Altered serum IgG levels to α-synuclein in dementia with Lewy bodies and Alzheimer's disease.

Natural self-reactive antibodies in the peripheral blood may play a considerable role in the control of potentially toxic proteins that may otherwise accumulate in the aging brain. The significance of serum antibodies reactive against α-synuclein is not well known. We explored serum IgG levels to mo...

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Autores principales: Niklas K U Koehler, Elke Stransky, Mona Shing, Susanne Gaertner, Mirjam Meyer, Brigitte Schreitmüller, Thomas Leyhe, Christoph Laske, Walter Maetzler, Phillipp Kahle, Maria S Celej, Thomas M Jovin, Andreas J Fallgatter, Anil Batra, Gerhard Buchkremer, Klaus Schott, Elke Richartz-Salzburger
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spelling oai:doaj.org-article:5e789229a17a412f996ecb93e4029b962021-11-18T07:43:36ZAltered serum IgG levels to α-synuclein in dementia with Lewy bodies and Alzheimer's disease.1932-620310.1371/journal.pone.0064649https://doaj.org/article/5e789229a17a412f996ecb93e4029b962013-01-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23741358/?tool=EBIhttps://doaj.org/toc/1932-6203Natural self-reactive antibodies in the peripheral blood may play a considerable role in the control of potentially toxic proteins that may otherwise accumulate in the aging brain. The significance of serum antibodies reactive against α-synuclein is not well known. We explored serum IgG levels to monomeric α-synuclein in dementia with Lewy bodies (DLB) and Alzheimer's disease (AD) with a novel and validated highly sensitive ELISA assay. Antibody levels revealed stark differences in patients compared to healthy subjects and were dependent on diagnosis, disease duration and age. Anti-α-synuclein IgG levels were increased in both patient groups, but in early DLB to a much greater extent than in AD. Increased antibody levels were most evident in younger patients, while with advanced age relatively low levels were observed, similar to healthy individuals, exhibiting stable antibody levels independent of age. Our data show the presence of differentially altered IgG levels against α-synuclein in DLB and AD, which may relate to a disturbed α-synuclein homeostasis triggered by the disease process. These observations may foster the development of novel, possibly preclinical biomarkers and immunotherapeutic strategies that target α-synuclein in neurodegenerative disease.Niklas K U KoehlerElke StranskyMona ShingSusanne GaertnerMirjam MeyerBrigitte SchreitmüllerThomas LeyheChristoph LaskeWalter MaetzlerPhillipp KahleMaria S CelejThomas M JovinAndreas J FallgatterAnil BatraGerhard BuchkremerKlaus SchottElke Richartz-SalzburgerPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 8, Iss 5, p e64649 (2013)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Niklas K U Koehler
Elke Stransky
Mona Shing
Susanne Gaertner
Mirjam Meyer
Brigitte Schreitmüller
Thomas Leyhe
Christoph Laske
Walter Maetzler
Phillipp Kahle
Maria S Celej
Thomas M Jovin
Andreas J Fallgatter
Anil Batra
Gerhard Buchkremer
Klaus Schott
Elke Richartz-Salzburger
Altered serum IgG levels to α-synuclein in dementia with Lewy bodies and Alzheimer's disease.
description Natural self-reactive antibodies in the peripheral blood may play a considerable role in the control of potentially toxic proteins that may otherwise accumulate in the aging brain. The significance of serum antibodies reactive against α-synuclein is not well known. We explored serum IgG levels to monomeric α-synuclein in dementia with Lewy bodies (DLB) and Alzheimer's disease (AD) with a novel and validated highly sensitive ELISA assay. Antibody levels revealed stark differences in patients compared to healthy subjects and were dependent on diagnosis, disease duration and age. Anti-α-synuclein IgG levels were increased in both patient groups, but in early DLB to a much greater extent than in AD. Increased antibody levels were most evident in younger patients, while with advanced age relatively low levels were observed, similar to healthy individuals, exhibiting stable antibody levels independent of age. Our data show the presence of differentially altered IgG levels against α-synuclein in DLB and AD, which may relate to a disturbed α-synuclein homeostasis triggered by the disease process. These observations may foster the development of novel, possibly preclinical biomarkers and immunotherapeutic strategies that target α-synuclein in neurodegenerative disease.
format article
author Niklas K U Koehler
Elke Stransky
Mona Shing
Susanne Gaertner
Mirjam Meyer
Brigitte Schreitmüller
Thomas Leyhe
Christoph Laske
Walter Maetzler
Phillipp Kahle
Maria S Celej
Thomas M Jovin
Andreas J Fallgatter
Anil Batra
Gerhard Buchkremer
Klaus Schott
Elke Richartz-Salzburger
author_facet Niklas K U Koehler
Elke Stransky
Mona Shing
Susanne Gaertner
Mirjam Meyer
Brigitte Schreitmüller
Thomas Leyhe
Christoph Laske
Walter Maetzler
Phillipp Kahle
Maria S Celej
Thomas M Jovin
Andreas J Fallgatter
Anil Batra
Gerhard Buchkremer
Klaus Schott
Elke Richartz-Salzburger
author_sort Niklas K U Koehler
title Altered serum IgG levels to α-synuclein in dementia with Lewy bodies and Alzheimer's disease.
title_short Altered serum IgG levels to α-synuclein in dementia with Lewy bodies and Alzheimer's disease.
title_full Altered serum IgG levels to α-synuclein in dementia with Lewy bodies and Alzheimer's disease.
title_fullStr Altered serum IgG levels to α-synuclein in dementia with Lewy bodies and Alzheimer's disease.
title_full_unstemmed Altered serum IgG levels to α-synuclein in dementia with Lewy bodies and Alzheimer's disease.
title_sort altered serum igg levels to α-synuclein in dementia with lewy bodies and alzheimer's disease.
publisher Public Library of Science (PLoS)
publishDate 2013
url https://doaj.org/article/5e789229a17a412f996ecb93e4029b96
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