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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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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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. 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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.</description><subject>Adjuvants</subject><subject>Antigen presentation</subject><subject>Antigens</subject><subject>Ataxia</subject><subject>Autoantibodies</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Cell death</subject><subject>Cell density</subject><subject>Cerebellum</subject><subject>Cerebrospinal fluid</subject><subject>Choroid plexus</subject><subject>Immune checkpoint inhibitors</subject><subject>Immune response</subject><subject>Infiltration</subject><subject>Inflammation</subject><subject>Life Sciences</subject><subject>Lymphocytes T</subject><subject>Metastases</subject><subject>Neurobiology</subject><subject>Neurodegeneration</subject><subject>Neurological diseases</subject><subject>Neurology</subject><subject>Neurosciences</subject><subject>Original Article</subject><subject>Ovarian carcinoma</subject><subject>Parenchyma</subject><subject>Pilot projects</subject><subject>Tumors</subject><issn>1473-4230</issn><issn>1473-4222</issn><issn>1473-4230</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNp9kU1P3DAQhq2qqHz1D_SAIvUCh9DxRzzkuFqgVCzqSsDZcpwJBGXjrZ0g7b_H21Ba9cDFtjzPvJ7XL2NfOJxyAPwWuZCc5yBkDrwQKtcf2B5XKHMlJHz857zL9mN8AhACFH5iu1KjKAXCHrueZcu280N2O4z1Jht8dk7P1Pl1trTB9uTXnY1D67I5Baqo62xIxAP1FOzQ-j678WOktNbUHbKdxnaRPr_uB-z-8uJufpUvfn7_MZ8tcic1DPmZRN1oUVeEsqnOatfYqpaqQKec5aK0Sqpaag5FpSRhU5aotNPOgiot1kIesJNJ99F2Zh3alQ0b421rrmYLs70DJQqJoJ95Yo8ndh38r5HiYFZtdFsfydsYjUDkpZKAkNCv_6FPfgx9cmLSZxWICmArKCbKBR9joOZtAg5mG4uZYjEpFvM7FqNT09Gr9FitqH5r-ZNDAuQExFTqHyj8ffsd2RfsYJVh</recordid><startdate>20240201</startdate><enddate>20240201</enddate><creator>Faure, Fabrice</creator><creator>Yshii, Lidia</creator><creator>Renno, Toufic</creator><creator>coste, Isabelle</creator><creator>Joubert, Bastien</creator><creator>Desestret, Virginie</creator><creator>Liblau, Roland</creator><creator>Honnorat, Jérôme</creator><general>Springer US</general><general>Springer Nature B.V</general><general>Springer</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TK</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>7X8</scope><scope>1XC</scope><scope>VOOES</scope><orcidid>https://orcid.org/0000-0002-4721-5952</orcidid><orcidid>https://orcid.org/0000-0001-6889-2920</orcidid><orcidid>https://orcid.org/0000-0002-9820-4452</orcidid><orcidid>https://orcid.org/0000-0001-5477-5475</orcidid></search><sort><creationdate>20240201</creationdate><title>A Pilot Study to Develop Paraneoplastic Cerebellar Degeneration Mouse Model</title><author>Faure, Fabrice ; 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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.</abstract><cop>New York</cop><pub>Springer US</pub><pmid>36729270</pmid><doi>10.1007/s12311-023-01524-6</doi><tpages>16</tpages><orcidid>https://orcid.org/0000-0002-4721-5952</orcidid><orcidid>https://orcid.org/0000-0001-6889-2920</orcidid><orcidid>https://orcid.org/0000-0002-9820-4452</orcidid><orcidid>https://orcid.org/0000-0001-5477-5475</orcidid><oa>free_for_read</oa></addata></record> |
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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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