Department of Internal Diseases, Pneumonology and Allergology, Medical University of Warsaw, Warsaw, Poland.
Transl Lung Cancer Res. 2015 Apr;4(2):177-90. doi: 10.3978/j.issn.2218-6751.2015.01.11.
Over a hundred years after the first description of this disease, lung cancer represents one of the major challenges in oncology. Radical treatment cannot be introduced in more than 70% of cases and overall survival rate does not exceed 15%. The immunosurveillance of lung cancer may be effective in early oncogenesis but is inhibited in the course of developing a clinically detectable tumor. Very low and heterogonous antigenicity of lung cancer cells leads to passive escape from anti-cancer immune defense. The cytotoxic lymphocytes (CTLs) that play a main role in the anticancer response are actively suppressed in the tumor environment and following regulatory mechanisms inhibit the recognition of tumor antigens by antigen presenting cells. The population of regulatory T cells (Tregs) is augmented and the expression of transcription factor-Foxp3 is markedly increased on tumor cells and tumor infiltrating lymphocytes (TIL). It is accomplished by M2 macrophage polarization, the activity of myeloid derived suppressor cells (MDSCs) and a significantly elevated concentration of cytokines: transforming growth factor beta (TGFβ) and IL-10 in the tumor microenvironment. Very active suppression of immune protection is the predominant role of the programmed death 1 (PD-1)-PD-L1 pathway. The blockage of this pathway was found to be an effective treatment approach; therefore the monoclonal antibodies are being intensively investigated in lung cancer patients. Cytotoxic T lymphocyte antigen-4 (CTLA-4) is the molecule capable of inhibiting the activation signal. The antibody anti-CTLA-4 improves CTLs function in solid tumors and lung cancer patients may benefit from use of this agent. The second way in lung cancer immunotherapy is production of anti-cancer vaccines using recognized cancer antigens: MAGE-A3, membrane associated glycoprotein (MUC-1), and EGF. It was recently shown in ongoing clinical trials that combined therapies: immune- and chemotherapy, radiotherapy or targeted therapy seem to be effective. Immunotherapy in lung cancer has an individual character-there is a need to assess the patient's immune status prior to implementation of immunomodulating therapy.
尽管在这种疾病首次被描述后的一百多年后,肺癌仍然是肿瘤学领域的主要挑战之一。激进的治疗方法不能应用于超过 70%的病例,整体存活率不超过 15%。肺癌的免疫监视可能在肿瘤发生的早期有效,但在发展为临床可检测肿瘤的过程中受到抑制。肺癌细胞的抗原性极低且异质性,导致其被动逃避抗癌免疫防御。在抗癌反应中起主要作用的细胞毒性 T 淋巴细胞(CTL)在肿瘤环境中被积极抑制,而以下调节机制抑制了抗原呈递细胞对肿瘤抗原的识别。调节性 T 细胞(Tregs)的数量增加,肿瘤细胞和肿瘤浸润淋巴细胞(TIL)上转录因子 Foxp3 的表达明显增加。这是通过 M2 巨噬细胞极化、髓源性抑制细胞(MDSC)的活性以及肿瘤微环境中转化生长因子β(TGFβ)和白细胞介素 10(IL-10)的浓度显著升高来实现的。在肿瘤微环境中,非常活跃的免疫保护抑制是程序性死亡 1(PD-1)-PD-L1 通路的主要作用。阻断该通路被发现是一种有效的治疗方法;因此,单克隆抗体在肺癌患者中正在被深入研究。细胞毒性 T 淋巴细胞抗原 4(CTLA-4)是能够抑制激活信号的分子。抗 CTLA-4 抗体可改善 CTLs 在实体瘤和肺癌患者中的功能,使这些患者受益于该药物的使用。肺癌免疫治疗的第二种方法是使用公认的癌症抗原生产抗癌疫苗:MAGE-A3、膜相关糖蛋白(MUC-1)和 EGF。最近在正在进行的临床试验中表明,联合治疗:免疫和化疗、放疗或靶向治疗似乎是有效的。肺癌的免疫治疗具有个体特征-在实施免疫调节治疗之前,需要评估患者的免疫状态。