Byrne G I, Stephens R S, Ada G, Caldwell H D, Su H, Morrison R P, Van der Pol B, Bavoil P, Bobo L, Everson S
Dept. of Medical Microbiology, University of Wisconsin, Madison 53706.
J Infect Dis. 1993 Aug;168(2):415-20. doi: 10.1093/infdis/168.2.415.
A task force evaluated an in vitro antibody-mediated chlamydial neutralization assay for its utility as a method to assess functional correlates of antibody responses to Chlamydia trachomatis. Two monoclonal antibodies that recognize different major outer membrane protein (MOMP) epitopes for a C. trachomatis serovar B strain exhibit good in vitro neutralizing activity, with a maximum of 90% neutralization. Calculations based on the 50% neutralization point indicated that 100% neutralization could theoretically be achieved when only 10% of the MOMP molecules bound antibody. Monoclonal antibodies that recognized either a heterologous MOMP or the genus-specific chlamydial lipopolysaccharide did not produce neutralizing activity. The standardized assay will be useful to establish if in vitro neutralizing antibody responses are predictive of protective immunity and will aid in defining chlamydial antigens and epitopes that may be attractive vaccine candidates.
一个特别工作组评估了一种体外抗体介导的衣原体中和试验,以确定其作为评估沙眼衣原体抗体反应功能相关性方法的实用性。两种识别沙眼衣原体B血清型菌株不同主要外膜蛋白(MOMP)表位的单克隆抗体表现出良好的体外中和活性,最大中和率为90%。基于50%中和点的计算表明,理论上仅10%的MOMP分子结合抗体时就能实现100%中和。识别异源MOMP或属特异性衣原体脂多糖的单克隆抗体未产生中和活性。该标准化试验将有助于确定体外中和抗体反应是否可预测保护性免疫,并将有助于确定可能是有吸引力的疫苗候选物的衣原体抗原和表位。