Zaldivar N M, Scher I
Infect Immun. 1979 Apr;24(1):127-31. doi: 10.1128/iai.24.1.127-131.1979.
Immune-defective and immunologically normal F1 mice derived from the CBA/N strain were used to study the influence of anti-endotoxin antibody on the lethal effects of endotoxin. Immune-defective F1 male mice were unable to make specific responses to purified preparations of E. coli O111:B4 endotoxin, whereas their immunologically normal F1 female littermates made excellent responses. The ability to form antibody to lipopolysaccharide (LPS) in these F1 mice did not influence either their natural resistance to endotoxin challenge or the effects of pretreatment with sublethal amounts of endotoxin on subsequent challenge with higher normally lethal doses. Furthermore, transfer of sera with high titers of anti-LPS antibody to mice prior to challenge with LPS failed to protect. Thus, anti-LPS antibody does not appear to play a critical role in protection of immune-defective (CBA/N X DBA/2) F1 male mice to the lethal effects of endotoxin or to the protective effects of a single sublethal dose of endotoxin on subsequent endotoxin challenge.
利用源自CBA/N品系的免疫缺陷型和免疫正常的F1小鼠,研究抗内毒素抗体对内毒素致死效应的影响。免疫缺陷型F1雄性小鼠无法对纯化的大肠杆菌O111:B4内毒素制剂产生特异性反应,而其免疫正常的F1雌性同窝小鼠则反应良好。这些F1小鼠中形成抗脂多糖(LPS)抗体的能力,既不影响它们对内毒素攻击的天然抵抗力,也不影响用亚致死量内毒素预处理对随后用更高通常致死剂量内毒素攻击的影响。此外,在LPS攻击前将高滴度抗LPS抗体的血清转移给小鼠并不能起到保护作用。因此,抗LPS抗体似乎在保护免疫缺陷型(CBA/N×DBA/2)F1雄性小鼠免受内毒素致死效应或单次亚致死剂量内毒素对随后内毒素攻击的保护作用方面,并不起关键作用。