栓系抗原抑制屏蔽血凝素头部结构域,并将抗体反应重新集中到茎结构域。

IF 2.4 Q3 CHEMISTRY, MULTIDISCIPLINARY
Chemistry-Switzerland Pub Date : 2025-02-01 Epub Date: 2025-01-21 DOI:10.3390/chemistry7010012
Donguk Kim, Kathryn Loeffler, Yixin Hu, Ammar Arsiwala, Steven Frey, Shruthi Murali, Vivek Hariharan, Alberto Moreno, Ravi S Kane
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引用次数: 0

摘要

过去一个世纪以来,流感一直是全球关注的健康问题。目前的季节性流感疫苗主要引发针对病毒糖蛋白血凝素(HA)免疫优势头部结构域的抗体反应,HA由于选择压力而不断发生突变。为了避免这个问题,我们引入了一种“栓系抗原抑制”策略来保护HA头部结构域,并将免疫反应重新聚焦于HA保守但免疫亚显性的茎结构域。具体来说,我们将一个识别HA头部区域Sb抗原位点的抗体片段(Fab)与HA蛋白连接在一起。我们分别用fab系结的透明质酸和常规的透明质酸免疫不同组的雌性小鼠,并观察引起的抗体反应。我们证明,用拴住的Fab屏蔽HA头结构域抑制了针对HA头结构域所有五个关键抗原位点的抗体滴度,同时引发了强大的抗茎抗体反应。我们的工作强调了栓系抗原抑制作为一种策略的潜力,将抗体反应重新聚焦于蛋白质抗原上的保守表位。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Tethered Antigenic Suppression Shields the Hemagglutinin Head Domain and Refocuses the Antibody Response to the Stalk Domain.

Influenza has been a global health concern for the past century. Current seasonal influenza vaccines primarily elicit an antibody response that targets the immunodominant head domain of the viral glycoprotein hemagglutinin (HA), which consistently mutates due to selective pressure. To circumvent this problem, we introduce a "tethered antigenic suppression" strategy to shield the HA head domain and refocus the immune response towards the conserved but immunosubdominant stalk domain of HA. Specifically, we tethered an antibody fragment (Fab) that recognizes the Sb antigenic site in the HA head domain to the HA protein with a linker. We immunized separate groups of female mice with the Fab-tethered HA or regular HA and characterized the elicited antibody response. We demonstrate that shielding the HA head domain with a tethered Fab suppresses the antibody titers towards all five key antigenic sites in the HA head domain while eliciting a robust anti-stalk antibody response. Our work highlights the potential of tethered antigenic suppression as a strategy to refocus the antibody response towards conserved epitopes on protein antigens.

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来源期刊
Chemistry-Switzerland
Chemistry-Switzerland CHEMISTRY, MULTIDISCIPLINARY-
CiteScore
3.20
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