Medical Department III, University Hospital Grosshadern, Ludwig-Maximilians-University, Munich, Germany.
Cell Immunol. 2010;263(1):88-98. doi: 10.1016/j.cellimm.2010.03.003. Epub 2010 Mar 6.
Animal-models are the basis of DC-based human immunotherapies. We describe the standardization of a canine-DC-generation protocol using different cytokines and characterize the quality and functional repertoire of the obtained canine-DCs. DCs were generated from healthy dog-PBMCs under serum-free and serum-containing conditions. DC-quality and -quantity was determined by FACS studying the expression-profiles of DC-/costimulatory- and maturation-antigens before/after culture with canine and human monoclonal-antibodies (cmabs/hmabs). Individual DCAgs-(DC-antigens)-expression-profiles were found before and after culture depending on the agents' mode-of-action. With at least one of three serum-free methods (Ca-Ionophore, Picibanil, Cytokines) sufficient DC-amounts were generated. So, canine-DCs can be regularly generated under serum-free conditions and hmabs additionally to cmabs qualify for staining/quantification of canine-cells/DCs. The canine-DCs were functional, shown by T-cell-activation, -proliferation and antigen-specific CTL-responses. In summary, successful, quantitative DC-generation is possible with serum-free methods. DC-based T-cell-vaccination-strategies evaluated for e.g. AML-patients can be tested in the dog and estimated in clinical studies for DC-vaccination-strategies.
动物模型是基于树突状细胞的人类免疫疗法的基础。我们描述了使用不同细胞因子标准化犬树突状细胞生成方案,并描述了获得的犬树突状细胞的质量和功能谱。在无血清和含血清条件下,从健康犬 PBMC 中生成 DC。通过流式细胞术研究 DC/共刺激和成熟抗原的表达谱,在使用犬和人单克隆抗体(cmabs/hmabs)培养前后,确定 DC 的质量和数量。根据作用方式,在培养前后发现个体 DCAgs(树突状细胞抗原)表达谱。使用至少三种无血清方法(钙离子载体、Picibanil、细胞因子)中的一种,可以产生足够数量的 DC。因此,犬树突状细胞可以在无血清条件下定期生成,并且 hmabs 除了 cmabs 之外,还可以用于染色/定量犬细胞/树突状细胞。犬树突状细胞具有功能,表现在 T 细胞激活、增殖和抗原特异性 CTL 反应。总之,使用无血清方法可以成功地进行定量的 DC 生成。可以在犬中测试评估例如 AML 患者的基于树突状细胞的 T 细胞疫苗接种策略,并在临床研究中评估用于树突状细胞疫苗接种策略的策略。