Editorial
Copyright ©The Author(s) 2015.
World J Biol Chem. Aug 26, 2015; 6(3): 71-77
Published online Aug 26, 2015. doi: 10.4331/wjbc.v6.i3.71
Figure 4
Figure 4 Compound Aspidasept® (Amino acid sequence GCKKYRRFRWKFKGKFWFWG; EU, United States, and Japan patent filed) is able to inhibit very efficiently the cytokine production induced by the pathogenicity factors endotoxin/lipoproteins or by the bacteria in vitro, in vivo (various mouse models), and ex vivo (human lung, see Figure 3). These inhibition properties of Aspidasept® comprise various relevant bacterial strains from Gram-negative and Gram-positive origin, as well as Mycobacteria, in particular M. tuberculosis. Aspidasept® has low toxicity (the NOAEL, no observed adverse effect level’ is 200 to 500 times higher than the planned therapeutical doses). Beside its inflammation-inhibiting activity, it is able to bind the multi-resistant bacteria thus limiting their spreading. LPS: Lipopolysaccharide.