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In order to distinguish cleavage-dependent and independent effects in SCA3 pathology, there is an urgent need for novel methodologies that enable the visualization of protein aggregates in living brains and allow effective discrimination of the triggers of nucleation, which could be achieved by developing radiotracers for positron emission tomography (PET) or similar procedure

We now demonstrate that targeting CD38 with heavy-chain antibodies that selectively inhibit NAD glycohydrolase activity without inducing cell death or global CD38 blockade will boost tissue NAD + and precursor levels and sirtuin activity, reduce cellular senescence and mitigate fibrosis and inflammation in multiple organs