nr. 477 - 2011 - Institut for Natur, Systemer og Modeller (NSM)
nr. 477 - 2011 - Institut for Natur, Systemer og Modeller (NSM)
nr. 477 - 2011 - Institut for Natur, Systemer og Modeller (NSM)
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3 Prospects <strong>for</strong> Therapy – A Mini Review<br />
As more in<strong>for</strong>mation about the etiol<strong>og</strong>y of diabetes has become available, several possible<br />
means of preventing/curing it have surfaced. In this chapter we give a brief account<br />
of some of these.<br />
3.1 Treatment Strategies<br />
Depending on the pr<strong>og</strong>ression of the disease different therapeutical approaches are relevant<br />
(Greenbaum and Harrison (2008)), though some of them are not confined to one<br />
stage. Figure 3.1 gives a qualitative indication of how the amount of β-cells left is<br />
related to treatment strategy, how prediction becomes more and more accurate with<br />
time while prevention of T1D becomes less and less possible.<br />
Firstly and most ideally every infant should be genetically screened to test <strong>for</strong> genes<br />
Figure 3.1 shows how different treatment strategies apply as β-cell mass is reduced over time.<br />
On the y-axis we have β-cell mass and along the x-axis we have time. As time passes the<br />
ability to prevent T1D becomes smaller and smaller. Figure was borrowed, with permission,<br />
from Staeva-Vieira et al. (2008)<br />
that are linked with T1D. This would permit <strong>for</strong> precautionary measures such as diet<br />
changes or antigen-based therapy. The only problem with this is that these genes need<br />
still be identified.<br />
Secondly, when autoimmunity is observed, antigen therapy is still an option, but also<br />
direct administration of regulatory cells (e.g. macrophages) has been suggested. At<br />
this stage the aim of the treatment is to prevent β-cell destruction.<br />
Unless the autoimmunity is treated it will inevitably lead to β-cell destruction, the<br />
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