Do thalidomides have a role in the treatment of multiple sclerosis?
Multiple sclerosis is an autoimmune inflammatory condition and so immunomodulators have been used in treatment. It is recognised that aberrant activation of the immune system and the associated network of its regulation are important events in the pathogenesis of the disease. This is the rationale for using immunomodulatory agents in disease control. Among immunomodulators of note are Fingolimod which prevents infiltration of auto-destructive lymphocytes into the CSF, Teriflunomide which reduces lymphocyte infiltration of the CNS, axonal loss and inflammatory demyelination, and dimethyl fumarate, which modulates the immune system by many mechanisms. Furthermore, much attention has been devoted to the immunomodulatory properties of MSCs (mesenchymal stem cells) (4,5). Thalidomides are also capable of modulating the function of key element of the immune system related to the pathogenesis of MS, but this brief article is intended to emphasise the potential of thalidomide and its analogues as potent inhibitors of angiogenesis and the latent possibility of their use as a therapeutic agent in the control of MS.
Thalidomide was introduced over four decades ago to treat respiratory infections and to combat morning sickness in pregnant women. It was withdrawn when it was found to be highly teratogenic. The teratogenic effects are a result of the binding of thalidomide to cereblon, a protein found in both embryonic and adult tissues. Cereblon is required for normal morphogenesis. It is inactivated by binding to thalidomide and this leads to teratogenesis (9). Thalidomide possesses immunomodulatory, anti-inflammatory, anti-angiogenesis and cell proliferation inhibitory properties and this has suggested its use in the treatment of cancer (5). Analogues of thalidomide, viz. lenalidomide and pomalidomide, have been synthesised and these possess reduced toxicity and greater efficacy (10,11). Recently, many studies have elucidated the signalling pathways which thalidomides inhibit and thereby suppress cell proliferation, promote apoptosis and inhibit angiogenesis. These have led to the suggestion of combining the modulators of these signalling pathways to synergise with thalidomides to deliver the suppressor effects with enhanced efficacy and at lower concentrations thus reducing the side effects (5) (Figure 1).
Most of the work on the efficacy of thalidomide and the analogues has been carried out in preclinical models. Quite understandably, in the clinical setting very little effort is seen to check whether thalidomide or the analogues provide any beneficial effects in MS or neuro-inflammation. Clinically orientated investigations so far relate mainly to multiple myeloma and some other forms of haematological malignancies but not solid tumours (5). Any perceived beneficial effects are probably outweighed by the side effects. We need to expend more effort and design and develop new analogues with reduced toxicity. In this context one should emphasise that pre-clinical exploration of the potential synergy between the thalidomides and the acknowledged modulators of the signalling pathways would be worthwhile. This might enable the delivery of benefits more effectively and at lower dosages. It is needless to say that safety of drug administration is of paramount importance.
G.V. SHERBET, DSc, FRSC, FRCPath, Institute for Molecular Medicine, Huntington Beach CA, USA and University of Newcastle upon Tyne UK.
CORRESPONDENCE: G.V. SHERBET, Institute for Molecular Medicine, Huntington Beach CA, USA and University of Newcastle upon Tyne UK.
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Table 1. Angiogenic mediators of MS Angiogenic agent/mediator Vascular endothelial growth factor (VEGF)/VEGF receptor 2 (VEGFR2) Nitric oxide (NO) and NOS (NO synthase) Transforming growth factor-[beta] (TGF-[beta]) Basic fibroblast growth factor (bFGF) [down arrow] Matrix metalloproteinases (MMP) Hepatocyte growth factor (HGF) [Note: Inhibitory effects of thalidomides were described by Sherbet (4); D'Amato et al. (6); Kenyon et al. (7); Lu et al. (8)]
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|Publication:||British Journal of Medical Practitioners|
|Date:||Sep 1, 2015|
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