Medizinische Universität Graz Austria/Österreich - Forschungsportal - Medical University of Graz
Gewählte Publikation:
SHR Neuro Krebs Kardio Lipid Stoffw Microb
Callegari, I; Oechtering, J; Schneider, M; Perriot, S; Mathias, A; Voortman, MM; Cagol, A; Lanner, U; Diebold, M; Holdermann, S; Kreiner, V; Becher, B; Granziera, C; Junker, A; Du, Pasquier, R; Khalil, M; Kuhle, J; Kappos, L; Sanderson, NSR; Derfuss, T.
Cell-binding IgM in CSF is distinctive of multiple sclerosis and targets the iron transporter SCARA5.
Brain. 2023;
Doi: 10.1093/brain/awad424
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- Co-Autor*innen der Med Uni Graz
- Khalil Michael
- Voortman Margarete Maria
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- Abstract:
- Intrathecal IgM production in multiple sclerosis (MS) is associated with a worse disease course. To investigate pathogenic relevance of autoreactive IgM in MS, CSF from two independent cohorts, including MS patients and controls, were screened for antibody binding to induced pluripotent stem cell-derived neurons and astrocytes, and a panel of CNS- related cell lines. IgM binding to a primitive neuro-ectodermal tumour cell line discriminated 10% of MS donors from controls. Transcriptomes of single IgM producing CSF B cells from patients with cell-binding IgM were sequenced and used to produce recombinant monoclonal antibodies for characterisation and antigen identification. We produced 5 cell-binding recombinant IgM antibodies, of which one, cloned from an HLA-DR + plasma-like B cell, mediated antigen-dependent complement activation. Immunoprecipitation and mass spectrometry, and biochemical and transcriptome analysis of the target cells identified the iron transport scavenger protein SCARA5 as the antigen target of this antibody. Intrathecal injection of a SCARA5 antibody led to an increased T cell infiltration in an EAE model. CSF IgM might contribute to CNS inflammation in MS by binding to cell surface antigens like SCARA5 and activating complement, or by facilitating immune cell migration into the brain.
- Find related publications in this database (Keywords)
- complement
- immunoprecipitation
- plasma cells
- iron metabolism