Immune activation in amyloid-β-related angiitis correlates with decreased parenchymal amyloid-β plaque load

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Immune activation in amyloid-β-related angiitis correlates with decreased parenchymal amyloid-β plaque load. / Bogner, S; Bernreuther, C; Matschke, J; Barrera-Ocampo, Alvaro A; Sepulveda-Falla, D; Leypoldt, F; Magnus, T; Haag, F; Bergmann, M; Brück, W; Vogelgesang, S; Glatzel, M.

in: NEURODEGENER DIS, Jahrgang 13, Nr. 1, 01.01.2014, S. 38-44.

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@article{ff6caa5e2df6468aa66ff94d72f5d7ba,
title = "Immune activation in amyloid-β-related angiitis correlates with decreased parenchymal amyloid-β plaque load",
abstract = "BACKGROUND: Primary angiitis of the central nervous system (PACNS) is a rare but serious condition. A fraction of patients suffering from PACNS concurrently exhibit pronounced cerebral amyloid angiopathy (CAA) which is characterized by deposits of amyloid-β (Aβ) in and around the walls of small and medium-sized arteries of the brain. PACNS with CAA has been identified as a distinct disease entity, termed Aβ-related angiitis (ABRA). Evidence points to an immune reaction to vessel wall Aβ as the trigger of vasculitis.OBJECTIVE: To investigate whether the inflammatory response to Aβ has (1) any effect on the status of immune activation in the brain parenchyma and (2) leads to clearance of Aβ from brain parenchyma.METHODS: We studied immune activation and Aβ load by quantitative immunohistochemical analysis in brain parenchyma adjacent to affected vessels in 11 ABRA patients and 10 matched CAA controls.RESULTS: ABRA patients showed significantly increased immune activation and decreased Aβ loads in the brain parenchyma adjacent to affected vessels.CONCLUSION: Our results are in line with the hypothesis of ABRA being the result of an excessive immune response to Aβ and show that this can lead to enhanced clearance of Aβ from the brain parenchyma by immune-mediated mechanisms.",
author = "S Bogner and C Bernreuther and J Matschke and Barrera-Ocampo, {Alvaro A} and D Sepulveda-Falla and F Leypoldt and T Magnus and F Haag and M Bergmann and W Br{\"u}ck and S Vogelgesang and M Glatzel",
note = "{\textcopyright} 2013 S. Karger AG, Basel.",
year = "2014",
month = jan,
day = "1",
doi = "10.1159/000352020",
language = "English",
volume = "13",
pages = "38--44",
journal = "NEURODEGENER DIS",
issn = "1660-2854",
publisher = "S. Karger AG",
number = "1",

}

RIS

TY - JOUR

T1 - Immune activation in amyloid-β-related angiitis correlates with decreased parenchymal amyloid-β plaque load

AU - Bogner, S

AU - Bernreuther, C

AU - Matschke, J

AU - Barrera-Ocampo, Alvaro A

AU - Sepulveda-Falla, D

AU - Leypoldt, F

AU - Magnus, T

AU - Haag, F

AU - Bergmann, M

AU - Brück, W

AU - Vogelgesang, S

AU - Glatzel, M

N1 - © 2013 S. Karger AG, Basel.

PY - 2014/1/1

Y1 - 2014/1/1

N2 - BACKGROUND: Primary angiitis of the central nervous system (PACNS) is a rare but serious condition. A fraction of patients suffering from PACNS concurrently exhibit pronounced cerebral amyloid angiopathy (CAA) which is characterized by deposits of amyloid-β (Aβ) in and around the walls of small and medium-sized arteries of the brain. PACNS with CAA has been identified as a distinct disease entity, termed Aβ-related angiitis (ABRA). Evidence points to an immune reaction to vessel wall Aβ as the trigger of vasculitis.OBJECTIVE: To investigate whether the inflammatory response to Aβ has (1) any effect on the status of immune activation in the brain parenchyma and (2) leads to clearance of Aβ from brain parenchyma.METHODS: We studied immune activation and Aβ load by quantitative immunohistochemical analysis in brain parenchyma adjacent to affected vessels in 11 ABRA patients and 10 matched CAA controls.RESULTS: ABRA patients showed significantly increased immune activation and decreased Aβ loads in the brain parenchyma adjacent to affected vessels.CONCLUSION: Our results are in line with the hypothesis of ABRA being the result of an excessive immune response to Aβ and show that this can lead to enhanced clearance of Aβ from the brain parenchyma by immune-mediated mechanisms.

AB - BACKGROUND: Primary angiitis of the central nervous system (PACNS) is a rare but serious condition. A fraction of patients suffering from PACNS concurrently exhibit pronounced cerebral amyloid angiopathy (CAA) which is characterized by deposits of amyloid-β (Aβ) in and around the walls of small and medium-sized arteries of the brain. PACNS with CAA has been identified as a distinct disease entity, termed Aβ-related angiitis (ABRA). Evidence points to an immune reaction to vessel wall Aβ as the trigger of vasculitis.OBJECTIVE: To investigate whether the inflammatory response to Aβ has (1) any effect on the status of immune activation in the brain parenchyma and (2) leads to clearance of Aβ from brain parenchyma.METHODS: We studied immune activation and Aβ load by quantitative immunohistochemical analysis in brain parenchyma adjacent to affected vessels in 11 ABRA patients and 10 matched CAA controls.RESULTS: ABRA patients showed significantly increased immune activation and decreased Aβ loads in the brain parenchyma adjacent to affected vessels.CONCLUSION: Our results are in line with the hypothesis of ABRA being the result of an excessive immune response to Aβ and show that this can lead to enhanced clearance of Aβ from the brain parenchyma by immune-mediated mechanisms.

U2 - 10.1159/000352020

DO - 10.1159/000352020

M3 - SCORING: Journal article

C2 - 24021982

VL - 13

SP - 38

EP - 44

JO - NEURODEGENER DIS

JF - NEURODEGENER DIS

SN - 1660-2854

IS - 1

ER -