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本文引用的文献

1
Simian immunodeficiency virus from the sooty mangabey and rhesus macaque is modified with O-linked carbohydrate.食蟹猴和恒河猴的猴免疫缺陷病毒经过 O-连接糖基化修饰。
J Virol. 2011 Jan;85(1):582-95. doi: 10.1128/JVI.01871-10. Epub 2010 Oct 20.
2
Fundamental difference in the content of high-mannose carbohydrate in the HIV-1 and HIV-2 lineages.HIV-1 和 HIV-2 谱系中高甘露糖碳水化合物含量的根本差异。
J Virol. 2010 Sep;84(18):8998-9009. doi: 10.1128/JVI.00996-10. Epub 2010 Jul 7.
3
Review: Soluble innate immune pattern-recognition proteins for clearing dying cells and cellular components: implications on exacerbating or resolving inflammation.综述:可溶性固有免疫模式识别蛋白清除死亡细胞和细胞成分:对炎症加重或消退的影响。
Innate Immun. 2010 Jun;16(3):191-200. doi: 10.1177/1753425910369271.
4
Microvirin, a novel alpha(1,2)-mannose-specific lectin isolated from Microcystis aeruginosa, has anti-HIV-1 activity comparable with that of cyanovirin-N but a much higher safety profile.微囊藻素,一种从铜绿微囊藻中分离得到的新型α(1,2)-甘露糖特异性凝集素,具有与环孢菌素 N 相当的抗 HIV-1 活性,但安全性更高。
J Biol Chem. 2010 Aug 6;285(32):24845-54. doi: 10.1074/jbc.M110.128546. Epub 2010 May 27.
5
HIV-1 assembly in macrophages.HIV-1 在巨噬细胞中的组装。
Retrovirology. 2010 Apr 7;7:29. doi: 10.1186/1742-4690-7-29.
6
HIV-1 exploits innate signaling by TLR8 and DC-SIGN for productive infection of dendritic cells.HIV-1 利用 TLR8 和 DC-SIGN 固有信号促进树突状细胞的感染。
Nat Immunol. 2010 May;11(5):419-26. doi: 10.1038/ni.1858. Epub 2010 Apr 4.
7
Relationships between plasma membrane microdomains and HIV-1 assembly.质膜微区与 HIV-1 组装之间的关系。
Biol Cell. 2010 Mar 25;102(6):335-50. doi: 10.1042/BC20090165.
8
Mucin-type O-glycosylation--putting the pieces together.粘蛋白型 O-糖基化——将各个部分组合在一起。
FEBS J. 2010 Jan;277(1):81-94. doi: 10.1111/j.1742-4658.2009.07429.x. Epub 2009 Nov 17.
9
Glycosyltransferase and sulfotransferase gene expression profiles in human monocytes, dendritic cells and macrophages.人单核细胞、树突状细胞和巨噬细胞中糖基转移酶和磺基转移酶基因表达谱。
Glycoconj J. 2009 Dec;26(9):1259-74. doi: 10.1007/s10719-009-9244-y.
10
Glycosylation of gp41 of simian immunodeficiency virus shields epitopes that can be targets for neutralizing antibodies.猿猴免疫缺陷病毒gp41的糖基化掩盖了可成为中和抗体靶点的表位。
J Virol. 2008 Dec;82(24):12472-86. doi: 10.1128/JVI.01382-08. Epub 2008 Oct 1.

碳水化合物对艾滋病病毒糖蛋白的功能贡献。

Functional contributions of carbohydrate on AIDS virus glycoprotein.

机构信息

New England Primate Research Center, Harvard Medical School, Southborough, Massachusetts 01772-9102, USA.

出版信息

Yale J Biol Med. 2010 Dec;83(4):201-8.

PMID:21165339
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3002149/
Abstract

Envelope glycoprotein spikes on the surface of the human immunodeficiency virus (HIV) are used by the virus to bind to cellular receptors to gain entry into target cells. As such, the envelope spikes are the targets of antibodies that can neutralize viral infectivity. Fifty percent or more of the mass of the viral-encoded surface glycoprotein of HIV, and of its close monkey relative simian immunodeficiency virus (SIV), is actually carbohydrate; it is one of the most heavily glycosylated proteins that can be found in mammals. It has been clearly demonstrated that one of the functions of this carbohydrate is to shield viral epitopes that would otherwise be the direct target of antibodies that could neutralize viral infection. In addition, it is now generally accepted that the carbohydrate on the viral envelope glycoprotein is recognized by multiple cellular lectins of the host lymphoreticular system, and these interactions play a role in the dissemination of virus within the host as well as the release of modulatory cytokines. Our work recently demonstrated fundamental differences in the composition of the carbohydrate on HIV type 1, the cause of the AIDS pandemic, versus the SIV in the sooty mangabey monkey, a natural host that does not develop disease from its infection. We now speculate that this fundamental difference in carbohydrate composition reflects evolutionary pressures on both virus and host. Furthermore, carbohydrate composition on the virus and genetic differences in carbohydrate-sensing proteins of the host could be critically important for the generalized lymphoid activation that characterizes the acquired immunodeficiency syndrome (AIDS).

摘要

人类免疫缺陷病毒 (HIV) 表面的包膜糖蛋白刺突被病毒用来结合细胞受体,从而进入靶细胞。因此,包膜刺突是可以中和病毒感染力的抗体的靶标。HIV 病毒编码的表面糖蛋白及其密切相关的猴免疫缺陷病毒 (SIV) 的 50%或更多质量实际上是碳水化合物;它是哺乳动物中糖基化程度最高的蛋白质之一。已经清楚地表明,这种碳水化合物的功能之一是屏蔽病毒表位,否则这些表位将成为中和病毒感染的抗体的直接靶标。此外,现在人们普遍认为,病毒包膜糖蛋白上的碳水化合物被宿主淋巴网状系统的多种细胞凝集素识别,这些相互作用在病毒在宿主中的传播以及调节性细胞因子的释放中发挥作用。我们最近的研究工作表明,引起艾滋病大流行的 HIV-1 与天然不发病的黑眉长尾猴中的 SIV 相比,在碳水化合物组成上存在根本差异。我们现在推测,这种碳水化合物组成上的根本差异反映了病毒和宿主所面临的进化压力。此外,病毒上的碳水化合物组成和宿主中碳水化合物感知蛋白的遗传差异对于以获得性免疫缺陷综合征 (AIDS) 为特征的广泛的淋巴激活可能至关重要。