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Titlebook: Gene Therapy for HIV Infection; Clay Smith Book 1998 Springer-Verlag Berlin Heidelberg 1998 AIDS.HIV.Immunsystem.diseases.gene therapy.gen

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發(fā)表于 2025-3-21 17:37:08 | 只看該作者 |倒序?yàn)g覽 |閱讀模式
書目名稱Gene Therapy for HIV Infection
編輯Clay Smith
視頻videohttp://file.papertrans.cn/382/381979/381979.mp4
概述How to develop effective gene therapy to fight HIV infection.
圖書封面Titlebook: Gene Therapy for HIV Infection;  Clay Smith Book 1998 Springer-Verlag Berlin Heidelberg 1998 AIDS.HIV.Immunsystem.diseases.gene therapy.gen
描述ince the early 1980s, the HIV epidemic has been raging within the S 1 United States and around the world. Drug therapy for HIV infection has not been curative, prompting the search for alternative strategies to control HIV infection within infected persons. One potential alterna- tive to drug therapy is a developing medical technology termed gene therapy. 2 Gene therapy involves introducing genetic elements into popu- lations of cells in order to correct or prevent a pathologic process. A large number of gene therapy strategies have been developed in an at- tempt to inhibit HIV expression and spread. These strategies fall into two general categories, genetic modification of cells in order to elicit an immune response against HIV and genetic modification of the target cells of HIV infection in order to block HIV expression and reproduction. In the first strategy, termed genetic immunotherapy by some, genetic material encoding HIV proteins is introduced into patient‘s cells in order to stimulate a cellular immune response above and beyond 3 5 that stimulated by the viral infection itself. - Two general genetic im- munotherapy strategies have been developed. Genes encoding HIV pro- te
出版日期Book 1998
關(guān)鍵詞AIDS; HIV; Immunsystem; diseases; gene therapy; gene transfer; hematopoietic stem cell; hematopoietic stem
版次1
doihttps://doi.org/10.1007/978-3-662-11821-4
isbn_softcover978-3-662-11823-8
isbn_ebook978-3-662-11821-4
copyrightSpringer-Verlag Berlin Heidelberg 1998
The information of publication is updating

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發(fā)表于 2025-3-21 23:43:23 | 只看該作者
C. M. Finlayson,A. G. van der Valke system durably protected from rampant viral multiplication. This chapter reviews different gene therapy approaches that have been taken to inhibit HIV replication, using either viral components or cellular proteins as targets.
板凳
發(fā)表于 2025-3-22 00:40:06 | 只看該作者
https://doi.org/10.1007/978-3-642-31635-7y of HIV-1 pathogenesis. Several model systems use immunodeficient mice engrafted with human immune cells while other models use one of several species of macaque infected with SIV, a virus which is highly related to HIV-2 and more distantly related to HIV-1.. Some of these animal models of HIV and
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Book 1998apy by some, genetic material encoding HIV proteins is introduced into patient‘s cells in order to stimulate a cellular immune response above and beyond 3 5 that stimulated by the viral infection itself. - Two general genetic im- munotherapy strategies have been developed. Genes encoding HIV pro- te
5#
發(fā)表于 2025-3-22 11:39:23 | 只看該作者
Gene Therapy Strategies for Inhibition of HIV,e system durably protected from rampant viral multiplication. This chapter reviews different gene therapy approaches that have been taken to inhibit HIV replication, using either viral components or cellular proteins as targets.
6#
發(fā)表于 2025-3-22 13:32:38 | 只看該作者
Animal Models of Gene Therapy for AIDS,y of HIV-1 pathogenesis. Several model systems use immunodeficient mice engrafted with human immune cells while other models use one of several species of macaque infected with SIV, a virus which is highly related to HIV-2 and more distantly related to HIV-1.. Some of these animal models of HIV and
7#
發(fā)表于 2025-3-22 19:59:46 | 只看該作者
https://doi.org/10.1007/978-3-662-11821-4AIDS; HIV; Immunsystem; diseases; gene therapy; gene transfer; hematopoietic stem cell; hematopoietic stem
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An Algorithm for Predictive Ordination,The goal of gene therapy for the treatment of acquired immuno deficiency syndrome (AIDS) is suppression of human immunodeficiency virus (HIV) replication at any stage of the viral life cycle in order to promote host survival. As described in chapter 2, most current gene therapy efforts focus on:
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