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一种针对改良安卡拉痘苗病毒(MVA)包膜蛋白的新型单克隆抗体,可用于流式细胞术测定 MVA 病毒滴度。

A Novel Monoclonal Antibody Against a Modified Vaccinia Ankara (MVA) Envelope Protein as a Tool for MVA Virus Titration by Flow Cytometry.

机构信息

Department of Immuno-Oncology, Beckman Research Institute of City of Hope, Duarte, CA 91010, USA.

Irell & Manella Graduate School of Biological Sciences, City of Hope, Duarte, CA 91010, USA.

出版信息

Viruses. 2024 Oct 17;16(10):1628. doi: 10.3390/v16101628.

Abstract

Modified vaccinia Ankara (MVA) virus is a widely used vaccine platform, making accurate titration essential for vaccination studies. However, the current plaque forming unit (PFU) assay, the standard for MVA titration, is prone to observer bias and other limitations that affect accuracy and precision. To address these challenges, we developed a new flow cytometry-based quantification method using a highly specific monoclonal antibody (mAb) for the detection of MVA-infected cells, as a more accurate titration assay. Through previous work, we serendipitously identified three MVA-specific hybridoma antibody clones, which we characterized through ELISA, immunoblot, and flow cytometry, confirming their specificity for MVA. Sequencing confirmed that each antibody was monoclonal, and mass spectrometry results revealed that all mAbs target the MVA cell surface binding protein (CSBP, MVA105L). We next optimized the titration protocol using the most effective mAb, 33C7 by refining culture conditions and staining protocols to enhance sensitivity and minimize background. Our optimized method demonstrated superior sensitivity, reliability, and reduced processing time when compared with the traditional PFU assay, establishing it as a more accurate and efficient approach for MVA titration.

摘要

改良安卡拉痘苗病毒(MVA)是一种广泛应用的疫苗平台,因此准确滴定对于疫苗研究至关重要。然而,目前的噬菌斑形成单位(PFU)测定法是 MVA 滴定的标准方法,但容易受到观察者偏差和其他影响准确性和精密度的限制。为了解决这些挑战,我们开发了一种新的基于流式细胞术的定量方法,使用针对 MVA 感染细胞的高度特异性单克隆抗体(mAb)作为更准确的滴定测定法。通过之前的工作,我们偶然发现了三个针对 MVA 的杂交瘤单克隆抗体克隆,通过 ELISA、免疫印迹和流式细胞术对其进行了表征,证实了它们对 MVA 的特异性。测序证实每种抗体都是单克隆的,质谱结果表明所有 mAb 都针对 MVA 细胞表面结合蛋白(CSBP,MVA105L)。接下来,我们通过优化培养条件和染色方案来提高灵敏度并最小化背景,使用最有效的 mAb 33C7 对滴定方案进行了优化。与传统的 PFU 测定法相比,我们的优化方法显示出更高的灵敏度、可靠性和减少的处理时间,确立了它作为 MVA 滴定的更准确和有效的方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/222a/11512277/32cfecc43b1f/viruses-16-01628-g001.jpg

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