Publications by authors named "Jonathan A B Villareal"

Article Synopsis
  • - Recent studies suggest that systemic infections, like COVID-19, may worsen Alzheimer's disease (AD) in vulnerable aging populations, prompting this research on brains from AD patients who survived COVID-19 compared to those who did not.
  • - Post-mortem analysis revealed that COVID-AD patients exhibited higher levels of amyloid beta (Aβ) in specific brain regions and significant disruptions in microglial and astrocytic function compared to non-COVID AD patients.
  • - Findings indicate lasting effects of COVID-19 on neuroimmune responses and glial health in AD patients, potentially contributing to disease progression long after infection, particularly involving pathways related to myelination and oligodendrocyte dysregulation.
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The disease-specific accumulation of pathological proteins has long been the major focus of research in neurodegenerative diseases (ND), including Alzheimer's disease (AD) and related dementias (RD), but the recent identification of a multitude of genetic risk factors for ND in immune-associated genes highlights the importance of immune processes in disease pathogenesis and progression. Studies in animal models have characterized the local immune response to disease-specific proteins in AD and ADRD, but due to the complexity of disease processes and the co-existence of multiple protein pathologies in human donor brains, the precise role of immune processes in ND is far from understood. To better characterize the interplay between different extracellular and intracellular protein pathologies and the brain's intrinsic immune system in ND, we set out to comprehensively profile the local immune response in postmortem brain samples of individuals with "pure" beta-Amyloid and tau pathology (AD), "pure" α-Synuclein pathology in Lewy body diseases (LBD), as well as cases with Alzheimer's disease neuropathological changes (ADNC) and Lewy body pathology (MIX).

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