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本文引用的文献

1
CIITA-driven MHC class II expressing tumor cells can efficiently prime naive CD4 TH cells and vaccinate the host against parental MHC-II-negative tumor cells.由CIITA驱动表达II类主要组织相容性复合体(MHC)的肿瘤细胞能够有效地激活初始CD4辅助性T细胞(TH细胞),并使宿主对亲本MHC-II阴性肿瘤细胞产生免疫。
Oncoimmunology. 2016 Nov 28;6(1):e1261777. doi: 10.1080/2162402X.2016.1261777. eCollection 2017.
2
Immunogenic cell death in cancer and infectious disease.肿瘤和传染病中的免疫原性细胞死亡
Nat Rev Immunol. 2017 Feb;17(2):97-111. doi: 10.1038/nri.2016.107. Epub 2016 Oct 17.
3
The untold story of IFN-γ in cancer biology.IFN-γ 在癌症生物学中的未解之谜。
Cytokine Growth Factor Rev. 2016 Oct;31:73-81. doi: 10.1016/j.cytogfr.2016.07.005. Epub 2016 Aug 1.
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Human leucocyte antigen class I-redirected anti-tumour CD4 T cells require a higher T cell receptor binding affinity for optimal activity than CD8 T cells.与CD8 T细胞相比,人白细胞抗原I类重定向抗肿瘤CD4 T细胞需要更高的T细胞受体结合亲和力才能实现最佳活性。
Clin Exp Immunol. 2017 Jan;187(1):124-137. doi: 10.1111/cei.12828. Epub 2016 Nov 14.
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Extracellular vesicles: masters of intercellular communication and potential clinical interventions.细胞外囊泡:细胞间通讯的掌控者及潜在的临床干预手段
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Different Subsets of T Cells, Memory, Effector Functions, and CAR-T Immunotherapy.T细胞的不同亚群、记忆、效应功能及嵌合抗原受体T细胞免疫疗法
Cancers (Basel). 2016 Mar 15;8(3):36. doi: 10.3390/cancers8030036.
7
Direct tumor recognition by a human CD4(+) T-cell subset potently mediates tumor growth inhibition and orchestrates anti-tumor immune responses.人类CD4(+) T细胞亚群对肿瘤的直接识别有力地介导肿瘤生长抑制并协调抗肿瘤免疫反应。
Sci Rep. 2015 Oct 8;5:14896. doi: 10.1038/srep14896.
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Developments in cancer vaccines for hepatocellular carcinoma.肝细胞癌癌症疫苗的进展
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Tertiary lymphoid structures in cancer and beyond.癌症中的三级淋巴结构及其他。
Trends Immunol. 2014 Nov;35(11):571-80. doi: 10.1016/j.it.2014.09.006. Epub 2014 Oct 22.
10
CD4 T-cell subsets and tumor immunity: the helpful and the not-so-helpful.CD4 T 细胞亚群与肿瘤免疫:有益与无益。
Cancer Immunol Res. 2014 Feb;2(2):91-8. doi: 10.1158/2326-6066.CIR-13-0216.

肿瘤免疫学遇见……免疫学:修饰的癌细胞作为专职抗原呈递细胞启动初始肿瘤特异性CD4+T细胞

Tumor Immunology meets…Immunology: Modified cancer cells as professional APC for priming naïve tumor-specific CD4+ T cells.

作者信息

Bou Nasser Eddine Farah, Ramia Elise, Tosi Giovanna, Forlani Greta, Accolla Roberto S

机构信息

Department of Medicine and Surgery, School of Medicine, University of Insubria, Varese, Italy.

出版信息

Oncoimmunology. 2017 Jul 31;6(11):e1356149. doi: 10.1080/2162402X.2017.1356149. eCollection 2017.

DOI:10.1080/2162402X.2017.1356149
PMID:29147609
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5674956/
Abstract

Although recent therapeutic approaches have revitalized the enthusiasm of the immunological way to combat cancer, still the comprehension of immunity against tumors is largely incomplete. Due to their specific function, CD8+ T cells with cytolytic activity (CTL) have attracted the attention of most investigators because CTL are considered the main effectors against tumor cells. Nevertheless, CTL activity and persistence is largely dependent on the action of CD4+ T helper cells (TH). Thus establishment of tumor-specific TH cell response is key to the optimal response against cancer. Here we describe emerging new strategies to increase the TH cell recognition of tumor antigens. In particular, we review recent data indicating that tumor cells themselves can act as surrogate antigen presenting cells for triggering TH response and how these findings can help in constructing immunotherapeutic protocols for anti-cancer vaccine development.

摘要

尽管最近的治疗方法重新激发了通过免疫途径对抗癌症的热情,但对肿瘤免疫的理解在很大程度上仍不完整。由于其特定功能,具有细胞溶解活性的CD8 + T细胞(CTL)吸引了大多数研究人员的关注,因为CTL被认为是对抗肿瘤细胞的主要效应细胞。然而,CTL的活性和持久性在很大程度上依赖于CD4 + T辅助细胞(TH)的作用。因此,建立肿瘤特异性TH细胞反应是对抗癌症的最佳反应的关键。在这里,我们描述了增加TH细胞对肿瘤抗原识别的新兴新策略。特别是,我们回顾了最近的数据,这些数据表明肿瘤细胞本身可以作为替代抗原呈递细胞来触发TH反应,以及这些发现如何有助于构建用于抗癌疫苗开发的免疫治疗方案。