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Immune checkpoint inhibitors in clinical practice: update on management of immune-related toxicities.免疫检查点抑制剂在临床实践中的应用:免疫相关毒性管理的最新进展。
Transl Lung Cancer Res. 2015 Oct;4(5):560-75. doi: 10.3978/j.issn.2218-6751.2015.06.06.
2
CCR 20th Anniversary Commentary: Immune-Related Response Criteria--Capturing Clinical Activity in Immuno-Oncology.CCR 20 周年述评:免疫相关缓解标准——捕捉免疫肿瘤学中的临床活动。
Clin Cancer Res. 2015 Nov 15;21(22):4989-91. doi: 10.1158/1078-0432.CCR-14-3128.
3
Cancer and the Immune System: Basic Concepts and Targets for Intervention.癌症与免疫系统:基本概念及干预靶点
Semin Oncol. 2015 Aug;42(4):523-38. doi: 10.1053/j.seminoncol.2015.05.003. Epub 2015 Jun 3.
4
Molecular and cellular insights into T cell exhaustion.对T细胞耗竭的分子和细胞层面的见解。
Nat Rev Immunol. 2015 Aug;15(8):486-99. doi: 10.1038/nri3862.
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Potency of Both Human Th1 and NK Helper Cell Activation is Determined by IL-12p70-Producing PAMP-Matured DCs.人Th1细胞和NK辅助细胞的激活效力由产生IL-12p70的模式识别受体成熟的树突状细胞决定。
J Interferon Cytokine Res. 2015 Sep;35(9):748-58. doi: 10.1089/jir.2015.0022. Epub 2015 Jul 2.
6
Trial Watch: Toll-like receptor agonists in oncological indications.试验观察:肿瘤适应症中的Toll样受体激动剂
Oncoimmunology. 2014 Aug 1;3:e29179. doi: 10.4161/onci.29179. eCollection 2014.
7
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J Natl Cancer Inst. 2014 May 29;106(6):dju124. doi: 10.1093/jnci/dju124. Print 2014 Jun.
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9
Durable Regression of Primary Cutaneous B-Cell Lymphoma Following Fever-inducing Mistletoe Treatment: Two Case Reports.发热性槲寄生治疗后原发性皮肤B细胞淋巴瘤的持久缓解:两例报告
Glob Adv Health Med. 2012 Mar;1(1):18-25. doi: 10.7453/gahmj.2012.1.1.006.
10
Mistletoe lectin has a shiga toxin-like structure and should be combined with other Toll-like receptor ligands in cancer therapy.槲寄生凝集素有志贺毒素样结构,应与其他 Toll 样受体配体联合用于癌症治疗。
Cancer Immunol Immunother. 2013 Aug;62(8):1283-92. doi: 10.1007/s00262-013-1455-1. Epub 2013 Jul 6.

铭记科利的经验教训:增强槲寄生疗法

Coley's Lessons Remembered: Augmenting Mistletoe Therapy.

作者信息

Orange Maurice, Reuter Uwe, Hobohm Uwe

机构信息

Klinik Arlesheim, Switzerland.

Klinik-im-LEBEN, Greiz, Germany.

出版信息

Integr Cancer Ther. 2016 Dec;15(4):502-511. doi: 10.1177/1534735416649916. Epub 2016 May 20.

DOI:10.1177/1534735416649916
PMID:27207233
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5739169/
Abstract

The following four observations point in the same direction, namely that there is an unleveraged potential for stimulating the innate immune system against cancer: (1) experimental treatments with bacterial extracts more than 100 years ago by Coley and contemporaries, (2) a positive correlation between spontaneous regressions and febrile infection, (3) epidemiological data suggesting an inverse correlation between a history of infection and the likelihood of developing cancer, and (4) our recent finding that a cocktail of pattern recognition receptor ligands (PRRLs) can eradicate solid tumors in cancer mice if applied metronomically. Because the main immunostimulating component of mistletoe extract (ME), mistletoe lectin, has been shown to be a PRRL as well, we suggest to apply ME in combination with additional PRRLs. Additional PRRLs can be found in approved drugs already on the market. Therefore, augmentation of ME might be feasible, with the aim of reattaining the old successes using approved drugs rather than bacterial extracts.

摘要

以下四点观察结果都指向同一个方向,即存在刺激先天免疫系统对抗癌症的未被利用的潜力:(1)100多年前科利及其同时代人用细菌提取物进行的实验性治疗;(2)自发消退与发热性感染之间的正相关;(3)流行病学数据表明感染史与患癌可能性之间呈负相关;(4)我们最近的发现,即模式识别受体配体(PRRL)鸡尾酒疗法若以节律性方式应用,可根除癌症小鼠体内的实体瘤。由于已证明槲寄生提取物(ME)的主要免疫刺激成分槲寄生凝集素也是一种PRRL,我们建议将ME与其他PRRL联合应用。其他PRRL可在已上市的获批药物中找到。因此,增强ME的效果可能是可行的,目的是利用获批药物而非细菌提取物重现过去的成功。