Shi Y, Xie L, Li C, Han J
Department of Parasitology, Tongji Medical University, Wuhan 430030, China.
Chin Med J (Engl). 1999 Aug;112(8):677-80.
To study protective immunity afforded by murine immunization with DNA vaccine of Schistosoma japonicum (S. japonicum) as measured by reduction in worm burden and host antibody, cytokines.
DNA vaccine pCD-Sj32 was constructed, identified and expressed. pCD-Sj32 could induce substantial protective immunity against infection of S. japonicum in BALB/c mice. The best efficacy can be produced with one injection of 100 micrograms DNA into the quadriceps muscle, combined with challenge for 8 weeks after immunization. T lymphocyte subsets of CD8+, IL-2. TNF and IFN-gamma of experimental animal could play important roles in regulating immune functions of schistosomiasis.
High titre of specific antibody IgG could be induced by vaccinated with pCD-Sj32, and antibody can mediate macrophage to produce ADCC effects in vitro.
pCD-Sj32 may represent a new approach to developing subunit vaccine.
通过检测虫负荷减少以及宿主抗体、细胞因子水平,研究日本血吸虫DNA疫苗免疫小鼠所提供的保护性免疫。
构建、鉴定并表达DNA疫苗pCD-Sj32。pCD-Sj32可诱导BALB/c小鼠对日本血吸虫感染产生显著的保护性免疫。将100微克DNA单次注射到股四头肌,并在免疫后8周进行攻击,可产生最佳效果。实验动物的CD8+、IL-2、TNF和IFN-γ等T淋巴细胞亚群在调节血吸虫病免疫功能中起重要作用。
接种pCD-Sj32可诱导产生高滴度的特异性抗体IgG,且该抗体可在体外介导巨噬细胞产生ADCC效应。
pCD-Sj32可能代表了一种开发亚单位疫苗的新方法。