PIK3R2, PIK3C2G) or associated with tumor aggressiveness (KRAS, INPP4B, SF3B1, SYNE1, TBL1XR1). These results indicate that CART-resistant B-cell non-Hodgkin lymphomas display genetic remodeling, which may result in profound dysregulation of B-cell differentiation. Acquired mutations in the PI3K and KRAS pathways suggest that some targeted therapies could be useful to overcome CART resistance.

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