Titzer S, Christensen O, Manzke O, Tesch H, Wolf J, Emmerich B, Carsten C, Diehl V, Bohlen H
Department of Internal Medicine I, University of Cologne, Joseph-Stelzmannstr. 9, 50924 Cologne, Germany.
Br J Haematol. 2000 Mar;108(4):805-16. doi: 10.1046/j.1365-2141.2000.01958.x.
Multiple myeloma (MM) is characterized by a clonal proliferation of malignant plasma cells in the bone marrow secreting a monoclonal immunoglobulin (paraprotein) with specific antigenic determinants, the idiotype (Id), which can be regarded as a tumour-associated antigen (TAA). In order to analyse the impact of a dendritic cell (DC)-based vaccine, 11 patients with advanced MM were treated with CD34 stem cell-derived dendritic cells that were pulsed with Id peptides. Subsequently, the patients received three boost immunizations every other week with a combination of Id and granulocyte-macrophage colony-stimulating factor (GM-CSF) (nine patients) or with Id peptide-pulsed dendritic cells again (two patients). The treatment was well tolerated with no side-effects. The present clinical study was a proof of concept analysis of dendritic cell-based vaccines in MM. The capacity of the dendritic cells to activate idiotype-specific T cells was verified by in vitro stimulation experiments before the vaccination therapy. Immunological effects of the Id vaccination were analysed by monitoring changes in anti-idiotype antibody titres and idiotype-specific T-cell activity. After vaccination, three out of 10 analysed patients showed increased anti-idiotype antibody serum titres, indicating the induction of an idiotype-specific humoral immune response. The idiotype-specific T-cell response analysed by ELISpot was increased in four out of 10 analysed patients after vaccination, and one patient had a decreased plasma cell infiltration in the bone marrow. In conclusion, five out of 11 patients showed a biological response after vaccination. Thus, our data indicate that immunotherapy with Id-pulsed DCs in MM patients is feasible and safe. DC generated from CD34+ progenitor cells can serve as a natural adjuvant for the induction of clinically relevant humoral and cellular idiotype-specific immune responses in patients suffering from advanced MM.
多发性骨髓瘤(MM)的特征是骨髓中恶性浆细胞的克隆性增殖,这些浆细胞分泌具有特定抗原决定簇(独特型,Id)的单克隆免疫球蛋白(副蛋白),该独特型可被视为肿瘤相关抗原(TAA)。为了分析基于树突状细胞(DC)的疫苗的影响,11例晚期MM患者接受了用Id肽脉冲处理的CD34干细胞衍生的树突状细胞治疗。随后,患者每隔一周接受三次加强免疫,分别使用Id与粒细胞-巨噬细胞集落刺激因子(GM-CSF)联合(9例患者)或再次使用Id肽脉冲处理的树突状细胞(2例患者)。该治疗耐受性良好,无副作用。本临床研究是对MM中基于树突状细胞的疫苗的概念验证分析。在疫苗接种治疗前,通过体外刺激实验验证了树突状细胞激活独特型特异性T细胞的能力。通过监测抗独特型抗体滴度和独特型特异性T细胞活性的变化来分析Id疫苗接种的免疫效果。接种疫苗后,10例接受分析的患者中有3例抗独特型抗体血清滴度升高,表明诱导了独特型特异性体液免疫反应。通过ELISpot分析的独特型特异性T细胞反应在10例接受分析的患者中有4例在接种疫苗后增加,并且1例患者骨髓中的浆细胞浸润减少。总之,11例患者中有5例在接种疫苗后出现生物学反应。因此,我们的数据表明,MM患者中用Id脉冲DC进行免疫治疗是可行且安全的。从CD34 +祖细胞产生的DC可作为天然佐剂,用于在晚期MM患者中诱导临床相关的体液和细胞独特型特异性免疫反应。