IL-12 as a therapeutic target for pharmacological modulation in immune-mediated and inflammatory diseases: regulation of T helper 1/T helper 2 responses

Authors
Citation
G. Hasko et C. Szabo, IL-12 as a therapeutic target for pharmacological modulation in immune-mediated and inflammatory diseases: regulation of T helper 1/T helper 2 responses, BR J PHARM, 127(6), 1999, pp. 1295-1304
Citations number
129
Categorie Soggetti
Pharmacology & Toxicology
Journal title
BRITISH JOURNAL OF PHARMACOLOGY
ISSN journal
00071188 → ACNP
Volume
127
Issue
6
Year of publication
1999
Pages
1295 - 1304
Database
ISI
SICI code
0007-1188(199907)127:6<1295:IAATTF>2.0.ZU;2-Q
Abstract
1 Interleukin-12 (IL-12) is a pivotal cytokine in driving the immune system towards a T helper (Th) 1 type response and preventing a Th2 type immune p rofile. Therefore, IL-12 is indispensable in the defense against certain, m ainly intracellular pathogens, but overproduction of this cytokine is cruci ally involved in the etiology of several inflammatory and autoimmune diseas es. 2 Hence, IL-12 is an ideal target for pharmacological intervention in the t herapy of autoimmune and inflammatory diseases. 3 The production of IL-12 and a resultant Th1 type immune response can be s uppressed with several pharmacological approaches including modulation of i ntracellular cyclic AMP levels, glucocorticoids and nuclear factor-kappa B inhibition. IL-12 responsiveness may be inhibited using anti-IL-12 antibodi es, soluble IL-12 receptors or the IL-12 p40 homodimer. 4 Exploitation of these approaches may provide novel means for the experime ntal therapy of a variety of pathophysiological states.