假基因RNA在抗肿瘤和抗病毒免疫中的新作用

Yoo Jane Han, Michaela U. Gack, O. Olopade
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摘要

肿瘤免疫和免疫疗法在各种恶性肿瘤的治疗策略中变得越来越重要,包括晚期癌症三阴性[1,2]。尽管免疫疗法已被证明是有效的,但患者的反应率差异很大,只有一小部分患者对治疗有良好反应[3]。癌症免疫疗法的疗效似乎取决于宿主免疫系统识别和消除癌症细胞[4]。越来越多的证据表明,宿主抗肿瘤免疫反应的存在与许多癌症的良好患者预后之间存在正相关[5-8]。例如,肿瘤微环境中肿瘤浸润性淋巴细胞(TIL)密度高的肿瘤更有可能对免疫检查点抑制剂产生反应,而TIL低或无TIL的肿瘤则不太可能对抑制剂产生反应[9-11]。因此,将无反应的肿瘤转化为有反应的肿瘤,从而促进抗肿瘤免疫的干预措施具有巨大的治疗潜力。
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Emerging Roles of Pseudogene RNAs in Antitumor and Antiviral Immunity
Tumor immunity and immunotherapy have become increasingly important in treatment strategies for a variety of malignancies including advanced triple negative breast cancer [1,2]. Although immunotherapy has been shown to be effective, patient response rates vary significantly and only a small fraction of patients respond favorably to the treatment [3]. The efficacy of cancer immunotherapy appears to depend on the host immune system recognizing and eliminating cancer cells [4]. Increasing evidence demonstrates a positive correlation between the presence of host antitumor immune responses and favorable patient outcomes for many cancers [5-8]. As an example, tumors with a high density of tumor-infiltrating lymphoid cells (TILs) in the tumor microenvironment are more likely to respond to immune checkpoint inhibitors, whereas those with low or no TILs are less likely to respond to the inhibitors [9-11]. Thus, interventions that render nonresponding tumors to become responding tumors and hence promote antitumor immunity bear tremendous therapeutic potential.
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