review article | Q7318358 |
scholarly article | Q13442814 |
P50 | author | Natalia B. Pikor | Q49130296 |
Alexandre Prat | Q56394627 | ||
Jennifer L Gommerman | Q56987206 | ||
Amit Bar-or | Q42885888 | ||
P2860 | cites work | Interrelationships of the pia mater and the perivascular (Virchow-Robin) spaces in the human cerebrum | Q24535884 |
A role for Th17 cells in the regulation of tertiary lymphoid follicles | Q26851559 | ||
Phenotypic and Morphological Properties of Germinal Center Dark Zone Cxcl12-Expressing Reticular Cells | Q27302285 | ||
Structural and functional features of central nervous system lymphatic vessels | Q27316769 | ||
Artery Tertiary Lymphoid Organs Control Aorta Immunity and Protect against Atherosclerosis via Vascular Smooth Muscle Cell Lymphotoxin β Receptors | Q30279169 | ||
Association of T-zone reticular networks and conduits with ectopic lymphoid tissues in mice and humans | Q30475578 | ||
Localizing central nervous system immune surveillance: meningeal antigen-presenting cells activate T cells during experimental autoimmune encephalomyelitis | Q30510541 | ||
Multiple sclerosis: T-cell receptor expression in distinct brain regions | Q33300045 | ||
Anatomy and imaging of the normal meninges | Q33526409 | ||
Th1, Th17, and Th9 effector cells induce experimental autoimmune encephalomyelitis with different pathological phenotypes | Q34066077 | ||
The development of inducible bronchus-associated lymphoid tissue depends on IL-17. | Q34191942 | ||
Tertiary lymphoid organ development coincides with determinant spreading of the myelin-specific T cell response | Q43887998 | ||
Microvasculature of the human cerebral meninges | Q44460014 | ||
Occurrence of tertiary lymphoid tissue is associated with T-cell infiltration and predicts better prognosis in early-stage colorectal cancers | Q45118047 | ||
Cortical grey matter demyelination can be induced by elevated pro-inflammatory cytokines in the subarachnoid space of MOG-immunized rats | Q45799560 | ||
IL-22 bridges the lymphotoxin pathway with the maintenance of colonic lymphoid structures during infection with Citrobacter rodentium | Q46485022 | ||
Characterization of a conduit system containing laminin-5 in the human thymus: a potential transport system for small molecules | Q46990518 | ||
In vivo detection of myelin proteins in cervical lymph nodes of MS patients using ultrasound-guided fine-needle aspiration cytology | Q47288465 | ||
Detection of ectopic B-cell follicles with germinal centers in the meninges of patients with secondary progressive multiple sclerosis. | Q47357498 | ||
Inflammation recapitulates the ontogeny of lymphoid stromal cells | Q47976120 | ||
Meningeal T cells associate with diffuse axonal loss in multiple sclerosis spinal cords | Q48099284 | ||
Meningeal B-cell follicles in secondary progressive multiple sclerosis associate with early onset of disease and severe cortical pathology. | Q48200750 | ||
Mast cell activation and neutrophil recruitment promotes early and robust inflammation in the meninges in EAE. | Q48240026 | ||
Dynamic changes in meningeal inflammation correspond to clinical exacerbations in a murine model of relapsing-remitting multiple sclerosis | Q48373501 | ||
A novel immune-to-CNS communication pathway: cells of the meninges surrounding the spinal cord CSF space produce proinflammatory cytokines in response to an inflammatory stimulus | Q48416184 | ||
Meningeal inflammation is not associated with cortical demyelination in chronic multiple sclerosis | Q48485900 | ||
A new focal EAE model of cortical demyelination: multiple sclerosis-like lesions with rapid resolution of inflammation and extensive remyelination | Q48530177 | ||
Cortical demyelination and diffuse white matter injury in multiple sclerosis. | Q48726181 | ||
