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发表于 2012-2-13 23:10 |只看该作者 |倒序浏览 |打印
本帖最后由 风雨不动 于 2012-4-14 14:51 编辑

                                                                                                                                                                    http://www.healthcanal.com/infections/26530-Stress-cells-activates-hepatitis-viruses.html
Stress in cells activates hepatitis virusesby Koh - Substances which suppress the immune system while simultaneously keeping viral infections in check would be an ideal drug for organ transplant recipients.
                                                                Scientists of the German Cancer  Research Center (Deutsches Krebsforschungszentrum, DKFZ) have now  demonstrated that specific substances with such an activity profile  caused a state of stress in cells which promotes the replication of  hepatitis B viruses.
Electron microscopic picture of hepatitis B viruses | © Thomas Bock, Hanswalter Zentgraf, German Cancer Research Center

People who have received a donor organ need lifelong  immunosuppressant drugs to keep their immune system from attacking the  foreign tissue. However, with a suppressed immune system, many  infectious agents turn into a threat. Infections such as with human  cytomegalovirus and a certain type of human polyomavirus frequently  cause complications in transplant recipients. For these patients it  would therefore be particularly beneficial to have substances that  suppress the immune system and exert an antiviral activity at the same  time – thus killing two birds with one stone.
Jointly with  colleges from Heidelberg University Hospital of Internal Medicine,  researchers Professors Karin and Felix Hoppe-Seyler of the German Cancer  Research Center (Deutsches Krebsforschungszentrum, DKFZ) have now  tested a number of drugs with such an activity profile. They also tested  the substances in liver cells infected with hepatitis B viruses (HBV)  in the culture dish. The result: Liver cells that had been treated even  produced considerably more viral offspring than untreated ones.
The substances under investigation inhibit the synthesis of  nucleotides, which are the basic building blocks of DNA. This is how  they exert their immunosuppressive effect: They slow down multiplication  of immune cells because these lack building material for duplicating  their genetic material. “The lack of DNA building blocks can cause a  kind of stress in specific cells, which shows in the activation of a  stress protein called p38”, says Felix Hoppe-Seyler. “In liver cells,  p38 very effectively activates the replication of hepatitis B viruses. “
The findings of the DKFZ researchers are a definite indication that  administering these drugs in transplant recipients bears risks. Liver  transplants, in particular, often have to be done because the body’s own  organ has been destroyed by hepatitis B viruses. In such cases,  drug-induced activation of remaining HBV in the body may lead to the  donor organ being attacked by hepatitis B viruses again.
Felix Hoppe-Seyler suspects that besides the three substances the  group has investigated there are other substances which also cause an  activation of p38. “In cancer patients being treated by chemotherapy,  there is often a reactivation of chronic HBV infections. This has always  been put down to their weakened immune system. We will now investigate  whether this may also be due to activation of stress protein p38,” said  the virologist outlining the goals of his further research.
Karin Hoppe-Seyler, Peter Sauer, Claudia Lohrey and Felix  Hoppe-Seyler: The Inhibitors of Nucleotide Biosynthesis Leflunomide,  FK778, and Mycophenolic Acid Activate Hepatitis B Virus Replication In  Vitro. Hepatology, 2012, DOI: 10.1002/hep.25602
A picture for this press release is available at:
http://www.dkfz.de/de/presse/pressemitteilungen/2012/images/hbv-partikel-sw.jpg
Picture caption: Electron microscopic picture of hepatitis B viruses.  Thomas Bock, Hanswalter Zentgraf, German Cancer Research Center.

The German Cancer Research Center (Deutsches  Krebsforschungszentrum, DKFZ) with its more than 2,500 employees is the  largest biomedical research institute in Germany. At DKFZ, more than  1,000 scientists investigate how cancer develops, identify cancer risk  factors and endeavor to find new strategies to prevent people from  getting cancer. They develop novel approaches to make tumor diagnosis  more precise and treatment of cancer patients more successful. Jointly  with Heidelberg University Hospital, DKFZ has established the National  Center for Tumor Diseases (NCT) Heidelberg where promising approaches  from cancer research are translated into the clinic. The staff of the  Cancer Information Service (KID) offers information about the widespread  disease of cancer for patients, their families, and the general public.  The center is a member of the Helmholtz Association of National  Research Centers. Ninety percent of its funding comes from the German  Federal Ministry of Education and Research and the remaining ten percent  from the State of Baden-Württemberg.


