Pyzer Athalia R, Avigan David E, Rosenblatt Jacalyn
a Beth Israel Deaconess Medical Center; Harvard Medical School ; Boston , MA USA.
Hum Vaccin Immunother. 2014;10(11):3125-31. doi: 10.4161/21645515.2014.982993.
The potential for the immune system to target hematological malignancies is demonstrated in the allogeneic transplant setting, where durable responses can be achieved. However, allogeneic transplantation is associated with significant morbidity and mortality related to graft versus host disease. Cancer immunotherapy has the capacity to direct a specific cytotoxic immune response against cancer cells, particularly residual cancer cells, in order to reduce the likelihood of disease relapse in a more targeted and tolerated manner. Ex vivo dendritic cells can be primed in various ways to present tumor associated antigen to the immune system, in the context of co-stimulatory molecules, eliciting a tumor specific cytotoxic response in patients. Several approaches to prime dendritic cells and overcome the immunosuppressive microenvironment have been evaluated in pre-clinical and early clinical trials with promising results. In this review, we summarize the clinical data evaluating dendritic cell based vaccines for the treatment of hematological malignancies.
在同种异体移植环境中,免疫系统针对血液系统恶性肿瘤的潜力得到了证明,在这种环境中可以实现持久的反应。然而,同种异体移植与移植物抗宿主病相关的显著发病率和死亡率有关。癌症免疫疗法有能力针对癌细胞,特别是残留癌细胞,引导特定的细胞毒性免疫反应,以便以更有针对性和耐受性的方式降低疾病复发的可能性。体外树突状细胞可以通过多种方式进行致敏,以便在共刺激分子的背景下向免疫系统呈递肿瘤相关抗原,从而在患者体内引发肿瘤特异性细胞毒性反应。在临床前和早期临床试验中,已经评估了几种致敏树突状细胞和克服免疫抑制微环境的方法,结果很有前景。在这篇综述中,我们总结了评估基于树突状细胞的疫苗治疗血液系统恶性肿瘤的临床数据。