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癌症免疫疗法:肿瘤与免疫系统之间的较量;有得有失。

Immunotherapy in Cancer: A Combat between Tumors and the Immune System; You Win Some, You Lose Some.

作者信息

Madorsky Rowdo Florencia Paula, Baron Antonela, Urrutia Mariela, Mordoh José

机构信息

Laboratorio de Cancerología, Fundación Instituto Leloir - IIBBA-CONICET , Buenos Aires , Argentina.

Laboratorio de Cancerología, Fundación Instituto Leloir - IIBBA-CONICET , Buenos Aires , Argentina ; Centro de Investigaciones Oncológicas, Fundación Cáncer and Instituto Alexander Fleming , Buenos Aires , Argentina.

出版信息

Front Immunol. 2015 Mar 26;6:127. doi: 10.3389/fimmu.2015.00127. eCollection 2015.

Abstract

Cancer immunotherapy has emerged as a treatment modality, mainly as the result of discoveries in the immune response regulation, including mechanisms that turn off immune responses. Immunogenic cutaneous melanoma is a canonical model for therapeutic immunotherapy studies. "Passive" immunotherapy with monoclonal antibodies (mAbs) has outpaced "active" immunotherapy with anti-tumor vaccines, and mAbs that antagonize the off responses have been recently introduced in clinical practice. Despite these recent successes, many unresolved practical and theoretical questions remain. Notably unknown are the identity of the lymphocytes that eliminate tumor cells, which white cells enter into tumors, through which endothelium, in what order, and how they perform their task. The parameters of size and location that could be used to determine in which tumors the immune response may be sufficient to eradicate the tumor are yet unknown. Immunotherapy has been so far more efficient to treat solid and hematologic tumors located outside the central nervous system, than primary brain tumors and brain metastases. In contrast to recent advances with mAbs, anti-tumor vaccine development has been lagging behind. The multiplicity of antigens that must be targeted to achieve significant clinical response is partially responsible for this lag, especially in melanoma, one of the most mutated tumors. Further hampering vaccination results is the fact that tumor elimination by the immune system is the result of a race between tumors with different growth rates and the relatively slow development of the adaptive immune response. The enhancement of the native arm of the immune response or the administration of targeted chemotherapy to slow tumor development, are approaches that should be studied. Finally, criteria used to analyze patient response to immunotherapeutic treatments must be perfected, and the patient populations that could benefit the most from this approach must be better defined.

摘要

癌症免疫疗法已成为一种治疗方式,这主要归功于免疫反应调节方面的发现,包括那些关闭免疫反应的机制。免疫原性皮肤黑色素瘤是治疗性免疫疗法研究的典型模型。单克隆抗体(mAb)的“被动”免疫疗法已超过抗肿瘤疫苗的“主动”免疫疗法,并且拮抗免疫反应关闭的单克隆抗体最近已应用于临床实践。尽管最近取得了这些成功,但许多尚未解决的实际和理论问题仍然存在。尤其未知的是消除肿瘤细胞的淋巴细胞的身份、哪些白细胞进入肿瘤、通过哪一层内皮、以何种顺序以及它们如何执行任务。可用于确定哪些肿瘤中的免疫反应足以根除肿瘤的大小和位置参数仍然未知。到目前为止,免疫疗法治疗中枢神经系统以外的实体瘤和血液系统肿瘤比原发性脑肿瘤和脑转移瘤更有效。与单克隆抗体的最新进展形成对比的是,抗肿瘤疫苗的开发一直滞后。为实现显著临床反应而必须靶向的多种抗原是造成这种滞后的部分原因,尤其是在黑色素瘤这种突变最多的肿瘤之一中。进一步阻碍疫苗接种效果的是,免疫系统消除肿瘤是不同生长速率的肿瘤与适应性免疫反应相对缓慢发展之间竞争的结果。增强免疫反应的天然分支或给予靶向化疗以减缓肿瘤发展,是应该研究的方法。最后,用于分析患者对免疫治疗反应的标准必须完善,并且最能从这种方法中受益的患者群体必须得到更好的界定。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1853/4374472/d57d665d77da/fimmu-06-00127-g001.jpg

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