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Immunoreactivity to astrocytes in different forms of dementia: High prevalence of autoantibodies to GFAP

OBJECTIVE: To study the prevalence of autoantibodies to glial and neuronal antigens with a focus on glial acidic fibrillary protein (GFAP) in patients with dementia. METHODS: Sera of 127 patients with different forms of dementia and sera of 82 age-matched patients with various neurological diseases...

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Autores principales: Barthel, Paula Charlotte, Staabs, Finja, Li, Lucie Y., Buthut, Maria, Otto, Carolin, Ruprecht, Klemens, Prüss, Harald, Höltje, Markus
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10008834/
https://www.ncbi.nlm.nih.gov/pubmed/36923695
http://dx.doi.org/10.1016/j.bbih.2023.100609
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author Barthel, Paula Charlotte
Staabs, Finja
Li, Lucie Y.
Buthut, Maria
Otto, Carolin
Ruprecht, Klemens
Prüss, Harald
Höltje, Markus
author_facet Barthel, Paula Charlotte
Staabs, Finja
Li, Lucie Y.
Buthut, Maria
Otto, Carolin
Ruprecht, Klemens
Prüss, Harald
Höltje, Markus
author_sort Barthel, Paula Charlotte
collection PubMed
description OBJECTIVE: To study the prevalence of autoantibodies to glial and neuronal antigens with a focus on glial acidic fibrillary protein (GFAP) in patients with dementia. METHODS: Sera of 127 patients with different forms of dementia and sera of 82 age-matched patients with various neurological diseases except for dementia, as well as sera from 15 age-matched healthy controls were analyzed for anti-glial or anti-neuronal IgG using 1) primary murine embryonic hippocampus cell cultures, 2) murine brain sections, 3) immunoblotting on mouse brain homogenates and 4) astrocyte cultures. Sera reacting with astrocytes in hippocampus cell cultures were further analyzed using HEK293 cells transfected with human GFAP. RESULTS: IgG in serum from 45 of 127 (35.5%) patients with dementia but only 8 of 97 (8.2%, p ≤ 0.001) controls bound to either glial or neuronal structures in cultured murine hippocampus cells. In these cultures antibodies to astrocytes were detected in 35 of 127 (27.5%) of the dementia patients, whereas in controls antibodies to astrocytes were detected in 4 sera only (4.1%, p ≤ 0.001). Among the sera exhibiting reactivity to astrocytes, 14 of 35 (40%) showed immunoreaction to HEK293 cells transfected with GFAP in dementia patients, representing 11% of all sera. Within the 4 immunoreactive control sera reacting with astrocytes one reacted with GFAP (1.0% of total immunoreactivity, p = 0.003). CONCLUSIONS: Autoantibodies to glial epitopes in general and to GFAP in particular are more frequent in patients with dementia than in age-matched controls without dementia, thus indicating the need for further investigations regarding the potential pathophysiological relevance of these antibodies.
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spelling pubmed-100088342023-03-14 Immunoreactivity to astrocytes in different forms of dementia: High prevalence of autoantibodies to GFAP Barthel, Paula Charlotte Staabs, Finja Li, Lucie Y. Buthut, Maria Otto, Carolin Ruprecht, Klemens Prüss, Harald Höltje, Markus Brain Behav Immun Health Full Length Article OBJECTIVE: To study the prevalence of autoantibodies to glial and neuronal antigens with a focus on glial acidic fibrillary protein (GFAP) in patients with dementia. METHODS: Sera of 127 patients with different forms of dementia and sera of 82 age-matched patients with various neurological diseases except for dementia, as well as sera from 15 age-matched healthy controls were analyzed for anti-glial or anti-neuronal IgG using 1) primary murine embryonic hippocampus cell cultures, 2) murine brain sections, 3) immunoblotting on mouse brain homogenates and 4) astrocyte cultures. Sera reacting with astrocytes in hippocampus cell cultures were further analyzed using HEK293 cells transfected with human GFAP. RESULTS: IgG in serum from 45 of 127 (35.5%) patients with dementia but only 8 of 97 (8.2%, p ≤ 0.001) controls bound to either glial or neuronal structures in cultured murine hippocampus cells. In these cultures antibodies to astrocytes were detected in 35 of 127 (27.5%) of the dementia patients, whereas in controls antibodies to astrocytes were detected in 4 sera only (4.1%, p ≤ 0.001). Among the sera exhibiting reactivity to astrocytes, 14 of 35 (40%) showed immunoreaction to HEK293 cells transfected with GFAP in dementia patients, representing 11% of all sera. Within the 4 immunoreactive control sera reacting with astrocytes one reacted with GFAP (1.0% of total immunoreactivity, p = 0.003). CONCLUSIONS: Autoantibodies to glial epitopes in general and to GFAP in particular are more frequent in patients with dementia than in age-matched controls without dementia, thus indicating the need for further investigations regarding the potential pathophysiological relevance of these antibodies. Elsevier 2023-03-02 /pmc/articles/PMC10008834/ /pubmed/36923695 http://dx.doi.org/10.1016/j.bbih.2023.100609 Text en © 2023 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Full Length Article
Barthel, Paula Charlotte
Staabs, Finja
Li, Lucie Y.
Buthut, Maria
Otto, Carolin
Ruprecht, Klemens
Prüss, Harald
Höltje, Markus
Immunoreactivity to astrocytes in different forms of dementia: High prevalence of autoantibodies to GFAP
title Immunoreactivity to astrocytes in different forms of dementia: High prevalence of autoantibodies to GFAP
title_full Immunoreactivity to astrocytes in different forms of dementia: High prevalence of autoantibodies to GFAP
title_fullStr Immunoreactivity to astrocytes in different forms of dementia: High prevalence of autoantibodies to GFAP
title_full_unstemmed Immunoreactivity to astrocytes in different forms of dementia: High prevalence of autoantibodies to GFAP
title_short Immunoreactivity to astrocytes in different forms of dementia: High prevalence of autoantibodies to GFAP
title_sort immunoreactivity to astrocytes in different forms of dementia: high prevalence of autoantibodies to gfap
topic Full Length Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10008834/
https://www.ncbi.nlm.nih.gov/pubmed/36923695
http://dx.doi.org/10.1016/j.bbih.2023.100609
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