Inflammatory Protein May Be Arthritis Drug

PLAD, a portion of the extracellular region of TNFRs (tumor necrosis factor receptors) that mediates receptor-chain association essential for signaling and guides the assembly of TNF cell surface receptors. Binding of TNF-alpha to the associated TNFR1 (also known as P60) and TNFR2 (also known as P80) complex initiates a cascade of reactions resulting in expression of symptoms of inflammation.

Results published in the October 2005 issue of Nature Medicine revealed that soluble versions of PLAD, especially those derived from P60, blocked the biochemical effects of TNF-alpha in vitro and potently inhibited arthritis in animal models. Furthermore, PLAD derived from P60 prevented TNF binding but did not inhibit other, beneficial functions of P80. PLAD did not seem to have any toxic effects.

"We found that P60 PLAD protein powerfully inhibited the symptoms of TNF-alpha-induced arthritis,” said senior author Dr. Michael Lenardo, a researcher at the [U.S.] National Institute of Allergy and Infectious Disease. "We are very hopeful that this could be good news for arthritis sufferers.”