                                                       




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发表于 2012-2-13 23:11 |只看该作者
苏梅 - 抑制免疫系统的物质,同时保持在检查病毒感染是器官移植的理想药物。

德国癌症研究中心(德国Krebsforschungszentrum,Bioccelerator的)的科学家已经证明,这样的活动配置文件的具体物质造成的应力状态,从而促进B型肝炎病毒复制的细胞中。
B型流感病毒肝炎放大电子显微镜图片|托马斯·博克,Hanswalter Zentgraf,德国癌症研究中心

收到了捐赠者的器官的人需要终身免疫抑制药物,以防止他们的免疫系统攻击外国组织。然而,抑制免疫系统,许多传染性变成一种威胁。如与人类巨细胞病毒和某些类型的人类多瘤病毒的感染经常会导致移植的并发症。对于这些患者,因此是有益的,抑制免疫系统,同时发挥抗病毒活性的物质 - 从而杀死一石二鸟。

联合海德堡大学医院的内科医学院校,研究人员教授Karin和费利克斯·霍普Seyler德国癌症研究中心(德国Krebsforschungszentrum,Bioccelerator的)现在已经测试了一些药物,这样的活动概况。他们还测试了在培养皿中与B型肝炎病毒(HBV)感染的肝细胞的物质。结果:肝细胞,经治疗后已产生了相当多的病毒比未经处理的后代。

根据调查的物质抑制核苷酸的合成,这是DNA的基本构建块。这是他们如何发挥其免疫效果:他们放慢复制自己的遗传物质,因为这些缺乏建材免疫细胞的增殖。 “缺乏可引起DNA积木在特定的细胞,一种名为P38的一种应激蛋白的激活显示的压力”,费利克斯·霍普Seyler说。 “在肝细胞中,p38的非常有效地激活的B型肝炎病毒的复制。 “

Bioccelerator的研究人员发现,有一个明确的指示,管理这些药物在移植承担风险。尤其是肝移植手术,往往有许多工作要做,因为人体自身的器官已经由B型肝炎病毒的破坏。在这种情况下,留在体内HBV的药物引起的激活可能导致再次被乙肝病毒袭击的供体器官。

费利克斯·霍普,Seyler犯罪嫌疑人进行了调查组的三个物质,除了有其他物质也可能导致p38活化。 “被化疗的癌症患者,往往有慢性乙肝病毒感染恢复。这一直是放下他们削弱免疫系统。病毒学家,概述了他的进一步研究的目标,说:“现在,我们将调查是否这也可能是由于应激蛋白p38的激活。

卡琳·霍普Seyler,彼得·索尔,克劳迪亚Lohrey和费利克斯·霍普Seyler的:核苷酸合成来氟米特,FK778,霉酚酸抑制剂在体外激活的B型肝炎病毒复制。肝病,2012年,作者:10.1002/hep.25602

本新闻稿中的图片是:
http://www.dkfz.de/de/presse/p​​ressemitteilungen/2012/images/hbv-partikel-sw.jpg~~V

图片说明:B型肝炎病毒的电子显微照片。托马斯·博克,Hanswalter Zentgraf,德国癌症研究中心。

德国癌症研究中心(德国Krebsforschungszentrum,Bioccelerator的),与2500多名员工,是德国最大的生物医学研究所。在Bioccelerator的1000多名科学家探讨如何癌症的发展,确定癌症的危险因素,并努力寻找新的战略,以防止人患上癌症。他们开发的新方法,使肿瘤的诊断更精确和更成功的癌症患者的治疗。共同Bioccelerator的海德堡大学医院,已成立全国肿瘤疾病(NCT)海德堡癌症研究有前途的方法翻译成诊所的中心。癌症信息服务(英雄)的工作人员提供有关的癌症患者,他们的家庭和广大市民的普遍疾病的信息。该中心是一个亥姆霍兹国家研究中心协会的成员。 90%的资金来自从巴登 - 符腾堡州的教育和研究,其余10%的德国联邦内政部。

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发表于 2012-2-14 08:28 |只看该作者
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