IL-17 and IL-22 elicited by a DNA vaccine encoding ROP13 associated with protection against Toxoplasma gondii <bold>in BALB/c mice</bold>

被引:17
|
作者
Alizadeh, Paria [1 ,2 ]
Ahmadpour, Ehsan [1 ]
Daryani, Ahmad [3 ]
Kazemi, Tohid [1 ]
Spotin, Adel [4 ]
Mahami-Oskouei, Mahmoud [5 ]
Flynn, Robin J. [6 ]
Azadi, Yaghob [2 ]
Rajabi, Saba [2 ]
Sandoghchian, Siamak [1 ]
机构
[1] Tabriz Univ Med Sci, Immunol Res Ctr, Tabriz, Iran
[2] Tabriz Univ Med Sci, Student Res Comm, Tabriz, Iran
[3] Mazandaran Univ Med Sci, Toxoplasmosis Res Ctr, Sari, Iran
[4] Tabriz Univ Med Sci, Infect & Trop Dis Res Ctr, Tabriz, Iran
[5] Tabriz Univ Med Sci, Dept Parasitol & Mycol, Tabriz, Iran
[6] Univ Liverpool, Inst Infect & Global Hlth, Dept Infect Biol, Liverpool, Merseyside, England
关键词
DNA vaccine; gene expression; interleukin (IL)-17; IL-22; ROP13; T-helper (Th) 17; Toxoplasma gondii; EXCRETORY-SECRETORY ANTIGENS; DENDRITIC CELLS; IMMUNE-RESPONSE; IMMUNIZATION; INFECTION; DEPLETION; PARASITE;
D O I
10.1002/jcp.27747
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Toxoplasma gondii, an intracellular parasitic protozoan, is capable of infecting man and all warm-blooded animals. Cell-mediated immunity is vital in mounting protective responses against T. gondii infection. Recent studies have shown that T-helper (Th) 17 responses may play a key role in parasite control. In this current study, we constructed a DNA vaccine encoding T. gondii ROP13 in a pcDNA vector. Groups of BALB/c mice were immunized intramuscularly with pcROP13 or controls and challenged with the RH strain of T. gondii. The results showed that immunization with pcROP13 could elicit an antibody response against T. gondii. The expression of the canonical Th17 cytokines, interleukin (IL)-17 and IL-22, were significantly increased after immunization with pcROP13 compared with control groups (p<0.05). Furthermore, vaccination resulted in a significant decrease in parasite load (p<0.05). The induction of Th17 related cytokines, using a ROP13 DNA vaccine, against T. gondii should be considered as a potential vaccine approach for the control of toxoplasmosis.
引用
收藏
页码:10782 / 10788
页数:7
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