| Literature DB >> 26402766 |
Stefan Busse1, Johann Steiner1,2, Juliane Alter1, Henrik Dobrowolny1, Christian Mawrin3, Bernhard Bogerts1,2, Roland Hartig4, Mandy Busse5.
Abstract
Although monocytes and macrophages could serve as new therapeutic targets for treatment of Alzheimer's disease (AD) and aging of the human innate immune system, its role in the pathogenesis of neurodegenerative disorders such as AD are only poorly understood. We have addressed this here by determining the number of CD14+ monocytes and the frequency of HLA-DR-, CD80-, and CD86-expression in peripheral blood from healthy volunteers aged 20-79 years, and in AD patients at diagnosis and after 12, 30, and 52 weeks of rivastigmine treatment. While the number of CD14+ monocytes remained constant, the expression of HLA-DR, CD80, and CD86 by monocytes increased with age. However, no differences were identified by comparing AD patients with age-matched healthy controls or following treatment of AD patients with rivastigmine. These results indicate that changes in the expression of HLA-DR, CD80, and CD86 are caused by immunosenescence rather than by AD pathology or treatment of AD patients with rivastigmine.Entities:
Keywords: Alzheimer’s disease; CD80; CD86; HLA-DR; monocytes
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Year: 2015 PMID: 26402766 DOI: 10.3233/JAD-150217
Source DB: PubMed Journal: J Alzheimers Dis ISSN: 1387-2877 Impact factor: 4.472