Meningeal inflammation is widespread and linked to cortical pathology in multiple sclerosis | Q48949792 | ||
Dendritic cells permit immune invasion of the CNS in an animal model of multiple sclerosis. | Q49014751 | ||
Integration of Th17- and Lymphotoxin-Derived Signals Initiates Meningeal-Resident Stromal Cell Remodeling to Propagate Neuroinflammation. | Q49130159 | ||
Group 3 innate lymphoid cells accumulate and exhibit disease-induced activation in the meninges in EAE. | Q50723182 | ||
Human solid tumors contain high endothelial venules: association with T- and B-lymphocyte infiltration and favorable prognosis in breast cancer. | Q50996147 | ||
Intracerebral expression of CXCL13 and BAFF is accompanied by formation of lymphoid follicle-like structures in the meninges of mice with relapsing experimental autoimmune encephalomyelitis. | Q51027456 | ||
A combination of fluorescent NFAT and H2B sensors uncovers dynamics of T cell activation in real time during CNS autoimmunity. | Q51035236 | ||
Complementarity-Determining Region 3 Spectratyping Analysis of the TCR Repertoire in Multiple Sclerosis | Q54777171 | ||
Effector T cell interactions with meningeal vascular structures in nascent autoimmune CNS lesions | Q59070288 | ||
Suppression of established experimental autoimmune encephalomyelitis and formation of meningeal lymphoid follicles by lymphotoxin β receptor-Ig fusion protein | Q60455093 | ||
A comparison of the pathology of primary and secondary progressive multiple sclerosis | Q72708285 | ||
Immunoglobulin class-switched B cells form an active immune axis between CNS and periphery in multiple sclerosis. | Q34251673 | ||
Meningeal inflammation plays a role in the pathology of primary progressive multiple sclerosis | Q34295012 | ||
Real-time in vivo analysis of T cell activation in the central nervous system using a genetically encoded calcium indicator | Q34345420 | ||
Extensive grey matter pathology in the cerebellum in multiple sclerosis is linked to inflammation in the subarachnoid space | Q34449329 | ||
Gadolinium-based MRI characterization of leptomeningeal inflammation in multiple sclerosis | Q34472457 | ||
Related B cell clones populate the meninges and parenchyma of patients with multiple sclerosis | Q34538912 | ||
Related B cell clones that populate the CSF and CNS of patients with multiple sclerosis produce CSF immunoglobulin | Q34960518 | ||
Organogenesis of lymphoid tissues | Q35096187 | ||
Lymphotoxin/light, lymphoid microenvironments and autoimmune disease | Q35219029 | ||
B cells populating the multiple sclerosis brain mature in the draining cervical lymph nodes | Q35298764 | ||
Inflammatory cortical demyelination in early multiple sclerosis | Q35764685 | ||
Inflammation-induced formation of fat-associated lymphoid clusters | Q35882546 | ||
Transcriptional profiling of stroma from inflamed and resting lymph nodes defines immunological hallmarks | Q36007057 | ||
Lymphotoxin controls the IL-22 protection pathway in gut innate lymphoid cells during mucosal pathogen challenge. | Q36031510 | ||
IL-22 regulates lymphoid chemokine production and assembly of tertiary lymphoid organs | Q36055624 | ||
Central Nervous System and Peripheral Expression of CCL19, CCL21 and Their Receptor CCR7 in Experimental Model of Multiple Sclerosis | Q36065424 | ||
Th17 cells induce ectopic lymphoid follicles in central nervous system tissue inflammation | Q36174679 | ||
Lymphoid neogenesis in chronic inflammatory diseases. | Q36405080 | ||
Lymphoid organ development: from ontogeny to neogenesis | Q36426808 | ||
B cell exchange across the blood-brain barrier in multiple sclerosis | Q36498036 | ||
Follicular dendritic cells emerge from ubiquitous perivascular precursors | Q36991851 | ||
Ectopic lymphoid tissues and local immunity | Q37075235 | ||
