Castanospermine:一种可能的艾滋病治疗方法

A. Gelbard
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引用次数: 0

摘要

HIV病毒以一种非常复杂的方式感染人体。它使用一种叫做CCR5的趋化因子受体,这种受体在称为CD4 t辅助细胞的特定类型的t辅助免疫细胞表面错误识别它。然后免疫系统的CD8 t辅助细胞系统地攻击被感染的CD4细胞并摧毁它们。这些细胞通过一个叫做MHC的系统进入降解和循环过程,但病毒持续存在,它的小肽通过MHC系统返回到t辅助细胞中,这一机制本质上是为了提高免疫力,由于CCR5受体失灵,再次感染CD4 t细胞。这一过程导致CD4 t细胞计数下降,并导致艾滋病明显的免疫缺陷,因为这些细胞是免疫系统功能所必需的。这种在t细胞表面错误识别病毒的趋化因子受体,CCR5,有有效的药物来阻止它的功能,CCR5拮抗剂已经在艾滋病治疗中使用,并产生了非常积极的影响。另一种治疗方法是通过增加新t细胞的产生来恢复免疫效率。这篇论文提出的是另一种随机研究的影响MHC过程的途径,以防止病毒持续感染CD t细胞。castanosperine是一种首次从澳洲Castanospermum australe种子中分离得到的吲哚吡啶类生物碱。它和它的衍生物已经在医学上使用了。多项研究表明,该物质抑制MHC循环过程并影响其分泌[2-4]。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Castanospermine a Possible AIDS Treatment
The HIV virus infects the body in a very sophisticated manner. It uses a chemokine receptor called CCR5 that mis-recognizes it on the surface of specific type of T-helper immune cells called CD4 T-helper cells. The immune system CD8 T-helper cells then systematically attack the infected CD4 cells and demolish them. These cells go to degradation and recycling process by a system called MHC but the virus persists and small peptides of it return to the T-helper cells through the MHC system, in a mechanism essentially designed to improve immunity, and because of the CCR5 receptor malfunction, infect the CD4 T-cells once again. This process leads to a decline in CD4 T-cells count and to the immunodeficiency evident in AIDS, because these cells are necessary for the immune system’s function. This chemokine receptor that misrecognizes the virus on the surface of the T-cells, CCR5, has effective drugs meant to block its function, CCR5 antagonists that are already in use in AIDS treatment and have a very positive impact. Another form of treatment is by enhancing the production of new T-cells to restore immune efficiency despite the disease. What this paper suggests is another pathway randomly researched to impact the MHC process, in order to prevent the virus from continuously infecting the CD T-cells. Castanospermine is an indolizidine alkaloid first isolated from the seeds of Castanospermum australe. It and substances deriving of it are already in use in medicine [1]. Several studies have shown this substance to inhibit the MHC recycling process and affect its secretion [2-4].
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