Vaccine therapy for pancreatic cancer

被引:63
作者
Salman, Bulent [1 ,2 ,3 ]
Zhou, Donger [3 ,4 ]
Jaffee, Elizabeth M. [2 ,3 ,4 ,5 ]
Edil, Barish H. [6 ]
Zheng, Lei [1 ,2 ,3 ,4 ,5 ]
机构
[1] Johns Hopkins Univ, Sch Med, Dept Surg, Baltimore, MD 21205 USA
[2] Johns Hopkins Univ, Sch Med, Sol Goldman Pancreat Canc Res Ctr, Baltimore, MD 21205 USA
[3] Johns Hopkins Univ, Sch Med, Sidney Kimmel Comprehens Canc Ctr, Baltimore, MD 21205 USA
[4] Johns Hopkins Univ, Sch Med, Dept Oncol, Baltimore, MD 21205 USA
[5] Johns Hopkins Univ, Sch Med, Skip Viragh Pancreat Canc Ctr, Baltimore, MD 21205 USA
[6] Univ Colorado, Dept Surg, Aurora, CO USA
关键词
pancreatic cancer; immunotherapy; cancer vaccine; clinical trials; immune checkpoint; COLONY-STIMULATING FACTOR; SECRETING TUMOR VACCINE; RAS PEPTIDE VACCINATION; PHASE-I; LISTERIA-MONOCYTOGENES; SAFETY; IMMUNOTHERAPY; CELLS; TRIAL; ADENOCARCINOMA;
D O I
10.4161/onci.26662
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Pancreatic cancer is a lethal disease and currently available therapies have significant limitations. Pancreatic cancer is thus an ideal setting for the development of novel treatment modalities such as immunotherapy. However, relevant obstacles must be overcome for immunotherapeutic regimens against pancreatic cancer to be successful. Vaccine therapy relies on the administration of biological preparations that include an antigen that (at least ideally) is specifically expressed by malignant cells, boosting the natural ability of the immune system to react against neoplastic cells. There are a number of ways to deliver anticancer vaccines. Potent vaccines stimulate antigen presentation by dendritic cells, hence driving the expansion of antigen-specific effector and memory T cells. Unlike vaccines given as a prophylaxis against infectious diseases, anticancer vaccines require the concurrent administration of agents that interfere with the natural predisposition of tumors to drive immunosuppression. The safety and efficacy of vaccines against pancreatic cancer are nowadays being tested in early phase clinical trials.
引用
收藏
页码:1 / 8
页数:8
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