1 Department of Urology, Affiliated Hospital of Qingdao University, Qingdao 266003, China ; 2 Department of Urology, People's Hospital of Linzi District, Zibo 255400, China ; 3 Medical College of Qingdao University, Qingdao 266021, China.
Chin J Cancer Res. 2015 Apr;27(2):128-37. doi: 10.3978/j.issn.1000-9604.2014.12.15.
In recent years, immunotherapy has been gradually established as the fourth frequently adopted antitumor therapy, following surgery, chemotherapy and radiotherapy, for advanced urologic malignancies with an improved understanding of theoretical basis, such as molecular biology and immunology. Thereinto, adoptive cellular immunotherapy (ACI) has become one of the hotspots, which comprises a variety of treatment approaches, such as TIL, CIK cell, γδ T cell, CAR-engineered T cell and Allogeneic stem cell transplantation (alloSCT). Although preclinical efficacy has been demonstrated remarkably, clinical trials could not consistently show the benefit due to multi-factors in complex immunosuppressive microenvironment in vivo compared to that of in vitro. Here we review some timely aspects of ACI for advanced urologic malignancies, and describe the current status and limitation of immunotherapy from the cellular level. It's our expectation to provide prompting consideration of novel combinatorial ACI strategies and a resurgence of interest in ACI for advanced urologic malignancies.
近年来,随着对分子生物学和免疫学等理论基础的深入理解,免疫疗法逐渐成为继手术、化疗和放疗之后治疗晚期泌尿系统恶性肿瘤的第四种常用抗肿瘤疗法。其中,过继性细胞免疫疗法(ACI)已成为热点之一,它包括多种治疗方法,如 TIL、CIK 细胞、γδ T 细胞、CAR 修饰 T 细胞和同种异体造血干细胞移植(alloSCT)。尽管临床前疗效显著,但由于体内复杂的免疫抑制微环境与体外相比存在多种因素,临床试验并不能始终显示出获益。本文我们就 ACI 治疗晚期泌尿系统恶性肿瘤的一些最新方面进行综述,并从细胞水平描述免疫治疗的现状和局限性。我们期望为新型联合 ACI 策略提供启示,并重新激发人们对晚期泌尿系统恶性肿瘤 ACI 的兴趣。