Martin Lluesma Silvia, Graciotti Michele, Chiang Cheryl Lai-Lai, Kandalaft Lana E
Center of Experimental Therapeutics, Ludwig Center for Cancer Research, Department of Oncology, University of Lausanne, Lausanne 1011, Switzerland.
Vaccine development laboratory, Ludwig Center for Cancer Research, Lausanne 1011, Switzerland.
Vaccines (Basel). 2018 Nov 23;6(4):79. doi: 10.3390/vaccines6040079.
Although different types of therapeutic vaccines against established cancerous lesions in various indications have been developed since the 1990s, their clinical benefit is still very limited. This observed lack of effectiveness in cancer eradication may be partially due to the often deficient immunocompetent status of cancer patients, which may facilitate tumor development by different mechanisms, including immune evasion. The most frequently used cellular vehicle in clinical trials are dendritic cells (DCs), thanks to their crucial role in initiating and directing immune responses. Viable vaccination options using DCs are available, with a positive toxicity profile. For these reasons, despite their limited therapeutic outcomes, DC vaccination is currently considered an additional immunotherapeutic option that still needs to be further explored. In this review, we propose potential actions aimed at improving DC vaccine efficacy by counteracting the detrimental mechanisms recognized to date and implicated in establishing a poor immunocompetent status in cancer patients.
自20世纪90年代以来,尽管已经开发出针对各种适应症中已形成的癌性病变的不同类型治疗性疫苗,但其临床益处仍然非常有限。在根除癌症方面观察到的这种有效性不足可能部分归因于癌症患者通常免疫功能低下的状态,这可能通过包括免疫逃逸在内的不同机制促进肿瘤发展。临床试验中最常用的细胞载体是树突状细胞(DC),这得益于它们在启动和指导免疫反应中的关键作用。使用DC的可行疫苗接种方案是可用的,且毒性特征良好。由于这些原因,尽管其治疗效果有限,但DC疫苗接种目前仍被视为一种仍需进一步探索的额外免疫治疗选择。在本综述中,我们提出了一些潜在的措施,旨在通过对抗迄今已认识到的、与癌症患者免疫功能低下状态相关的有害机制来提高DC疫苗的疗效。