A Pilot Study to Develop Paraneoplastic Cerebellar Degeneration Mouse Model

Modeling paraneoplastic neurological diseases to understand the immune mechanisms leading to neuronal death is a major challenge given the rarity and terminal access of patients’ autopsies. Here, we present a pilot study aiming at modeling paraneoplastic cerebellar degeneration with Yo autoantibodie...

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Veröffentlicht in:Cerebellum (London, England) England), 2024-02, Vol.23 (1), p.181-196
Hauptverfasser: Faure, Fabrice, Yshii, Lidia, Renno, Toufic, coste, Isabelle, Joubert, Bastien, Desestret, Virginie, Liblau, Roland, Honnorat, Jérôme
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container_issue 1
container_start_page 181
container_title Cerebellum (London, England)
container_volume 23
creator Faure, Fabrice
Yshii, Lidia
Renno, Toufic
coste, Isabelle
Joubert, Bastien
Desestret, Virginie
Liblau, Roland
Honnorat, Jérôme
description Modeling paraneoplastic neurological diseases to understand the immune mechanisms leading to neuronal death is a major challenge given the rarity and terminal access of patients’ autopsies. Here, we present a pilot study aiming at modeling paraneoplastic cerebellar degeneration with Yo autoantibodies (Yo-PCD). Female mice were implanted with an ovarian carcinoma cell line expressing CDR2 and CDR2L, the known antigens recognized by anti-Yo antibodies. To boost the immune response, we also immunized the mice by injecting antigens with diverse adjuvants and immune checkpoint inhibitors. Ataxia and gait instability were assessed in treated mice as well as autoantibody levels, Purkinje cell density, and immune infiltration in the cerebellum. We observed the production of anti-Yo antibodies in the CSF and serum of all immunized mice. Brain immunoreaction varied depending on the site of implantation of the tumor, with subcutaneous administration leading to a massive infiltration of immune cells in the meningeal spaces, choroid plexus, and cerebellar parenchyma. However, we did not observe massive Purkinje cell death nor any motor impairments in any of the experimental groups. Self-sustained neuro-inflammation might require a longer time to build up in our model. Unusual tumor antigen presentation and/or intrinsic, species-specific factors required for pro-inflammatory engagement in the brain may also constitute strong limitations to achieve massive recruitment of antigen-specific T-cells and killing of antigen-expressing neurons in this mouse model.
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subjects Adjuvants
Antigen presentation
Antigens
Ataxia
Autoantibodies
Biomedical and Life Sciences
Biomedicine
Cell death
Cell density
Cerebellum
Cerebrospinal fluid
Choroid plexus
Immune checkpoint inhibitors
Immune response
Infiltration
Inflammation
Life Sciences
Lymphocytes T
Metastases
Neurobiology
Neurodegeneration
Neurological diseases
Neurology
Neurosciences
Original Article
Ovarian carcinoma
Parenchyma
Pilot projects
Tumors
title A Pilot Study to Develop Paraneoplastic Cerebellar Degeneration Mouse Model
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