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应中央军委要求,2022年9月起,《药学实践杂志》将更名为《药学实践与服务》,双月刊,正文96页;2023年1月起,拟出版月刊,正文64页,数据库收录情况与原《药学实践杂志》相同。欢迎作者踊跃投稿!

免疫治疗在肝细胞癌治疗中的进展

郭玲玲 仇金荣

郭玲玲, 仇金荣. 免疫治疗在肝细胞癌治疗中的进展[J]. 药学实践与服务, 2017, 35(4): 362-366. doi: 10.3969/j.issn.1006-0111.2017.04.019
引用本文: 郭玲玲, 仇金荣. 免疫治疗在肝细胞癌治疗中的进展[J]. 药学实践与服务, 2017, 35(4): 362-366. doi: 10.3969/j.issn.1006-0111.2017.04.019
GUO Lingling, QIU Jinrong. Progress in immunotherapy for hepatocellular carcinoma[J]. Journal of Pharmaceutical Practice and Service, 2017, 35(4): 362-366. doi: 10.3969/j.issn.1006-0111.2017.04.019
Citation: GUO Lingling, QIU Jinrong. Progress in immunotherapy for hepatocellular carcinoma[J]. Journal of Pharmaceutical Practice and Service, 2017, 35(4): 362-366. doi: 10.3969/j.issn.1006-0111.2017.04.019

