Kirkland T N, Ziegler E J
J Immunol. 1984 May;132(5):2590-2.
The ability of antisera against lipopolysaccharide (LPS) raised by immunization with gram-negative bacteria to prevent LPS toxicity and death from gram-negative bacteremia is well established. To demonstrate conclusively that the protective antibody is specific for LPS, we tested an anti-LPS monoclonal antibody (mAb) in three animal models. 7G is an IgG3 mAb directed against an oligosaccharide side chain determinant of LPS from E. coli 0111:B4. This anti-LPS mAb increased the LD50 of 0111:B4 LPS in mice and protected rabbits against the dermal Shwartzman reaction elicited by 0111:B4 LPS. 7G mAb also protected mice against lethal infection with mucin-enhanced E. coli 0111:B4. Pretreatment with 250 micrograms of 7G increased the LD50 by more than 1.5 logs. These studies prove that oligosaccharide side chain-specific antibody to LPS confers protection against LPS toxicity in vivo and against experimental gram-negative infection. In addition, these studies suggest the potential of anti-LPS monoclonal antibody as therapy for gram-negative infection.
用革兰氏阴性菌免疫产生的抗脂多糖(LPS)抗血清预防LPS毒性及革兰氏阴性菌血症致死的能力已得到充分证实。为了确凿地证明保护性抗体对LPS具有特异性,我们在三种动物模型中测试了一种抗LPS单克隆抗体(mAb)。7G是一种IgG3 mAb,针对大肠杆菌0111:B4 LPS的寡糖侧链决定簇。这种抗LPS mAb提高了小鼠对0111:B4 LPS的半数致死剂量(LD50),并保护兔子免受0111:B4 LPS引发的皮肤施瓦茨曼反应。7G mAb还保护小鼠免受黏蛋白增强型大肠杆菌0111:B4的致死性感染。用250微克7G进行预处理使LD50增加了超过1.5个对数级。这些研究证明,针对LPS的寡糖侧链特异性抗体在体内可抵御LPS毒性,并抵御实验性革兰氏阴性菌感染。此外,这些研究表明抗LPS单克隆抗体作为革兰氏阴性菌感染治疗方法的潜力。