In the News
As reported by the Silicon Valley / San Jose Business Journal, February 18, 2008.
Stanford Researchers ID Therapy Targets For MS
Treatment
By American City Business Journals Inc.
Researchers from the Stanford University School of Medicine said
Sunday that they have identified therapy targets that could lead to
personalized treatments for multiple sclerosis patients.
The team said it cataloged all of the brain-tissue proteins that
they found were distinct to three discrete stages of multiple
sclerosis.
"This is a gold mine," said Dr. Lawrence Steinman, professor of
neurology and neurological sciences. "Knowing what proteins are most
important at a discrete stage of the multiple sclerosis process is
the first step toward being able to 'personalize' treatment."
Steinman, whose team worked with researchers at the University of
Connecticut Health Center, is one of two senior authors of an
article published in the new issue of the journal Nature.
In the study, the team found many unexpected proteins involved in
the disease progression. When they tested drugs that block two of
these proteins in a mouse model of multiple sclerosis, the mice
improved dramatically.
"If our hypothesis is correct, the findings can be directly
applied to patients," said Dr. May Han, a postdoctoral scholar at
Stanford and co-first author of the paper. She emphasized that
researchers are still very early in the process of being able to
tailor drug therapies for humans.
In multiple sclerosis, the immune system launches an attack
against the myelin sheath surrounding nerve cells, causing them to
misfire. The resulting variety of neurological disorders affects
more than 2.5 million people worldwide, according to the Multiple
Sclerosis International Federation.
The work was funded by the National Institute of Health and the
National Multiple Sclerosis Society. Others from Stanford who
contributed to this study are: graduate student Jordan Price;
postdoctoral scholar Shalina Ousman; Dr. William Robinson, an
assistant professor of immunology and rheumatology, and Dr. Raymond
Sobel, professor of pathology.
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