Rivera V R, Poli M A, Bignami G S
U.S. Army Medical Research Institute of Infectious Diseases, Fort Detrick, Frederick, MD 21702, USA.
Toxicon. 1995 Sep;33(9):1231-7. doi: 10.1016/0041-0101(95)00060-y.
The ability of a tetrodotoxin (TTX)-specific monoclonal antibody to confer passive protection against lethal TTX challenge was investigated. The monoclonal antibody, T20G10, has an estimated affinity for TTX of approximately 10(-9) M and is about 50-fold less reactive with anhydrotetrodotoxin and unreactive with tetrodonic acid by competitive immunoassay. T20G10 specifically inhibited TTX binding in an in vitro radioligand receptor binding assay, but had no effect on the binding of saxitoxin to the sodium channel on rat brain membranes. In prophylaxis studies, mice were administered T20G10 via the tail vein 30 min prior to i.p. TTX challenge (10 micrograms/kg). Under these conditions, 100 micrograms T20G10 protected 6/6 mice, whereas 3/6 mice were protected with 50 micrograms T20G10. Non-specific control monoclonal antibody did not protect against lethality. Therapy studies simulating oral intoxication were performed with mice given a lethal dose of TTX by gavage in a suspension of non-fat dry milk in phosphate-buffered saline. Death occurred within 25-35 min in 6/6 mice not treated with T20G10. However, 500 micrograms T20G10 administered via the tail vein 10-15 min after oral TTX exposure prevented death in 6/6 mice. Lower doses of mAb conferred less protection.
研究了一种河豚毒素(TTX)特异性单克隆抗体对致死性TTX攻击提供被动保护的能力。单克隆抗体T20G10对TTX的估计亲和力约为10^(-9) M,通过竞争性免疫测定,其与脱水河豚毒素的反应性约低50倍,与河豚酸无反应。在体外放射性配体受体结合试验中,T20G10特异性抑制TTX结合,但对石房蛤毒素与大鼠脑膜上钠通道的结合没有影响。在预防研究中,小鼠在腹腔注射TTX攻击(10微克/千克)前30分钟经尾静脉给予T20G10。在这些条件下,100微克T20G10保护了6/6只小鼠,而50微克T20G10保护了3/6只小鼠。非特异性对照单克隆抗体不能预防致死性。通过在磷酸盐缓冲盐水中的脱脂干奶悬浮液中灌胃给予小鼠致死剂量的TTX,进行了模拟口服中毒的治疗研究。未用T20G10治疗的6/6只小鼠在25 - 35分钟内死亡。然而,口服TTX暴露后10 - 15分钟经尾静脉给予500微克T20G10可防止6/6只小鼠死亡。较低剂量的单克隆抗体提供的保护较少。