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本文引用的文献

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Programmed death-1 blockade enhances the antitumor effects of peptide vaccine-induced peptide-specific cytotoxic T lymphocytes.程序性死亡-1阻断增强肽疫苗诱导的肽特异性细胞毒性T淋巴细胞的抗肿瘤作用。
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Efficacy and toxicity management of 19-28z CAR T cell therapy in B cell acute lymphoblastic leukemia.19-28z嵌合抗原受体T细胞疗法治疗B细胞急性淋巴细胞白血病的疗效及毒性管理
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Breakthrough of the year 2013. Cancer immunotherapy.2013年度重大突破。癌症免疫疗法。
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Donor-derived CD19-targeted T cells cause regression of malignancy persisting after allogeneic hematopoietic stem cell transplantation.供者来源的 CD19 靶向 T 细胞可导致异基因造血干细胞移植后持续存在的恶性肿瘤消退。
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Human CD14+ CTLA-4+ regulatory dendritic cells suppress T-cell response by cytotoxic T-lymphocyte antigen-4-dependent IL-10 and indoleamine-2,3-dioxygenase production in hepatocellular carcinoma.人源 CD14+ CTLA-4+ 调节性树突状细胞通过细胞毒性 T 淋巴细胞抗原-4 依赖性白细胞介素-10 和吲哚胺 2,3-双加氧酶的产生来抑制肝癌中的 T 细胞反应。
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Combination of radiofrequency ablation and sequential cellular immunotherapy improves progression-free survival for patients with hepatocellular carcinoma.射频消融联合序贯细胞免疫治疗改善肝癌患者无进展生存期。
Int J Cancer. 2014 Jan 15;134(2):342-51. doi: 10.1002/ijc.28372. Epub 2013 Aug 5.
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Increase in CD14+HLA-DR -/low myeloid-derived suppressor cells in hepatocellular carcinoma patients and its impact on prognosis.肝癌患者中 CD14+HLA-DR-/low 髓源抑制细胞的增加及其对预后的影响。
Cancer Immunol Immunother. 2013 Aug;62(8):1421-30. doi: 10.1007/s00262-013-1447-1. Epub 2013 Jun 14.
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Nivolumab plus ipilimumab in advanced melanoma.纳武利尤单抗联合伊匹单抗治疗晚期黑色素瘤。
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Targeting MAPK pathway in melanoma therapy.靶向丝裂原活化蛋白激酶(MAPK)通路用于黑色素瘤治疗。
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免疫疗法治疗肝细胞癌的潜力。

Potentiality of immunotherapy against hepatocellular carcinoma.

作者信息

Tsuchiya Nobuhiro, Sawada Yu, Endo Itaru, Uemura Yasushi, Nakatsura Tetsuya

机构信息

Nobuhiro Tsuchiya, Yasushi Uemura, Tetsuya Nakatsura, Division of Cancer Immunotherapy, Exploratory Oncology Research and Clinical Trial Center, National Cancer Center, Kashiwa 277-8577, Japan.

出版信息

World J Gastroenterol. 2015 Sep 28;21(36):10314-26. doi: 10.3748/wjg.v21.i36.10314.

DOI:10.3748/wjg.v21.i36.10314
PMID:26420958
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4579878/
Abstract

Hepatocellular carcinoma (HCC), the predominant form of primary liver cancer, is the fifth most common cancer worldwide and the second leading cause of cancer-related death. Despite the high incidence, treatment options remain limited for advanced HCC, and as a result prognosis continues to be poor. Current therapeutic options, surgery, chemotherapy and radiotherapy, have only modest efficacy. New treatment modalities to prolong survival and to minimize the risk of adverse response are desperately needed for patients with advanced HCC. Tumor immunotherapy is a promising, novel treatment strategy that may lead to improvements in both treatment-associated toxicity and outcome. The strategies have developed in part through genomic studies that have yielded candidate target molecules and in part through basic biology studies that have defined the pathways and cell types regulating immune response. Here, we summarize the various types of HCC immunotherapy and argue that the new-found field of HCC immunotherapy might provide critical advantages in the effort to improve prognosis of patients with advanced HCC. Already several immunotherapies, such as tumor-associated antigen therapy, immune checkpoint inhibitors and cell transfer immunotherapy, have demonstrated safety and feasibility in HCC patients. Unfortunately, immunotherapy currently has low efficacy in advanced stage HCC patients; overcoming this challenge will place immunotherapy at the forefront of HCC treatment, possibly in the near future.

摘要

肝细胞癌(HCC)是原发性肝癌的主要形式,是全球第五大常见癌症,也是癌症相关死亡的第二大主要原因。尽管发病率很高,但晚期HCC的治疗选择仍然有限,因此预后仍然很差。目前的治疗选择,手术、化疗和放疗,疗效都很一般。对于晚期HCC患者,迫切需要新的治疗方法来延长生存期并将不良反应风险降至最低。肿瘤免疫疗法是一种有前景的新型治疗策略,可能会改善治疗相关毒性和治疗结果。这些策略部分是通过产生候选靶分子的基因组研究发展而来,部分是通过定义调节免疫反应的途径和细胞类型的基础生物学研究发展而来。在这里,我们总结了HCC免疫疗法的各种类型,并认为新发现的HCC免疫疗法领域可能会在改善晚期HCC患者预后的努力中提供关键优势。已经有几种免疫疗法,如肿瘤相关抗原疗法、免疫检查点抑制剂和细胞转移免疫疗法,在HCC患者中证明了安全性和可行性。不幸的是,免疫疗法目前在晚期HCC患者中的疗效较低;克服这一挑战将使免疫疗法在不久的将来可能处于HCC治疗的前沿。