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单克隆抗体对实验性大肠杆菌感染的预防与治疗

Prevention and therapy of experimental Escherichia coli infection with monoclonal antibody.

作者信息

Kim K S, Cross A S, Zollinger W, Sadoff J

出版信息

Infect Immun. 1985 Dec;50(3):734-7. doi: 10.1128/iai.50.3.734-737.1985.

Abstract

Mouse hybridoma antibody of immunoglobulin class M prepared with live group B meningococci was evaluated for its ability to protect against and treat Escherichia coli infections in a newborn-rat model. In these studies, antibody was administered intraperitoneally and bacteria were administered subcutaneously to avoid introducing the antibody and bacteria to the same site. The activity of this hybridoma antibody was specific; the antibody provided protection against the K-1 strain, but not against the K-92 strain. In addition, the amount of the antibody required for protection was dependent upon the size of bacterial challenge. With an increase of the bacterial inocula from the 100% lethal dose to 10 times the 100% lethal dose there was a threefold increase in the amount of the antibody required for 50% protection. Similarly, therapeutic efficacy of the antibody was also dependent upon the magnitude of bacteremia before therapy. The antibody successfully cleared the bacteremia only when the pretherapy bacterial counts in blood were less than 10(4) CFU/ml. These findings suggest that the monoclonal immunoglobulin M antibody against the capsular polysaccharide of the group B meningococcus may be useful in the prevention and treatment of K-1 E. coli infections.

摘要

用活的B群脑膜炎球菌制备的免疫球蛋白M类小鼠杂交瘤抗体,在新生大鼠模型中评估其预防和治疗大肠杆菌感染的能力。在这些研究中,抗体通过腹腔注射给药,细菌通过皮下注射给药,以避免将抗体和细菌引入同一部位。这种杂交瘤抗体的活性具有特异性;该抗体能提供针对K-1菌株的保护,但不能针对K-92菌株。此外,提供保护所需的抗体量取决于细菌攻击的规模。随着细菌接种量从100%致死剂量增加到10倍100%致死剂量,50%保护所需的抗体量增加了三倍。同样,抗体的治疗效果也取决于治疗前菌血症的程度。只有当治疗前血液中的细菌计数低于10(4) CFU/ml时,该抗体才能成功清除菌血症。这些发现表明,针对B群脑膜炎球菌荚膜多糖的单克隆免疫球蛋白M抗体可能对预防和治疗K-1大肠杆菌感染有用。

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