Pepys M B
Immunology. 1975 Feb;28(2):369-77.
The effect of the isolated C3-cleaving factor (CoF) of cobra venom on murine C3 in vivo and in vitro was studied. Optimal quantities of 100-200 units (0.5 minus 1.0 mg) of CoF per kg administered to mice by intraperitoneal injection in divided doses caused plasma C3 levels to fall to less than 5 per cent of normal from 1 to at least 4 days afterwards. Passive anti-CoF serum promptly abrogated the in vivo plasma C3 depletion, and under optimal conditions C3 levels reached 50 per cent of normal after approximately 15 hours. Injection of as little as 20 mug per mouse of CoF in saline induced a precipitating anti-CoF antibody response which prevented subsequent depletion of plasma C3 by CoF. The in vivo half-life of 125I-labelled CoF in normal mice estimated by whole body elimination and clearance from the blood was 24 hours. The presence in vivo of antibodies to CoF caused rapid clearance from the blood and elimination of 125I-labelled CoF, and also localization of some CoF in the spleen, liver and kidneys.
研究了眼镜蛇毒中分离出的C3裂解因子(CoF)对小鼠体内和体外C3的影响。以每千克100 - 200单位(0.5至1.0毫克)的最佳剂量将CoF分剂量腹腔注射给小鼠,可使血浆C3水平在随后1至至少4天内降至正常水平的5%以下。被动抗CoF血清可迅速消除体内血浆C3的消耗,在最佳条件下,约15小时后C3水平可达到正常水平的50%。每只小鼠注射低至20微克的CoF生理盐水溶液可诱导产生沉淀性抗CoF抗体反应,从而阻止CoF随后对血浆C3的消耗。通过全身清除和血液清除估算,正常小鼠体内125I标记的CoF的半衰期为24小时。体内存在抗CoF抗体可导致血液中125I标记的CoF迅速清除和消除,同时部分CoF在脾脏、肝脏和肾脏中定位。