Esslinger Christoph, Chapatte Laurence, Finke Daniela, Miconnet Isabelle, Guillaume Philippe, Lévy Frédéric, MacDonald H Robson
Ludwig Institute for Cancer Research, Lausanne Branch, University of Lausanne, Epalinges, Switzerland.
J Clin Invest. 2003 Jun;111(11):1673-81. doi: 10.1172/JCI17098.
The present study evaluates the potential of third-generation lentivirus vectors with respect to their use as in vivo-administered T cell vaccines. We demonstrate that lentivector injection into the footpad of mice transduces DCs that appear in the draining lymph node and in the spleen. In addition, a lentivector vaccine bearing a T cell antigen induced very strong systemic antigen-specific cytotoxic T lymphocyte (CTL) responses in mice. Comparative vaccination performed in two different antigen models demonstrated that in vivo administration of lentivector was superior to transfer of transduced DCs or peptide/adjuvant vaccination in terms of both amplitude and longevity of the CTL response. Our data suggest that a decisive factor for efficient T cell priming by lentivector might be the targeting of DCs in situ and their subsequent migration to secondary lymphoid organs. The combination of performance, ease of application, and absence of pre-existing immunity in humans make lentivector-based vaccines an attractive candidate for cancer immunotherapy.
本研究评估了第三代慢病毒载体作为体内给药的T细胞疫苗的潜力。我们证明,将慢病毒载体注射到小鼠足垫可转导引流淋巴结和脾脏中出现的树突状细胞(DCs)。此外,携带T细胞抗原的慢病毒载体疫苗在小鼠中诱导了非常强烈的全身性抗原特异性细胞毒性T淋巴细胞(CTL)反应。在两种不同抗原模型中进行的比较疫苗接种表明,就CTL反应的幅度和持续时间而言,体内给予慢病毒载体优于转导的DCs转移或肽/佐剂疫苗接种。我们的数据表明,慢病毒载体有效启动T细胞的一个决定性因素可能是原位靶向DCs及其随后迁移至次级淋巴器官。慢病毒载体疫苗的性能、易于应用以及人类不存在预先存在的免疫等因素使其成为癌症免疫治疗的有吸引力的候选者。