Academic Journal
Lymphotoxin-dependent elevated meningeal CXCL13:BAFF ratios drive gray matter injury.
| Τίτλος: | Lymphotoxin-dependent elevated meningeal CXCL13:BAFF ratios drive gray matter injury. |
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| Συγγραφείς: | Naouar, Ikbel, Pangan, Andrei, Sayeed, Faizah N, Zhu, Jingwen, Pössnecker, Elisabeth, Spring, Shoshana, Sled, John G, Cenni, Bruno, Nuesslein-Hildesheim, Barbara, Browning, Jeffrey L, Pröbstel, Anne-Katrin, Reich, Daniel S, Zuo, Michelle, Gommerman, Jennifer L, Ramaglia, Valeria, Raza, Syed Ali, Champagne-Jorgensen, Kevin, Patel, Jyot, Wang, Angela, Pu, Annie, Ward, Lesley, Ahn, Jennifer S Y |
| Πηγή: | Nature immunology 27(1), 48 - 60 (2026). doi:10.1038/s41590-025-02359-5 |
| Στοιχεία εκδότη: | Springer Nature Limited |
| Έτος έκδοσης: | 2026 |
| Θεματικοί όροι: | info:eu-repo/classification/ddc/610, Animals, Chemokine CXCL13: metabolism, Chemokine CXCL13: immunology, Gray Matter: immunology, Gray Matter: pathology, Gray Matter: metabolism, Humans, Mice, Encephalomyelitis, Autoimmune, Experimental: immunology, Experimental: pathology, Meninges: immunology, Meninges: metabolism, Meninges: pathology, B-Cell Activating Factor: metabolism, B-Cell Activating Factor: immunology, Multiple Sclerosis: immunology, Multiple Sclerosis: pathology, Multiple Sclerosis: metabolism, Female, Male, Inbred C57BL, Lymphotoxin-alpha: metabolism, Th17 Cells: immunology, Tertiary Lymphoid Structures: immunology, Tertiary Lymphoid Structures: pathology, B-Lymphocytes: immunology, Chemokine CXCL13 |
| Θέμα γεωγραφικό: | DE |
| Περιγραφή: | In multiple sclerosis (MS), B cell-rich tertiary lymphoid tissues (TLTs) in the brain leptomeninges associate with cortical gray matter injury. Using a model of Th17 cell-driven experimental autoimmune encephalomyelitis in mice, we found that inhibitors of Bruton's tyrosine kinase (BTKi) prevented TLT formation and cortical pathology in a B cell activating factor (BAFF)-dependent manner. BTKi reduced expression of lymphotoxin ligands, and cotreatment with a lymphotoxin-β receptor agonist abrogated the benefits of BTKi. TLT and cortical pathology tracked with a high CXCL13:BAFF ratio in the leptomeninges, which was reduced by BTKi. Moreover, we observed high CXCL13:BAFF ratios in post mortem cerebral spinal fluid from patients with MS and pathologically confirmed leptomeningeal inflammation, as well as in living patients with MS and radiologically confirmed paramagnetic rim lesions. In summary, using experimental autoimmune encephalomyelitis, we revealed a molecular circuit that leads to TLT formation and cortical injury with translational relevance for detection of this pathology in patients with MS. |
| Τύπος εγγράφου: | article in journal/newspaper |
| Γλώσσα: | English |
| ISSN: | 1529-2916 1529-2908 |
| Relation: | info:eu-repo/semantics/altIdentifier/issn/1529-2916; info:eu-repo/semantics/altIdentifier/pmid/pmid:41482555; info:eu-repo/semantics/altIdentifier/issn/1529-2908; https://pub.dzne.de/record/283126 |
| Διαθεσιμότητα: | https://pub.dzne.de/record/283126 https://pub.dzne.de/search?p=id:%22DZNE-2026-00022%22 |
| Rights: | info:eu-repo/semantics/openAccess |
| Αριθμός Καταχώρησης: | edsbas.74063273 |
| Βάση Δεδομένων: | BASE |
| ISSN: | 15292916 15292908 |
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