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A Molecularly Cloned Schwarz Strain of Measles Virus Vaccine Induces Strong Immune Responses in Macaques and Transgenic Mice

机译:麻疹病毒疫苗的分子克隆的施瓦茨菌株在猕猴和转基因小鼠中诱导强烈的免疫反应。

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摘要

Live attenuated RNA viruses make highly efficient vaccines. Among them, measles virus (MV) vaccine has been given to a very large number of children and has been shown to be highly efficacious and safe. Therefore, this vaccine might be a very promising vector to immunize children against both measles and other infectious agents, such as human immunodeficiency virus. A vector was previously derived from the Edmonston B strain of MV, a vaccine strain abandoned 25 years ago. Sequence analysis revealed that the genome of this vector diverges from Edmonston B by 10 amino acid substitutions not related to any Edmonston subgroup. Here we describe an infectious cDNA for the Schwarz/Moraten strain, a widely used MV vaccine. This cDNA was constructed from a batch of commercial vaccine. The extremities of the cDNA were engineered in order to maximize virus yield during rescue. A previously described helper cell-based rescue system was adapted by cocultivating transfected cells on primary chicken embryo fibroblasts, the cells used to produce the Schwarz/Moraten vaccine. After two passages the sequence of the rescued virus was identical to that of the cDNA and of the published Schwarz/Moraten sequence. Two additional transcription units were introduced in the cDNA for cloning foreign genetic material. The immunogenicity of rescued virus was studied in macaques and in mice transgenic for the CD46 MV receptor. Antibody titers and T-cell responses (ELISpot) in animals inoculated with low doses of rescued virus were identical to those obtained with commercial Schwarz MV vaccine. In contrast, the immunogenicity of the previously described Edmonston B strain-derived MV clone was much lower. This new molecular clone will allow for the production of MV vaccine without having to rely on seed stocks. The additional transcription units allow expressing heterologous antigens, thereby providing polyvalent vaccines based on an approved, safe, and efficient MV vaccine strain that is used worldwide.
机译:减毒活RNA病毒可制成高效疫苗。其中,麻疹病毒(MV)疫苗已被接种给大量儿童,并被证明是高度有效和安全的。因此,这种疫苗可能是一种非常有前途的载体,可以使儿童针对麻疹和其他传染原,例如人类免疫缺陷病毒,进行免疫。该载体先前源自MV的Edmonston B株,这是25年前放弃的疫苗株。序列分析表明,该载体的基因组与埃德蒙斯顿B有10个与任何埃德蒙斯顿亚组均不相关的氨基酸取代。在这里,我们描述了Schwarz / Moraten菌株(一种广泛使用的MV疫苗)的感染性cDNA。该cDNA由一批商业疫苗构建而成。对cDNA的末端进行了改造,以便在营救过程中最大化病毒产量。通过在原代鸡胚成纤维细胞(用于生产Schwarz / Moraten疫苗的细胞)上共转染转染的细胞来适应先前描述的基于辅助细胞的拯救系统。经过两次传代后,所拯救病毒的序列与cDNA和已发表的Schwarz / Moraten序列相同。在cDNA中引入了两个额外的转录单位,用于克隆外源遗传物质。在猕猴和CD46 MV受体转基因小鼠中研究了拯救病毒的免疫原性。用低剂量抢救病毒接种的动物中的抗体滴度和T细胞应答(ELISpot)与市售Schwarz MV疫苗所获得的相同。相反,先前描述的Edmonston B菌株衍生的MV克隆的免疫原性低得多。这种新的分子克隆将无需依赖种子储备即可生产MV疫苗。额外的转录单位允许表达异源抗原,从而提供基于在世界范围内使用的批准,安全和有效的MV疫苗株的多价疫苗。

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