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Immune privilege of the CNS is not the consequence of limited antigen sampling
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/(sici)1097-4547(19980815)53:4<393::aid-jnr1>3.0.co;2-1openalex-snapshot
Four-kilobase sequence of the mouse CNP gene directs spatial and temporal expression of lacZ in transgenic mice
inferredcites →https://doi.org/10.1002/eji.200839019openalex-snapshot
Antigens expressed by myelinating glia cells induce peripheral cross‐tolerance of endogenous CD8+ T cells
inferredcites →https://doi.org/10.1002/gene.10154openalex-snapshot
Inducible site‐specific recombination in myelinating cells
inferredcites →https://doi.org/10.1002/glia.1101openalex-snapshot
Basic principles of immunological surveillance of the normal central nervous system
inferredcites →https://doi.org/10.1002/jnr.10368openalex-snapshot
Expression of the green fluorescent protein in the oligodendrocyte lineage: A transgenic mouse for developmental and physiological studies
inferredcites →https://doi.org/10.1007/3-540-29714-6_2openalex-snapshot
Breaking Ignorance: The Case of the Brain
inferredcites →https://doi.org/10.1007/bf00965533openalex-snapshot
Proteolipid protein and DM-20 are synthesized by Schwann cells, present in myelin membrane, but they are not fatty acylated
inferredcites →https://doi.org/10.1007/s11481-013-9470-8openalex-snapshot
Drainage of Cells and Soluble Antigen from the CNS to Regional Lymph Nodes
inferredcites →https://doi.org/10.1016/0165-5728(89)90136-7openalex-snapshot
Role of cervical lymph nodes in the systemic humoral immune response to human serum albumin microinfused into rat cerebrospinal fluid
inferredcites →https://doi.org/10.1016/0165-5728(91)90160-9openalex-snapshot
Myelin basic protein infused into cerebrospinal fluid suppresses experimental autoimmune encephalomyelitis
inferredcites →https://doi.org/10.1016/0167-5699(92)90027-5openalex-snapshot
Cervical lymphatics, the blood-brain barrier and the immunoreactivity of the brain: a new view
inferredcites →https://doi.org/10.1016/0896-6273(94)90450-2openalex-snapshot
Embryonic expression of myelin genes: Evidence for a focal source of oligodendrocyte precursors in the ventricular zone of the neural tube
inferredcites →https://doi.org/10.1016/j.coph.2008.07.009openalex-snapshot
Sensing the microenvironment of the central nervous system: immune cells in the central nervous system and their pharmacological manipulation
inferredcites →https://doi.org/10.1016/j.immuni.2011.10.015openalex-snapshot
Th17 Cells Induce Ectopic Lymphoid Follicles in Central Nervous System Tissue Inflammation
inferredcites →https://doi.org/10.1016/j.it.2006.11.004openalex-snapshot
What is immune privilege (not)?
inferredcites →https://doi.org/10.1016/s0165-5728(03)00249-2openalex-snapshot
In situ processing and distribution of intracerebrally injected OVA in the CNS
inferredcites →https://doi.org/10.1016/s1044-7431(03)00029-0openalex-snapshot
Tamoxifen-inducible glia-specific Cre mice for somatic mutagenesis in oligodendrocytes and Schwann cells
inferredcites →https://doi.org/10.1038/ng1095openalex-snapshot
Disruption of Cnp1 uncouples oligodendroglial functions in axonal support and myelination
inferredcites →https://doi.org/10.1038/ni.1716openalex-snapshot
C-C chemokine receptor 6–regulated entry of TH-17 cells into the CNS through the choroid plexus is required for the initiation of EAE
inferredcites →https://doi.org/10.1038/ni.2513openalex-snapshot
MHC class I–restricted myelin epitopes are cross-presented by Tip-DCs that promote determinant spreading to CD8+ T cells
inferredcites →https://doi.org/10.1038/ni1427openalex-snapshot
Peripheral antigen display by lymph node stroma promotes T cell tolerance to intestinal self
inferredcites →https://doi.org/10.1038/nm1197openalex-snapshot
Dendritic cells permit immune invasion of the CNS in an animal model of multiple sclerosis
inferredcites →https://doi.org/10.1038/nri1786openalex-snapshot
Lymphoid neogenesis in chronic inflammatory diseases
inferredcites →https://doi.org/10.1038/nri2438openalex-snapshot
Immunotherapy of autoimmunity and cancer: the penalty for success
inferredcites →https://doi.org/10.1038/nri2550openalex-snapshot
Autoimmune T cell responses in the central nervous system
inferredcites →https://doi.org/10.1038/nri3265openalex-snapshot
The anatomical and cellular basis of immune surveillance in the central nervous system
inferredcites →https://doi.org/10.1056/nejmoa051586openalex-snapshot
Progressive Multifocal Leukoencephalopathy after Natalizumab Therapy for Crohn's Disease
inferredcites →https://doi.org/10.1056/nejmoa051782openalex-snapshot
Progressive Multifocal Leukoencephalopathy Complicating Treatment with Natalizumab and Interferon Beta-1a for Multiple Sclerosis
inferredcites →https://doi.org/10.1056/nejmoa051847openalex-snapshot
Progressive Multifocal Leukoencephalopathy in a Patient Treated with Natalizumab
inferredcites →https://doi.org/10.1073/pnas.1433000100openalex-snapshot
Human cerebrospinal fluid central memory CD4 + T cells: Evidence for trafficking through choroid plexus and meninges via P-selectin
inferredcites →https://doi.org/10.1073/pnas.84.16.5665openalex-snapshot
Splice site selection in the proteolipid protein (PLP) gene transcript and primary structure of the DM-20 protein of central nervous system myelin.
