| Literature DB >> 29438713 |
Wangqian Zhang1, Shuning Wang1, Jintao Gu1, Yuan Gao1, Zhaowei Wang1, Kuo Zhang1, Nan Mu1, Tonglie Huang1, Weina Li1, Qiang Hao1, Xiaochang Xue1, Wei Zhang1, Yingqi Zhang1, Cun Zhang2.
Abstract
Immunotherapy is gathering momentum as a kind of important therapy for cancer patients. However, monotherapies have limited efficacy in improving outcomes and benefit only in a small subset of patients. Combination therapies targeting multiple pathways often can augment an immune response to improve survival further. Here, the tumoricidal effects of the dual hPD-L1(human programmed cell death ligand 1) vaccination/HER2(human epidermal growth factor receptor 2) gene vaccination immunotherapy against the established HER2-expressed cancers were observed. Animals treated with combination therapy using hPD-L1 vaccine and HER2 gene vaccine had significantly improved survival in a mammary carcinoma model. We observed an increase in tumor growth inhibition following treatment. The percentage of the tumor-free mice (%) was much higher in the combined PD-L1/HER2 group. Furthermore, under the tumor-burden condition, hPD-L1 vaccine enhanced humoral immunity of HER2 gene vaccine. And the combination treatment increased the IFN-γ-producing effector T cells. Additionally, splenocytes from the combined PD-L1/HER2 group immunized mice possessed higher CTL activity. Notably, vaccination with combination therapy induced a significant decrease in the percentage of CD4+CD25+ Treg cells. Collectively, these data demonstrate that PD-L1/HER2 gene vaccine combination therapy synergistically generates marked tumoricidal effects against established HER2-expressing cancers.Entities:
Keywords: CD4(+) Foxp3(+) regulatory T cells; HER2; Immune evasion; PD-L1; Vaccine
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Year: 2018 PMID: 29438713 DOI: 10.1016/j.bbrc.2018.02.092
Source DB: PubMed Journal: Biochem Biophys Res Commun ISSN: 0006-291X Impact factor: 3.575