The innate immune system, however, does possess a capacity for the clearance of Aβ and can play a beneficial role in AD. This would explain the detrimental effects of knocking out completely the innate immune response, while beneficial effects of inhibiting selective parts of it can prove to be an efficient therapeutic strategy. This was highlighted by the failure of nonsteroidogenic anti-inflammatory drugs (NSAIDs) to treat AD in large-scale clinical trials (Imbimbo, 2009). Initial reports have shown that subjects on recurring treatments of NSAIDs had lower incidence of AD (McGeer et al., 1996). The reason for the clinical failure was that it had been forgotten why the subjects on

NSAIDs needed to receive these drugs in the first place: they have an overly active innate immune system that was helping prevent the development of AD. As such, a tightly regulated Alisertib stimulation of innate immune processes, selleck chemicals rather than its complete inhibition, is another way of designing new treatment options for AD. This can be achieved with the use of novel TLR ligands that can stimulate the clearance of Aβ without inducing overt inflammatory processes. We have recently demonstrated the beneficial effects of monophosphoryl lipid A (MPL) in mouse models of AD (Michaud et al., 2013). MPL, a detoxified

TLR4 ligand, induced a high phagocytic potential in microglia, as much as LPS, while showing almost undetectable production of inflammatory cytokines or ROS. In AD mouse models, a chronic treatment with MPL reduced Aβ production by up to 80% in some cases and normalized their cognitive behavior. This paves the way for the development of safe

immunomodulatory therapies in AD as a monotherapy but also as complements to other Aβ-lowering strategies such as vaccination. Although most of the work in AD has focused on neurodegeneration and inflammatory processes, accumulating evidence shows that a dysregulation of the vasculature is just as important in the development of AD (Zlokovic, 2011). Most of the work on the implication of innate immunity in AD has focused on the role of MYO10 microglia. However, novel exciting research shows that the rest of the NVU is a prime candidate for the creation of new therapeutic strategies for AD. Pioneer work from the team of Zlokovic has shown that LRP-1, a specific transporter at the BBB, is critical in the clearance of Aβ from the CNS into the circulation (Deane et al., 2004). In further studies, the authors found that LRP-1 was upregulated upon LPS stimulation, therefore presumably enhancing pericytes and endothelial cells’ capacity to internalize the toxic peptide Aß given the major role of LRP-1 in Aß processing (Deane et al., 2008). Moreover, ABCB1 and ABCG2 have been shown to be involved in the elimination of Aβ from the CNS (Xiong et al., 2009; Cirrito et al., 2005; van Assema et al., 2012).