Raff H V, Siscoe P J, Wolff E A, Maloney G, Shuford W
Oncogen, Seattle, Washington 98121.
J Exp Med. 1988 Sep 1;168(3):905-17. doi: 10.1084/jem.168.3.905.
Group B streptococcal (GBS) infections cause significant mortality and morbidity among infants. Passive antibody immunotherapy has been proposed as treatment for infected infants. To this end, two human mAb-secreting cell lines were produced by EBV immortalization of human B cells. The mAbs were specific for the group B polysaccharide and bound to strains of all five serotypes as demonstrated by ELISA and crossed immunoelectrophoresis. The mAbs reacted and opsonized 100% (132/132) of the clinical isolates tested which represented all four capsule types. Both prophylactic and therapeutic protection with these mAbs were demonstrated in neonatal rats given lethal infections of types Ia and III human clinical isolates. These data indicate that a single human mAb directed against the group B carbohydrate can protect against GBS infections caused by the different serotypes. This antibody may be useful in the passive immunotherapy of infants infected with GBS.
B族链球菌(GBS)感染在婴儿中导致显著的死亡率和发病率。被动抗体免疫疗法已被提议用于治疗受感染的婴儿。为此,通过EBV永生化人B细胞产生了两种分泌人单克隆抗体的细胞系。这些单克隆抗体对B族多糖具有特异性,并通过ELISA和交叉免疫电泳证明能与所有五种血清型的菌株结合。这些单克隆抗体与所测试的100%(132/132)临床分离株发生反应并进行调理,这些分离株代表了所有四种荚膜类型。在给予Ia型和III型人类临床分离株致死性感染的新生大鼠中,证明了这些单克隆抗体的预防和治疗保护作用。这些数据表明,一种针对B族碳水化合物的单一人类单克隆抗体可以预防由不同血清型引起的GBS感染。这种抗体可能对感染GBS的婴儿的被动免疫治疗有用。