免疫治疗在肝细胞癌治疗中的进展

doi: 10.3969/j.issn.1006-0111.2017.04.019

Progress in immunotherapy for hepatocellular carcinoma

  • 摘要: 肝细胞癌(HCC)是全球发病率和致死率都很高的恶性肿瘤。目前以手术治疗为主的治疗方法远难以达到理想的效果。肿瘤免疫治疗,包括树突状细胞诱导的杀伤细胞(DC-CIK)、肿瘤浸润淋巴细胞(TIL)、嵌合抗原受体T细胞(CAR-T)、免疫检查点阻滞剂(如PD-1阻滞剂、CTL4阻滞剂)等,是近年发展迅速且具有良好前景的肿瘤治疗新方法。本综述着重介绍PD-1阻滞剂、DC-CIK细胞、TIL细胞在治疗肝细胞癌中取得的进展,并对本课题组发明的多能免疫杀伤转基因细胞(PIK)做简要介绍。
  • [1] Torre LA, Bray F, Siegel RL,et al. Global cancer statistics,2012[J]. CA Cancer J Clin,2015,65(2): 87-108.
    [2] Car BI. Hepatocellular carcinoma: current management and future trends[J]. Gastroenterology,2004,127(5 Suppl 1): S218-224.
    [3] Llovet JM, Ricci S, Mazzaferro V,et al. Sorafenib in advanced hepatocellular carcinoma[J]. N Engl J Med,2008,359(4): 378-390.
    [4] Killock D. Liver cancer: Regorafenib-a new RESORCE in HCC[J]. Nat Rev Clin Oncol, 2017, 14(2): 70-71.
    [5] Couzin-Frankel J. Breakthrough of the year 2013. Cancer immunotherapy[J]. Science,2013,342(6165): 1432-1433.
    [6] Robert C, Ribas A, Wolchok JD, et al. Anti-programmed-death-receptor-1 treatment with pembrolizumab in ipilimumab-refractory advanced melanoma: a randomised dose-comparison cohort of a phase 1 trial[J]. Lancet,2014,384(9948): 1109-1117.
    [7] Robert C, Schachter J, Long GV,et al. Pembrolizumab versus ipilimumab in advanced melanoma[J]. N Engl J Med,2015,372(26): 2521-2532.
    [8] Garon EB, Rizvi NA, Hui R,et al. Pembrolizumab for the treatment of non-small-cell lung cancer[J]. N Engl J Med,2015,372(21): 2018-2028.
    [9] Harding JJ, El Dika I, Abou-Alfa GK. Immunotherapy in hepatocellular carcinoma: Primed to make a difference[J]. Cancer,2016,122(3): 367-377.
    [10] Gravitz L. Cancer immunotherapy[J]. Nature, 2013,504(7480): S1.
    [11] Kim HM, Lim J, Yoon YD,et al. Anti-tumor activity of ex vivo expanded cytokine-induced killer cells against human hepatocellular carcinoma[J]. Int Immunopharmacol,2007,7(13): 1793-1801.
    [12] Schmidt-Wolf IG, Negrin RS, Kiem HP,et al. Use of a SCID mouse/human lymphoma model to evaluate cytokine-induced killer cells with potent antitumor cell activity[J]. J Exp Med,1991,174(1): 139-149.
    [13] Banchereau J, Steinman RM. Steinman. Dendritic cells and the control of immunity[J]. Nature,1998, 392(6673): 245-252.
    [14] Zhang L, Zhu W, Li J,et al. Clinical outcome of immunotherapy with dendritic cell vaccine and cytokine-induced killer cell therapy in hepatobiliary and pancreatic cancer[J]. Mol Clin Oncol,2016,4(1): 129-133.
    [15] Lin T, Song C, Chuo DY,et al. Clinical effects of autologous dendritic cells combined with cytokine-induced killer cells followed by chemotherapy in treating patients with advanced colorectal cancer: a prospective study[J]. Tumour Biol,2016,37(4): 4367-4372.
    [16] Wang S, Wang Z. Efficacy and safety of dendritic cells co-cultured with cytokine-induced killer cells immunotherapy for non-small-cell lung cancer[J]. Int Immunopharmacol,2015,28(1): 22-28.
    [17] Jiang JT, Shen YP, Wu CP,et al. Increasing the frequency of CIK cells adoptive immunotherapy may decrease risk of death in gastric cancer patients[J]. World J Gastroenterol,2010,16(48): 6155-6162.
    [18] Hui D, Qiang L, Jian W,et al. A randomized,controlled trial of postoperative adjuvant cytokine-induced killer cells immunotherapy after radical resection of hepatocellular carcinoma[J]. Dig Liver Dis,2009,41(1): 36-41.
    [19] Pan K, Li YQ, Wang W,et al. The efficacy of cytokine-induced killer cell infusion as an adjuvant therapy for postoperative hepatocellular carcinoma patients[J]. Ann Surg Oncol, 2013,20(13): 4305-4311.
    [20] Xie F, Zhang X, Li H,et al. Adoptive immunotherapy in postoperative hepatocellular carcinoma: a systemic review[J]. PLoS One,2012,7(8): e42879.
    [21] Niu LZ, Li JL, Zeng JY,et al. Combination treatment with comprehensive cryoablation and immunotherapy in metastatic hepatocellular cancer[J]. World J Gastroenterol,2013,19(22): 3473-3480.
    [22] Cui J, Wang N, Zhao H,et al. Combination of radiofrequency ablation and sequential cellular immunotherapy improves progression-free survival for patients with hepatocellular carcinoma[J]. Int J Cancer,2014,134(2): 342-351.
    [23] Hao MZ, Lin HL, Chen Q,et al. Efficacy of transcatheter arterial chemoembolization combined with cytokine-induced killer cell therapy on hepatocellular carcinoma: a comparative study[J]. Chin J Cancer,2010,29(2): 172-177.
    [24] 郭伟伟, 刘 莉, 吴德华. DC-CIK细胞免疫治疗联合TACE术治疗原发性肝癌[J]. 南方医科大学学报,2014,34(5): 674-678.
    [25] He G, Zheng C, Huo H,et al. TACE combined with dendritic cells and cytokine-induced killer cells in the treatment of hepatocellular carcinoma: A meta-analysis[J]. Int Immunopharmacol,2016,40: 436-442.
    [26] Rosenberg SA, Restifo NP, Yang JC,et al. Adoptive cell transfer: a clinical path to effective cancer immunotherapy[J]. Nat Rev Cancer,2008,8(4): 299-308.
