MS is considered to be an autoimmune disorder. I believe that all autoimmune disorders are a result of a virus (not bacteria) that has invaded your body for an extended amount of time giving it a chance to cross a barrier and manage to mimic specific cells, tissues, and/or organs in our body. In the case of MS, I believe some sort of virus crosses the blood brain barrier to enter the central nervous system. Our immune system is aware of it's presence and in it's attempt to destroy the virus, our nerve cells become collateral damage. Collateral damage is defined as "[the] unintentional damage or incidental damage affecting facilities, equipment, or personnel, occurring as a result of military actions directed against targeted enemy forces or facilities. Such damage can occur to friendly, neutral, and even enemy forces. An autoimmune disorder is caused by the body producing an inappropriate immune response against its own tissues. Sometimes the immune system will cease to recognize one or more of the body's normal constituents as "self" and will create autoantibodies – antibodies that attack its own cells, tissues, and/or organs. This causes inflammation and damage and it leads to autoimmune disorders. In the case of MS, RA (Rheumatoid Arthritis), Chron's disease and other autoimmune diseases, our bodies are being attacked by friendly fire (immune system) in an attempt to get to the enemy (virus).
MS therapies are designed to weaken the immune system or modify the disease. Tysabri, my current choice of therapy, prevents white blood cells from crossing the blood brain barrier where they attack nerve cells. This helps to slow the progression of MS. The downside to this gives the JC virus an opportunity to cross the blood brain barrier as well and cause worse damage than the white blood cells. This causes a rare infection of the brain called PML (Primary Multifocal Leukoecephalopathy) which I have written about in some of my past postings. Tysabri is a bit of a double edged sword but a risk that I am willing to take until a cure for MS has been found. That is why I am so passionate about sharing my world with the world. I believe a cure for MS can and will be found and the more awareness we raise about MS, the better off we will be in creating a world free of MS.
The human body is a magnificent wonder of many systems designed to collaborate and work together for the common good. Like soldiers in the military the cells in our body do their best to protect human life. But as we know, nothing or no one is perfect except God who knows the plans that He has for us all. Whether we have MS, Cancer, ALS or any other disease of the body, put all your trust in God, who causes ALL things to work together for the good of those who love Him.
This blog is about me, my MS and I. It is my way of sharing my personal MS journey with my friends, my family and the world.
Showing posts with label JC Virus. Show all posts
Showing posts with label JC Virus. Show all posts
Monday, June 20, 2011
Saturday, January 1, 2011
Risky Business
Tysabri is my current MS therapy. As an African American MS tends to be more aggressive for us so we must be equally aggressive with our treatment. Tysabri is the most aggressive treatment that I am aware of. Since it is so aggressive, there is a down side of course. With it comes the risk of developing a fatal brain disorder called PML caused by JC Virus or JCV. JC Virus was first isolated from the brain of a person suffering from Hodgkin's disease & PML . PML tissue contains virus-like particles in the nuclei of abnormal oligodendrocytes, which is the pathognomonic cell of the disease. JCV will only grow in a very restricted range of cells, mainly in the brain. JCV is known as a DNA virus that maintains a latent infection in the body which can be reactivated from time to time. The oligodendrocytes in the peripheral zone surrounding an area of demyelination are grossly abnormal. The nuclei of abnormal oligodendrocytes are packed with JCV. Typically, PML evolves gradually, with impairment of mental function and disturbance of speech and vision. Movement may also be affected. The disease then progresses rapidly and patient is severely disabled, eventually becoming demented, blind, paralyzed and finally, coma and death.
Antibodies of JC virus in the Cerebral Spinal Fluid (CSF) is rare but if detected, it suggests active multiplication of JCV in the Central Nervous System (CNS). Cytarbine is an anti-viral drug that has proven to be somewhat effective against PML. Out of 8 cases, long term improvement was only seen in 2 cases. Another case had a dramatic response within 24 hours but was not maintained. Rapid progression was halted in 1 case but the neurological damage was severe. The other 4 cases did not show any improvement.
Our immune system routinely keeps the virus in check. Anyone with a weak immune system run the risk of developing PML. Life is risky every day. I am too blessed to be stressed.
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