TY - JOUR
T1 - Cerebellar presence of immune cells in patients with neuro-coeliac disease
AU - Rouvroye, Maxine D.
AU - Bontkes, Hetty J.
AU - Bol, John G. J. M.
AU - Lissenberg-Witte, Birgit
AU - Byrnes, Valerie
AU - Bennani, Fadel
AU - Jordanova, Ekaterina S.
AU - Wilhelmus, Micha M. M.
AU - Mulder, Chris J.
AU - van der Valk, Paul
AU - Rozemuller, Annemieke J. M.
AU - Bouma, Gerd
AU - van Dam, Anne-Marie
N1 - Funding Information: We thank the Netherlands Brain Bank, The VU medical centre biobank and the UMC biobank for their human post mortem material. We thank Dr. Byrnes of the University College Hospital Galway and the families that gave their permission for autopsy and donation of cerebellar tissue for this study. Publisher Copyright: © 2023, The Author(s).
PY - 2023/12/1
Y1 - 2023/12/1
N2 - Although various neurodegenerative disorders have been associated with coeliac disease (CD), the underlying neuropathological link between these brain and gut diseases remains unclear. We postulated that the neuronal damage sporadically observed in CD patients is immune-mediated. Our aim was to determine if the loss of neurons, especially Purkinje cells, coincides with microglia activation and T- and B-cell infiltration in the cerebellum of patients with CD and a concomitant idiopathic neurological disease affecting the cerebellum (NeuroCD). Post-mortem cerebellar tissue was collected of validated NeuroCD cases. Gender- and age-matched genetic spinocerebellar ataxia (SCA) controls and non-neurological controls (NNC) were selected based on clinical reports and pathological findings. Cerebellar tissue of seventeen patients was included (6 NeuroCD, 5 SCA, 6 NNC). In SCA cases we found that the Purkinje cell layer was 58.6% reduced in comparison with NNC. In NeuroCD cases this reduction was even more prominent with a median reduction of 81.3% compared to NNC. Marked increased numbers of both CD3+ and CD8+ cells were observed in the NeuroCD but not in SCA patients. This coincided with significantly more microglial reactivity in NeuroCD patients. These findings demonstrate that the massive loss of Purkinje cells in the cerebellum of neuro CD patients is accompanied by local innate and T-cell mediated immune responses.
AB - Although various neurodegenerative disorders have been associated with coeliac disease (CD), the underlying neuropathological link between these brain and gut diseases remains unclear. We postulated that the neuronal damage sporadically observed in CD patients is immune-mediated. Our aim was to determine if the loss of neurons, especially Purkinje cells, coincides with microglia activation and T- and B-cell infiltration in the cerebellum of patients with CD and a concomitant idiopathic neurological disease affecting the cerebellum (NeuroCD). Post-mortem cerebellar tissue was collected of validated NeuroCD cases. Gender- and age-matched genetic spinocerebellar ataxia (SCA) controls and non-neurological controls (NNC) were selected based on clinical reports and pathological findings. Cerebellar tissue of seventeen patients was included (6 NeuroCD, 5 SCA, 6 NNC). In SCA cases we found that the Purkinje cell layer was 58.6% reduced in comparison with NNC. In NeuroCD cases this reduction was even more prominent with a median reduction of 81.3% compared to NNC. Marked increased numbers of both CD3+ and CD8+ cells were observed in the NeuroCD but not in SCA patients. This coincided with significantly more microglial reactivity in NeuroCD patients. These findings demonstrate that the massive loss of Purkinje cells in the cerebellum of neuro CD patients is accompanied by local innate and T-cell mediated immune responses.
KW - Ataxia
KW - Cerebellum
KW - Coeliac disease
KW - Encephalopathy
KW - Gluten
KW - Immunohistochemistry
KW - Lymphocyte
KW - Microglia
KW - Neurological disorders
KW - Purkinje cell
UR - http://www.scopus.com/inward/record.url?scp=85150952324&partnerID=8YFLogxK
UR - https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85150952324&origin=inward
UR - https://www.ncbi.nlm.nih.gov/pubmed/36966322
U2 - https://doi.org/10.1186/s40478-023-01538-5
DO - https://doi.org/10.1186/s40478-023-01538-5
M3 - Article
C2 - 36966322
SN - 2051-5960
VL - 11
JO - Acta Neuropathologica Communications
JF - Acta Neuropathologica Communications
IS - 1
M1 - 51
ER -