From Our 2010 Archives

'Ghostly' Drug May Help Fight RA

Study Shows Molecule Can Infiltrate Immune Cells to Treat Rheumatoid Arthritis

By Daniel J. DeNoon
WebMD Health News

Reviewed By Louise Chang, MD

Jan. 28, 2010 -- A ghostly "suicide" drug wafts into immune cells in joints, making the cells self-destruct and reducing rheumatoid arthritis in mice.

The drug, technically a BH3 mimetic dubbed TAT-BH3, is a man-made molecule. One part of the molecule lets it drift through cell walls. The other part mimics a chemical signal missing in the macrophage immune cells that build up inside joints afflicted by rheumatoid arthritis (RA).

Because they are missing this signal, macrophages in RA joints don't die off as they are supposed to do. They live on, destroying bone and inflaming the joint, says Harris Perlman, PhD, associate professor of medicine at Chicago's Northwestern University Feinberg School of Medicine.

"In RA, there is this persistent inflammation that never shuts down. Part of the reason is these macrophages are missing a protein they need to die off," Perlman tells WebMD. "So this drug says OK, let's replace this protein. Let's bring back the death pathway."

Perhaps because normal cells aren't clinging to life like the zombie macrophages involved in RA, the drug doesn't kill normal macrophages. The drug was not toxic to mice.

But in mice with RA, injections of TAT-BH3 cut bone erosion by as much as 39% and thinned the too-thick lining of the joint by up to 34%.

Perlman says that by hitting it's Bim-protein target, TAT-BH3 has therapeutic effects that go beyond just killing macrophages.

"This drug does far more than cause cell death," he says. "We think this Bim protein has multiple functions and may be a great target for disease."

Perlman's team and others are making their molecule more appropriate for human treatment. One approach they are trying is to use tiny nanoparticles to speed the BH3 mimetic through cell walls. Much work remains before their drug prototype is ready for human studies.

Other BH3 mimetics, with targets different from the so-called Bim protein that is the focus of the Perlman study, are being developed as cancer treatments. Some already are showing promising results in clinical trials.

The Perlman study appears in the February issue of Arthritis & Rheumatism.

SOURCES: Perlman, H. Arthritis & Rheumatism, February 2010; published online Jan. 28, 2010.

Harris Perlman, PhD, associate professor of medicine, Northwestern University Feinberg School of Medicine, Chicago.

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