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美国国立卫生研究院给出SLU $ 220万设计治愈乙肝 [复制链接]

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发表于 2015-12-15 09:14 |只看该作者 |倒序浏览 |打印
NIH gives SLU $2.2 million to design a cure for Hepatitis B


ST. LOUIS-- With proof-of-principle in his pocket and a new $2.2 million grant from the National Institutes of Health (NIH), SLU scientist John Tavis, Ph.D., will take his 25 year mission to finally develop a cure for the hepatitis B virus into the next phase.

Tavis, who is professor of molecular microbiology and immunology at Saint Louis University, says his team has built a warhead that will kill the virus; now, it's time to design a cruise missile that will deliver the drug.

After exposure, the hepatitis B virus can linger, causing chronic infection in many people. Over time, the illness causes liver damage. While current treatments can suppress the virus, they cannot fully kill it, and it will return if treatments are stopped.

More than 350 million people are chronically infected with the hepatitis B virus. Of those infected, up to 1.2 million die from liver failure and liver cancer each year.

Because current treatments are costly, lifetime medications, scientists are keen to develop better options, likely in the form of combination therapies, to knock out the virus for good.

Tavis and his team have finished one stage of research and are moving on to another in their quest to design a new drug.

"We've achieved the first stage of the laboratory research. We've developed the warhead of a drug, the portion that does the actual activity that the drug is designed to do. We did this with a class of compounds called alpha hydroxyl tropolones.

"We have advanced beyond what is called 'target identification and validation'," Tavis said. "We found something to hit in the virus and proved that it is a good thing to hit. Then, we identified about 35 inhibitors. This tells us about the types of compounds needed to block the viral activity. This is the first step to drug development. Now, we're done with proof-of-principle part of the work.

"The inhibitors we found are the warhead of the drug, but this is only one portion of a drug. The next part is the delivery, which involves all kinds of things. We must design a molecule for minimal toxicity, that can be absorbed by the body and that can last long enough for therapeutic benefit. Then, we've got to package it so people can take it in a pill. Ideally, we'd like to avoid injectables, which are difficult for people to take.

"So, now we've got to design the package -- the cruise missile -- that will hold and deliver the warhead."

The recent NIH grant will allow Tavis, his key collaborators Ryan Murelli, Ph.D., of the City University of New York and Marvin Meyers, Ph.D., director of medicinal chemistry at SLU's Center for World Health and Medicine, and the rest of his team to take their promising findings a step closer toward drug development. This stage will focus on medicinal chemistry, testing the drug in repetitive cycles aimed at optimizing the drug and limiting toxicity.

"We need an inhibitor that is safe enough and good enough to give to people," Tavis said. "This is very hard work. While this new grant won't get us all the way there, if we are very successful we will get deep into the preclinical stage in preparation for clinical trials."

Tavis credits early support from the NIH and SLU, as well as the unique collaborations possible through partnership with SLU's Center for World Health and Medicine (CWHM) with allowing his work to progress.

"Drug design has not traditionally been done in academia," Tavis said. "The work is not always compatible with academic duties and it requires an interdisciplinary team. It can be difficult to organize the workflow. But, the Center for World Health and Medicine at SLU is a unique resource. It has enabled those of us in the basic sciences to advance our work."

Initial research funding for Tavis's work included seed grants that allowed him to gather enough data to publish early findings and attract NIH funding.

"This project is a result of 25 years of background studies in basic science funded by the NIH," he said. "And, the initial stages of the more recent work were generously supported by seed grants from SLU through the President's Research Fund. We also received funding from the "Friends of the Saint Louis University Liver Center" and from SLU Cancer Center, as well as Washington University's Institute of Clinical and Translational Sciences. All of those different organizations saw value in this work at an early stage, invested, and now we are seeing the payoff."

Read about the 19-year problem Tavis cracked that led to his scientific breakthrough in the search for a cure for hepatitis B here: http://www.slu.edu/rel-tavis-24.

Established in 1836, Saint Louis University School of Medicine has the distinction of awarding the first medical degree west of the Mississippi River. The school educates physicians and biomedical scientists, conducts medical research, and provides health care on a local, national and international level. Research at the school seeks new cures and treatments in five key areas: cancer, liver disease, heart/lung disease, aging and brain disease, and infectious diseases.

SLU's Center for World Health and Medicine is dedicated to the development of medicines to treat diseases that affect the world's poor and underserved populations. The center consists of a multidisciplinary team of former pharmaceutical company scientists with extensive translational research experience. They have the skills to discover and develop small molecule drugs, and they are experienced in advancing such agents into clinical trials.

