Chemokines as molecular targets for therapeutic intervention

Citation
Omz. Howard et al., Chemokines as molecular targets for therapeutic intervention, J CLIN IMM, 19(5), 1999, pp. 280-292
Citations number
98
Categorie Soggetti
Immunology
Journal title
JOURNAL OF CLINICAL IMMUNOLOGY
ISSN journal
02719142 → ACNP
Volume
19
Issue
5
Year of publication
1999
Pages
280 - 292
Database
ISI
SICI code
0271-9142(199909)19:5<280:CAMTFT>2.0.ZU;2-R
Abstract
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.