Pal S, Peterson E M, de la Maza L M
Department of Pathology, University of California, Irvine 92697-4800, USA.
Infect Immun. 1996 Dec;64(12):5341-8. doi: 10.1128/iai.64.12.5341-5348.1996.
In an attempt to confer long-term protective immunity, BALB/c female mice were immunized intranasally with 10(4) inclusion-forming units (IFU) of the Chlamydia trachomatis mouse pneumonitis biovar (MoPn). Animals were subsequently challenged in the ovarian bursa with 10(5) C. trachomatis MoPn IFU at 60, 120, or 180 days post-intranasal immunization. Two control groups were included in the study. One control was sham immunized and mock challenged, and another group was sham immunized and challenged with 10(5) C. trachomatis MoPn IFU. Vaginal cultures were collected at regular intervals following the intrabursal challenge. In comparison with the sham-immunized mice, the animals that were intranasally immunized with C. trachomatis had significant protection, as shown by a reduction in the number of animals that had positive vaginal cultures and by a decrease in the intensity and length of the shedding. Furthermore, histopathological characterization of the genital tract following challenge, in the three groups of mice, showed a minimal inflammatory infiltrate in the C. trachomatis-immunized animals, when compared with the sham-immunized control group. Subsequently, the three groups of female mice that were challenged at 60, 120 and 180 days postimmunization were mated at 6 weeks following the challenge. Overall, in the mice intranasally immunized with C. trachomatis the fertility rates and the number of embryos were similar to those in the sham-immunized and mock-challenged group. In contrast, there was a significant increase in infertility in the groups of mice that were sham immunized and C. trachomatis challenged. In conclusion, intranasal immunization with C. trachomatis induces long-term protection against a genital challenge as shown by a decrease in the infection and infertility rates when compared with sham-immunized animals. Thus, this model may help to characterize the parameters of the immune response that are important in maintaining long-term protection and may aid in identifying the antigenic determinants involved in eliciting protection.
为了赋予长期保护性免疫,用10⁴个沙眼衣原体小鼠肺炎生物变种(MoPn)的包涵体形成单位(IFU)对BALB/c雌性小鼠进行鼻内免疫。随后在鼻内免疫后60、120或180天,用10⁵个沙眼衣原体MoPn IFU对动物的卵巢囊进行攻毒。研究中纳入了两个对照组。一个对照组进行假免疫和假攻毒,另一组进行假免疫并用10⁵个沙眼衣原体MoPn IFU进行攻毒。在囊内攻毒后定期收集阴道培养物。与假免疫小鼠相比,用沙眼衣原体进行鼻内免疫的动物具有显著的保护作用,表现为阴道培养物阳性的动物数量减少,以及排菌强度和持续时间降低。此外,在攻毒后对三组小鼠的生殖道进行组织病理学特征分析,结果显示,与假免疫对照组相比,沙眼衣原体免疫的动物炎症浸润最少。随后,在免疫后60、120和180天接受攻毒的三组雌性小鼠在攻毒后6周进行交配。总体而言,用沙眼衣原体进行鼻内免疫的小鼠的生育率和胚胎数量与假免疫和假攻毒组相似。相比之下,假免疫并用沙眼衣原体攻毒的小鼠组不育率显著增加。总之,与假免疫动物相比,用沙眼衣原体进行鼻内免疫可诱导对生殖道攻毒的长期保护,表现为感染率和不育率降低。因此,该模型可能有助于确定在维持长期保护中起重要作用的免疫反应参数,并可能有助于识别引发保护作用的抗原决定簇。