dna疫苗
质粒
表位
生物
生育率
病毒学
啮齿动物
DNA
免疫学
遗传学
医学
抗体
生态学
人口
环境卫生
作者
Md. Abu Hadi Noor Ali Khan,Kazuhide Ogita,Valerie A. Ferro,Keiichi Kumasawa,Tateki Tsutsui,Tadashi Kimura
出处
期刊:Vaccine
[Elsevier]
日期:2008-03-01
卷期号:26 (10): 1365-1374
被引量:35
标识
DOI:10.1016/j.vaccine.2007.12.052
摘要
Research into active immunisation against gonadotrophin releasing hormone (GnRH-I) has gained widespread acceptance as a means of controlling reproduction and behaviour of farm, companion and wild animals. Many studies describe the use of multiple copies of the self-peptide in linear alignment and conjugation with a large carrier protein to increase the immune response to the peptide. However, problems resulting from carrier protein epitope suppression have seen a diversion of interest into the use of genetic materials to elicit an optimum immune response. In this study, a 533-bp long DNA vaccine was constructed in pcDNAV5-HisB coding for 18.871 kDa GnRH-I-T-helper-V5 epitopes fusion protein. COS1 cells transfected with the vaccine construct were found to release fusion protein into culture supernatant. The vaccine construct (100 μg/mice) in saline solution administered into the anterior quadriceps muscle of ICR male and female mice stimulated antigen-specific IgG antibody responses. Testosterone levels in the vaccinated male mice were significantly (p = 0.021) reduced. A significant reduction in uterine implants were noted following mating between immunised males and control females (p = 0.028), as well as between immunised females and control males (p = 0.004). Histological examination of both the male and female gonads in study week 13 showed atrophy of the seminiferous epithelium and suppression of folliculogenesis.
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