    [27] Shirabe K, Motomura T, Muto J,et al. Tumor-infiltrating lymphocytes and hepatocellular carcinoma: pathology and clinical management[J]. Int J Clin Oncol,2010,15(6): 552-558.
    [28] Jiang SS, Tang Y, Zhang YJ,et al. A phase I clinical trial utilizing autologous tumor-infiltrating lymphocytes in patients with primary hepatocellular carcinoma[J]. Oncotarget,2015,6(38): 41339-41349.
    [29] Dolan DE, Gupta S. PD-1 pathway inhibitors: changing the landscape of cancer immunotherapy[J]. Cancer Control,2014,21(3): 231-237.
    [30] Zou W, Wolchok JD, Chen L. PD-L1 (B7-H1) and PD-1 pathway blockade for cancer therapy: Mechanisms,response biomarkers,and combinations[J]. Sci Transl Med,2016, 8(328): 328rv324.
    [31] Wu K, Kryczek I, Chen L,et al. Kupffer cell suppression of CD8+ T cells in human hepatocellular carcinoma is mediated by B7-H1/programmed death-1 interactions[J]. Cancer Res,2009,69(20): 8067-8075.
    [32] Finkelmeier F, Canli Ö, Tal A,et al. High levels of the soluble programmed death-ligand (sPD-L1) identify hepatocellular carcinoma patients with a poor prognosis[J]. Eur J Cancer,2016,59: 152-159.
    [33] Gao Q, Wang XY, Qiu SJ,et al. Overexpression of PD-L1 significantly associates with tumor aggressiveness and postoperative recurrence in human hepatocellular carcinoma[J]. Clin Cancer Res,2009,15(3): 971-979.
    [34] Kuang DM, Zhao Q, Peng C,et al. Activated monocytes in peritumoral stroma of hepatocellular carcinoma foster immune privilege and disease progression through PD-L1[J]. J Exp Med,2009,206(6): 1327-1337.
    [35] Ouyang FZ, Wu RQ, Wei Y,et al. Dendritic cell-elicited B-cell activation fosters immune privilege via IL-10 signals in hepatocellular carcinoma[J]. Nat Commun,2016,7: 13453.
    [36] Powles T, Eder JP, Fine GD, et al. MPDL3280A (anti-PD-L1) treatment leads to clinical activity in metastatic bladder cancer[J]. Nature,2014,515(7528): 558-562.
    [37] Brahmer JR, Tykodi SS, Chow LQ,et al. Safety and activity of anti-PD-L1 antibody in patients with advanced cancer[J]. N Engl J Med,2012,366(26): 2455-2465.
    [38] Armand P, Nagler A, Weller EA,et al. Disabling immune tolerance by programmed death-1 blockade with pidilizumab after autologous hematopoietic stem-cell transplantation for diffuse large B-cell lymphoma: results of an international phase Ⅱ trial[J]. J Clin Oncol,2013,31(33): 4199-4206.
    [39] Westin JR, Chu F, Zhang M,et al. Safety and activity of PD1 blockade by pidilizumab in combination with rituximab in patients with relapsed follicular lymphoma: a single group,open-label,phase 2 trial[J]. Lancet Oncol,2014,15(1): 69-77.
    [40] Ansell SM, Lesokhin AM, Borrello I,et al. PD-1 blockade with nivolumab in relapsed or refractory Hodgkin's lymphoma[J]. N Engl J Med,2015,372(4): 311-319.
    [41] Herbst RS, Soria JC, Kowanetz M,et al. Predictive correlates of response to the anti-PD-L1 antibody MPDL3280A in cancer patients[J]. Nature,2014,515(7528): 563-567.
    [42] El-Khoueiry A B, Melero I, Crocenzi T S, et al.Phase Ⅰ/Ⅱ safety and antitumor activity of nivolumab in patients with advanced hepatocellular carcinoma (HCC): CA209-040[J]. Clin Oncol 2015,33(18): LBA101.
    [43] Chen CL, Pan QZ, Zhao JJ,et al. PD-L1 expression as a predictive biomarker for cytokine-induced killer cell immunotherapy in patients with hepatocellular carcinoma[J]. Oncoimmunology,2016,5(7): e1176653.
    [44] Le DT, Uram JN, Wang H,et al. PD-1 blockade in tumors with mismatch-repair deficiency[J]. N Engl J Med,2015,372(26): 2509-2520.
    [45] Sun TW, Gao Q, Qiu SJ,et al. B7-H3 is expressed in human hepatocellular carcinoma and is associated with tumor aggressiveness and postoperative recurrence[J]. Cancer Immunol Immunother,2012,61(11): 2171-2182.
    [46] Pan QZ, Wang QJ, Dan JQ,et al. A nomogram for predicting the benefit of adjuvant cytokine-induced killer cell immunotherapy in patients with hepatocellular carcinoma[J]. Sci Rep,2015,5: 9202.
    [47] Tang H, Qiao J, Fu YX. Immunotherapy and tumor microenvironment[J]. Cancer Lett,2016,370(1): 85-90.
    [48] Sivan A, Corrales L, Hubert N,et al. Commensal Bifidobacterium promotes antitumor immunity and facilitates anti-PD-L1 efficacy[J]. Science,2015,350(6264): 1084-1089.
    [49] Vétizou M, Pitt JM, Daillère R,et al. Anticancer immunotherapy by CTLA-4 blockade relies on the gut microbiota[J]. Science,2015,350(6264): 1079-1084.
    [50] Wang XP, Xu M, Gao HF,et al. Intraperitoneal perfusion of cytokine-induced killer cells with local hyperthermia for advanced hepatocellular carcinoma[J]. World J Gastroenterol,2013, 19(19): 2956-2962.
    [51] Qiu Y, Xu MB, Yun MM,et al. Hepatocellular carcinoma-specific immunotherapy with synthesized alpha1,3- galactosyl epitope-pulsed dendritic cells and cytokine-induced killer cells[J]. World J Gastroenterol,2011,17(48): 5260-5266.
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  • 收稿日期:  2017-01-18
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免疫治疗在肝细胞癌治疗中的进展

