| Literature DB >> 24225642 |
Qingwen Zhang1, Qiong Wang2, Guang Tian3, Zhizhen Qi4, Xuecan Zhang3, Xiaohong Wu3, Yefeng Qiu5, Yujing Bi3, Xiaoyan Yang4, Youquan Xin4, Jian He4, Jiyuan Zhou3, Lin Zeng5, Ruifu Yang3, Xiaoyi Wang2.
Abstract
Yersinia pestis biovar Microtus is considered to be a virulent to larger mammals, including guinea pigs, rabbits and humans. It may be used as live attenuated plague vaccine candidates in terms of its low virulence. However, the Microtus strain's protection against plague has yet to be demonstrated in larger mammals. In this study, we evaluated the protective efficacy of the Microtus strain 201 as a live attenuated plague vaccine candidate. Our results show that this strain is highly attenuated by subcutaneous route, elicits an F1-specific antibody titer similar to the EV and provides a protective efficacy similar to the EV against bubonic plague in Chinese-origin rhesus macaques. The Microtus strain 201 could induce elevated secretion of both Th1-associated cytokines (IFN-γ, IL-2 and TNF-α) and Th2-associated cytokines (IL-4, IL-5, and IL-6), as well as chemokines MCP-1 and IL-8. However, the protected animals developed skin ulcer at challenge site with different severity in most of the immunized and some of the EV-immunized monkeys. Generally, the Microtus strain 201 represented a good plague vaccine candidate based on its ability to generate strong humoral and cell-mediated immune responses as well as its good protection against high dose of subcutaneous virulent Y. pestis challenge.Entities:
Keywords: Rhesus macaques; Yersinia pestis; live attenuated vaccine; plague; protection
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Year: 2013 PMID: 24225642 PMCID: PMC4185917 DOI: 10.4161/hv.27060
Source DB: PubMed Journal: Hum Vaccin Immunother ISSN: 2164-5515 Impact factor: 3.452