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

机译:癌症中的免疫疗法:肿瘤与免疫系统之间的斗争;你赢了一些,你输了一些

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摘要

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.
机译:癌症免疫疗法已成为一种治疗方式,主要是由于免疫应答调节的发现,包括关闭免疫应答的机制。免疫原性皮肤黑色素瘤是用于治疗性免疫疗法研究的典型模型。单克隆抗体(mAbs)的“被动”免疫疗法已超过抗肿瘤疫苗的“主动”免疫疗法,最近在临床实践中引入了拮抗关闭反应的mAb。尽管取得了这些最近的成功,但仍然存在许多未解决的实践和理论问题。消除肿瘤细胞的淋巴细胞的身份尤其未知,白细胞进入肿瘤,内皮细胞以什么顺序,如何执行任务的淋巴细胞的身份。可用于确定在哪些肿瘤中免疫反应可能足以根除肿瘤的大小和位置参数尚不清楚。迄今为止,免疫疗法比原发性脑部肿瘤和脑转移瘤更有效地治疗位于中枢神经系统外的实体和血液肿瘤。与mAb的最新进展相比,抗肿瘤疫苗的开发一直滞后。导致这种滞后的原因部分是必须针对的抗原才能实现显着的临床反应,尤其是在黑色素瘤(突变最多的肿瘤之一)中。进一步阻碍疫苗接种结果的事实是,免疫系统清除肿瘤的原因是不同生长速率的肿瘤之间的竞争以及适应性免疫反应的发展相对缓慢。应当增强免疫反应的天然能力或靶向化疗以减缓肿瘤的发展。最后,必须完善用于分析患者对免疫疗法反应的标准,并且必须更好地定义可以从该方法中受益最大的患者人群。

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