Abstract

Trained immunity was recently discovered in innate immune cells and shown to facilitate the clearance of pathogens at the time of occurrence of the second insult. However, it exacerbates several aspects of neuropathologies, and proper therapy is needed to rectify this abnormal immune reaction. Mesenchymal-stem cells (MSCs) exhibit a distinct capability for brain repair but are associated with safety concerns. Extracellular vesicles derived from MSCs are a promising alternative therapy. In this study, we used lipopolysaccharides to activate trained immunity in the brain and examined the therapeutic potential of MSC-derived extracellular vesicles in mitigating the trained-immunity-induced exacerbated neuropathology. We found that MSC-derived extracellular vesicles showed comparable effects to those of MSCs in the mitigation of trained immunity in the brain. Moreover, the administration of MCS-derived extracellular vesicles mitigated the aggregated inflammatory responses in the acute stage of stroke and alleviated the trained-immunity-induced increased load of amyloid-β in APP/PS1 mice. We further investigated the molecular machinery of MSC-derived extracellular vesicles and found that IL-10 is important for the mediation of the therapeutic potential of MSC-derived extracellular vesicles toward the alleviation of trained immunity. Our study indicates that extracellular-vesicle-based regenerative strategies might be useful to mitigate trained immunity in the brain.

Highlights

  • Immune memory has long been believed to exist only in the adaptive immune system

  • These results suggest that peripherally administered Mesenchymal-stem cells (MSCs)-derived extracellular vesicles (EVs) were able to cross the BBB and were engulfed by microglia in the central nervous system (CNS)

  • We uncovered the therapeutic potential of MSCderived EVs in mitigating trained immunity in the CNS

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Summary

Introduction

Immune memory has long been believed to exist only in the adaptive immune system. Recent evidence indicates that innate immune cells display memory effects, namely trained immunity (Netea et al, 2015, 2016; Wendeln et al, 2018). Certain inflammatory stimuli, such as lipopolysaccharides (LPS), prime peripheral monocytes, leading them to respond more efficiently when the second inflammatory insult occurs (Biswas and Lopez-Collazo, 2009; Saeed et al, 2014). Trained immunity triggers the more efficient clearance of pathogens by myeloid cells. In the central nervous system (CNS), microglia, which are the brain-resident macrophages, exhibit a different aspect of trained immunity. It has been demonstrated that mice subjected to initial inflammatory stimuli, such as LPS, exhibit activation of the innate immune memory in the brain, which exacerbated stroke prognosis and deteriorated the pathology of MSC-Derived EVs Mitigate Trained Immunity

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