Volp K, Mathews S, Timms P, Hafner L
Centre for Molecular Biotechnology, School of Life Sciences, Queensland University of Technology, Brisbane, Queensland, Australia.
Immunol Cell Biol. 2001 Jun;79(3):245-50. doi: 10.1046/j.1440-1711.2001.01005.x.
Immunization of female guinea pigs with a chimeric peptide consisting of variable domain IV (VDIV) and a region known as GP8 from the major outer membrane protein of Chlamydophila caviae, formerly Chlamydia psittaci guinea pig inclusion conjunctivitis strain, was performed to assess whether humoral immune responses could be elicited in the reproductive tracts of immunized animals. The C. caviae strain is able to cause a sexually transmitted infection in the guinea pig that closely parallels C. trachomatis infections in humans. The best anti-VDIV antibody response in vaginal secretions was achieved by intraperitoneal priming with subsequent intravaginal boosting (P < 0.001). Dot-blot analyses of vaginal secretions confirmed that these anti-VDIV antibodies, produced against a linear peptide, were able to recognize and bind to whole conformational C. caviae elementary bodies. Following live intravaginal challenge with C. caviae, a significant reduction in the intensity (P = 0.01) and an apparent reduction in the duration of the infection was evident between the guinea pigs immunized with VDIV-GP8 and non-immunized controls.
用一种嵌合肽对雌性豚鼠进行免疫,该嵌合肽由可变结构域IV(VDIV)和来自豚鼠嗜衣原体(以前称为鹦鹉热衣原体豚鼠包涵体结膜炎菌株)主要外膜蛋白的一个名为GP8的区域组成,以评估免疫动物的生殖道中是否能引发体液免疫反应。豚鼠嗜衣原体菌株能够在豚鼠中引起性传播感染,这与人类沙眼衣原体感染非常相似。通过腹腔初次免疫随后阴道加强免疫,在阴道分泌物中获得了最佳的抗VDIV抗体反应(P < 0.001)。对阴道分泌物的斑点印迹分析证实,这些针对线性肽产生的抗VDIV抗体能够识别并结合完整构象的豚鼠嗜衣原体原体。在用豚鼠嗜衣原体进行阴道活体攻击后,在用VDIV-GP8免疫的豚鼠和未免疫的对照之间,感染强度显著降低(P = 0.01),感染持续时间明显缩短。