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October 11th, 2010, 10:31 GMT · By

News on Multiple Sclerosis and Guillain-Barré Syndrome

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Researchers could develop a vaccination for people who are at risk of developing autoimmune diseases.
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A thesis from the Sahlgrenska Academy concluded that a flaw in one of the immune system's enzymes determines the degree of the severity of autoimmune diseases like multiple sclerosis (MS) and Guillain-Barré syndrome (GBS).

These new findings can explain the way that this enzyme deficiency can be diagnosed and also why these diseases can vary so much.

The immune system is based on white blood cells, that play a vital role in fighting against pathogens.

The white blood cells contain an enzyme that transforms oxygen into reactive oxygen radicals – which break down microorganisms and stop infections, called NADPH oxidase.

These new studies have used animal models to show that an inadequate production of oxygen radicals can favor the development of autoimmune diseases, as the patient's immune system would attack itself.

The body has an ability of producing reactive oxygen radicals at an early stage in the immune defense against pathogens, and this has a serious impact on the way that these illnesses develop.

Natalia Mossberg, doctoral student at the Institute of Neuroscience and Physiology at the Sahlgrenska Academy, said that “a strong but controlled production of oxygen radicals by the immune system is important for subduing illnesses such as MS and GBS.”

These are the two autoimmune diseases that were covered by this thesis, as they can vary from insignificant to life-threatening, and their mechanism needed to be revealed.

Mossberg says that they “wanted to look at this in humans, and examined the NADPH oxidase in the white blood cells of patients with MS, GBS and recurring GBS (RGBS).

“The results show that patients with more severe forms of the illness have lower levels of oxygen radical production in their white blood cells as a result of deficient NADPH oxidase function.”

Other autoimmune diseases can be investigated through this method, and this could help diagnose their severity.

Also, early stages of MS treatment could benefit from a new approach, and use drugs that trigger the production of NADPH oxidase.

Furthermore, researchers could develop a vaccination for people who are at risk of developing this kind of diseases.

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READER COMMENTS:


Comment #1 by: afs on 21 Oct 2010, 13:08 UTC reply to this comment

I believe this track is promising. My son has MS, and I remember that when he was a child, his blood tests always came in showing low white blood cell count.


Comment #2 by: momof3 on 18 Mar 2012, 14:51 UTC reply to this comment

I had total paralysis from gbs in 2006. I recovered for 2 years with residual numbness and weakness. In 2009 I started having right sided weakness in arm, leg, and face with no signs of stroke or heart problems. I have some neurological dysfunction and severe weakness when I am fatigued. The neurologist I was going to said she did not think it was gbs but infact a bout of ms. My qusetion is I had the classic symptoms of gbs, starting from feet up and was totally paralyzed within 3 days, could my symptoms be from gbs still this long after or ms? Or could it infact be both? I know it is rare for it to be both but I need to know if gbs lingures for years afterwards.

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