Reddy M V, Parkhe K A, Piessens W F, Harinath B C
Department of Biochemistry, Mahatma Gandhi Institute of Medical Sciences, Sevagram, Maharashtra, India.
J Clin Lab Anal. 1989;3(5):277-81. doi: 10.1002/jcla.1860030504.
The Wb E34 monoclonal antibody raised against Wuchereria bancrofti microfilarial excretory secretory (mf ES) antigen was reported to be useful in detecting the filarial antigen in W. bancrofti and Brugia malayi infected sera. Further studies in this laboratory showed that this monoclonal antibody reacts with a stage-specific antigen of W. bancrofti filarial parasite. Wb E34 identified three antigenic components with molecular weights, 55, 57.5, and 63 kilodaltons (Kd) in western blot analysis. The target antigen of Wb E34 was found to be located in the cytoplasm of microfilariae by indirect immunofluorescence technique. The inhibitory antibodies to Wb E34 were detected in a higher percentage of microfilaraemic sera (81%) than in clinical filarial (33%) or tropical eosinophilia sera (35%). Thus the inhibition ELISA using W. bancrofti mf ES antigen and Wb E34-penicillinase may be useful in detecting the filarial antibody associated with the active stage of infection.
据报道,针对班氏吴策线虫微丝蚴排泄分泌(mf ES)抗原产生的Wb E34单克隆抗体可用于检测班氏吴策线虫和马来布鲁线虫感染血清中的丝虫抗原。本实验室的进一步研究表明,该单克隆抗体与班氏吴策线虫寄生虫的阶段特异性抗原发生反应。在蛋白质印迹分析中,Wb E34鉴定出三种分子量分别为55、57.5和63千道尔顿(Kd)的抗原成分。通过间接免疫荧光技术发现,Wb E34的靶抗原位于微丝蚴的细胞质中。与临床丝虫病(33%)或热带嗜酸性粒细胞增多症血清(35%)相比,在更高比例的微丝蚴血症血清(81%)中检测到了针对Wb E34的抑制性抗体。因此,使用班氏吴策线虫mf ES抗原和Wb E34 - 青霉素酶的抑制性ELISA可能有助于检测与感染活跃阶段相关的丝虫抗体。