inferredcites →https://doi.org/10.1093/brain/awn148openalex-snapshot
Naïve CD8 T-cells initiate spontaneous autoimmunity to a sequestered model antigen of the central nervous system
inferredcites →https://doi.org/10.1111/j.1600-065x.2011.01016.xopenalex-snapshot
Immune tolerance in multiple sclerosis
inferredcites →https://doi.org/10.1111/j.1750-3639.2004.tb00049.xopenalex-snapshot
Detection of Ectopic B‐cell Follicles with Germinal Centers in the Meninges of Patients with Secondary Progressive Multiple Sclerosis
inferredcites →https://doi.org/10.1152/ajpheart.1991.261.4.h1197openalex-snapshot
Albumin outflow into deep cervical lymph from different regions of rabbit brain
inferredcites →https://doi.org/10.1152/ajprenal.1981.240.4.f329openalex-snapshot
Drainage of cerebral interstitial fluid into deep cervical lymph of the rabbit
inferredcites →https://doi.org/10.1159/000048712openalex-snapshot
Unraveling Oligodendrocyte Origin and Function by Cell-Specific Transgenesis
inferredcites →https://doi.org/10.1182/blood-2002-10-3309openalex-snapshot
CD8+ T cells from patients with acute multiple sclerosis display selective increase of adhesiveness in brain venules: a critical role for P-selectin glycoprotein ligand-1
inferredcites →https://doi.org/10.1182/blood-2005-01-0154openalex-snapshot
How to drain without lymphatics? Dendritic cells migrate from the cerebrospinal fluid to the B-cell follicles of cervical lymph nodes
inferredcites →https://doi.org/10.1371/journal.pone.0011453openalex-snapshot
Dendritic Cells in Chronic Mycobacterial Granulomas Restrict Local Anti-Bacterial T Cell Response in a Murine Model
inferredcites →https://doi.org/10.1371/journal.pone.0017988openalex-snapshot
Intracerebral Human Regulatory T Cells: Analysis of CD4+CD25+FOXP3+ T Cells in Brain Lesions and Cerebrospinal Fluid of Multiple Sclerosis Patients
inferredcites →https://doi.org/10.1523/jneurosci.07-09-02703.1987openalex-snapshot
Molecular cloning of a 2',3'-cyclic nucleotide 3'-phosphodiesterase: mRNAs with different 5' ends encode the same set of proteins in nervous and lymphoid tissues
inferredcites →https://doi.org/10.1523/jneurosci.2199-08.2009openalex-snapshot
Intracerebral Dendritic Cells Critically Modulate Encephalitogenic versus Regulatory Immune Responses in the CNS
inferredcites →https://doi.org/10.1523/jneurosci.22-03-00876.2002openalex-snapshot
Proteolipid Promoter Activity Distinguishes Two Populations of NG2-Positive Cells throughout Neonatal Cortical Development
inferredcites →https://doi.org/10.4049/jimmunol.166.10.6099openalex-snapshot
Cell-Associated Ovalbumin Is Cross-Presented Much More Efficiently than Soluble Ovalbumin In Vivo
inferredcites →https://doi.org/10.4049/jimmunol.169.10.5415openalex-snapshot
Transfer of Central Nervous System Autoantigens and Presentation in Secondary Lymphoid Organs
inferredcites →https://doi.org/10.4049/jimmunol.169.2.1000openalex-snapshot
Overlapping Roles of P-Selectin and α4 Integrin to Recruit Leukocytes to the Central Nervous System in Experimental Autoimmune Encephalomyelitis
inferredcites →https://doi.org/10.4049/jimmunol.173.4.2353openalex-snapshot
Initiation of Immune Responses in Brain Is Promoted by Local Dendritic Cells
inferredcites →https://doi.org/10.4049/jimmunol.178.10.6038openalex-snapshot
Cutting Edge: Cross-Presented Intracranial Antigen Primes CD8+ T Cells
inferredcites →https://doi.org/10.4049/jimmunol.181.3.1617openalex-snapshot
Cutting Edge: Multiple Sclerosis-Like Lesions Induced by Effector CD8 T Cells Recognizing a Sequestered Antigen on Oligodendrocytes
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Incoming claims: where this work appears in other papers’ reference lists and arguments.
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TGFα controls checkpoints in CNS resident and infiltrating immune cells to promote resolution of inflammation
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VEGF-C-driven lymphatic drainage enables immunosurveillance of brain tumours
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Neuroinflammation creates an immune regulatory niche at the meningeal lymphatic vasculature near the cribriform plate
inferred← citeshttps://doi.org/10.1038/s41593-022-01060-2openalex-snapshot
Cerebrospinal fluid can exit into the skull bone marrow and instruct cranial hematopoiesis in mice with bacterial meningitis
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Contraction of T cell richness in lung cancer brain metastases
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Single-dose radiotherapy is more effective than fractionation when combined with anti-PD-1 immunotherapy in glioblastoma
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CCR7 deficient inflammatory Dendritic Cells are retained in the Central Nervous System
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A novel tumor-promoting mechanism of IL6 and the therapeutic efficacy of tocilizumab: Hypoxia-induced IL6 is a potent autophagy initiator in glioblastoma via the p-STAT3-MIR155-3p-CREBRF pathway
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Ryanodine receptors in experimental autoimmune encephalomyelitis, an animal model of multiple sclerosis
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Meningeal lymphatic drainage promotes T cell responses against Toxoplasma gondii but is dispensable for parasite control in the brain
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