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Immune Characteristics of Chinese Diffuse Large B-Cell Lymphoma Patients: Implications for Cancer Immunotherapies

机译:中国弥漫性大B细胞淋巴瘤患者的免疫特性:对癌症免疫治疗的意义。

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Immunotherapeutic agents have demonstrated encouraging signs of clinical utility in non-Hodgkin lymphoma. The goal of this study is to analyze the immune characteristics of Chinese patients with diffuse large B-cell lymphoma (DLBCL) to inform the development of immunotherapies in this patient population. Tumor samples from 211 DLBCL patients were analyzed for cell of origin (COO) and immune characteristics using the NanoString platform as well as MYC protein expression through immunohistochemistry. Lower incidence of the germinal center B-cell (GCB) subtype (93/211, 44.1%) was observed in this cohort. Compared to the GCB subtype, the activated B-cell (ABC) subtype was associated with significantly increased expression of multiple pro-inflammatory gene signatures and decreased expression of anti-inflammatory gene signatures. Instead of affecting the pro-inflammatory genes, MYC protein overexpression showed a negative correlation with the expression of T-cell receptor (TCR) and T regulatory genes as well as the OX40 gene. Regardless of COO, higher PD-L1 or IDO1 gene expression correlated with increased expression of T effector and Interferon-γ gene signatures while the expression of multiple oncogenes including ACTR3B, ERBB2, AKT2 and SMARCD1 was down-regulated. Our findings may thus be helpful in guiding further development of immunotherapies for the different subsets of Chinese DLBCL patients.
机译:免疫治疗剂已在非霍奇金淋巴瘤中显示出令人鼓舞的临床效用迹象。这项研究的目的是分析中国弥漫性大B细胞淋巴瘤(DLBCL)患者的免疫特性,为该患者人群的免疫疗法发展提供信息。使用NanoString平台分析了211名DLBCL患者的肿瘤样品的起源细胞(COO)和免疫特性,并通过免疫组织化学分析了MYC蛋白的表达。在该队列中观察到生发中心B细胞(GCB)亚型的发生率较低(93 / 211,44.1%)。与GCB亚型相比,激活的B细胞(ABC)亚型与多个促炎基因标记的表达显着增加和抗炎基因标记的表达减少有关。 MYC蛋白过表达没有影响促炎基因,而是与T细胞受体(TCR)和T调节基因以及OX40基因的表达呈负相关。无论COO如何,较高的PD-L1或IDO1基因表达都与T效应子和干扰素-γ基因签名的表达增加相关,而包括ACTR3B,ERBB2,AKT2和SMARCD1在内的多种癌基因的表达均被下调。因此,我们的发现可能有助于指导中国DLBCL患者不同亚型免疫治疗的进一步发展。

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