Raff H V, Shuford W, Wolff E, Rubens C E
Infectious Disease Therapy, Oncogen, Seattle, Washington 98121.
Pediatr Res. 1991 Mar;29(3):310-4. doi: 10.1203/00006450-199103000-00018.
We have developed a human MAb that opsonizes group B streptococci, the major cause of gram-positive bacterial sepsis in newborns. It is an IgM class human MAb that possess unique protective activity against experimental infections caused by the predominant group B capsule serotypes III and I. Preliminary preclinical studies with the IgM human MAb were designed to provide initial information useful for predicting its safety and pharmacokinetic properties. Two neonatal Macaca fascicularis monkeys were infused with the human MAb at either 17.8 or 230 mg/kg. Safety was evaluated by visually monitoring postinfusion clinical status and by standard clinical chemistry analyses and quantitative hematology on blood samples collected for 30 d. The serum antibody levels were determined by ELISA and antibody functional activity in serum samples by opsonophagocytic assays. The IgM human MAb appeared safe (normal laboratory values and clinical status) with a half-life of 2.5 d, a period compatible with the 5-d half-life reported for human IgM in adult serum. In addition, the human MAb retained functional opsonic activity for at least 30 d. Human MAb may offer a safe alternative for treating severe bacterial infections.
我们已经研发出一种人源单克隆抗体(MAb),它能调理B族链球菌,而B族链球菌是新生儿革兰氏阳性菌败血症的主要病因。这是一种IgM类人源单克隆抗体,对由主要的B族III型和I型荚膜血清型引起的实验性感染具有独特的保护活性。对该IgM人源单克隆抗体进行的初步临床前研究旨在提供有助于预测其安全性和药代动力学特性的初始信息。给两只新生食蟹猴分别注射17.8或230 mg/kg的人源单克隆抗体。通过目视监测注射后的临床状态以及对采集30天的血样进行标准临床化学分析和定量血液学检查来评估安全性。通过酶联免疫吸附测定(ELISA)测定血清抗体水平,并通过调理吞噬试验测定血清样本中的抗体功能活性。该IgM人源单克隆抗体似乎是安全的(实验室值和临床状态正常),半衰期为2.5天,这与成年血清中人IgM报道的5天半衰期相符。此外,该人源单克隆抗体至少在30天内保持功能性调理活性。人源单克隆抗体可能为治疗严重细菌感染提供一种安全的替代方法。