Despite the youth of the chemokine field, many antagonists of chemokine fun
ction have already been identified and tested at the preclinical level. The
se include neutralizing antibodies, peptidyl and non-peptidyl antagonists a
nd non-specific immunosuppressive agents. These early studies suggest that
chemokine agonists have the potential to regulate many diseases, ranging fr
om HIV-1 infection and tumor growth to acute and chronic inflammation. Clin
ical application will depend on pharmaceutical development. Great strides h
ave been made in defining structural domains of the chemokines involved in
receptor binding and activation. The identification of receptors is rapidly
progressing, but with 50 potential ligands and 15 characterized receptors,
it is obvious that additional molecular studies are needed. The intriguing
observation that several pathogens either use chemokine receptors as entry
portals or produce chemokine decoys to subvert the immune system suggests
that there is much to be learned about the immune system from studies of "v
irokines." Future studies should lead to the discovery and design of more e
ffective inhibitors and antagonists with therapeutic benefit.