Poehlein Christian H, Rüttinger Dominik, Ma Jun, Hu Hong-Ming, Urba Walter J, Fox Bernard A
Laboratory of Molecular and Tumor Immunology, Robert W. Franz Cancer Research Center, Earle A. Chiles Research Institute, 4805 N.E. Glisan, Portland, OR 97213, USA.
Curr Oncol Rep. 2005 Sep;7(5):383-92. doi: 10.1007/s11912-005-0066-1.
The past 20 years have seen remarkable advances in our understanding of the molecular and cellular processes controlling the development of an anticancer immune response. These advances have spawned a renaissance in the field of cancer immunotherapy, the original targeted therapy, during which investigators have pushed the envelope and translated promising strategies into investigational therapeutics in patients with cancer. An approach that combined nonmyeloablative lymphodepleting chemotherapy with adoptive transfer of tumor-specific CD4 and CD8 T cells exhibited an initial objective response rate of 51% for patients with stage IV melanoma. Although this strategy is extremely challenging, one can expect technological advances that may simplify this approach and further improve outcome.
在过去20年里,我们对控制抗癌免疫反应发展的分子和细胞过程的理解取得了显著进展。这些进展催生了癌症免疫治疗领域的复兴,癌症免疫治疗是最初的靶向治疗方法,在此期间,研究人员不断突破界限,将有前景的策略转化为针对癌症患者的研究性治疗方法。一种将非清髓性淋巴细胞清除化疗与肿瘤特异性CD4和CD8 T细胞的过继转移相结合的方法,对IV期黑色素瘤患者的初始客观缓解率为51%。尽管这种策略极具挑战性,但人们可以期待技术进步,这可能会简化这种方法并进一步改善治疗效果。