[1]王玲,王燕,冯琛,等.骨肉瘤免疫治疗的研究进展[J].中华老年骨科与康复电子杂志,2017,(06):381-384.[doi:10.3877/cma.j.issn.2096-0263.2017.06.013]
 Wang Ling,Wang Yan,Feng Chen,et al.Advancement of the research on the immunotherapy for osteosarcoma[J].Chin J Geriatr Orthop Rehabil(Electronic Edition),2017,(06):381-384.[doi:10.3877/cma.j.issn.2096-0263.2017.06.013]
点击复制

骨肉瘤免疫治疗的研究进展()
分享到:

中华老年骨科与康复电子杂志[ISSN:1674-3911/CN:11-9292/R]

卷:
期数:
2017年06期
页码:
381-384
栏目:
综述
出版日期:
2017-11-27

文章信息/Info

Title:
Advancement of the research on the immunotherapy for osteosarcoma
作者:
王玲 12王燕 3冯琛 1潘禹铮 1张英泽 1
050051 石家庄,河北省骨科研究所 1;050051 石家庄,河北医科大学第三医院骨与软组织肿瘤科 2;050011 石家庄,河北医科大学第一医院变态反应科 3
Author(s):
Wang Ling12 Wang Yan3 Feng Chen1 Pan Yuzheng1 Zhang Yingze1
1Orthopedic Research Institution of Hebei Province, Shijiazhuang 050051, China; 2Department of Orthopedic Oncology, the Third Hospital of Hebei Medical University, Shijiazhuang 050051, China; 3Department of Allergy, the First Hospital of Hebei Medical University, Shijiazhuang 050011, China
关键词:
骨肉瘤 适应性免疫 免疫疗法主动
Keywords:
Osteosarcoma Adaptive immunity Immunotherapy active
DOI:
10.3877/cma.j.issn.2096-0263.2017.06.013
文献标志码:
A
摘要:
骨肉瘤是骨恶性肿瘤中最常见的一种,常常危害儿童和青少年,易发生早期转移,病情进展快、预后差。新辅助化疗结合手术治疗使骨肉瘤患者的 5年生存期提高到 50%~60%,但仍有部分患者会复发及转移。近年来随着免疫学技术的发展,以及对骨肉瘤的发病机制认识的深入,免疫治疗在骨肉瘤综合治疗中发挥着越来越重要的作用。
Abstract:
Osteosarcoma is one of the most common malignant bone tumors that often jeopardize children and adolescents. The prognosis of osteosarcoma is poor because of its early metastasis. Neoadjuvant chemotherapy combined with surgery can improve the 5-year survival of patients with osteosarcoma up to 50%- 60% , but some patients are still likely to relapse and metastasis. With the rapid development of immunology technology in recent years, and more in- depth pathogenesis of osteosarcoma are conducted, immunotherapy may play more and more important role in the comprehensive treatment of osteosarcoma.

参考文献/References:

