Cyclosporine A

 
Cyclosporine A is an immunosuppressive agent used to improve the effectiveness of the success rate of the heart, kidneys and liver. It has also proven to be helpful in the treatment of certain autoimmune diseases. It in a series of studies on MS, the largest of which were analyzed workforce of 547 patients suffering from Multiple Sclerosis chronic progressive, it was found that a slight decrease in the rate of disease progression and a slight increase in the time before using the wheelchair. This modest or marginal benefits, and comes at the expense of long-term toxicity (kidney weakness and high blood pressure).

Cyclophosphamide

 
Cyclophosphamide is another immunosuppressive agent used for many years in the treatment of MS. It was originally uncontrolled studies that evaluated often, but not always, and show that improvement. Product in chronic progressive MS, particularly in patients who suffer from a disability is very light at the beginning of treatment the largest study so far, multicenter showed any positive effect. Cyclophosphamide has many side effects such as hair loss, nausea, vomiting, hemorrhagic cystitis, infertility, infections and cancer. Some doctors. Cyclophosphamide also still with shock therapy in the case of patients who deteriorate quickly, citing allegations that the stability of the disease treatment requires close monitoring and ongoing patient, including blood count, liver function tests and urinalysis.

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Azathioprine

Azathioprine is an immunosuppressant used widely in the treatment of various autoimmune diseases. He was extracted from the analysis of the results of randomized trials 7 (five and two double-blind, single blind) with patients who suffer from MS 793 by oral azathioprine (1-3 mg/kg/m2) reduces the frequency of relapses and little impact very EDSS. These results have been criticized on the grounds that used a sufficient dose of azathioprine in some studies. Side effects of azathioprine toxicity, gastrointestinal tract, and blood and liver. Another risk potential long-term cancer, but in the controlled trial, case-control, short-term (less than 5 years) are not associated with significantly increased risk. Treatment requires close monitoring and ongoing patient, including blood counts and liver function tests.

Treatment with IVIG

Has large multicenter study in Europe and Canada for IVIG (1.0 g / kg / month) in secondary progressive MS. Results on the clinical and magnetic resonance imaging (MRI) is negative.
Treatment with IVIG rarely cause serious side effects. Including aseptic meningitis, kidney failure, and vascular injury and viral infections, eczema and anaphylaxis. Another potential problem associated with its use is high contrast composition of supplements on the market, confirmed by many studies.

Can exercise and in addition to the immunosuppressive effects (due to the fact that the suppression of the production of proinflammatory cytokines, or they contain antibodies to fight different styles self) promotion of IVIG leaning back, and according to some studies. However, small studies are performed at the Mayo Clinic does not support the hypothesis that IVIG can reverse neurological deficits and visual long.

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Protocol Optimization

In addition, reduces treatment nearly half the pace of setbacks has no obvious effect on the severity of the outbreak. However, it is possible that not blind protocol optimization, which may be biased study results. Unfortunately, MRI are not included in the protocol, and the book did not produce any data on changes EDSS "confirmed" the three months and six months.

In another clinical study, we investigate the effect of high doses of IVIG (2.0 g / kg / month for 6 months) to assess disease activity as measured by magnetic resonance imaging (MRI), but there was a high dropout rate due to side effects.

In double-blind study, 40 patients Israeli with RRMS random IVIG because of loading dose (0.4 mg / kg / day for 5 days), followed by enhanced access to a unique (0.4 mg / kg) or placebo, administered every two months for two years. Treatment was reduced almost 40 percent. Percent in annual relapse rate, in addition to its impact on the EDSS. However, it did not differ significantly between the two groups in total lesion load on magnetic resonance imaging (MRI) of the brain.

Intravenous Immunoglobulin

Immunoglobulins (IgG) for intravenous administration (IVIG) have different effects on the immune system.

During the first small studies that did not show multicenter study wide effectiveness convincing Australian found that the monthly management of low-dose IVIG effective and well tolerated. A group of patients 148 RRMS (EDSS 1-6) randomly into two groups, one treated with IVIG monthly dose of 0.15 to 0.20 kg / g split and the other received a placebo for two years. Was ultimately the main effects of treatment on clinical disability (as measured by the change in EDSS), and the proportion of patients who have debilitating disability, remained stable or deteriorating (difference of one point at least on EDSS). The analysis is based on the plan showed that IVIG therapy have a significant positive impact, albeit modest, in EDSS.

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Demyelinating Disease

The study showed Enyoropathologyekal MS lesions clearly that the process of demyelination occurs in the presence of inflammatory cells and cytokines. Traditionally, demyelination and inflammation MS tie (MS often known as inflammatory demyelinating disease). Research has confirmed recently. Was a significant correlation between the deficit and the clinical onset of permanent nerve cells themselves (especially on the axon)

These insights into the functioning of the immune system led to the development of therapeutic strategies, conducted consisting, for example, prevents management of anti-inflammatory cytokines in patients with MS or treatments that pro-inflammatory cytokines. However, limited ability to predict the effect of such an intervention by the complexity of the network formed by the immune system, with many interrelated factors and mechanisms that vary depending on the stage of the disease. Even more difficult than outside entity heterogeneous MS patients, and that we will see a variety of phenomena such as the masses of the destruction of the cells, and the process of demyelination with or without the participation of the principal cells work as oligodendrogliopathie 'primary.

Given our limited understanding of the pathogenesis of MS, generally or in a particular person, can not be achieved any specific therapeutic progress to be achieved at the expense of clinical trials. These tests are to be carried out on large numbers for a long time, because the path is highly variable and unpredictable disease, and the difficulty in accurately measure neurological disability.