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Intranasal Protollin-formulated recombinant SARS S-protein elicits respiratory and serum neutralizing antibodies and protection in mice

机译:鼻内Protollin配制的重组SARS S蛋白引起小鼠呼吸道和血清中和抗体及保护作用

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摘要

The feasibility of developing a prophylactic vaccine against SARS was assessed by comparing the immune responses elicited by immunizing mice with a recombinant SARS spike glycoprotein (S-protein) formulated with different adjuvants, given by different routes. In both young and aged mice, an intranasal Protollin-formulated S-protein vaccine elicited high levels of antigen-specific IgG in serum, comparable to those elicited by an intramuscular Alum-adsorbed S-protein vaccine. Serum antibodies were shown to be virus neutralizing. Intranasal immunization of young mice with the Protollin-formulated vaccine elicited significant levels of antigen-specific lung IgA in contrast to mice immunized with the intramuscular vaccine in which no antigen-specific lung IgA was detected. Following live virus challenge of aged mice, no virus was detected in the lungs of intranasally immunized mice, in contrast to intramuscularly immunized mice whose lung virus titers were comparable to those observed in control mice.
机译:通过比较用不同途径配制的不同佐剂配制的重组SARS穗糖蛋白(S蛋白)对小鼠进行免疫诱导的免疫反应,评估开发针对SARS的预防性疫苗的可行性。在年轻和老年小鼠中,鼻内Protollin配制的S蛋白疫苗在血清中均能引起高水平的抗原特异性IgG,这与肌肉内明矾吸附的S蛋白疫苗所引起的相当。血清抗体显示出病毒中和作用。与未检测到抗原特异性肺IgA的肌内疫苗免疫的小鼠相比,用Protollin配制的疫苗对年轻小鼠进行鼻内免疫可引起显着水平的抗原特异性肺IgA。与衰老小鼠进行活病毒攻击后,鼻内免疫小鼠的肺中未检测到病毒,而肌肉内免疫小鼠的肺病毒滴度与对照组小鼠相当。

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