Yoshizaki Shinji, Nishi Mayuko, Kondo Asami, Kojima Yoshitsugu, Yamamoto Naoki, Ryo Akihide
Department of Microbiology, Yokohama City University Graduate School of Medicine Yokohama, Kanagawa, Japan.
Front Microbiol. 2011 Feb 22;2:27. doi: 10.3389/fmicb.2011.00004. eCollection 2011.
Induced pluripotent stem cells (iPSCs) are artificially derived from somatic cells that have been transduced with defined reprogramming factors. A previous report has indicated the possibility of using iPSCs as an immune stimulator to generate antigen-specific immunity. In our current study, we have investigated whether human iPSCs (hiPSCs) have the ability to enhance specific immune response against a human immunodeficiency virus type 1 (HIV-1) antigen in a xenogenic mouse model. Our results show that BALB/c mice immunized with hiPSCs transduced with an adenoviral vector encoding HIV-1 gp160 exhibited prominent antigen-specific cellular immune responses. We further found that pre-treatment of hiPSCs with ionizing radiation promotes the secretion of pro-inflammatory cytokines such as interleukin-1 alpha (IL-1α), IL-12, and IL-18. These cytokines might promote the activation of antigen-presenting cells and the effective induction of cellular immunity. Our present findings thus demonstrate that a hiPSCs-based vaccine has the potential to generate cellular immunity against viral antigens such as HIV-1 gp160 in a xenogenic condition.
诱导多能干细胞(iPSC)是通过用特定重编程因子转导的体细胞人工衍生而来的。先前的一份报告表明,有可能将iPSC用作免疫刺激剂来产生抗原特异性免疫。在我们目前的研究中,我们调查了人类iPSC(hiPSC)在异种小鼠模型中是否有能力增强针对1型人类免疫缺陷病毒(HIV-1)抗原的特异性免疫反应。我们的结果表明,用编码HIV-1 gp160的腺病毒载体转导的hiPSC免疫的BALB/c小鼠表现出显著的抗原特异性细胞免疫反应。我们进一步发现,用电离辐射预处理hiPSC可促进促炎细胞因子如白细胞介素-1α(IL-1α)、IL-12和IL-18的分泌。这些细胞因子可能促进抗原呈递细胞的活化和细胞免疫的有效诱导。因此,我们目前的研究结果表明,基于hiPSC的疫苗有可能在异种条件下产生针对病毒抗原如HIV-1 gp160的细胞免疫。