ELEVATED T- CELL RESPONSE IN LIVER OF MICE VACCINATED WITH ATTENUATED KOREA VACCINIA VIRAL VACCINE EXPRESSING PLASMODIUM VIVAX CIRCUMSPOROZOITE PROTEIN

被引:0
|
作者
Kim, Tae Yun [1 ]
Yang, Eun-Jeong [2 ,3 ]
Shin, Hyun-Il [1 ]
Lee, Sang-Won [4 ]
Cho, Shin-Hyeong [1 ]
Lee, Sang-Eun [1 ]
Kim, Jung-Yeon [1 ]
机构
[1] Ctr Dis Control & Prevent, Div Vectors & Parasit Dis, 187 Osongsaengmyeong 2 Ro, Cheongju 28159, Chungcheongbuk, South Korea
[2] Korea Univ, Coll Med, Dept Microbiol, Seoul, South Korea
[3] Korea Univ, Coll Med, Inst Viral Dis, Seoul, South Korea
[4] Ctr Dis Control & Prevent, Div Publ Hlth Emergency & Bioterrorism, Chungcheongbuk Do, South Korea
关键词
Plasmodium vivax; circumsporozoite protein; malaria; vaccine; vaccinia virus; MALARIA VACCINE; ANTIBODIES; EPIDEMIOLOGY; PLATFORMS; VECTORS; BINDING;
D O I
暂无
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Relapse and recurrence of vivax malaria is still a major issue in temperate regions including Korea. Recombinant attenuated vaccinia virus KVAC103 expressing circumsporozoite protein (CSP), one of the main antigenic proteins of Plasmodium vivax, (KVAC-PvCSP) was generated and evaluated for its potential as an anti- malarial vaccine. Mice were subcutaneously inoculated twice with KVAC-PvCSP, with a three-week interval between injections, and cellular as well as humoral immune responses, including memory B cell response, were examined. Serial inoculation of KVAC-PvCSP elicited strong IgG production in mice. Moreover, CD3(+), CD4(+) and CD8(+) T-cells were increased by vaccination in mouse hepatocytes, but not in splenocytes. Thus, serial KVAC-PvCSP vaccination elicited CD4(+) and CD8(+) T-cell responses in the liver of mice. These results suggest KVAC103-based vaccination may be useful for targeting pre-erythrocytic stages of vivax malaria.
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页码:147 / 154
页数:8
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