Gorina L G, Drobyshevskaia E I
Gamaleya Research Institute of Epidemiology and Microbiology, Moscow, Russia.
Zh Mikrobiol Epidemiol Immunobiol. 1999 Mar-Apr(2):81-4.
Approaches to obtaining stable mouse hybridomas, capable of producing monoclonal antibodies (McAb) to M. pneumoniae key antigens, were developed. As the result of hybridization experiments, 7 clones were obtained; of these, 4 clones stably synthesized IgG McAb. Clones H1/H9 and H9/B2 synthesized antibodies to thermolabile, proteinase-sensitive K protein, produced by cytoplasmic membranes of M. pneumoniae cells. The molecular weight of this protein was found to be 90 kD. McAb of clone H1/H9, labeled with horse-radish peroxidase and fluorescein isothiocyanate, specifically reacted with M. pneumoniae antigens in the immunofluorescence test and the enzyme immunoassay (EIA). The sensitivity of EIA was 0.25 ng/ml of antigen protein. These data are prerequisites for the development of diagnostic test systems for the detection of M. pneumoniae antigens in different biological substances obtained from patients with respiratory pathology.
已开发出获得稳定小鼠杂交瘤的方法,这些杂交瘤能够产生针对肺炎支原体关键抗原的单克隆抗体(McAb)。作为杂交实验的结果,获得了7个克隆;其中,4个克隆稳定合成IgG McAb。克隆H1/H9和H9/B2合成了针对肺炎支原体细胞质膜产生的热不稳定、蛋白酶敏感K蛋白的抗体。发现该蛋白的分子量为90 kD。用辣根过氧化物酶和异硫氰酸荧光素标记的克隆H1/H9的McAb,在免疫荧光试验和酶免疫测定(EIA)中与肺炎支原体抗原发生特异性反应。EIA的灵敏度为0.25 ng/ml抗原蛋白。这些数据是开发用于检测从呼吸道疾病患者获得的不同生物物质中肺炎支原体抗原的诊断测试系统的前提条件。