Completed Genetics & Molecular Biology Infection & Immunity

Disease susceptibility Pathways in Multiple Sclerosis

In plain English

AI plain-English summary

Multiple sclerosis patients carry a handful of genetic variants that make their immune cells more likely to attack the brain and spinal cord, but researchers cannot tell which of these closely packed genes actually cause the disease. The problem is that several MS-linked genes—including those controlling natural killer cells, inflammation receptors, and a key immune regulator called EOMES—sit right next to each other on the chromosome. Standard genetic studies cannot separate their individual effects, leaving a gap in understanding which ones truly drive disease and which are merely along for the ride. This research group has developed methods to isolate each gene and test its role in MS independently. If the team succeeds, drug developers will know exactly which immune pathways to target. Instead of broadly suppressing the immune system, future therapies could block only the specific molecular steps that trigger MS. This is fundamental science—it will not produce a new drug tomorrow—but it provides the genetic roadmap needed to design treatments that are more precise and less harmful than current options.

View original technical description
My group is studying the genes involved in the pathogenesis of multiple sclerosis so that effective therapies may be developed. Several genes have been shown to contribute to MS susceptibility – for example the KIR receptors that are expressed on immune cells called NK cells, tumour necrosis factor-receptor 1, the interleukin-7 receptor alpha chain, and the (e) the T-box transcription factor eomesodermin (EOMES) gene region. These genes are very close to each other on the chromosomes, and so it has been difficult to work out their relative importance. We have developed methods that will allow us to study each of these genes in isolation, and determine how each contributes to the pathogenecity of MS. Data from our studies will be used in the development of new and more effective therapies for this debilitating disease.

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Researchers

Lars Fugger (Principal Investigator)

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Original classification

Intramural

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