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Reduced Immunosenescence of Peripheral Blood T Cells in Parkinson’s Disease with CMV Infection Background
Authors:Julia D Vavilova  Anna A Boyko  Natalya V Ponomareva  Vitaly F Fokin  Ekaterina Y Fedotova  Maria A Streltsova  Sofya A Kust  Maria V Grechikhina  Ekaterina V Bril  Olga S Zimnyakova  Elena I Kovalenko  Alexander M Sapozhnikov
Affiliation:1.Shemyakin and Ovchinnikov Institute of Bioorganic Chemistry, Russian Academy of Sciences, 117997 Moscow, Russia; (J.D.V.); (A.A.B.); (M.A.S.); (S.A.K.); (M.V.G.); (A.M.S.);2.Research Center of Neurology, 125367 Moscow, Russia; (N.V.P.); (V.F.F.); (E.Y.F.);3.Burnasyan Federal Medical Biophysical Center of Federal Medical Biological Agency, 123098 Moscow, Russia; (E.V.B.); (O.S.Z.)
Abstract:Immunosenescence is a process of remodeling the immune system under the influence of chronic inflammation during aging. Parkinson’s disease (PD) is a common age-associated neurodegenerative disorder and is frequently accompanied by neuroinflammation. On the other hand, cytomegalovirus (CMV), one of the most spread infections in humans, may induce chronic inflammation which contributes to immunosenescence, differentiation and the inflation of T cells and NK cells. Currently, there is no clear understanding of immunosenescence severity in PD patients infected with CMV. In this study, we analyzed differentiation stages and immunosenescence characteristics of T cells and NK cells in 31 patients with mild and moderate PD severity, 33 age-matched and 30 young healthy donors. The PD patients were 100% CMV-seropositive compared to 76% age-matched and 73% young CMV-infected healthy donors. The proportion of effector memory T cells re-expressing CD45RA, CD57+CD56 T cells and CD57+CD56+ T cells was significantly reduced in PD patients compared with CMV-seropositive age-matched healthy individuals. The CD57+CD56 T cell proportion in PD patients was similar to that of CMV-seropositive young healthy donors. Thus, PD is characterized by reduced peripheral blood T cell immunosenescence, even against the background of CMV infection.
Keywords:Parkinson’  s disease  cytomegalovirus  peripheral immune system  neuroinflammation  differentiation of immune cells
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