Human blood plasma has been reported to possess nonspecific antiviral activ
ity. This activity is due to several preexisting naturally occurring molecu
les that are either active against individual members or a family of viruse
s. These molecules, however, have not been adequately studied to reveal the
ir molecular structures and mechanisms of action presumably because of thei
r low and nonspecific antiviral action. Therefore, their possible role agai
nst viraemia remains unknown. Recently, two naturally occurring nonspecific
broad-spectrum antiviral agents, University of Texas Inhibitor beta (UTI b
eta) glycoprotein and high density lipoprotein, have been described in huma
n serum. They are active against DNA and RNA viruses and one of them, UTI b
eta, possesses significant antiviral activity of 40 units/mL. Since preexis
ting antiviral molecules in serum appear to be the only defence mechanisms
available at the onset of viral infection they may have protective signific
ance against viraemia. In view of this potential, we have undertaken to rev
iew the properties of these innate viral inhibitory molecules. Copyright (C
) 2000 John Wiley & Sons, Ltd.