Department of Medicine, Division of Infectious Diseases, New York University Langone Medical Center, New York, NY 10016, USA; Department of Microbiology, New York University Langone Medical Center, New York, NY 10016, USA.
Department of Medicine, Division of Infectious Diseases, New York University Langone Medical Center, New York, NY 10016, USA.
Mol Ther. 2020 Aug 5;28(8):1795-1805. doi: 10.1016/j.ymthe.2020.05.018. Epub 2020 May 20.
Dendritic cell vaccines are a promising strategy for the treatment of cancer and infectious diseases but have met with mixed success. We report on a lentiviral vector-based dendritic cell vaccine strategy that generates a cluster of differentiation 8 (CD8) T cell response that is much stronger than that achieved by standard peptide-pulsing approaches. The strategy was tested in the mouse lymphocytic choriomeningitis virus (LCMV) model. Bone marrow-derived dendritic cells from SAMHD1 knockout mice were transduced with a lentiviral vector expressing the GP33 major-histocompatibility-complex (MHC)-class-I-restricted peptide epitope and CD40 ligand (CD40L) and injected into wild-type mice. The mice were highly protected against acute and chronic variant CL-13 LCMVs, resulting in a 100-fold greater decrease than that achieved with peptide epitope-pulsed dendritic cells. Inclusion of an MHC-class-II-restricted epitope in the lentiviral vector further increased the CD8 T cell response and resulted in antigen-specific CD8 T cells that exhibited a phenotype associated with functional cytotoxic T cells. The vaccination synergized with checkpoint blockade to reduce the viral load of mice chronically infected with CL-13 to an undetectable level. The strategy improves upon current dendritic cell vaccine strategies; is applicable to the treatment of disease, including AIDS and cancer; and supports the utility of Vpx-containing vectors.
树突状细胞疫苗是治疗癌症和传染病的一种很有前途的策略,但取得的效果喜忧参半。我们报告了一种基于慢病毒载体的树突状细胞疫苗策略,该策略可产生比标准肽脉冲方法更强的簇分化 8(CD8)T 细胞反应。该策略在小鼠淋巴细胞脉络丛脑膜炎病毒(LCMV)模型中进行了测试。用表达 GP33 主要组织相容性复合物(MHC)-I 限制性肽表位和 CD40 配体(CD40L)的慢病毒载体转导 SAMHD1 敲除小鼠的骨髓来源树突状细胞,并注射到野生型小鼠中。这些小鼠对急性和慢性变异 CL-13 LCMV 高度保护,导致病毒载量下降 100 倍,而肽表位脉冲树突状细胞的下降幅度则小得多。在慢病毒载体中加入 MHC-II 限制性表位进一步增强了 CD8 T 细胞反应,并产生了具有与功能细胞毒性 T 细胞相关表型的抗原特异性 CD8 T 细胞。该疫苗与检查点阻断协同作用,可将慢性感染 CL-13 的小鼠的病毒载量降低至无法检测的水平。该策略改进了现有的树突状细胞疫苗策略;可应用于治疗疾病,包括艾滋病和癌症;并支持含有 Vpx 的载体的实用性。