Immunotherapy with autologous, human dendritic cells transfected with carcinoembryonic antigen mRNA

被引:126
作者
Morse, MA
Nair, SK
Mosca, PJ
Hobeika, AC
Clay, TM
Deng, YP
Boczkowski, D
Proia, A
Neidzwiecki, D
Clavien, PA
Hurwitz, HI
Schlom, J
Gilboa, E
Lyerly, HK
机构
[1] Duke Univ, Med Ctr, Dept Med, Durham, NC 27710 USA
[2] Duke Univ, Med Ctr, Dept Surg, Durham, NC 27710 USA
[3] Duke Univ, Med Ctr, Dept Pathol, Durham, NC 27710 USA
[4] Duke Univ, Med Ctr, Dept Biostat, Durham, NC 27710 USA
[5] Eastern Virginia Med Sch, Dept Internal Med, Yorktown, VA USA
[6] Natl Inst Hlth, Bethesda, MD USA
关键词
dendritic cells; immunotherapy; CEA; hepatic metastases;
D O I
10.1081/CNV-120018224
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Immunizations with dendritic cells (DC) transfected with RNA encoding tumor antigens induce potent tumor antigen-specific immune responses in vitro and in murine models. We performed a phase I study of patients with advanced carcinoembryonic antigen (CEA)-expressing malignancies followed by a phase II study of patients with resected hepatic metastases of colon cancer to assess safety and feasibility of administering autologous DC loaded with CEA mRNA. The immunizations were well tolerated. Of the 24 evaluable patients in the dose-escalation phase, there was I complete response (by tumor marker), 2 minor responses, 3 with stable disease, and 18 with progressive disease. In the phase II study, 9 of 13 patients have relapsed at a median of 122 days. Evidence of an immunologic response was demonstrated in biopsies of DC injection sites and peripheral blood of selected patients. We conclude that it is feasible and safe to administer mRNA-loaded DC to patients with advanced malignancies.
引用
收藏
页码:341 / 349
页数:9
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