1 Anninga JK, Gelderblom H, Fiocco M, et al. Chemotherapeutic adjuvant treatment for osteosarcoma: where do we stand? [J]. Eur J Cancer, 2011, 47(16): 2431-2445.
2 Moore DD, Luu HH. Osteosarcoma [J]. Cancer Treat Res, 2014,162: 65-92.
3 Isakoff MS, Bielack SS, Meltzer P, et al. Osteosarcoma: Current Treatment and a Collaborative Pathway to Success [J]. J Clin Oncol, 2015, 33(27):3029-3035.
4 Dai X, Ma W, He X, et al. Review of therapeutic strategies for osteosarcoma, chondrosarcoma, and Ewing’s sarcoma [J]. Med Sci Monit, 2011, 17(8): RA177-RA190.
5 Hong CW, Zeng Q. Awaiting a new era of cancer immunotherapy [J]. Cancer Res, 2012, 72(15): 3715-3719.
6 Ghafouri- Fard S, Ghafouri- Fard S. siRNA and cancer immunotherapy [J]. Immunotherapy, 2012, 4(9): 907-917.
7 Beard RE, Zheng Z, Lagisetty KH, et al. Multiple chimeric antigen receptors successfully target chondroitin sulfate proteoglycan 4 in several different cancer histologies and cancer stem cells [J]. Immunother Cancer, 2014, 2(25).
8 Toledo SR, Zago MA, Oliveira ID, et al. Insights on PRAME and osteosarcoma by means of gene expression profiling [J]. J Orthop Sci, 2011, 16(4): 458-466.
9 Liu Y, He Z, Feng D, et al. Cytotoxic T- lymphocyte antigen- 4 polymorphisms and susceptibility to osteosarcoma [J]. DNA Cell Biol, 2011, 30(12):1051-1055.
10 Dong Q, Ma X. B7- H4 expression is associated with tumor progression and prognosis in patients with osteosarcoma [J]. Biomed Res Int, 2015: 156432.
11 Wang L, Zhang Q, Chen W, et al. B7-H3 is overexpressed in patients suffering osteosarcoma and associated with tumor aggressiveness and metastasis [J]. PLoS One, 2013, 8(8): e70689.
12 Mitchison N. Studies on the immunological response to foreign tumor transplants in the mouse I.The role of lymph node cells in conferring immunity by adoptive transfer [J]. J Exp Med, 1955, 102 (2): 157-177.
13 Seton- Rogers S. Tumour immunology: An exhausting metabolic competition [J]. Nat Rev Cancer, 2015, 15(10): 573.
14 Schmeel FC, Schmeel LC, Gast SM, et al. Adoptive immunotherapy strategies with cytokine-induced killer (CIK) cells in the treatment of hematological malignancies [J]. Int J Mol Sci, 2014, 15(8): 14632- 14648.
15 Wongkajornsilp A, Sangsuriyong S, Hongeng S, et al. Effective osteosarcoma cytolysis using cytokine- induced killer cells preinoculated with tumor RNA-pulsed dendritic cells [J]. J Orthop Res, 2005, 23(6): 1460-1466.
16 Todorovic M, Mesiano G, Gammaitoni L, et al. Ex vivo allogeneic stimulation significantly improves expansion of cytokine- induced killer cells without increasing their alloreactivity across HLA barriers [J]. J Immunother, 2012, 35(7): 579-586.
17 Rosenberg S, Packard BS, Aebersold PM, et al. Use of tumorinfiltrating lymphocytes and interleukin- 2 in the immunotherapy of patients with metastatic melanoma. A preliminary report [J]. N Engl J Med, 1988, 319(25): 1676-1680.
18 Théoleyre S, Mori K, Cherrier B, et al. Phenotypic and functional analysis of lymphocytes infiltrating osteolytic tumors:use as a possible therapeutic approach of osteosarcoma [J]. BMC Cancer, 2005, 5: 123.
19 Fritzsching B, Fellenberg J, Moskovszky L, et al. CD8(+)/FOXP3(+)- ratio in osteosarcoma microenvironment separates survivors from non- survivors: a multicenter validated retrospective study [J]. Oncoimmunology, 2015, 4(3): e990800.
20 Karimi S, Chattopadhyay S, Chakraborty NG. Manipulation of regulatory T cells and antigen-specific cytotoxic T lymphocyte-based tumour immunotherapy [J]. Immunology, 2015, 144(2): 186-196.
21 Wang W, Wang J, Song H, et al. Cytotoxic T-lymphocyte antigen-4 + 49G/A polymorphism is associated with increased risk of osteosarcoma [J]. Genet Test Mol Biomarkers, 2011, 15(7/8): 503-506.
22 Liu S, Geng P, Cai X, et al. Comprehensive evaluation of the cytotoxic T- lymphocyte antigen- 4 gene polymorphisms in risk of bone sarcoma [J]. Genet Test Mol Biomarkers, 2014, 18(8): 574-579.
23 Contardi E, Palmisano GL, Tazzari PL, et al. CTLA- 4 is constitutively expressed on tumor cells and can trigger apoptosis upon ligand interaction [J]. Int J Cancer, 2005, 117(4): 538-550.
24 Lussier DM, O’neill L, Nieves LM, et al. Enhanced T-cell immunity to osteosarcoma through antibody blockade of PD- 1/PD- L1 interactions [J]. J Immunother, 2015, 38(3): 96-106.
