Zhang Shimin, Feng Shaw-Huey, Li Bingjie, Kim Hyung-Yong, Rodriguez Joe, Tsai Shien, Lo Shyh-Ching
Department of Environmental and Infectious Disease Sciences, American Registry of Pathology, Armed Forces Institute of Pathology, Washington, DC 20306, USA.
Clin Vaccine Immunol. 2011 May;18(5):825-34. doi: 10.1128/CVI.00533-10. Epub 2011 Mar 30.
Our laboratory has developed more than a hundred mouse monoclonal antibodies (MAbs) against Burkholderia pseudomallei and Burkholderia mallei. These antibodies have been categorized into different groups based on their specificities and the biochemical natures of their target antigens. The current study first examined the bactericidal activities of a number of these MAbs by an in vitro opsonic assay. Then, the in vivo protective efficacy of selected MAbs was evaluated using BALB/c mice challenged intranasally with a lethal dose of the bacteria. The opsonic assay using dimethyl sulfoxide-treated human HL-60 cells as phagocytes revealed that 19 out of 47 tested MAbs (40%) have prominent bactericidal activities against B. pseudomallei and/or B. mallei. Interestingly, all MAbs with strong opsonic activities are those with specificity against either the capsular polysaccharides (PS) or the lipopolysaccharides (LPS) of the bacteria. On the other hand, none of the MAbs reacting to bacterial proteins or glycoproteins showed prominent bactericidal activity. Further study revealed that the antigenic epitopes on either the capsular PS or LPS molecules were readily available for binding in intact bacteria, while the epitopes on proteins/glycoproteins were less accessible to the MAbs. Our in vivo study showed that four MAbs reactive to either the capsular PS or LPS were highly effective in protecting mice against lethal bacterial challenge. The result is compatible with that of our in vitro study. The MAbs with the highest protective efficacy are those reactive to either the capsular PS or LPS of the Burkholderia bacteria.
我们实验室已开发出一百多种针对伯克霍尔德菌属假鼻疽杆菌和鼻疽杆菌的小鼠单克隆抗体(MAb)。这些抗体已根据其特异性和靶抗原的生化性质被分为不同组。本研究首先通过体外调理吞噬试验检测了其中多种单克隆抗体的杀菌活性。然后,使用经鼻内接种致死剂量细菌攻击的BALB/c小鼠评估了所选单克隆抗体的体内保护效果。以二甲基亚砜处理的人HL-60细胞作为吞噬细胞的调理吞噬试验表明,47种测试单克隆抗体中有19种(40%)对假鼻疽杆菌和/或鼻疽杆菌具有显著的杀菌活性。有趣的是,所有具有强调理活性的单克隆抗体都是那些对细菌的荚膜多糖(PS)或脂多糖(LPS)具有特异性的抗体。另一方面,与细菌蛋白或糖蛋白反应的单克隆抗体均未显示出显著的杀菌活性。进一步研究表明,荚膜PS或LPS分子上的抗原表位在完整细菌中易于结合,而蛋白/糖蛋白上的表位则较难被单克隆抗体识别。我们的体内研究表明,四种对荚膜PS或LPS有反应的单克隆抗体在保护小鼠免受致死性细菌攻击方面非常有效。该结果与我们的体外研究结果一致。保护效果最高的单克隆抗体是那些对伯克霍尔德菌属细菌的荚膜PS或LPS有反应的抗体。