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本文引用的文献

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Neo-adjuvant chemotherapy alone or with regional hyperthermia for localised high-risk soft-tissue sarcoma: a randomised phase 3 multicentre study.新辅助化疗联合或不联合区域热疗治疗局限性高危软组织肉瘤的随机 3 期多中心研究。
Lancet Oncol. 2010 Jun;11(6):561-70. doi: 10.1016/S1470-2045(10)70071-1. Epub 2010 Apr 29.
2
Radiofrequency thermal ablation for hepatocellular carcinoma stimulates autologous NK-cell response.射频热消融治疗肝细胞癌可刺激自体自然杀伤细胞反应。
Gastroenterology. 2010 May;138(5):1931-42. doi: 10.1053/j.gastro.2009.12.051. Epub 2010 Jan 11.
3
Diverse immune mechanisms may contribute to the survival benefit seen in cancer patients receiving hyperthermia.多种免疫机制可能有助于解释接受热疗的癌症患者的生存获益。
Immunol Res. 2010 Mar;46(1-3):137-54. doi: 10.1007/s12026-009-8115-8.
4
Hyperthermia as an immunotherapy strategy for cancer.热疗作为一种癌症免疫治疗策略。
Curr Opin Investig Drugs. 2009 Jun;10(6):550-8.
5
Expression of intracellular cytokines, HSP72, and apoptosis in monocyte subsets during exertional heat stress in trained and untrained individuals.训练有素和未经训练个体在运动性热应激期间单核细胞亚群中细胞内细胞因子、热休克蛋白72(HSP72)的表达及细胞凋亡情况
Am J Physiol Regul Integr Comp Physiol. 2009 Mar;296(3):R575-86. doi: 10.1152/ajpregu.90683.2008. Epub 2009 Jan 21.
6
Heat shock protein 70, released from heat-stressed tumor cells, initiates antitumor immunity by inducing tumor cell chemokine production and activating dendritic cells via TLR4 pathway.热应激肿瘤细胞释放的热休克蛋白70通过诱导肿瘤细胞产生趋化因子并经由Toll样受体4(TLR4)途径激活树突状细胞来启动抗肿瘤免疫。
J Immunol. 2009 Feb 1;182(3):1449-59. doi: 10.4049/jimmunol.182.3.1449.
7
Molecular responses of Jurkat T-cells to 1763 MHz radiofrequency radiation.Jurkat T细胞对1763兆赫兹射频辐射的分子反应。
Int J Radiat Biol. 2008 Sep;84(9):734-41. doi: 10.1080/09553000802317760.
8
Febrile-range hyperthermia accelerates caspase-dependent apoptosis in human neutrophils.发热范围的高温加速人中性粒细胞中半胱天冬酶依赖性凋亡。
J Immunol. 2008 Aug 15;181(4):2636-43. doi: 10.4049/jimmunol.181.4.2636.
9
Fever-range whole-body thermal therapy combined with cisplatin, gemcitabine, and daily interferon-alpha: a description of a phase I-II protocol.热程全身热疗联合顺铂、吉西他滨及每日一次的α干扰素:一项I-II期方案描述
Int J Hyperthermia. 2008 Dec;24(8):649-62. doi: 10.1080/02656730802104740.
10
Microvascular injury, thrombosis, inflammation, and apoptosis in the pathogenesis of heatstroke: a study in baboon model.中暑发病机制中的微血管损伤、血栓形成、炎症及细胞凋亡:狒狒模型研究
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为建立人类热暴露对免疫影响的温度阈值。

Toward establishment of temperature thresholds for immunological impact of heat exposure in humans.

机构信息

Genetics Branch, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, Maryland, USA.

出版信息

Int J Hyperthermia. 2011;27(4):344-52. doi: 10.3109/02656736.2011.562873.

DOI:10.3109/02656736.2011.562873
PMID:21591898
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3620730/
Abstract

There is interest in understanding the health impact of thermal effects as a result of exposure of humans to radiofrequency/microwave (RF/MW) fields. Immune cells and responses are affected by modest changes in temperature and it is important to quantify these effects and establish safety thresholds similar to what has been done with other tissue targets. Since previous summaries of thresholds for thermal damage to normal tissues have not focused much attention to cells of the immune system, this summary highlights recent studies which demonstrate positive and some negative effects of temperature shifts on human immune cells. We emphasise literature reporting adverse immunological endpoints (such as cell damage, death and altered function) and provide the temperature at which these effects were noted. Whereas there have been many in vitro studies of adverse temperature effects on immune cells, there has been limited validation of these temperature effects in vivo. However, data from heat stress/stroke patients do provide some information regarding core temperatures (40°C) at which thermal damage to immunological processes can begin to occur. We conclude that there is considerable need for more quantitative time temperature assessments using relevant animal models, more complete kinetic analyses to determine how long immunological effects persist, and for analysis of whether frequency of exposure has impact on immune function. To date, no attempt to categorise effects by using cumulative thermal dose measurements (e.g. cumulative equivalent minutes at a given temperature) has been conducted for cells or tissues of the immune system, representing a major gap in this field.

摘要

人们对了解人类暴露于射频/微波(RF/MW)场时热效应的健康影响很感兴趣。免疫细胞和反应会受到体温适度变化的影响,因此量化这些影响并建立类似于已对其他组织靶标所做的安全阈值非常重要。由于以前对正常组织热损伤阈值的总结没有太多关注免疫系统的细胞,因此本总结重点介绍了最近的研究,这些研究表明体温变化对人类免疫细胞有积极和一些负面影响。我们强调报告不良免疫学终点(如细胞损伤、死亡和功能改变)的文献,并提供注意到这些影响的温度。虽然已经有许多关于免疫细胞不良温度影响的体外研究,但在体内对这些温度影响的验证有限。然而,来自热应激/中风患者的数据确实提供了一些关于可能开始发生免疫过程热损伤的核心温度(40°C)的信息。我们得出的结论是,非常需要使用相关动物模型进行更定量的时间-温度评估,更完整的动力学分析以确定免疫效应持续多长时间,以及分析暴露频率是否对免疫功能有影响。迄今为止,尚未对免疫细胞或组织进行累积热剂量测量(例如在给定温度下累积等效分钟数)来对其进行分类,这是该领域的一个主要空白。