25 Lussier DM, Johnson JL, Hingorani P, et al. Combination immunotherapy with α- CTLA- 4 and α- PD- L1 antibody blockade prevents immune escape and leads to complete control of metastatic osteosarcoma [J]. J Immunother Cancer, 2015, 3: 21.
26 Sun C, Sun HY, Xiao WH, et al. Natural killer cell dysfunction in hepatocellular carcinoma and NK cell- based immunotherapy [J]. Acta Pharmacol Sin, 2015, 36(10): 1191-1199.
27 Kubista B, Trieb K, Blahovec H, et al. Hyperthermia increases the susceptibility of chondro- and osteosarcoma cells to natural killer cell-mediated lysis [J]. Anticancer Res, 2002, 22(2A): 789-792.
28 Guma SR, Lee DA, Yu L, et al. Natural killer cell therapy and aerosol interleukin- 2 for the treatment of osteosarcoma lung metastasis [J]. Pediatr Blood Cancer, 2014, 61(4): 618-626.
29 Chang YH, Connolly J, Shimasaki N, et al. A chimeric receptor with NKG2D specificity enhances natural killer cell activation and killing of tumor cells [J]. Cancer Res, 2013, 73(6): 1777-1786.
30 Buddingh EP, Schilham MW, Ruslan SE, et al. Chemotherapyresistant osteosarcoma is highly susceptible to IL- 15- activated allogeneic and autologous NK cells [J]. Cancer Immunol Immunother, 2011, 60(4): 575-586.
31 Kubo T, Shimose S, Matsuo T, et al. Interferon- α/β receptor as a prognostic marker in osteosarcoma [J]. J Bone Joint Surg Am, 2011, 93(6): 519-526.
32 Zhao J, Wang M, Li Z, et al. Interferon-α suppresses invasion and enhances cisplatin- mediated apoptosis and autophagy in human osteosarcoma cells [J]. Oncol Lett, 2014, 7(3): 827-833.
33 Li Z, Xu Q, Peng H, et al. IFN-γ enhances HOS and U2OS cell lines susceptibility to γδ T cell- mediated killing through the Fas/Fas ligand pathway [J]. Int Immunopharmacol, 2011, 11(4): 496-503.
34 Pahl JH, Kwappenberg KM, Varypataki EM, et al. Macrophages inhibit human osteosarcoma cell growth after activation with the bacterial cell wall derivative liposomal muramyltripeptide in combination with interferon-γ [J]. J Exp Clin Cancer Res, 2014, 33: 27.
35 Hirohashi Y, Torigoe T, Tsukahara T, et al. Immune responses to human cancer stem-like cells/cancer-initiating cells [J]. Cancer Sci, 2015.
36 Kissick HT, Sanda MG. The role of active vaccination in cancer immunotherapy: lessons from clinical trials [J]. Curr Opin Immunol, 2015, 35: 15-22.
37 Marcove RC, Southam CM, Levin A, et al. A clinical trial of autogenous vaccine in osteogenic sarcoma in patients under the age of twenty-five [J]. Surg Forum, 1971, 22: 434-435.
38 Southam CM, Marcove RC, Levin AG, et al. Proceedings: Clinical trial of autogenous tumor vaccine for treatment of osteogenic sarcoma [J]. ProcNatl Cancer Conf. 1972, 7:91-100.
39 Krishnadas DK, Shusterman S, Bai F, et al. A phase I trial combining decitabine/dendritic cell vaccine targeting MAGE- A1, MAGE- A3 and NY- ESO- 1 for children with relapsed or therapy- refractory neuroblastoma and sarcoma [J]. Cancer Immunol Immunother, 2015, 64(10): 1251-1260.
40 Domingo-Musibay E, Allen C, Kurokawa C, et al. Measles edmonston vaccine strain derivatives have potent oncolytic activity against osteosarcoma [J]. Cancer Gene Ther, 2014, 21(11): 483-490.
41 王臻, 彭磊, 肖毅, 等. 骨肉瘤细胞与活化 B淋巴细胞融合疫苗的制备及其诱导的抗瘤活性 [J]. 中华骨科杂志, 2001, 21(10): 622-625.
42 郝新保, 范清宇, 张殿忠, 等. 巨噬细胞融合瘤苗对大鼠骨肉瘤的主动性免疫治疗[J]. 第四军医大学学报. 1999, 20(12):1042-1044.
43 Tanaka T, Yui Y, Naka N, et al. Dynamic analysis of lung metastasis by mouse osteosarcoma LM8: VEGF is a candidate for antimetastasis therapy [J]. Clin Exp Metastasis, 2013, 30(4): 369-379.
44 Broadhead ML, Dass CR, Choong PF. Systemically administered PEDF against primary and secondary tumours in a clinically relevant osteosarcoma model [J]. Br J Cancer, 2011, 105(10): 1503-1511.
45 Seto M, Yamazaki T, Sonoda J, et al. Suppression of tumor growth and pulmonary metastasis in murine osteosarcoma using gene therapy [J]. Oncol Rep, 2002, 9(2): 337-340.
46 Pellinen R, Hakkarainen T, Wahlfors T, et al. Cancer cells as targets for lentivirus- mediated gene transfer and gene therapy [J]. Int J Oncol, 2004, 25(6): 1753-1762.
47 Zhang Y, Yang CQ, Gao Y, et al. Knockdown of CXCR7 inhibits proliferation and invasion of osteosarcoma cells through inhibition of the PI3K/Akt and β- arrestin pathways [J]. Oncol Rep, 2014, 32 (3): 965-972.
48 Zhao Q, Wang C, Zhu J, et al. RNAi- mediated knockdown of cyclooxygenase2 inhibits the growth,invasion and migration of SaOS2 human osteosarcoma cells:a case control study [J]. J Exp Clin Cancer Res, 2011, 30: 26.

