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单域 CD4 融合到人抗 CD16 抗体结构域介导对 HIV-1 感染细胞的有效杀伤。

One-domain CD4 Fused to Human Anti-CD16 Antibody Domain Mediates Effective Killing of HIV-1-Infected Cells.

机构信息

Protein Interactions Section, Cancer and Inflammation Program, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Frederick, Maryland, 21702, USA.

Key Laboratory of Medical Molecular Virology of Ministries of Education and Health, School of Basic Medical Sciences, Fudan University, Shanghai, 200032, China.

出版信息

Sci Rep. 2017 Aug 22;7(1):9130. doi: 10.1038/s41598-017-07966-3.

Abstract

Bispecific killer cells engagers (BiKEs) which can bind to natural killer (NK) cells through the activating receptor CD16A and guide them to cells expressing the HIV-1 envelope glycoprotein (Env) are a promising new weapon for elimination of infected cells and eradication of the virus. Here we report the design, generation and characterization of BiKEs which consist of CD16A binding human antibody domains fused through a flexible linker to an engineered one-domain soluble human CD4. In presence of cells expressing HIV-1 envelope glycoproteins (Envs), these BiKEs activated specifically CD16A-expressing Jurkat T cells, degranulated NK cells, induced cytokine production and killed Env-expressing cells. They also effectively mediated killing of chronically and acutely HIV-1 infected T cells by human peripheral blood mononuclear cells. The presumed ability of these CD4-based BiKEs to bind all HIV-1 isolates, their small size and fully human origin, combined with high efficacy suggest their potential for HIV-1 eradication.

摘要

双特异性杀伤细胞接合器(BiKEs)可以通过激活受体 CD16A 与自然杀伤(NK)细胞结合,并引导它们靶向表达 HIV-1 包膜糖蛋白(Env)的细胞,是消除感染细胞和根除病毒的有前途的新武器。在这里,我们报告了 BiKEs 的设计、生成和表征,它们由与人 NK 细胞上的 CD16A 结合的人抗体结构域通过柔性接头融合到人源单结构域可溶性 CD4 组成。在表达 HIV-1 包膜糖蛋白(Envs)的细胞存在的情况下,这些 BiKEs 特异性地激活了表达 CD16A 的 Jurkat T 细胞、脱颗粒 NK 细胞,诱导细胞因子产生并杀伤表达 Env 的细胞。它们还能有效介导人外周血单个核细胞对慢性和急性 HIV-1 感染 T 细胞的杀伤。这些基于 CD4 的 BiKEs 结合所有 HIV-1 分离株的假定能力、它们的小尺寸和完全人源化,以及高效性,提示它们有用于 HIV-1 根除的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95a9/5567353/7848fbbff52f/41598_2017_7966_Fig1_HTML.jpg

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