期刊
FRONTIERS IN IMMUNOLOGY
卷 11, 期 -, 页码 -出版社
FRONTIERS MEDIA SA
DOI: 10.3389/fimmu.2020.01495
关键词
nucleotide exchange factor (GrpE); Ureaplasma urealyticum; immunogenicity; immune protection; BALB; c mice
类别
资金
- National Natural Science Foundation of China [31500156]
- University of South China Innovation Foundation for Postgraduate [193YXC034]
- Hunan Science and Technology Innovation Project [2018SK50302]
- Research Project of Hunan Provincial Health and Wellness Commission [B2019003]
- Chenzhou Science and Technology Bureau Science and Technology Development Plan Project [zdyf201844]
Nucleotide exchange factor (GrpE), a highly conserved antigen, is rapidly expressed and upregulated whenUreaplasma urealyticuminfects a host, which could act as a candidative vaccine if it can induce an anti-U. urealyticumimmune reaction. Here, we evaluated the vaccine potential of recombinant GrpE protein adjuvanted by Freund's adjuvant (FA), to protect againstU. urealyticumgenital tract infection in a mouse model. After booster immunization in mice with FA, the GrpE can induced both humoral and cellular immune response after intramuscular injection into BALB/c mice. A strong humoral immune response was detected in the GrpE-immunized mice characterized by production of high titers of antigen-specific serum IgG (IgG1, IgG2a, and IgG3) antibodies. At the same time, the GrpE also induced a Th1-biased cytokine spectrum with high levels of IFN-gamma and TNF-alpha after re-stimulation with immunogen GrpEin vitro, suggesting that GrpE could trigger the Th1 response when used for vaccination in the presence of FA. Although GrpE vaccination in the presence of a Th1-type adjuvant-induced had readily detectable Th1 responses, there wasn't increase inflammation in response to the infection. More importantly, the robust immune responses in mice after immunization with GrpE showed a significantly reducedU. urealyticumburden in cervical tissues. Histopathological analysis confirmed that tissues of GrpE-immunized BALB/c mice were protected against the pathological effects ofU. urealyticuminfection. In conclusion, this study preliminarily reveals GrpE protein as a promising new candidate vaccine for preventingU. urealyticumreproductive tract infection.
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