A Pilot Study to Develop Paraneoplastic Cerebellar Degeneration Mouse Model

被引:3
作者
Faure, Fabrice [1 ]
Yshii, Lidia [2 ,3 ,4 ,5 ]
Renno, Toufic [6 ]
Coste, Isabelle [6 ]
Joubert, Bastien [1 ,7 ]
Desestret, Virginie [1 ,7 ]
Liblau, Roland [2 ,3 ]
Honnorat, Jerome [1 ,7 ]
机构
[1] Univ Lyon, Univ Claude Bernard Lyon 1, Inst NeuroMyoGene INMG MeLis, Synaptopathies & Autoantibodies SynatAc Team,INSER, F-69373 Lyon, France
[2] Univ Toulouse, Toulouse Inst Infect & Inflammatory Dis Infin, CNRS, INSERM,UPS, F-31024 Toulouse, France
[3] Toulouse Univ Hosp, Dept Immunol, F-31300 Toulouse, France
[4] Katholieke Univ Leuven, Dept Microbiol, Immunol & Transplantat, B-3000 Louvain, Belgium
[5] Katholieke Univ Leuven, Dept Neurosci, B-3000 Louvain, Belgium
[6] Univ Lyon, Canc Res Ctr Lyon, INSERM 1052, CNRS 5286, F-69008 Lyon, France
[7] Hosp Civils Lyon, Hop Neurol Pierre Wertheimer, French Reference Ctr Paraneoplast Neurol Syndromes, 59 Blvd Pinel, F-69677 Bron, France
关键词
Paraneoplastic cerebellar degeneration; Autoantibodies; Anti-Yo autoantibodies; CDR2L protein; Immune checkpoint inhibitors; RECOMBINANT YO PROTEIN; T-CELL RESPONSES; ANTI-YO; PERTUSSIS TOXIN; DENDRITIC CELLS; ANIMAL-MODEL; AUTOIMMUNE ENCEPHALOMYELITIS; PASSIVE TRANSFER; IMMUNE-RESPONSE; PURKINJE-CELLS;
D O I
10.1007/s12311-023-01524-6
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
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.
引用
收藏
页码:181 / 196
页数:16
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