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人类对HIV的免疫反应及其对灭活HIV疫苗潜在研发的影响。

The Human Immune Response to HIV and its Impact in the Potential Development of an Inactivated HIV Vaccine.

作者信息

Rios Adan, Pottet Ethan C, Siwak Edward B, Anderson Dallas W, Yao Qizhi C

机构信息

PhotoImmune Biotechnology Inc., Houston, TX, USA.

University of Texas Medical School at Houston. Houston, TX, USA.

出版信息

AIDS Rev. 2016 Jul-Sep;18(3):151-157.

Abstract

There is evidence that the transmission and acute phase of HIV infection triggers an immune response capable of controlling HIV subverted by the process of virus integration, essential to the replicative cycle of retroviruses. We review here two aspects that deserve consideration in light of recent developments concerning HIV transmission and vaccine development: vaccines directed against transmitted/founder viruses, and a reconsideration of inactivation as a viable means to obtain a preventive HIV vaccine. Since 80% of sexually transmitted HIV infections are caused by a single transmitted/founder variant, it is appropriate to target transmitted/founder viruses for vaccine development. Transmitted/founder virus transmission is subject to strong natural selection based on conserved signatures present in all forms of transmitted/founder HIV viruses. This provides an opportunity to pursue inactivation methods of vaccine development that allow antigenic preservation of HIV transmitted/founder viruses. The presentation to the immune system of an inactivated but antigenically preserved transmitted/founder virus should allow the development of an effective immune response against transmitted/founder viruses. This could be the base for an inactivated transmitted/founder virus HIV vaccine. We have devised a method of inactivation of HIV reverse transcriptase through the use of a novel photo-labeling procedure based on the use of photo-labeled analogs of antiretroviral compounds with specific affinity for HIV reverse transcriptase. We believe this method fulfills the required conditions for an effective preventive vaccine development: inactivation and antigenic preservation.

摘要

有证据表明,HIV感染的传播和急性期会引发一种免疫反应,这种免疫反应能够控制被病毒整合过程颠覆的HIV,而病毒整合是逆转录病毒复制周期所必需的。鉴于近期在HIV传播和疫苗研发方面的进展,我们在此回顾两个值得考虑的方面:针对传播/奠基者病毒的疫苗,以及重新审视灭活作为获得预防性HIV疫苗的可行手段。由于80%的性传播HIV感染是由单一的传播/奠基者变体引起的,因此将传播/奠基者病毒作为疫苗研发的靶点是合适的。传播/奠基者病毒的传播受到基于所有形式的传播/奠基者HIV病毒中存在的保守特征的强烈自然选择的影响。这为寻求疫苗研发的灭活方法提供了机会,这种方法能够保留HIV传播/奠基者病毒的抗原性。将灭活但抗原性保留的传播/奠基者病毒呈递给免疫系统,应该能够引发针对传播/奠基者病毒的有效免疫反应。这可能是灭活的传播/奠基者病毒HIV疫苗的基础。我们通过使用一种基于对抗逆转录病毒化合物进行光标记的新型光标记程序,设计了一种灭活HIV逆转录酶的方法,该化合物对HIV逆转录酶具有特异性亲和力。我们相信这种方法满足了有效预防性疫苗研发的必要条件:灭活和抗原性保留。

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