Tumor-Specific T-Cells Engineered to Overcome Tumor Immune Evasion Induce Clinical Responses in Patients With Relapsed Hodgkin Lymphoma
医学
免疫系统
抗原
肿瘤微环境
癌症研究
CD30
淋巴瘤
免疫学
作者
Catherine M. Bollard,Tamara Tripic,Conrad Russell Y. Cruz,Gianpietro Dotti,Stephen Gottschalk,Vicky Torrano,Olga Dakhova,George Carrum,Carlos A. Ramos,Hao Liu,Meng-Fen Wu,Andrea N. Marcogliese,Cecilia Barese,Youli Zu,Daniel Y. Lee,Owen A. O’Connor,Adrian P. Gee,Malcolm K. Brenner,Helen E. Heslop,Cliona M. Rooney
出处
期刊:Journal of Clinical Oncology [American Society of Clinical Oncology] 日期:2018-01-09卷期号:36 (11): 1128-1139被引量:153
Purpose Transforming growth factor-β (TGF-β) production in the tumor microenvironment is a potent and ubiquitous tumor immune evasion mechanism that inhibits the expansion and function of tumor-directed responses; therefore, we conducted a clinical study to discover the effects of the forced expression of a dominant-negative TGF-β receptor type 2 (DNRII) on the safety, survival, and activity of infused tumor-directed T cells. Materials and Methods In a dose escalation study, eight patients with Epstein Barr virus-positive Hodgkin lymphoma received two to 12 doses of between 2 × 10