DeCathelineau Aimee M, Bokoch Gary M
Department of Immunology, The Scripps Research Institute, La Jolla, CA 92037, USA.
Biochem J. 2006 Apr 1;395(1):e1-3. doi: 10.1042/bj20060245.
The pathogenesis of anthrax is such that unless antibiotic treatment is initiated at an early stage in the disease, it is ineffective against the bacteria-induced toxaemia that subverts the immune response, inflicts massive tissue damage and is ultimately the major factor contributing to death during anthrax infection. As current events have demonstrated the feasibility of the use of anthrax as a bioterrorism agent, and exemplified the difficulty of treating the ensuing infection, inhibition of anthrax toxin has become a major focus of research for the design of antitoxin therapeutics. In this issue of Biochemical Journal, Bracci and co-workers describe the discovery by competitive screening of a phage-display library of a peptide inhibitor of anthrax toxin assembly that shows great promise towards the treatment of anthrax.
炭疽的发病机制是,除非在疾病早期开始抗生素治疗,否则它对细菌诱导的毒血症无效,这种毒血症会破坏免疫反应,造成大规模组织损伤,最终是导致炭疽感染期间死亡的主要因素。正如当前事件所表明的,使用炭疽作为生物恐怖主义制剂是可行的,也例证了治疗后续感染的困难,因此抑制炭疽毒素已成为抗毒素治疗药物设计研究的主要焦点。在本期《生物化学杂志》中,布拉奇及其同事描述了通过竞争性筛选噬菌体展示文库发现一种炭疽毒素组装肽抑制剂,该抑制剂在治疗炭疽方面显示出巨大潜力。