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炭疽芽孢杆菌与抗菌剂。

Bacillus anthracis and antibacterial agents.

作者信息

Bryskier A

机构信息

Aventis Pharma SA, Infectious Disease Group, Romainville, France.

出版信息

Clin Microbiol Infect. 2002 Aug;8(8):467-78. doi: 10.1046/j.1469-0691.2002.00527.x.

Abstract

Anthrax is one of the oldest threats to humankind, and remains endemic in animals in many parts of the world. Human cases are infrequent, and some result from biological warfare. This review summarizes the current knowledge on the antibacterial activity of available antibiotics. For potential use in the most severe cases of anthrax, antibacterials need to exhibit potent in vitro activity, intracellular bioactivity, and suitable locations in lymph nodes. In animal models, it has been shown that doxycycline and fluoroquinolones are the most active compounds. There is a lack of data for animal models for macrolides and ketolides, some of them exhibiting good in vitro activity. However, systemic anthrax (inhalation or gastrointestinal) is mainly due to anthrax toxin, and therapy directed against intoxication is needed as basic treatment.

摘要

炭疽是对人类最古老的威胁之一,在世界许多地区的动物中仍然流行。人类病例并不常见,有些是由生物战导致的。本综述总结了现有抗生素抗菌活性的当前知识。对于炭疽最严重病例的潜在用途,抗菌药物需要在体外表现出强效活性、细胞内生物活性以及在淋巴结中的合适定位。在动物模型中,已表明强力霉素和氟喹诺酮类是活性最强的化合物。关于大环内酯类和酮内酯类在动物模型中的数据不足,其中一些在体外表现出良好活性。然而,全身性炭疽(吸入性或胃肠道性)主要是由炭疽毒素引起的,针对中毒的治疗作为基础治疗是必需的。

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