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本文引用的文献

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First-in-class, first-in-human phase I results of targeted agents: highlights of the 2008 American society of clinical oncology meeting.首创新药、人体首用一期临床试验结果:2008 年美国临床肿瘤学会会议重点。
J Hematol Oncol. 2008 Oct 29;1:20. doi: 10.1186/1756-8722-1-20.
2
OX40 costimulatory signals potentiate the memory commitment of effector CD8+ T cells.OX40共刺激信号增强效应性CD8 + T细胞的记忆形成。
J Immunol. 2008 Nov 1;181(9):5990-6001. doi: 10.4049/jimmunol.181.9.5990.
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CTLA-4 control over Foxp3+ regulatory T cell function.细胞毒性T淋巴细胞相关抗原4对叉头框蛋白3阳性调节性T细胞功能的调控
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Combination therapy with cisplatin and anti-4-1BB: synergistic anticancer effects and amelioration of cisplatin-induced nephrotoxicity.顺铂与抗4-1BB联合治疗:协同抗癌作用及对顺铂诱导的肾毒性的改善
Cancer Res. 2008 Sep 15;68(18):7264-9. doi: 10.1158/0008-5472.CAN-08-1365.
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Cell intrinsic mechanisms of T-cell inhibition and application to cancer therapy.T细胞抑制的细胞内在机制及其在癌症治疗中的应用。
Immunol Rev. 2008 Aug;224:141-65. doi: 10.1111/j.1600-065X.2008.00649.x.
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Limited tumor infiltration by activated T effector cells restricts the therapeutic activity of regulatory T cell depletion against established melanoma.活化的T效应细胞对肿瘤的浸润有限,限制了调节性T细胞耗竭对已建立的黑色素瘤的治疗活性。
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7
CD137 costimulation of CD8+ T cells confers resistance to suppression by virus-induced regulatory T cells.CD8⁺ T细胞的CD137共刺激赋予其对病毒诱导的调节性T细胞介导的抑制作用的抗性。
J Immunol. 2008 Apr 15;180(8):5267-74. doi: 10.4049/jimmunol.180.8.5267.
8
The promise of 4-1BB (CD137)-mediated immunomodulation and the immunotherapy of cancer.4-1BB(CD137)介导的免疫调节作用及癌症免疫治疗前景。
Immunol Rev. 2008 Apr;222:277-86. doi: 10.1111/j.1600-065X.2008.00621.x.
9
OX40 triggering blocks suppression by regulatory T cells and facilitates tumor rejection.OX40激活可阻止调节性T细胞的抑制作用,并促进肿瘤排斥反应。
J Exp Med. 2008 Apr 14;205(4):825-39. doi: 10.1084/jem.20071341. Epub 2008 Mar 24.
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4-1BB engagement costimulates NKT cell activation and exacerbates NKT cell ligand-induced airway hyperresponsiveness and inflammation.4-1BB参与共刺激NKT细胞活化,并加剧NKT细胞配体诱导的气道高反应性和炎症。
J Immunol. 2008 Feb 15;180(4):2062-8. doi: 10.4049/jimmunol.180.4.2062.

癌症免疫疗法:共刺激激动剂和共抑制拮抗剂。

Cancer immunotherapy: co-stimulatory agonists and co-inhibitory antagonists.

作者信息

Peggs K S, Quezada S A, Allison J P

机构信息

Department of Haematology, UCL Cancer Institute, Paul O'Gorman Building, University College London, London, UK.

出版信息

Clin Exp Immunol. 2009 Jul;157(1):9-19. doi: 10.1111/j.1365-2249.2009.03912.x. Epub 2009 Feb 18.

DOI:10.1111/j.1365-2249.2009.03912.x
PMID:19659765
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2710587/
Abstract

The generation and maintenance of immune responses are controlled by both co-stimulatory and co-inhibitory signalling through T cell co-receptors, many of which belong to the immunoglobulin-like superfamily or the tumour necrosis factor receptor superfamily. Agonistic or antagonistic monoclonal antibodies targeting these co-receptors have the potential to enhance immunity. Furthermore, their activity on the immunosuppressive regulatory T cell populations which are prevalent within many tumours provides an additional rationale for their use as anti-cancer therapies. This review summarizes the interactions between cancer and the immune system, highlighting the ways in which these new classes of immunostimulatory antibodies might enhance anti-tumour immunity and summarizing early clinical experience with their use.

摘要

免疫反应的产生和维持由通过T细胞共受体的共刺激和共抑制信号控制,其中许多共受体属于免疫球蛋白样超家族或肿瘤坏死因子受体超家族。靶向这些共受体的激动性或拮抗性单克隆抗体有可能增强免疫力。此外,它们对许多肿瘤中普遍存在的免疫抑制调节性T细胞群体的作用为其作为抗癌疗法的应用提供了额外的理论依据。本综述总结了癌症与免疫系统之间的相互作用,强调了这些新型免疫刺激抗体增强抗肿瘤免疫力的方式,并总结了其使用的早期临床经验。