Bunse R, Heinz H P
Institute for Medical Microbiology and Virology, Heinrich Heine University, Düsseldorf, Germany.
J Immunol Methods. 1994 Dec 28;177(1-2):89-99. doi: 10.1016/0022-1759(94)90146-5.
Monoclonal antibodies to polyribosylribitolphosphate (PRP), the capsular polysaccharide of Haemophilus influenzae type b (Hib), are useful tools in the investigation of the molecular and cellular mechanisms causing Hib meningitis. A better understanding of these mechanisms may lead to improved therapeutic strategies. A number of different in vivo immunization techniques in BALB/c mice were used, which did not however reveal detectable serum levels of antibodies to PRP. Therefore a modified in vitro immunization technique, originally established for in vitro immunization of human B lymphocytes, was used for this weak immunogen in mice. After 5 days of in vitro stimulation with purified PRP the splenic lymphocytes of BALB/c mice were fused with the mouse myeloma line P3-X63-Ag8.653. One hybridoma produced an IgM antibody (12E7) which recognized the capsular polysaccharide in ELISA and specifically labelled all tested Hib strains in immune fluorescent microscopy. The blotted polysaccharide PRP was immunostained with monoclonal antibody 12E7. Preincubation of Hib with this antibody enhanced the oxygen radical metabolism of polymorphnuclear leucocytes in a chemiluminescence assay. There was no cross-reactivity with the supernatants of other Haemophilus influenzae serotypes and other bacterial species, as shown by counterimmunoelectrophoresis.
针对b型流感嗜血杆菌(Hib)的荚膜多糖多聚核糖基核糖醇磷酸(PRP)的单克隆抗体,是研究导致Hib脑膜炎的分子和细胞机制的有用工具。对这些机制的更好理解可能会带来改进的治疗策略。在BALB/c小鼠中使用了多种不同的体内免疫技术,但未检测到血清中PRP抗体水平。因此,一种最初为体外免疫人B淋巴细胞建立的改良体外免疫技术,被用于小鼠的这种弱免疫原。用纯化的PRP进行5天体外刺激后,将BALB/c小鼠的脾淋巴细胞与小鼠骨髓瘤细胞系P3-X63-Ag8.653融合。一个杂交瘤产生了一种IgM抗体(12E7),该抗体在ELISA中可识别荚膜多糖,并在免疫荧光显微镜下特异性标记所有测试的Hib菌株。印迹的多糖PRP用单克隆抗体12E7进行免疫染色。在化学发光分析中,Hib与该抗体预孵育可增强多形核白细胞的氧自由基代谢。免疫对流电泳显示,与其他流感嗜血杆菌血清型和其他细菌种类的上清液无交叉反应。