首页> 外文期刊>Vaccine >Synthetic peptides coupled to the surface of liposomes effectively induce SARS coronavirus-specific cytotoxic T lymphocytes and viral clearance in HLA-A*0201 transgenic mice.
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Synthetic peptides coupled to the surface of liposomes effectively induce SARS coronavirus-specific cytotoxic T lymphocytes and viral clearance in HLA-A*0201 transgenic mice.

机译:在HLA-A * 0201转基因小鼠中,与脂质体表面偶联的合成肽可有效诱导SARS冠状病毒特异性细胞毒性T淋巴细胞和病毒清除。

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摘要

We investigated whether the surface-linked liposomal peptide was applicable to a vaccine based on cytotoxic T lymphocytes (CTLs) against severe acute respiratory syndrome (SARS) coronavirus (SARS-CoV). We first identified four HLA-A*0201-restricted CTL epitopes derived from SARS-CoV using HLA-A*0201 transgenic mice and recombinant adenovirus expressing predicted epitopes. These peptides were coupled to the surface of liposomes, and inoculated into mice. Two of the liposomal peptides were effective for peptide-specific CTL induction, and one of them was efficient for the clearance of vaccinia virus expressing epitopes of SARS-CoV, suggesting that the surface-linked liposomal peptide might offer an effective CTL-based vaccine against SARS.
机译:我们调查了表面连接的脂质体肽是否适用于针对严重急性呼吸综合征(SARS)冠状病毒(SARS-CoV)的基于细胞毒性T淋巴细胞(CTL)的疫苗。我们首先使用HLA-A * 0201转基因小鼠和表达预测表位的重组腺病毒鉴定了四个源自SARS-CoV的HLA-A * 0201限制性CTL表位。这些肽偶联至脂质体表面,并接种到小鼠中。脂质体肽中的两种对肽特异性CTL诱导有效,其中一种对清除表达SARS-CoV的痘苗病毒的表位有效,这表明表面连接的脂质体肽可能提供针对CTL的有效疫苗非典。

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