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Towards Personalized Therapy
In a 15-min lecture, Dr. Pierre Lemaitre presented results on the mechanisms of teplizumab therapy resistance in the NOD mouse model and blood samples from individuals with type 1 diabetes (T1D). Mice were treated for 5 days with an anti-CD3 therapy from the onset of T1D symptoms and were then divided into two groups based on a positive effect (47%, responders) or no effect of the treatment (53%, non-responders). The transcriptomic properties of the immune cells were compared between the groups. It was found that responders and non-responders showed significant gene differences in a specific subgroup of immune cells, namely neutrophils, both in the blood and pancreas. These results were confirmed in blood samples from newly diagnosed individuals with T1D, treated with teplizumab, and followed up for 12 months. Nine genes were identified that could distinguish non-responders even before therapy starts. These findings promote personalized therapy choices in the future.
In addition, team members Amber Wouters, Pieter-Jan Martens, and Laure Degroote presented their posters. PhD student Amber Wouters demonstrated that redosing with anti-CD3 does not enhance therapy responsiveness in the NOD mouse model. Dr. Pieter-Jan Martens presented his results on verapamil in combination with low-dose murine anti-thymocyte globulin (mATG) therapy in newly diagnosed diabetic NOD mice. PhD student Laure Degroote presented dose-dependent effects of mATG on T1D development in the NOD mouse model.
Recap of IDS 2024 in photo gallery.