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GT160 - 246,一种用于治疗艰难梭菌结肠炎的毒素结合聚合物。

GT160-246, a toxin binding polymer for treatment of Clostridium difficile colitis.

作者信息

Kurtz C B, Cannon E P, Brezzani A, Pitruzzello M, Dinardo C, Rinard E, Acheson D W, Fitzpatrick R, Kelly P, Shackett K, Papoulis A T, Goddard P J, Barker R H, Palace G P, Klinger J D

机构信息

GelTex Pharmaceuticals, Inc., Waltham, Massachusetts 02451, USA.

出版信息

Antimicrob Agents Chemother. 2001 Aug;45(8):2340-7. doi: 10.1128/AAC.45.8.2340-2347.2001.

Abstract

GT160-246, a high-molecular-weight soluble anionic polymer, was tested in vitro and in vivo for neutralization of Clostridium difficile toxin A and B activities. Five milligrams of GT160-246 per ml neutralized toxin-mediated inhibition of protein synthesis in Vero cells induced by 5 ng of toxin A per ml or 1.25 ng of toxin B per ml. In ligated rat ileal loops, 1 mg of GT160-246 neutralized fluid accumulation caused by 5 microg of toxin A. At doses as high as 80 mg/loop, cholestyramine provided incomplete neutralization of fluid accumulation caused by 5 microg of toxin A. GT160-246 protected 80% of the hamsters from mortality caused by infection with C. difficile, whereas cholestyramine protected only 10% of animals. Treatment of C. difficile-infected hamsters with metronidazole initially protected 100% of the hamsters from mortality, but upon removal of treatment, 80% of the hamsters had relapses and died. In contrast, removal of GT160-246 treatment did not result in disease relapse in the hamsters. GT160-246 showed no antimicrobial activity in tests with a panel of 16 aerobic bacteria and yeast and 22 anaerobic bacteria and did not interfere with the in vitro activities of most antibiotics. GT160-246 offers a novel, nonantimicrobial treatment of C. difficile disease in humans.

摘要

GT160 - 246是一种高分子量可溶性阴离子聚合物,已在体外和体内测试其对艰难梭菌毒素A和B活性的中和作用。每毫升5毫克的GT160 - 246可中和每毫升5纳克毒素A或每毫升1.25纳克毒素B诱导的Vero细胞中毒素介导的蛋白质合成抑制。在结扎的大鼠回肠袢中,1毫克的GT160 - 246可中和5微克毒素A引起的液体蓄积。在剂量高达80毫克/袢时,消胆胺对5微克毒素A引起的液体蓄积的中和作用不完全。GT160 - 246可保护80%的仓鼠免受艰难梭菌感染导致的死亡,而消胆胺仅保护10%的动物。用甲硝唑治疗艰难梭菌感染的仓鼠最初可100%保护仓鼠免于死亡,但停止治疗后,80%的仓鼠复发并死亡。相比之下,停止GT160 - 246治疗并未导致仓鼠疾病复发。GT160 - 246在对16种需氧菌和酵母菌以及22种厌氧菌的测试中未显示抗菌活性,并且不干扰大多数抗生素的体外活性。GT160 - 246为人类艰难梭菌病提供了一种新型的非抗菌治疗方法。

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