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B 细胞恶性肿瘤中的表观遗传学特征分析与 CD19 CAR-T 细胞治疗应答

英文原题:Epigenetic Profiling and Response to CD19 Chimeric Antigen Receptor T-Cell Therapy in B-Cell Malignancies.

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Epigenetic Profiling and Response to CD19 Chimeric Antigen Receptor T-Cell Therapy in B-Cell Malignancies.

PubMed 2022/03/08(内容时间) J Natl Cancer Inst Q1 · IF 7.7(JCR 2025)

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研究概要

我们表明,患者 CAR-T19 细胞的 DNA 甲基化图谱影响 B 细胞恶性肿瘤患者细胞免疫治疗的疗效。

研究思路结论见上方概要

针对CD19的嵌合抗原受体(CAR)T细胞(CAR-T19)在B细胞恶性肿瘤中有效,但预测CAR-T19治疗临床结局的分子因素知之甚少。表观遗传改变在癌症免疫学中的相关性日益被认识到,这促使我们确定CAR-T19细胞的DNA甲基化谱对临床病程的影响。

我们招募了114例B细胞恶性肿瘤患者,包括77例急性淋巴细胞白血病患者和37例非霍奇金淋巴瘤患者,这些患者接受了CAR-T19细胞治疗。使用全面的DNA甲基化微阵列,我们确定了患者T细胞在转导CAR载体后发生的表观基因组变化。评估了所识别的DNA甲基化位点对临床反应、细胞因子释放综合征、免疫效应细胞相关神经毒性综合征、无事件生存期和总生存期的影响。所有统计检验均为双侧检验。

我们在输注到患者体内之前,在CAR未转导和CAR转导的T细胞之间鉴定出984个差异DNA甲基化基因组位点。经多重检验校正后,其中18个不同的表观遗传位点与完全缓解(CR)相关。利用与CR相关的位点,在初始发现队列(n = 79)中建立了一种表观遗传特征,以下称为EPICART特征,该特征与CR相关(Fisher精确检验,P < .001),并与改善的无事件生存期(风险比[HR] = 0.36;95%置信区间[CI] = 0.19至0.70;P = .002;log-rank P = .003)和总生存期(HR = 0.45;95% CI = 0.20至0.99;P = .047;log-rank P = .04)相关。最重要的是,EPICART特征在验证队列(n = 35)中保持了其临床病程预测价值,在该队列中它与CR相关(Fisher精确检验,P < .001),并与改善的总生存期相关(HR = 0.31;95% CI = 0.11至0.84;P = .02;log-rank P = .02)。

展开英文摘要原文

Chimeric antigen receptor (CAR) T cells directed against CD19 (CART19) are effective in B-cell malignancies, but little is known about the molecular factors predicting clinical outcome of CART19 therapy. The increasingly recognized relevance of epigenetic changes in cancer immunology prompted us to determine the impact of the DNA methylation profiles of CART19 cells on the clinical course.

We recruited 114 patients with B-cell malignancies, comprising 77 patients with acute lymphoblastic leukemia and 37 patients with non-Hodgkin lymphoma who were treated with CART19 cells. Using a comprehensive DNA methylation microarray, we determined the epigenomic changes that occur in the patient T cells upon transduction of the CAR vector. The effects of the identified DNA methylation sites on clinical response, cytokine release syndrome, immune effector cell-associated neurotoxicity syndrome, event-free survival, and overall survival were assessed. All statistical tests were 2-sided.

We identified 984 genomic sites with differential DNA methylation between CAR-untransduced and CAR-transduced T cells before infusion into the patient. Eighteen of these distinct epigenetic loci were associated with complete response (CR), adjusting by multiple testing. Using the sites linked to CR, an epigenetic signature, referred to hereafter as the EPICART signature, was established in the initial discovery cohort (n = 79), which was associated with CR (Fisher exact test, P < .001) and enhanced event-free survival (hazard ratio [HR] = 0.36; 95% confidence interval [CI] = 0.19 to 0.70; P = .002; log-rank P = .003) and overall survival (HR = 0.45; 95% CI = 0.20 to 0.99; P = .047; log-rank P = .04;). Most important, the EPICART profile maintained its clinical course predictive value in the validation cohort (n = 35), where it was associated with CR (Fisher exact test, P < .001) and enhanced overall survival (HR = 0.31; 95% CI = 0.11 to 0.84; P = .02; log-rank P = .02).

We show that the DNA methylation landscape of patient CART19 cells influences the efficacy of the cellular immunotherapy treatment in patients with B-cell malignancy.

论文信息

作者
Garcia-Prieto CA、Villanueva L、Bueno-Costa A、Davalos V、González-Navarro EA、Juan M、Urbano-Ispizua Á、Delgado J
单位
Cancer and Leukemia Epigenetics and Biology Program (PEBCL), Josep Carreras Leukaemia Research Institute (IJC), Badalona, Spain.Spain
文献类型
非美国政府资助研究
期刊
Journal of the National Cancer Institute2022 Mar 8
原文标识
PubMed 34581788 · DOI 10.1093/jnci/djab194