Ts-Hsp70 induces protective immunity against Trichinella spiralis infection in mouse by activating dendritic cells through TLR2 and TLR4

被引:16
|
作者
Zhang, Rui [1 ,2 ]
Sun, Qing [1 ]
Chen, Yi [1 ,2 ]
Sun, Ximeng [1 ,2 ]
Gu, Yuan [1 ]
Zhao, Zhang [1 ,2 ]
Cheng, Yuli [1 ]
Zhao, Limei [1 ,2 ]
Huang, Jingjing [1 ]
Zhan, Bin [3 ]
Zhu, Xinping [1 ,2 ]
机构
[1] Capital Med Univ, Sch Basic Med Sci, Dept Med Microbiol & Parasitol, Beijing, Peoples R China
[2] Capital Med Univ, Res Ctr Microbiome, Beijing, Peoples R China
[3] Baylor Coll Med, Natl Sch Trop Med, Dept Pediat, Houston, TX 77030 USA
来源
PLOS NEGLECTED TROPICAL DISEASES | 2018年 / 12卷 / 05期
基金
中国国家自然科学基金; 北京市自然科学基金;
关键词
TOLL-LIKE-RECEPTORS; HEAT-SHOCK PROTEINS; BALB/C MICE; MOLECULAR-CLONING; IN-VITRO; RESPONSES; TRICHINOSIS; HEAT-SHOCK-PROTEIN-70; SYSTEM; RECOGNITION;
D O I
10.1371/journal.pntd.0006502
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Background Trichinellosis is a serious food -borne parasitic zoonosis worldwide. In the effort to develop vaccine against Trichinella infection, we have identified Trichinella spiralis Heat shock protein 70 (Ts-Hsp70) elicits partial protective immunity against T. spiralis infection via activating dendritic cells (DCs) in our previous study. This study aims to investigate whether DCs were activated by Ts-Hsp70 through TLR2 and/or TLR4 pathways. Methods and findings After blocking with anti-TLR2 and TLR4 antibodies, the binding of Ts-Hsp70 to DCs was significantly reduced. The reduced binding effects were also found in TLR2 and TLR4 knockout (TLR2(-/)- and TLR4(-/-)) DCs. The expression of TLR2 and TLR4 on DCs was upregulated after treatment with Ts-Hsp70 in vitro. These results suggest that Ts-Hsp70 is able to directly bind to TLR2 and TLR4 on the surface of mouse bone morrow-derived DCs. In addition, the expression of the co-stimulatory molecules (CD80, CD83) on Ts-Hsp70-induced DCs was reduced in TLR2(-/-) and TLR4(-/-) mice. More evidence showed that Ts-Hsp70 reduced its activation on TLR2/4 knockout DCs to subsequently activate the nave T-cells. Furthermore, Ts-Hsp70 elicited protective immunity against T. spiralis infection was reduced in TLR2(-/-) and TLR4(-/-) mice correlating with the reduced humoral and cellular immune responses. Conclusion This study demonstrates that Ts-Hsp70 activates DCs through TLR2 and TLR4, and TLR2 and TLR4 play important roles in Ts-Hsp70-induced DCs activation and immune responses.
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页数:19
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