Trapping of naive lymphocytes triggers rapid growth and remodeling of the fibroblast network in reactive murine lymph nodes | Q37475213 | ||
Lymphatic vessels and tertiary lymphoid organs | Q37602241 | ||
B cells in multiple sclerosis: connecting the dots. | Q37943607 | ||
Interdependence of stromal and immune cells for lymph node function | Q37966310 | ||
The anatomical and cellular basis of immune surveillance in the central nervous system. | Q38035711 | ||
Capture, crawl, cross: the T cell code to breach the blood-brain barriers | Q38038445 | ||
Mesenchymal cell differentiation during lymph node organogenesis | Q38068182 | ||
Stromal infrastructure of the lymph node and coordination of immunity | Q38286890 | ||
Maturation of lymph node fibroblastic reticular cells from myofibroblastic precursors is critical for antiviral immunity | Q38408658 | ||
Stromal cells in chronic inflammation and tertiary lymphoid organ formation | Q38415281 | ||
IL-17-induced CXCL12 recruits B cells and induces follicle formation in BALT in the absence of differentiated FDCs | Q38641655 | ||
Multiple sclerosis: presence of lymphatic capillaries and lymphoid tissue in the brain and spinal cord | Q41466361 | ||
A Gradient of neuronal loss and meningeal inflammation in multiple sclerosis. | Q42847184 | ||
P407 | language of work or name | English | Q1860 |
P921 | main subject | multiple sclerosis | Q8277 |
P304 | page(s) | 657 | |
P577 | publication date | 2015-01-01 | |
P1433 | published in | Frontiers in Immunology | Q27723748 |
P1476 | title | Meningeal Tertiary Lymphoid Tissues and Multiple Sclerosis: A Gathering Place for Diverse Types of Immune Cells during CNS Autoimmunity | |
P478 | volume | 6 |
Q48325814 | Activated B Cells Participating in the Anti-Myelin Response Are Excluded from the Inflamed Central Nervous System in a Model of Autoimmunity that Allows for B Cell Recognition of Autoantigen |
Q40530656 | Activated GL7+ B cells are maintained within the inflamed CNS in the absence of follicle formation during viral encephalomyelitis. |
Q92712543 | Central Nervous System Inflammatory Aggregates in the Theiler's Virus Model of Progressive Multiple Sclerosis |
Q37729523 | Emerging Approaches for Validating and Managing Multiple Sclerosis Relapse |
Q47546882 | Epstein-Barr virus is present in the brain of most cases of multiple sclerosis and may engage more than just B cells |
Q39314770 | IL-17+ γδ T cells as kick-starters of inflammation. |
Q91723047 | Identification of novel non-myelin biomarkers in multiple sclerosis using an improved phage-display approach |
Q90540880 | Immune cells in the retina and choroid: Two different tissue environments that require different defenses and surveillance |
Q28067334 | Inebilizumab, a B Cell-Depleting Anti-CD19 Antibody for the Treatment of Autoimmune Neurological Diseases: Insights from Preclinical Studies |
Q63363253 | Innate, innate-like and adaptive lymphocytes in the pathogenesis of MS and EAE |
Q47839893 | Mass cytometry analysis of immune cells in the brain |
Q47846433 | Multiple Sclerosis Pathology |
Q28071670 | Potential of Cells and Cytokines/Chemokines to Regulate Tertiary Lymphoid Structures in Human Diseases |
Q91842191 | Siponimod therapy implicates Th17 cells in a preclinical model of subpial cortical injury |
Q39201665 | Tertiary lymphoid organs in systemic autoimmune diseases: pathogenic or protective? |
Q50175862 | The Interleukin (IL)-23/T helper (Th)17 Axis in Experimental Autoimmune Encephalomyelitis and Multiple Sclerosis |
Q102379386 | The frequency of follicular T helper cells differs in acute and chronic neuroinflammation |
Q47552983 | Transcriptional profile and Epstein-Barr virus infection status of laser-cut immune infiltrates from the brain of patients with progressive multiple sclerosis |
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