| Literature DB >> 28620692 |
Marie Wunsch1, Samir Jabari2, Barbara Voussen3, Michael Enders2, Shanthi Srinivasan4, François Cossais5, Thilo Wedel5, Martina Boettner5, Anna Schwarz6, Linda Weyer6, Oktay Göcer1, Michael Schroeter7, Mathias Maeurer8, Matthias Woenckhaus9, Karolin Pollok10, Helena Radbruch11, Luisa Klotz12, Claus-Jürgen Scholz13,14, Joachim Nickel15, Andreas Friebe3, Klaus Addicks6, Süleyman Ergün1, Paul V Lehmann16, Stefanie Kuerten17,18.
Abstract
Multiple sclerosis (MS) is a chronic autoimmune disease of the central nervous system (CNS) in young adults that has serious negative socioeconomic effects. In addition to symptoms caused by CNS pathology, the majority of MS patients frequently exhibit gastrointestinal dysfunction, which was previously either explained by the presence of spinal cord lesions or not directly linked to the autoimmune etiology of the disease. Here, we studied the enteric nervous system (ENS) in a B cell- and antibody-dependent mouse model of MS by immunohistochemistry and electron microscopy at different stages of the disease. ENS degeneration was evident prior to the development of CNS lesions and the onset of neurological deficits in mice. The pathology was antibody mediated and caused a significant decrease in gastrointestinal motility, which was associated with ENS gliosis and neuronal loss. We identified autoantibodies against four potential target antigens derived from enteric glia and/or neurons by immunoprecipitation and mass spectrometry. Antibodies against three of the target antigens were also present in the plasma of MS patients as confirmed by ELISA. The analysis of human colon resectates provided evidence of gliosis and ENS degeneration in MS patients compared to non-MS controls. For the first time, this study establishes a pathomechanistic link between the well-established autoimmune attack on the CNS and ENS pathology in MS, which might provide a paradigm shift in our current understanding of the immunopathogenesis of the disease with broad diagnostic and therapeutic implications.Entities:
Keywords: Autoantibodies; CNS; EAE; ENS; Multiple sclerosis
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Year: 2017 PMID: 28620692 DOI: 10.1007/s00401-017-1742-6
Source DB: PubMed Journal: Acta Neuropathol ISSN: 0001-6322 Impact factor: 17.088