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发表于 2015-12-15 09:15 |只看该作者
美国国立卫生研究院给出SLU $ 220万设计治愈乙肝


ST。 LOUIS--通过验证性原则,在他的口袋里,一个新的$ 2.2万美元的赠款,从健康(NIH),SLU科学家约翰·塔维斯博士的国家机构,将他的25年的使命,终于开发出治疗乙肝病毒进入下一个阶段。

塔维斯,谁是分子微生物学和免疫学圣路易斯大学的教授,他说他的团队已经建立了一个弹头,将杀死病毒;现在,它的时间来设计巡航导弹,将提供药物。

曝光后,将乙肝病毒可以停留,引起慢性感染的许多人。随着时间的推移,这种疾病会导致肝脏损伤。虽然目前的治疗可以抑制病毒,他们不能完全杀死它,如果治疗被停止,将返回。

超过3.5亿人为慢性感染了乙肝病毒。感染者,高达120万死于肝功能衰竭和每年肝癌。

由于目前的治疗是昂贵的,终身的药物,科学家们都热衷于开发更好的选择,有可能在联合疗法的形式,敲出来的病毒为好。

塔维斯和他的团队已经完成了一个研究阶段,正在转向另一个在寻求设计一种新的药物。

“我们已经实现了实验室研究的第一阶段,我们已经制定了药物的弹头,那确实该药物是专门做的实际活动的部分。我们这样做是有一类化合物称为阿尔法羟基tropolones 。

“我们拥有先进的超越了被称为”目标识别和确认“,”塔维斯说。 “我们发现一些在病毒击中并证明了它是个好东西打了。然后,我们确定了约35抑制剂。这告诉我们需要阻止病毒活性的化合物的类型。这是第一步药物发展。现在,我们有证明性的原则工作的一部分完成。

“我们找到的抑制剂是药物的弹头,但是这是一种药物的仅一个部分中。接下来的部分是递送,这涉及到各种事情,我们必须设计一个分子为毒性最小,能够由吸收身体和可以持续足够长的治疗效果,那么,我们一定要打包,以便人们可以把它在一个药丸。理想情况下,我们想避免注射,这是难以让人拿。

“所以,现在我们已经有了设计包 - 巡航导弹 - 将保存并提供弹头”

最近美国国立卫生研究院资助将让纽约和马文·迈尔斯博士,药物化学,在圣路易斯的中心为世界卫生和医学主任城市大学的Tavis,他的主要合作者瑞安Murelli,博士,和他的团队的其余部分采取他们希望的结果更接近了一步走向药物研发。这个阶段将集中于药物化学,测试药物在重复循环旨在优化药物和限制性毒性。

“我们需要的抑制剂是足够安全的不够好,给的人,”塔维斯说。 “这是非常艰苦的工作,而这个新的赠款将不会得到我们所有的方式出现,如果我们都是非常成功的,我们将深入到准备进行临床试验,临床前研究阶段。”

塔维斯归功于来自美国国立卫生研究院和SLU,以及通过与SLU的中心世界卫生和医学(CWHM)的合作可能的独特合作初期支持,让他的工作取得进展。

“药物设计工作传统上并未在学术界做了,”塔维斯说。 “这项工作并不总是与学术职务兼容,它需要一个跨学科的团队。它可以是难以组织的工作流程。但是,该中心为世界卫生和医学在圣路易斯大学是一个独特的资源,它使我们这些在基础科学推进我们的工作。“

初步研究经费塔维斯的工作包括种子基金,使他收集足够的数据来发布的初步结果,并吸引NIH资助。

“这个项目是25年由美国国立卫生研究院资助的基础科学背景研究的结果,”他说。 “而且,最近的工作的初始阶段都慷慨地从SLU通过总统的研究基金支持的种子基金。我们也获得了资金从”圣路易斯大学肝病中心之友“,并从SLU癌症中心,以及临床和转化科学华盛顿大学的研究所。所有这些不同的组织看到了这项工作的价值在早期阶段,投入资金,而现在我们看到了回报。“

阅读关于19年的问题塔维斯破裂,导致他的科学突破中寻找治愈这里乙型肝炎http://www.slu.edu/rel-tavis-24

成立于1836年,圣路易斯大学医学院有授予密西西比河的第一个医学学位西部的区别。学校教育的医生和生物医学科学家,开展医学研究,并提供一个地方,国家和国际一级卫生保健。研究在学校寻求新的治疗方法和治疗的五个关键领域:癌症,肝病,心脏/肺疾病,衰老和脑疾病和传染病。

SLU的中心世界卫生和医学专门用于药物开发治疗影响世界上的穷人和弱势人群疾病。该中心由以前的制药公司的科学家具有广泛的转化研究经验的多学科团队。他们有能力发现和开发小分子药物,他们都是经验丰富的在推进这类药物进入临床试验阶段。

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发表于 2015-12-15 10:02 |只看该作者
回复 StephenW 的帖子

希望早点成功,如果中国有些仁人志士能够投身于其中,就更好了,那点小钱,对了土豪来说,太少了
拉米(5年)耐藥,恩替(7年)耐藥, 2015.10.21服下第1顆替諾的超瘦大三羊,替诺进行时....

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发表于 2015-12-15 12:21 |只看该作者
目标是开发RNAseH抑制剂,本质上和RT抑制剂(NUC)没有太大区别,号称“ design a cure”,这个牛皮吹得略微有点大。

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发表于 2015-12-15 13:52 |只看该作者
回复 HBVCURER 的帖子

所以还是更看好。杨梅一些。
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