Wang Yang, Kern Aurélie, Boatright Naomi K, Schiller Zachary A, Sadowski Andrew, Ejemel Monir, Souders Colby A, Reimann Keith A, Hu Linden, Thomas William D, Klempner Mark S
MassBiologics, University of Massachusetts Medical School.
Sackler School of Graduate Biomedical Sciences, Tufts University School of Medicine, Boston, Massachusetts.
J Infect Dis. 2016 Jul 15;214(2):205-11. doi: 10.1093/infdis/jiw151. Epub 2016 Apr 18.
Tick transmission of Borrelia spirochetes to humans results in significant morbidity from Lyme disease worldwide. Serum concentrations of antibodies against outer surface protein A (OspA) were shown to correlate with protection from infection with Borrelia burgdorferi, the primary cause of Lyme disease in the United States.
Mice transgenic for human immunoglobulin genes were immunized with OspA from B. burgdorferi to generate human monoclonal antibodies (HuMabs) against OspA. HuMabs were generated and tested in in vitro borreliacidal assays and animal protection assays.
Nearly 100 unique OspA-specific HuMabs were generated, and 4 HuMabs (221-7, 857-2, 319-44, and 212-55) were selected as lead candidates on the basis of borreliacidal activity. HuMabs 319-44, 857-2, and 212-55 were borreliacidal against 1 or 2 Borrelia genospecies, whereas 221-7 was borreliacidal (half maximal inhibitory concentration, < 1 nM) against B. burgdorferi, Borrelia afzelii, and Borrelia garinii, the 3 main genospecies endemic in the United States, Europe, and Asia. All 4 HuMabs completely protected mice from infection at 10 mg/kg in a murine model of tick-mediated transmission of B. burgdorferi
Our study indicates that OspA-specific HuMabs can prevent the transmission of Borrelia and that administration of these antibodies could be employed as preexposure prophylaxis for Lyme disease.
蜱将疏螺旋体传播给人类会在全球范围内导致莱姆病引发严重发病。研究表明,抗外膜蛋白A(OspA)的血清抗体浓度与预防感染伯氏疏螺旋体相关,伯氏疏螺旋体是美国莱姆病的主要病因。
用来自伯氏疏螺旋体的OspA免疫转人免疫球蛋白基因的小鼠,以产生抗OspA的人单克隆抗体(HuMabs)。在体外杀螺旋体试验和动物保护试验中产生并测试HuMabs。
产生了近100种独特的OspA特异性HuMabs,基于杀螺旋体活性选择了4种HuMabs(221 - 7、857 - 2、319 - 44和212 - 55)作为主要候选抗体。HuMabs 319 - 44、857 - 2和212 - 55对1种或2种疏螺旋体基因种具有杀螺旋体作用,而221 - 7对伯氏疏螺旋体、阿氏疏螺旋体和伽氏疏螺旋体具有杀螺旋体作用(半数最大抑制浓度,<1 nM),这3种主要基因种分别在美国、欧洲和亚洲流行。在蜱介导的伯氏疏螺旋体传播的小鼠模型中,所有4种HuMabs在10 mg/kg时都能完全保护小鼠免受感染。
我们的研究表明,OspA特异性HuMabs可以预防疏螺旋体的传播,并且给予这些抗体可作为莱姆病的暴露前预防措施。