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Multiple antigens of Yersinia pestis delivered by live recombinant attenuated Salmonella vaccine strains elicit protective immunity against plague

机译:活重组减毒沙门氏菌疫苗株传递的鼠疫耶尔森氏菌多种抗原引发针对鼠疫的保护性免疫

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摘要

Based on our improved >novel Salmonella vaccine delivery platform, we optimized the recombinant attenuated Salmonella Typhimurium vaccine (RASV) χ12094 to deliver multiple Y. pestis antigens. These included LcrV196 (amino acids, 131 to 326), Psn encoded on pYA5383 and F1 encoded in the chromosome, >their synthesis did not cause adverse effects on bacterial growth. Oral immunization with χ12094(pYA5383) simultaneously stimulated high antibody titers to LcrV, Psn and F1 in mice and presented complete protection against both subcutaneous (s.c.) and intranasal (i.n.) challenges with high lethal doses of Y. pestis CO92. Moreover, no deaths or other disease symptoms were observed in SCID mice orally immunized with χ12094(pYA5383) over a 60 day period. Therefore, the trivalent S. Typhimurium-based live vaccine shows promise for a next-generation plague vaccine.
机译:基于改进的>新型沙门氏菌疫苗递送平台,我们优化了重组减毒鼠伤寒沙门氏菌疫苗(RASV)χ12094,以递送多种鼠疫耶尔森氏菌抗原。其中包括LcrV196(氨基酸131至326),pYA5383上编码的Psn和染色体上编码的F1,>它们的合成对细菌的生长没有不利影响。用χ12094(pYA5383)进行的口服免疫可同时刺激小鼠中对LcrV,Psn和F1的高抗体滴度,并通过高致死剂量的鼠疫杆菌CO92对皮下(s.c.)和鼻内(i.n.)攻击提供了完全保护。此外,在60天内口服χ12094(pYA5383)免疫的SCID小鼠中未观察到死亡或其他疾病症状。因此,基于三价鼠伤寒沙门氏菌的活疫苗显示出下一代鼠疫疫苗的前景。

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