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本文引用的文献

1
Adenovirus-mediated ING4 Gene Transfer in Osteosarcoma Suppresses Tumor Growth via Induction of Apoptosis and Inhibition of Tumor Angiogenesis.腺病毒介导的ING4基因转移在骨肉瘤中通过诱导凋亡和抑制肿瘤血管生成来抑制肿瘤生长。
Technol Cancer Res Treat. 2015 Aug;14(4):369-78. doi: 10.1177/1533034614500424. Epub 2014 Oct 16.
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Combination therapy with dendritic cell vaccine and IL-2 encapsulating polymeric micelles enhances intra-tumoral accumulation of antigen-specific CTLs.树突状细胞疫苗与包裹白细胞介素-2的聚合物胶束联合治疗可增强肿瘤内抗原特异性细胞毒性T淋巴细胞的聚集。
Int Immunopharmacol. 2014 Dec;23(2):499-504. doi: 10.1016/j.intimp.2014.09.025. Epub 2014 Oct 3.
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Expression of programmed death 1 is correlated with progression of osteosarcoma.程序性死亡蛋白1的表达与骨肉瘤的进展相关。
APMIS. 2015 Feb;123(2):102-7. doi: 10.1111/apm.12311. Epub 2014 Sep 25.
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Tumor-specific oncolytic adenoviruses expressing granulocyte macrophage colony-stimulating factor or anti-CTLA4 antibody for the treatment of cancers.表达粒细胞巨噬细胞集落刺激因子或抗CTLA4抗体的肿瘤特异性溶瘤腺病毒用于癌症治疗。
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Ipilimumab augments antitumor activity of bispecific antibody-armed T cells.伊匹单抗增强双特异性抗体武装T细胞的抗肿瘤活性。
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Genital infection with herpes simplex virus types 1 and 2 in women from natal, Brazil.巴西纳塔尔地区女性感染1型和2型单纯疱疹病毒的生殖器感染情况。
ISRN Obstet Gynecol. 2014 Mar 11;2014:323657. doi: 10.1155/2014/323657. eCollection 2014.
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Comprehensive evaluation of the cytotoxic T-lymphocyte antigen-4 gene polymorphisms in risk of bone sarcoma.
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Genetically modified T-cell therapy for osteosarcoma.骨肉瘤的基因修饰 T 细胞治疗。
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Oncolytic viruses for potential osteosarcoma therapy.溶瘤病毒在骨肉瘤治疗中的应用。
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The addition of mifamurtide to chemotherapy improves lifetime effectiveness in children with osteosarcoma: a Markov model analysis.在化疗中添加米伐木肽可提高骨肉瘤患儿的终生疗效:一项马尔可夫模型分析。
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骨肉瘤免疫治疗的策略与进展

Strategies and developments of immunotherapies in osteosarcoma.

作者信息

Wan Jia, Zhang Xianghong, Liu Tang, Zhang Xiangsheng

机构信息

Department of Orthopedics, The Second Xiangya Hospital, Central South University, Changsha, Hunan 410011, P.R. China.

出版信息

Oncol Lett. 2016 Jan;11(1):511-520. doi: 10.3892/ol.2015.3962. Epub 2015 Nov 24.

DOI:10.3892/ol.2015.3962
PMID:26834853
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4727173/
Abstract

Osteosarcoma (OS) is a frequently observed primary malignant tumor. Current therapy for osteosarcoma consists of comprehensive treatment. The long-term survival rate of patients exhibiting nonmetastatic OS varies between 65-70%. However, a number of OS cases have been observed to be resistant to currently used therapies, leading to disease recurrence and lung metastases, which are the primary reasons leading to patient mortality. In the present review, a number of pieces of evidence provide support for the potential uses of immunotherapy, including immunomodulation and vaccine therapy, for the eradication of tumors via upregulation of the immune response. Adoptive T-cell therapy and oncolytic virotherapy have been used to treat OS and resulted in objective responses. Immunologic checkpoint blockade and targeted therapy are also potentially promising therapeutic tools. Immunotherapy demonstrates significant promise with regard to improving the outcomes for patients exhibiting OS.

摘要

骨肉瘤(OS)是一种常见的原发性恶性肿瘤。目前骨肉瘤的治疗包括综合治疗。非转移性骨肉瘤患者的长期生存率在65%至70%之间。然而,已观察到一些骨肉瘤病例对目前使用的治疗方法耐药,导致疾病复发和肺转移,这是导致患者死亡的主要原因。在本综述中,大量证据支持免疫疗法(包括免疫调节和疫苗疗法)通过上调免疫反应来根除肿瘤的潜在用途。过继性T细胞疗法和溶瘤病毒疗法已用于治疗骨肉瘤并产生了客观反应。免疫检查点阻断和靶向治疗也是潜在有前景的治疗工具。免疫疗法在改善骨肉瘤患者的治疗结果方面显示出巨大潜力。