Poly(I:C) as cancer vaccine adjuvant: Knocking on the door of medical breakthroughs

被引:131
作者
Ammi, Rachid [1 ]
De Waele, Jorrit [2 ]
Willemen, Yannick [3 ]
Van Brussel, Ilse [1 ]
Schrijvers, Dorien M. [1 ]
Lion, Eva [3 ,4 ]
Smits, Evelien L. J. [2 ,3 ,4 ]
机构
[1] Univ Antwerp, Lab Physiopharmacol, B-2610 Antwerp, Belgium
[2] Univ Antwerp VIB, Oncol Res Ctr, B-2610 Antwerp, Belgium
[3] Univ Antwerp, Vaccine & Infect Dis Inst VAXINFECTIO, Lab Expt Hematol, Tumor Immunol Grp, B-62650 Edegem, Belgium
[4] Univ Antwerp Hosp, Ctr Cell Therapy & Regenerat Med, B-2650 Edegem, Belgium
关键词
Poly(I:C); Poly-ICLC; Cancer vaccine; Adjuvant; TLR; Anti-tumor immunity; TOLL-LIKE RECEPTOR-3; POLYRIBOINOSINIC-POLYRIBOCYTIDYLIC ACID; T-CELL RESPONSES; NK CELLS; POLYCYTIDYLIC ACID; DENDRITIC CELLS; PHASE-I; OVARIAN-CANCER; L-LYSINE; COMBINED IMMUNIZATION;
D O I
10.1016/j.pharmthera.2014.09.010
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Although cancer vaccination has yielded promising results in patients, the objective response rates are low. The right choice of adjuvant might improve the efficacy. Here, we review the biological rationale, as well as the preclinical and clinical results of polyinosinic:polycytidylic acid and its derivative poly-ICLC as cancer vaccine adjuvants. These synthetic immunological danger signals enhanced vaccine-induced anti-tumor immune responses and contributed to tumor elimination in animal tumor models and patients. Supported by these results, poly-ICLC-containing cancer vaccines are currently extensively studied in the ongoing trials, making it highly plausible that poly-ICLC will be part of the future approved cancer immunotherapies. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:120 / 131
页数:12
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