Direct antimicrobial activity of antithrombin?

a study by Hofstra and colleagues [1] in a recent issue of Critical Care, nebulization of drotrecogin-alfa (activated), antithrombin, heparin, or danaparoid attenuated pulmonary coagulopathy during Streptococcus pneumoniae pneumonia in rats; only antithrombin additionally exerted lung-protective eff ects and reduced bacterial outgrowth. Adding antithrombin to culture medium had no eff ect on the outgrowth of S. pneumoniae in vitro; thus, less neutralizing of endogenous antimicrobicidals by reduced bronchoalveolar fl uid levels of infl ammatory proteins could have permitted better endogenous microbicidal eff ects in the antithrombin group [1]. Direct microbicidal eff ects of antithrombin would not have been surprising since antimicrobial peptides are known to bind to glycosaminoglycans similar to anti-thrombin [2]. Structural motifs associated with heparin affi nity confer antimicrobial properties to a given peptide [3]. Th us, heparin-binding peptides (for example, from laminin isoforms, von Willebrand factor, vitronectin, protein C inhibitor, complement factor C3, and fi bro-nectin) exerted antimicrobial activities against bacteria [3]. Similar results had been obtained using consensus sequences for heparin binding (Cardin and Weintraub motifs) determined as-X-B-B-X-B-X-and-X-B-B-B-X-X-B-X-(B: probability of a basic residue; X: hydropathic residue) [4]. Antithrombin contains such a consensus sequence (130L-Y-R-K-AN -K-S) [4,5]. When investigating the ligation of glycosaminoglycans with endogenous antimicrobials [2], we also studied the direct eff ects of antithrombin on bacterial growth, and growth inhibition was found (C.J. Wiedermann, A. Djanani, unpublished data). It is therefore unclear why Hofstra and colleagues [1] failed to observe a direct inhibition of bacterial growth by antithrombin. Reasons may include (a) dose and duration of antithrombin exposure of bacteria and (b) microbial species. Given the authors' interesting observation, however, to further explore the direct antimicrobial potential of nebulized anti thrombin in the lung would be worthwhile. Wiedermann CJ: Heparan sulfate proteoglycan-dependent neutrophil chemotaxis toward PR-39 cathelicidin.