Department of Immunology, School of Basic Medical Sciences, Fudan University, Building 13, No. 130, Dongan Road, Shanghai, 200032, China.
Department of Biochemistry and Molecular Biology, School of Basic Medical Sciences, Fudan University, Building 7, No. 130, Dongan Road, Shanghai, 200032, China.
Cancer Immunol Immunother. 2019 Jan;68(1):45-56. doi: 10.1007/s00262-018-2250-9. Epub 2018 Sep 26.
CD19 tumor-infiltrating B-cells (CD19 TIB) play a crucial role in tumorigenesis, but their clinical relevance in muscle-invasive bladder cancer (MIBC) remains unknown. This study aimed to investigate the prognostic value of CD19 TIB for post-surgery survival and adjuvant chemotherapy response in MIBC.
We assessed TIB by immunohistochemical staining of CD19 in 246 MIBC patients from Zhongshan Hospital and Shanghai Cancer Center. We evaluated the survival benefit of platinum-based chemotherapy according to CD19 TIB. The mechanism underlying CD19 TIB antitumor immunity was explored through the Cancer Genome Atlas (TCGA) dataset analysis and an in vitro Ag presentation assay.
CD19 TIB extensively infiltrated into the tumor stroma of MIBC. Adjuvant chemotherapy (ACT) led to a significantly increased benefit in the high CD19 TIB MIBC patients (P = 0.003). In multivariate analysis, high CD19 TIB MIBC patients had significantly longer OS with ACT in the discovery set (HR = 0.487, P = 0.038). TCGA gene expression analyses showed enrichment of adaptive immunity, T-cell-mediated immunity, and antigen-presentation signaling pathways in high CD19 TIB MIBC patients. Moreover, CD19 TIB co-localized with activated CD4 TIT and expressed surface markers characteristic of antigen-presenting cells. Finally, an antigen-presentation assay demonstrated the antigen-presentation function of CD19 TIB.
CD19 TIB was identified as an independent prognostic factor, which could predict for post-surgery survival and platinum-based ACT benefits in MIBC. CD19 TIB serve as antigen-presenting cells (APCs) to activate CD4 TIT in the tumor environment of MIBC.
CD19 肿瘤浸润 B 细胞(CD19 TIB)在肿瘤发生中起着至关重要的作用,但它们在肌层浸润性膀胱癌(MIBC)中的临床相关性尚不清楚。本研究旨在探讨 CD19 TIB 在 MIBC 术后生存和辅助化疗反应中的预后价值。
我们通过免疫组化染色法检测了来自中山医院和上海癌症中心的 246 例 MIBC 患者的 TIB。我们根据 CD19 TIB 评估了铂类化疗的生存获益。通过癌症基因组图谱(TCGA)数据集分析和体外 Ag 呈递测定,探讨了 CD19 TIB 抗肿瘤免疫的机制。
CD19 TIB 广泛浸润 MIBC 的肿瘤基质。辅助化疗(ACT)显著增加了高 CD19 TIB MIBC 患者的获益(P=0.003)。在多变量分析中,高 CD19 TIB MIBC 患者在发现组中接受 ACT 治疗后具有显著更长的 OS(HR=0.487,P=0.038)。TCGA 基因表达分析显示,高 CD19 TIB MIBC 患者中适应性免疫、T 细胞介导的免疫和抗原呈递信号通路富集。此外,CD19 TIB 与活化的 CD4 TIT 共定位,并表达抗原呈递细胞的表面标志物。最后,抗原呈递测定显示了 CD19 TIB 的抗原呈递功能。
CD19 TIB 被确定为一个独立的预后因素,可预测 MIBC 术后生存和基于铂类的 ACT 获益。CD19 TIB 在 MIBC 的肿瘤微环境中作为抗原呈递细胞(APC)激活 CD4 TIT。