相似文献/References:

[1]卢军丽,包超恩,赵建,等.老年腓骨近端骨肉瘤影像诊断与鉴别诊断[J].中华老年骨科与康复电子杂志,2018,(03):175.[doi:10.3877/cma.j.issn.2096-0263.2018.03.010]
 Lu Junli,Bao Chaoen,Zhao Jian,et al.Imaging diagnosis and differential diagnosis of proximal fibula osteosarcoma[J].Chin J Geriatr Orthop Rehabil(Electronic Edition),2018,(06):175.[doi:10.3877/cma.j.issn.2096-0263.2018.03.010]
[2]邱明宪,康肖,王磊.LncRNA NEAT1靶向miR-185-5p调控骨肉瘤的机制研究[J].中华老年骨科与康复电子杂志,2023,(04):233.[doi:10.3877/cma.j.issn.2096-0263.2023.04.006]
 Qiu Mingxian,Kang Xiao,Wang Lei..Expression of LncRNA NEAT1 in osteosarcoma cells and study of the mechanism of cellular activity via miR-185-5p[J].Chin J Geriatr Orthop Rehabil(Electronic Edition),2023,(06):233.[doi:10.3877/cma.j.issn.2096-0263.2023.04.006]

备注/Memo

备注/Memo:
基金项目:国家自然基金面上项目(81772858);国家自然基金青年基金(81402228);河北省自然基金青年基金(H2015206216)
更新日期/Last Update: 2017-11-28