ABOUT this BLOG and How to use it

WELCOME to Stu's Views & MS News. A product of MS Views and News, a Not-for-Profit [501c3] organization. Founded in 2008, we provide educational Multiple Sclerosis information via live seminars and via the internet.

Key-Notes: Our live seminars average approx 60 people per educational program. Our blog is visited over 2900 times per week and our website is visited by thousands each month.

Register at our website to receive our globally transmitted Multiple Sclerosis e-newsletter, currently being received in (90) Countries.

On this blog see our Directory, Archives, recent Blog Posts & so much more. Use the Blog Search box (enter a keyword). See our Facebook information AND Links to other MS Organizations & bloggers. Scroll through entire page, to find information that could EMPOWER You. At the Bottom of this page, see informational videos and some for fun.

Disclaimer: "Stu's Views & MS News" / 'MS Views and News' does not endorse any products or services found on this blog. It is up to you to seek advice from your healthcare provider. The intent of this blog is to provide information on various medical conditions, medications, treatments, and procedures for your personal knowledge and to keep you informed of current health-related issues. It is not intended to be complete or exhaustive, nor is it a substitute for the advice of your physician. Should you or your family members have any specific medical problem, seek medical care promptly

~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~

Like this blog? - CLICK "LIKE"

Tuesday, December 22, 2009

ImmunoSupressive vs Immunomodulator Therapies for Multiple Sclerosis

What are immunosuppressive drugs?

Research indicates that MS is an autoimmune disease. As immunosuppressants have been proven to be beneficial in other autoimmune diseases such as rheumatoid arthritis and psoriasis, drugs that have an immunosuppressant function have shown to be potentially beneficial in controlling disease progression in patients with MS.

Immunosuppressive drugs work by suppressing the body’s immune reaction, and they prevent the body’s ‘good’ white cells (leukocytes) from attacking each other. Normally, leukocytes help regulate the immune system. Immunosuppressive drugs offer another way of treating MS but they are normally used if the disease is progressing in spite of immunomodulatory treatment.

There are a variety of immunosuppressive drugs that have been used in cancer treatment and that have proved effective in treating advanced forms of MS. Specific immunosuppressive drugs used in MS therapy include azathioprine, mitoxantrone and occasionally cyclophosphamide or methotrexate.

However, only Tysabri® (Natalizumab) (in the USA) and Novantrone® (Mitoxantrone) (in the USA, France and Switzerland) are currently licensed specifically for use in the treatment of MS.


+++++++++++++++++++++++++++

What are immunomodulatory drugs?

Immunomodulatory drugs are Disease Modifying Drugs(DMDs), which alter the course of the disease.

Treatments for MS have been considerably advanced by the availability of Disease Modifying Drugs. Positive outcomes in people with relapsing forms of the disease have been demonstrated, including:

  • reduction in the frequency and severity of relapses; and
  • reduction of brain lesion development, as evidenced by Magnetic Resonance Imaging, (MRI), and (for some DMDs) the possibility of future disability.

As the name suggests, immunomodulatory drugs ‘modulate’, i.e. change, the disordered immune processes of MS, and have a corrective effect on the immune system. Interferons belong to this group of drugs.

Interferons are small soluble proteins or glycoproteins that, as ‘messenger substances’, modulate immune responses.

Read more about Interferons and the role they play in treating MS.

Recent results from clinical studies indicate that therapy should begin as soon as possible after diagnosis.

Dosage and route of administration of current available immunomodulatory drugs

Proprietary name

Rebif®

Avonex®

Betaferon®

Copaxone®

International
non-proprietary name

Interferon beta-1a

Interferon beta-1a

Interferon beta-1b

Glatiramer Acetate

Delivery systems

Ready to use Pre-filled syringe

Reconstitution needed / pre-filled syringe

Reconstitution needed

Ready to use pre-filled syringe

Available dosage

22 mcg three times a week or 44 mcg three times a week

30 mcg once a week

0,25 mg every other day

20 mg daily

Route of administration

Subcutaneous injection

Intramuscular injection

Subcutaneous injection

Subcutaneous injection

Other characteristics, such as indications, format, etc. may vary from one country to another. Always consult the product leaflet.


SOURCE for the above data comes from the MS-Network - However, their information has not been updated in a couple of years.

Such the case that Cytoxan and Imuran are also being used for MS and are immunosupressants


============================================

2 comments:

Gerry C. said...

When newly dx. I was not given an option as to what meds would help me, such was the severity of my disease. I was put on cytoxan, which created severe negative side effects, i.e. blisters throughout my body (which then was thought I might have sclererdoma:which is usually fatal); then was prescribed the Imuran 50 mgs./day for about 6mos.until I had a relapse and was placed on 100 mgs/day for one(1) year. I empowered myself by researching these chemotherapuetic agents and found out they were doing more harm than good in the long road, not to mention going from 194 lbs of lean,mean, muscular Marine to a 134 lb. "weakling, from a 36" waist to a 29-30" waist. So I respectfully requested my M.D. to stop all chemo. I have been on Tysabri for 16 mos. now and I feel like a new man. I'm walking, (which I was told I would never be able to again and I'm also driving myself around on my own accord. Thanks to the great neurologist here at the veteran's hospital in Miami.

Stuart said...

You are a GOOD MAN Gerry. Thanks for the remarks.
will see you soon..