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Chemokine receptor plays key role in pathogenesis of encephalomyelitis.

Vaccine Weekly

| October 06, 2004 | COPYRIGHT 2004 NewsRX. This material is published under license from the publisher through the Gale Group, Farmington Hills, Michigan.  All inquiries regarding rights should be directed to the Gale Group. (Hide copyright information)Copyright

2004 OCT 6 - (NewsRx.com & NewsRx.net) -- The CXC chemokine ligand 16/scavenger receptor that binds phosphatidylserine and oxidized lipoprotein plays a critical role in the pathogenesis of both acute and adoptive transfer experimental autoimmune encephalomyelitis.

According to a study from Japan, "The scavenger receptor that binds phosphatidylserine and oxidized lipoprotein (SR-PSOX)/CXCL16 is a chemokine expressed on macrophages and dendritic cells, while its receptor expresses on T and NK T cells. We-investigated the role of SR-PSOX/CXCL16 on acute and adoptive experimental autoimmune encephalomyelitis (EAE), which is Th1-polarized T cell-mediated autoimmune disease of the CNS. Administration of mAb against SR-PSOX/CXCL16 around the primary immunization decreased disease incidence of acute EAE with associated reduced infiltration of mononuclear cells into the CNS."

"Its administration was also shown to inhibit elevation of serum IFN-gamma level at primary immune response, as well as subsequent generation of antigen-specific T cells," reported Noriko Fukumoto and colleagues at Kyoto University and Osaka University. "In adoptive transfer EAE, treatment of recipient mice with anti-SR-PSOX/CXCL16 mAb also induced not only decreased clinical disease incidence, but also diminished traffic of mononuclear cells into the CNS. In addition, histopathological analyses showed that ...

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