Health & Medical Immune System Disorders

New Target for Lupus Treatment?

´╗┐New Target for Lupus Treatment?

New Target for Lupus Treatment?


Key Chemical Signal Lets Lupus Immune Cells Hide in Spleen

Sept. 14, 2006 -- An exciting new study shows a new target for future lupus treatments.

Lupus is an autoimmune disease: The body is attacked by its own immune system. In lupus, that attack may come from a kind of immune cell called a B cell.

As the body makes new B cells, a few of them go haywire and try to attack the body. Normally, the body quickly eliminates these cells. But in lupus, they somehow survive.

A special hormone called B-cell-activating factor -- or BAFF -- helps these self-attacking B cells survive. And people with lupus and some other autoimmune diseases overproduce BAFF. Eventually, these B cells build up to dangerous levels and cause lupus.

Hiding in the Spleen


Now a research team, including Michael Karin, PhD, of the University of California, San Diego, finds that B cells build up in a specific part of the spleen called the marginal zone. Mouse studies suggest that if the B cells can't hide in the spleen, they can't cause lupus.

What lets lupus-causing B cells lurk in the spleen is a chain of chemical signals called the NF-kB pathway. You need a functional NF-kB pathway for your immune system to fight infections. But this pathway is made up of two parts: the classical NF-kB pathway and the alternative NF-kB pathway.

In mouse experiments, Karin's team now finds that partial disruption of just the alternative NF-kB pathway is enough to keep lupus-causing B cells from hiding in the spleen.

"Our findings suggest that incomplete inhibition of the alternative NF-kB pathway ... may be a sufficient therapeutic option for patients suffering from autoimmune disease associated with BAFF overproduction," the researchers suggest. "Inhibition of the alternative NF-kB pathway is less likely to cause an immune deficiency, which is commonly seen after blockade of the classical NF-kB pathway."

The findings appear in the September issue of the journal Immunity.

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