Shirwan Haval, Sharma Rajesh K, Srivastava Abhishek K, Yolcu Esma S
Institute for Cellular Therapeutics; Department of Microbiology and Immunology; University of Louisville; Louisville, KY USA ; James Graham Brown Cancer Center; University of Louisville; Louisville, KY USA.
Oncoimmunology. 2013 Apr 1;2(4):e23440. doi: 10.4161/onci.23440.
Tumor-associated antigen (TAA) subunit-based vaccines constitute promising tools for the anticancer immunotherapy. Given the weak antigenic nature of most TAAs, however, the efficacy of TAA-based vaccines requires adjuvants exerting potent immunostimulatory functions. Co-stimulatory members of the tumor necrosis factor ligand (TNFL) family may be used in this sense due to their pleiotropic and robust effects on cells of innate, adaptive and regulatory immune responses.
基于肿瘤相关抗原(TAA)亚基的疫苗是抗癌免疫治疗的有前景的工具。然而,鉴于大多数TAA的抗原性较弱,基于TAA的疫苗的疗效需要具有强大免疫刺激功能的佐剂。肿瘤坏死因子配体(TNFL)家族的共刺激成员由于其对先天性、适应性和调节性免疫反应细胞具有多效性和强大作用,因此可用于此目的。