Hersey Peter
Sydney and Newcastle Melanoma Units, Newcastle, New South Wales, Australia.
Asia Pac J Clin Oncol. 2010 Mar;6 Suppl 1:S2-8. doi: 10.1111/j.1743-7563.2010.01269.x.
A number of studies have shown that melanoma is a particularly immunogenic tumour, at least in the early stages of its development. A range of clinical phenomena also suggests that immune responses play an important role in the natural history of the disease, including the total or partial regression of primary melanomas associated with lymphoid infiltrates. Immunization with a variety of vaccines can increase immune responses to melanoma, but whether this is of therapeutic benefit remains unclear. Various trials of melanoma vaccines have shown benefits but their significance has been marginal to date. Two trials have actually shown an adverse effect on survival. Stimulation of immune responses by blocking down-regulatory mechanisms in the immune system has evolved as a potential therapeutic approach following studies that have shown that immune responses are finely regulated by a series of receptors and ligands on lymphocytes and antigen presenting cells. The best studied of these approaches is the blockade of the cytotoxic T-lymphocyte antigen 4 receptor on T cells, which allows the generation of more effector cells for longer periods. Agents targeting this receptor have shown promising results and continue to be studied.
多项研究表明,黑色素瘤是一种具有高度免疫原性的肿瘤,至少在其发展的早期阶段如此。一系列临床现象也表明,免疫反应在该疾病的自然病程中起着重要作用,包括与淋巴细胞浸润相关的原发性黑色素瘤的完全或部分消退。用多种疫苗进行免疫接种可增强对黑色素瘤的免疫反应,但这是否具有治疗益处仍不清楚。黑色素瘤疫苗的各种试验已显示出益处,但迄今为止其意义不大。两项试验实际上显示对生存有不利影响。在研究表明免疫反应受到淋巴细胞和抗原呈递细胞上一系列受体和配体的精细调节之后,通过阻断免疫系统中的下调调节机制来刺激免疫反应已发展成为一种潜在的治疗方法。这些方法中研究得最充分的是阻断T细胞上的细胞毒性T淋巴细胞抗原4受体,这使得能够在更长时间内产生更多效应细胞。针对该受体的药物已显示出有希望的结果,并仍在继续研究。