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A prime-boost vaccination protocol optimizes immune responses against the nucleocapsid protein of the SARS coronavirus

机译:初免-加强疫苗接种方案可优化针对SARS冠状病毒核衣壳蛋白的免疫反应

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摘要

Severe acute respiratory syndrome (SARS) is a serious infectious disease caused by the SARS coronavirus. We assessed the potential of prime-boost vaccination protocols based on the nucleocapsid (NC) protein co-administered with a derivative of the mucosal adjuvant MALP-2 or expressed by modified Vaccinia virus Ankara (MVA–NC) to stimulate humoral and cellular immune responses at systemic and mucosal levels. The obtained results demonstrated that strong immune responses can be elicited both at systemic and mucosal levels following a heterologous prime-boost vaccination protocol consisting in priming with NC protein add-mixed with MALP-2 by intranasal route and boosting with MVA–NC by intramuscular route.
机译:严重急性呼吸系统综合症(SARS)是由SARS冠状病毒引起的严重传染病。我们评估了基于核衣壳(NC)蛋白与粘膜佐剂MALP-2衍生物共同施用或经修饰的痘苗病毒安卡拉(MVA–NC)刺激体液和细胞免疫反应的初免加强免疫接种方案的潜力在全身和粘膜水平。获得的结果表明,异源的初免-加强接种方案包括通过鼻内途径与NCLP混合添加与MALP-2混合的NC蛋白引发和通过肌内途径与MVA-NC增强混合,可以在全身和粘膜水平上引起强烈的免疫反应。 。

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