doi: 10.3969/j.issn.1006-0111.2017.04.019

摘要: 肝细胞癌(HCC)是全球发病率和致死率都很高的恶性肿瘤。目前以手术治疗为主的治疗方法远难以达到理想的效果。肿瘤免疫治疗,包括树突状细胞诱导的杀伤细胞(DC-CIK)、肿瘤浸润淋巴细胞(TIL)、嵌合抗原受体T细胞(CAR-T)、免疫检查点阻滞剂(如PD-1阻滞剂、CTL4阻滞剂)等,是近年发展迅速且具有良好前景的肿瘤治疗新方法。本综述着重介绍PD-1阻滞剂、DC-CIK细胞、TIL细胞在治疗肝细胞癌中取得的进展,并对本课题组发明的多能免疫杀伤转基因细胞(PIK)做简要介绍。

English Abstract

郭玲玲, 仇金荣. 免疫治疗在肝细胞癌治疗中的进展[J]. 药学实践与服务, 2017, 35(4): 362-366. doi: 10.3969/j.issn.1006-0111.2017.04.019
引用本文: 郭玲玲, 仇金荣. 免疫治疗在肝细胞癌治疗中的进展[J]. 药学实践与服务, 2017, 35(4): 362-366. doi: 10.3969/j.issn.1006-0111.2017.04.019
GUO Lingling, QIU Jinrong. Progress in immunotherapy for hepatocellular carcinoma[J]. Journal of Pharmaceutical Practice and Service, 2017, 35(4): 362-366. doi: 10.3969/j.issn.1006-0111.2017.04.019
Citation: GUO Lingling, QIU Jinrong. Progress in immunotherapy for hepatocellular carcinoma[J]. Journal of Pharmaceutical Practice and Service, 2017, 35(4): 362-366. doi: 10.3969/j.issn.1006-0111.2017.04.019
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