More MS news articles for September 2002

Experimental autoimmune encephalitis and inflammation in the absence of interleukin-12

http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=12189243&dopt=Abstract

Full Text available free at:
http://www.jci.org/cgi/content/full/110/4/493

J Clin Invest 2002 Aug;110(4):493-7
Becher B, Durell BG, Noelle RJ.
Department of Microbiology and Immunology, Dartmouth Medical School, Lebanon, New Hampshire 03756, USA.

IL-12 is considered a critical proinflammatory cytokine for autoimmune diseases such as multiple sclerosis and its animal model, experimental autoimmune encephalomyelitis (EAE).

IL-12 is a heterodimer composed of a p35 subunit and a common p40 subunit shared by other cytokines.

Both IL-12 p40(-/-) and p35(-/-) mice fail to produce IL-12 p70 heterodimer.

However, in contrast to p40(-/-) mice, p35(-/-) mice are highly susceptible to the induction of EAE, establishing that IL-12 p70 is not essential for the development of EAE.

When compared with wild-type mice, both p40(-/-) and p35(-/-) mice show deficiencies in primary IFN-gamma responses by lymph node cells.

Expression profiling of the inflamed CNS revealed that Th2 cytokines such as IL-4 and IL-10 are upregulated in p35(-/-) mice, whereas LT-alpha and TNF-alpha levels are reduced.

These studies show that a molecule other than IL-12 p70, which uses the p40 subunit, fulfills the functions previously attributed to IL-12 with regard to the development and pathogenesis of this autoimmune disease.