棉鼠对含有呼吸道合胞病毒融合蛋白前融合形式的病毒样颗粒的免疫反应。

Lori McGinnes Cullen, Jorge C G Blanco, Trudy G Morrison
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引用次数: 0

摘要

背景:病毒样颗粒(VLPs)以新城疫病毒(NDV)核心蛋白M和NP为基础,并含有两种嵌合蛋白F/F和H/G,这两种嵌合蛋白由呼吸道合胞病毒(RSV)融合蛋白(F)和糖蛋白(G)外域组成,分别与NDV F蛋白和HN蛋白的跨膜结构域和胞质结构域融合。此外,用含有 F/F 嵌合体蛋白的 VLP 免疫小鼠,与含有野生型 F 蛋白的 VLP 相比,含有 F/F 嵌合体蛋白的 VLP 免疫小鼠的中和抗体滴度明显提高。本研究的目的是确定含有 RSV F 蛋白前融合形式的 VLPs 是否能刺激棉鼠(一种比小鼠更易感染 RSV 的动物模型)产生保护性免疫反应:方法:用含有稳定的前融合F/F嵌合体蛋白和H/G嵌合体蛋白的VLPs对棉鼠进行肌肉免疫。用 ELISA 法测定抗 RSV F 和 RSV G 的抗体反应。免疫动物血清中的中和抗体滴度是通过斑块还原试验测定的。评估了动物对 RSV 挑战的保护作用。通过监测免疫动物接受 RSV 挑战时的肺部病理变化,确定了 VLP 疫苗的安全性:结果:Pre-F/F VLP诱导的中和滴度远高于之前提出的成功疫苗所需的最低水平,而且滴度明显高于RSV感染所激发的滴度。此外,与 RSV 感染相比,Pre-F/F VLP 免疫可激发更高的可溶性前融合 F 蛋白 IgG 滴度。用前融合F/F VLP免疫棉鼠可免受RSV挑战,重要的是,VLP免疫不会导致RSV挑战时呼吸道疾病的加重:结论:含有前融合 RSV F 蛋白的 VLP 具有安全、有效的 RSV 疫苗所需的特征。
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Cotton rat immune responses to virus-like particles containing the pre-fusion form of respiratory syncytial virus fusion protein.

Background: Virus-like particles (VLPs) based on Newcastle disease virus (NDV) core proteins, M and NP, and containing two chimera proteins, F/F and H/G, composed of the respiratory syncytial virus (RSV) fusion protein (F) and glycoprotein (G) ectodomains fused to the transmembrane and cytoplasmic domains of the NDV F and HN proteins, respectively, stimulate durable, protective anti-RSV neutralizing antibodies in mice. Furthermore, immunization of mice with a VLP containing a F/F chimera protein with modifications previously reported to stabilize the pre-fusion form of the RSV F protein resulted in significantly improved neutralizing antibody titers over VLPs containing the wild type F protein. The goal of this study was to determine if VLPs containing the pre-fusion form of the RSV F protein stimulated protective immune responses in cotton rats, a more RSV permissive animal model than mice.

Methods: Cotton rats were immunized intramuscularly with VLPs containing stabilized pre-fusion F/F chimera protein as well as the H/G chimera protein. The anti-RSV F and RSV G antibody responses were determined by ELISA. Neutralizing antibody titers in sera of immunized animals were determined in plaque reduction assays. Protection of the animals from RSV challenge was assessed. The safety of the VLP vaccine was determined by monitoring lung pathology upon RSV challenge of immunized animals.

Results: The Pre-F/F VLP induced neutralizing titers that were well above minimum levels previously proposed to be required for a successful vaccine and titers significantly higher than those stimulated by RSV infection. In addition, Pre-F/F VLP immunization stimulated higher IgG titers to the soluble pre-fusion F protein than RSV infection. Cotton rats immunized with Pre-F/F VLPs were protected from RSV challenge, and, importantly, the VLP immunization did not result in enhanced respiratory disease upon RSV challenge.

Conclusions: VLPs containing the pre-fusion RSV F protein have characteristics required for a safe, effective RSV vaccine.

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3.80%
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12
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