Sulfated K5 Escherichia coli polysaccharide derivatives: A novel class of candidate antiviral microbicides

Pharmacol Ther. 2009 Sep;123(3):310-22. doi: 10.1016/j.pharmthera.2009.05.001. Epub 2009 May 14.


Antiviral microbicides, topical agents that prevent sexually transmitted infections, mainly work by blocking the interaction between viral proteins and cell surface components. In many instances, virus-cell interaction is mediated by cell surface heparan sulfate proteoglycans (HSPGs). HSPGs are exploited as attachment receptors by three sexually transmitted viruses: Human Immunodeficiency Virus (HIV), Herpes Simplex Virus (HSV) and Human Papilloma Virus (HPV). Since these viruses can either infect or co-infect humans, virus/HSPGs interaction is a preferential target for the development of wide-spectrum antiviral microbicides. Several polyanionic compounds prevent HIV, HSV and HPV infections in cell culture models by acting as heparan sulfate (HS)-antagonists. However, three promising polyanionic compounds recently failed to pass phase III clinical trials designed to establish their efficacy in preventing HIV acquisition. In this scenario, new polyanionic compounds must be added to the pipeline of candidate microbicides and their development as effective drugs reconsidered. The capsular K5 polysaccharide from Escherichia coli has the same structure as the heparin/HS biosynthetic precursor. Chemical and enzymatic modifications have led to the synthesis of K5 derivatives with different degrees of sulfation and charge distribution and devoid of anticoagulant activity and cell toxicity. Recently attracting attention as candidate microbicides, they potently inhibit a broad spectrum of HIV-1 strains and genital types of HPV and HSV-1 and 2 in vitro. With a focus on the K5 derivatives, this article reviews the literature on polyanions as antiviral microbicides and discusses the possible therapeutic implications of this novel class of compounds.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Antiviral Agents / chemistry
  • Antiviral Agents / pharmacology*
  • Bacterial Capsules / chemistry
  • Bacterial Capsules / pharmacology*
  • Clinical Trials as Topic
  • Escherichia coli / chemistry*
  • HIV Infections / drug therapy
  • HIV Infections / physiopathology
  • Herpes Simplex / drug therapy
  • Herpes Simplex / physiopathology
  • Humans
  • Papillomavirus Infections / drug therapy
  • Papillomavirus Infections / physiopathology


  • Antiviral Agents
  • capsular polysaccharide K5