Institute of Health & Biomedical Innovation, Cell & Molecular Biosciences, Faculty of Science, Queensland University of Technology, 60 Musk Ave, Kelvin Grove, QLD 4059, Australia.
Vaccine. 2011 Sep 2;29(38):6505-13. doi: 10.1016/j.vaccine.2011.07.012. Epub 2011 Jul 19.
Research into an efficacious Chlamydia trachomatis vaccine is ongoing, however, there has been no examination into the timing of vaccine administration to either asymptomatically or previously infected individuals. Using the female Chlamydia muridarum genital tract mouse model, we examined this aspect of vaccine development. Our results show timing of vaccination affected the production of systemic antibodies, but had minimal effects on mucosal antibody production. Vaccination during an active infection or after a resolved infection did not provide protection against re-exposure to Chlamydia, and did not exacerbate the development of pathological sequelae in infected mice. This demonstrates that vaccination may not be protective in individuals who are seropositive for an acute or previous chlamydial infection.
针对有效的沙眼衣原体疫苗的研究正在进行中,然而,尚未有研究检查疫苗接种的时间,无论是针对无症状或先前感染的个体。本研究使用雌性鼠生殖道沙眼衣原体感染模型,研究了疫苗开发的这一方面。我们的结果表明,疫苗接种的时间影响了系统抗体的产生,但对粘膜抗体的产生影响很小。在急性感染期或感染恢复后进行疫苗接种并不能提供针对再次接触衣原体的保护,也不会加重感染小鼠的病理后遗症的发展。这表明,对于急性或先前衣原体感染的血清阳性个体,疫苗接种可能没有保护作用。