ImmPORT Therapeutics, 1 Technology Drive, Suite E309, Irvine, CA 92618, USA.
Vaccine. 2010 Apr 9;28(17):3014-24. doi: 10.1016/j.vaccine.2009.12.020. Epub 2009 Dec 29.
Chlamydia trachomatis is the most common bacterial sexually transmitted pathogen in the world. In order to control this infection there is an urgent need to formulate a vaccine. Identification of protective antigens is required to implement a subunit vaccine. To identify potential antigen vaccine candidates, three strains of mice, BALB/c, C3H/HeN and C57BL/6, were inoculated with live and inactivated C. trachomatis mouse pneumonitis (MoPn) by different routes of immunization. Using a protein microarray, serum samples collected after immunization were tested for the presence of antibodies against specific chlamydial antigens. A total of 225 open reading frames (ORF) of the C. trachomatis genome were cloned, expressed, and printed in the microarray. Using this protein microarray, a total of seven C. trachomatis dominant antigens were identified (TC0052, TC0189, TC0582, TC0660, TC0726, TC0816 and, TC0828) as recognized by IgG antibodies from all three strains of animals after immunization. In addition, the microarray was probed to determine if the antibody response exhibited a Th1 or Th2 bias. Animals immunized with live organisms mounted a predominant Th1 response against most of the chlamydial antigens while mice immunized with inactivated Chlamydia mounted a Th2-biased response. In conclusion, using a high throughput protein microarray we have identified a set of novel proteins that can be tested for their ability to protect against a chlamydial infection.
沙眼衣原体是世界上最常见的细菌性性传播病原体。为了控制这种感染,迫切需要制定一种疫苗。要实施亚单位疫苗,就需要鉴定保护性抗原。为了鉴定潜在的抗原疫苗候选物,用不同的免疫途径给 BALB/c、C3H/HeN 和 C57BL/6 三种小鼠接种活的和灭活的沙眼衣原体鼠肺炎(MoPn)。用蛋白质微阵列检测免疫后收集的血清样本中针对特定沙眼衣原体抗原的抗体存在情况。克隆、表达并打印了沙眼衣原体基因组的 225 个开放阅读框(ORF)到微阵列上。使用这种蛋白质微阵列,鉴定出了七种沙眼衣原体优势抗原(TC0052、TC0189、TC0582、TC0660、TC0726、TC0816 和 TC0828),这些抗原被三种动物的 IgG 抗体识别。此外,还探测了微阵列以确定抗体反应是否表现出 Th1 或 Th2 偏向。用活生物体免疫的动物针对大多数衣原体抗原产生了主要的 Th1 反应,而用灭活的衣原体免疫的小鼠则产生了 Th2 偏向的反应。总之,我们使用高通量蛋白质微阵列鉴定了一组新的蛋白质,这些蛋白质可以测试其预防衣原体感染的能力。