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为什么基因治疗能成为消灭HIV的合理工具 - David Baltimore P2

本视频由科普中国和生物医学大讲堂出品

David Baltimore (Caltech) Part 2: Why Gene Therapy Might be a Reasonable Tool for Attacking HIV

Lecture Overview:
In this set of lectures, I describe the threat facing the world from the human immunodeficiency virus (HIV) and a bold proposal on how we might meet the challenge of eliminating this disease by engineering the immune system.

In part 1, I provide a broad introduction to viruses, describing their basic properties and my own history of studying the replication of RNA viruses which led to the discovery of reverse transcriptase. I also illustrate the distinguishing features of equilibrium viruses (e.g. the common cold) that have adapted to co-exist with their host and non-equilibrium viruses (e.g. HIV) that have recently jumped from another species, are not adapted to the new host, and which can lead to disastrous outcomes (e.g. loss of immune function with potential lethality in the case of HIV).

In part 2, I describe the growing health problem that is facing the world with the spread of HIV and the limitations of current drug therapies and vaccine strategies. We need new ideas for tackling this problem. Here and in the next segment, I describe bold strategies of using gene therapy to conquer HIV, The approach that I describe in this segment involves gene therapy to produce short hairpin RNAs (siRNA) that target the destruction of a critical co-receptor of HIV, which the viruses that needs to infect cells. I discuss initial proof-of-principle experiments that suggest this approach might be feasible and the next steps needed to develop this idea into a real therapy.

In this last segment, I describe another gene therapy strategy for HIV in which we propose to develop antibody-like proteins that can be expressed by a patient's B cells and will target the HIV virus for destruction. To achieve this objective, hematopoietic (blood) stem cells must to be targeted with the gene, which will ultimately develop into B cells that express the therapeutic molecule. The ultimate goal is to produce a life-long supply of anti-HIV neutralizing antibodies. In this lecture, I describe the molecular methods underlying this strategy and a development path from proof-of-principle studies in mouse to safe trials in humans. This project receives funding from the Bill and Melinda Gates Foundation.

Speaker Bio: After serving as President of the California Institute of Technology for nine years, in 2006 David Baltimore was appointed President Emeritus and the Robert Andrews Millikan Professor of Biology. Born in New York City, he received his B.A. in Chemistry from Swarthmore College in 1960 and a Ph.D. in 1964 from Rockefeller University, where he returned to serve as President from 1990-91 and faculty member until 1994.

For almost 30 years, Baltimore was a faculty member at Massachusetts Institute of Technology. While his early work was on poliovirus, in 1970 he identified the enzyme reverse transcriptase in tumor virus particles, thus providing strong evidence for a process of RNA to DNA conversion, the existence of which had been hypothesized some years earlier. Baltimore and Howard Temin (with Renato Dulbecco, for related research) shared the 1975 Nobel Prize in Physiology or Medicine for their discovery, which provided the key to understanding the life-cycle of HIV. In the following years, he has contributed widely to the understanding of cancer, AIDS and the molecular basis of the immune response. His present research focuses on control of inflammatory and immune responses as well as on the use of gene therapy methods to treat HIV and cancer in a program called "Engineering Immunity".

Baltimore played an important role in creating a consensus on national science policy regarding recombinant DNA research. He served as founding director of the Whitehead Institute for Biomedical Research at MIT from 1982 until 1990. He co-chaired the 1986 National Academy of Sciences committee on a National Strategy for AIDS and was appointed in 1996 to head the National Institutes of Health AIDS Vaccine Research Committee.

In addition to receiving the Nobel Prize, Baltimore's numerous honors include the 1999 National Medal of Science, election to the National Academy of Sciences in 1974, the Royal Society of London, and the French Academy of Sciences. For 2007/8, he is President of the AAAS. He has published more than 600 peer-reviewed articles.

2015-12-14 课时:31分钟

丁秋蓉:基因组编辑在干细胞疾病模型建立和基因治疗中的应用

介绍了人群疾病基因组学的研究,尤其是全基因 组关联分析(GWAS)和罕见病研究,提示多个基因以及基因组区域和代谢综合征的发病显著相关。深入解析这类遗传发现,我们从基因组学研究出发,综合人多能干细胞疾病模拟、基因组编辑技术和模 式动物平台,对SORT1、AKT2、KLF14等代谢疾病相关基因组位点进行了功能和分子机制的深入解读;并研究利用基因组编辑技术体内直接靶向成体细胞,建立高效、特异和安全的核酸酶体内运输方式,探索潜在的代谢疾病新基因治疗方案。

2017-09-15 课时:41分钟

基因编辑技术与基因治疗讲坛

基因编辑技术正处于迅速发展的时期,编辑效率和精确性不断提高的同时,作为一项工具,在基因筛查、动物模型构建及疾病的基因治疗中都发挥着重要的作用。随着人们对疾病的新的有效靶点的不断认识和新的基因编辑技术的不断发展,基因编辑治疗方案的大规模临床应用将成为可能,特别是对那些传统疗法难以治愈的疾病,基因编辑技术的临床转化和应用研究值得拭目以待。

2020-06-08 课时:95分钟

2020杰克森实验室肿瘤免疫与基因治疗论坛

自2018年首款PD1单抗药物获得CFDA批准在中国上市起,国内肿瘤免疫药物的创新研发进入高速发展阶段。伴随药物研发的不断深入,研究者也面临诸多挑战。例如,PD-1单抗在肿瘤治疗领域虽取得了显著进展,但仅对一小部分病人有效。如何开发包括非T细胞靶点在内的新肿瘤免疫靶点;如何快速筛选可与PD-1联用的组合疗法等都依然有待探索。在临床前研究中,越来越多的研究者希望找到一个能够高效和稳定地实现多种人源免疫细胞重建的动物模型平台,为研究新靶点提供有力的支持。同时,研究者们也希望找到合适的动物疾病模型,实现不依赖于靶点的基因修饰而对组合疗法的体内药效进行快速评估。 在罕见病及神经疾病领域,能够在基因水平上模拟人患病机制的动物模型依然匮乏。药物开发者们希望能够拥有更多可模拟病人的突变类型和疾病进程的动物模型,为基因疗法提供具有临床转化意义的平台。 针对这些挑战,杰克森实验室将在9月2号于上海举办“2020肿瘤免疫与基因治疗论坛”,我们诚挚地邀请药物研发从业人员参加此次论坛,希望借此机会与您及业内专家们共同深入探讨相关解决方案,助力您的药物研发进程。

2020-09-07 课时:127分钟