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本文引用的文献

1
Vector-mediated gene transfer engenders long-lived neutralizing activity and protection against SIV infection in monkeys.载体介导的基因转移在猴子体内产生了长期的中和活性并提供了针对猴免疫缺陷病毒感染的保护。
Nat Med. 2009 Aug;15(8):901-6. doi: 10.1038/nm.1967. Epub 2009 May 17.
2
Phase 2 gene therapy trial of an anti-HIV ribozyme in autologous CD34+ cells.抗HIV核酶在自体CD34+细胞中的2期基因治疗试验。
Nat Med. 2009 Mar;15(3):285-92. doi: 10.1038/nm.1932. Epub 2009 Feb 15.
3
Long-term control of HIV by CCR5 Delta32/Delta32 stem-cell transplantation.通过CCR5 Δ32/Δ32干细胞移植实现对HIV的长期控制。
N Engl J Med. 2009 Feb 12;360(7):692-8. doi: 10.1056/NEJMoa0802905.
4
Optimization of human immunodeficiency virus type 1 envelope glycoproteins with V1/V2 deleted, using virus evolution.利用病毒进化对缺失V1/V2的1型人类免疫缺陷病毒包膜糖蛋白进行优化。
J Virol. 2009 Jan;83(1):368-83. doi: 10.1128/JVI.01404-08. Epub 2008 Oct 15.
5
Evaluation of safety and efficacy of RNAi against HIV-1 in the human immune system (Rag-2(-/-)gammac(-/-)) mouse model.在人类免疫系统(Rag-2(-/-)gammac(-/-))小鼠模型中评估RNA干扰对HIV-1的安全性和有效性。
Gene Ther. 2009 Jan;16(1):148-53. doi: 10.1038/gt.2008.124. Epub 2008 Jul 31.
6
The aftermath of the Merck's HIV vaccine trial.默克公司艾滋病疫苗试验的后续情况。
Retrovirology. 2008 Jul 2;5:56. doi: 10.1186/1742-4690-5-56.
7
Replicating viral vectors as HIV vaccines Summary Report from IAVI Sponsored Satellite Symposium, International AIDS Society Conference, July 22, 2007.
Biologicals. 2008 Sep;36(5):277-86. doi: 10.1016/j.biologicals.2008.04.004. Epub 2008 Jun 13.
8
RNA interference against viruses: strike and counterstrike.针对病毒的RNA干扰:攻击与反击
Nat Biotechnol. 2007 Dec;25(12):1435-43. doi: 10.1038/nbt1369.
9
Stable reduction of CCR5 by RNAi through hematopoietic stem cell transplant in non-human primates.通过造血干细胞移植在非人灵长类动物中利用RNA干扰稳定降低CCR5水平。
Proc Natl Acad Sci U S A. 2007 Aug 7;104(32):13110-5. doi: 10.1073/pnas.0705474104. Epub 2007 Aug 1.
10
Generation of neutralizing activity against human immunodeficiency virus type 1 in serum by antibody gene transfer.通过抗体基因转移在血清中产生针对1型人类免疫缺陷病毒的中和活性。
J Virol. 2002 Sep;76(17):8769-75. doi: 10.1128/jvi.76.17.8769-8775.2002.

迈向基因艾滋病疫苗。

Towards a genetic AIDS vaccine.

机构信息

Laboratory of Experimental Virology, Department of Medical Microbiology, Center for Infectious Diseases and Immunology Amsterdam, Academic Medical Center, University of Amsterdam, the Netherlands.

出版信息

Retrovirology. 2009 Oct 16;6:93. doi: 10.1186/1742-4690-6-93.

DOI:10.1186/1742-4690-6-93
PMID:19835599
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2766360/
Abstract

We discuss a recent Nature Medicine publication by Philip Johnson and co-workers (Vector-mediated gene transfer engenders long-lived neutralizing activity and protection against SIV infection in monkeys. Nat. Med. 2009, 15: 901-906) in which an effective HIV-1 vaccine was designed that is based on gene therapy. The introduced gene produces an antibody-like immunoadhesin in the blood that neutralizes the virus.

摘要

我们讨论了最近发表在《自然医学》杂志上的一篇文章,这篇文章由 Philip Johnson 及其同事撰写(Vector-mediated gene transfer engenders long-lived neutralizing activity and protection against SIV infection in monkeys. Nat. Med. 2009, 15: 901-906),文中设计了一种基于基因治疗的有效 HIV-1 疫苗。引入的基因在血液中产生一种类似抗体的免疫黏附素,可中和病毒。