Chapuis Aude G, Lee Sylvia M, Thompson John A, Roberts Ilana M, Margolin Kim A, Bhatia Shailender, Sloan Heather L, Lai Ivy, Wagener Felecia, Shibuya Kendall, Cao Jianhong, Wolchok Jedd D, Greenberg Philip D, Yee Cassian
Program in Immunology, Fred Hutchinson Cancer Research Center (FHCRC), Seattle, WA 98109.
Division of Medical Oncology, Department of Medicine, University of Washington Medical Center/FHCRC/Seattle Cancer Care Alliance, Seattle, WA 98109.
J Exp Med. 2016 Jun 27;213(7):1133-9. doi: 10.1084/jem.20152021. Epub 2016 May 30.
Adoptive transfer of peripheral blood-derived, melanoma-reactive CD8(+) cytotoxic T lymphocytes (CTLs) alone is generally insufficient to eliminate bulky tumors. Similarly, monotherapy with anti-CTLA4 infrequently yields sustained remissions in patients with metastatic melanoma. We postulated that a bolus of enhanced IL-21-primed polyclonal antigen-specific CTL combined with CTLA4 blockade might boost antitumor efficacy. In this first-in-human case study, the combination successfully led to a durable complete remission (CR) in a patient whose disease was refractory to both monoclonal CTL and anti-CTLA4. Long-term persistence and sustained anti-tumor activity of transferred CTL, as well as responses to nontargeted antigens, confirmed mutually beneficial effects of the combined treatment. In this first-in-human study, Chapuis et al. demonstrate that the combination of adoptive cellular therapy with CTLA4 blockade induces long-term remission in a melanoma patient resistant to both modalities administered serially and individually.
单独过继转移外周血来源的、黑色素瘤反应性CD8(+) 细胞毒性T淋巴细胞(CTL)通常不足以消除体积较大的肿瘤。同样,抗CTLA4单药治疗在转移性黑色素瘤患者中很少能产生持续缓解。我们推测,一剂增强型IL-21预激的多克隆抗原特异性CTL与CTLA4阻断相结合可能会提高抗肿瘤疗效。在这项首例人体病例研究中,该联合治疗成功使一名对单克隆CTL和抗CTLA4均难治的患者实现了持久的完全缓解(CR)。转移的CTL的长期持续存在和持续抗肿瘤活性,以及对非靶向抗原的反应,证实了联合治疗的互利效果。在这项首例人体研究中,沙皮伊等人证明,过继性细胞疗法与CTLA4阻断相结合可使一名对两种单独和序贯给药方式均耐药的黑色素瘤患者实现长期缓解。