首页> 外文期刊>British Journal of Haematology >Optimizing dendritic cell-based immunotherapy in multiple myeloma: intranodal injections of idiotype-pulsed CD40 ligand-matured vaccines led to induction of type-1 and cytotoxic T-cell immune responses in patients
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Optimizing dendritic cell-based immunotherapy in multiple myeloma: intranodal injections of idiotype-pulsed CD40 ligand-matured vaccines led to induction of type-1 and cytotoxic T-cell immune responses in patients

机译:在多发性骨髓瘤中优化基于树突细胞的免疫疗法:结节内注射独特型脉冲CD40配体成熟的疫苗可诱导患者诱发1型和细胞毒性T细胞免疫反应

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SummaryVaccination with idiotype (Id) protein-pulsed dendritic cells (DCs) has been explored in multiple myeloma and the results have been disappointing. To improve the efficacy of DC vaccination in myeloma, we investigated the use of Id- and keyhole limpet haemocyanin (KLH)-pulsed, CD40 ligand-matured DCs administered intranodally. Nine patients with smouldering or stable myeloma without treatment were enrolled and DC vaccines were administered at weekly intervals for a total of four doses. Following vaccination, all patients mounted Id-specific -interferon T-cell response. Interleukin-4 response was elicited in two, and skin delayed-type hypersensitivity reaction occurred in seven patients. More importantly, Id-specific cytotoxic T-cell responses were also detected in five patients. Most if not all patients mounted a positive T-cell response to KLH following vaccination. At 1-year follow-up, six of the nine patients had stable disease, while three patients had slowly progressive disease even during the vaccination period. At 5-year follow-up, four of the six patients continued with stable disease. No major side effects were noted. In summary, intranodal administration of Id-pulsed CD40 ligand-matured DCs was able to induce Id-specific T and B-cell responses in patients. Current efforts are geared towards breaking tumour-mediated immune suppression and improving clinical efficacy of this immunotherapy.
机译:总结已在多发性骨髓瘤中探索了用独特型(Id)蛋白脉冲树突状细胞(DC)进行的疫苗接种,其结果令人失望。为了提高DC疫苗接种在骨髓瘤中的疗效,我们调查了经IDd和匙孔血蓝蛋白(KLH)脉冲,CD40配体成熟的DC结节内给药的使用。招募了9名未经治疗的闷热或稳定的骨髓瘤患者,并且每周间隔接种DC疫苗,共四剂。接种疫苗后,所有患者均接受Id特异性干扰素T细胞应答。在两次中引起白介素4反应,并且在七名患者中发生了皮肤迟发型超敏反应。更重要的是,在5例患者中也检测到了Id特异性细胞毒性T细胞反应。接种疫苗后,大多数(如果不是全部)患者对KLH呈阳性T细胞反应。在一年的随访中,九名患者中有六名病情稳定,而三名患者即使在疫苗接种期间也进展缓慢。在5年的随访中,六名患者中有四名继续病情稳定。没有发现主要的副作用。总之,对Id脉冲的CD40配体成熟的DC进行节点内给药能够诱导患者产生Id特异性的T细胞和B细胞应答。当前的努力旨在打破肿瘤介导的免疫抑制并提高这种免疫疗法的临床功效。

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