scholarly article | Q13442814 |
P356 | DOI | 10.1038/NRI.2017.100 |
P698 | PubMed publication ID | 28869253 |
P50 | author | Giulia Fornasa | Q58924256 |
P2093 | author name string | Maria Rescigno | |
Ilaria Spadoni | |||
P2860 | cites work | Pericytes Control Key Neurovascular Functions and Neuronal Phenotype in the Adult Brain and during Brain Aging | Q24600644 |
Goblet cells deliver luminal antigen to CD103+ dendritic cells in the small intestine | Q24609125 | ||
Pericytes are required for blood-brain barrier integrity during embryogenesis | Q24627396 | ||
CNS immune privilege: hiding in plain sight | Q24642697 | ||
Lack of pericytes leads to endothelial hyperplasia and abnormal vascular morphogenesis | Q24681191 | ||
Breaking down the barriers: the gut microbiome, intestinal permeability and stress-related psychiatric disorders | Q26777279 | ||
Sleep and gastrointestinal disturbances in autism spectrum disorder in children | Q26783381 | ||
Role of gut microbiota in the modulation of atherosclerosis-associated immune response | Q26801649 | ||
Development and functions of the choroid plexus-cerebrospinal fluid system | Q26801821 | ||
Retinoic acid induces blood-brain barrier development. | Q39205654 | ||
Connecting dysbiosis, bile-acid dysmetabolism and gut inflammation in inflammatory bowel diseases. | Q39275409 | ||
The predominant site of bacterial translocation across the intestinal mucosal barrier occurs at the advancing disease margin in Crohn's disease | Q39600588 | ||
Recruitment of pericytes and astrocytes is closely related to the formation of tight junction in developing retinal vessels | Q39935875 | ||
Gene expression profile of endothelial cells during perturbation of the gut vascular barrier. | Q40471016 | ||
Effect of short-chain fatty acids on paracellular permeability in Caco-2 intestinal epithelium model | Q41118303 | ||
Characterization of suppressor cells in anterior chamber-associated immune deviation (ACAID) induced by soluble antigen. Evidence of two functionally and phenotypically distinct T-suppressor cell populations | Q41138099 | ||
Identification of transforming growth factor-beta as an immunosuppressive factor in aqueous humor. | Q41675605 | ||
Mesenteric lymph nodes at the center of immune anatomy | Q42108522 | ||
Origin of the lamina propria dendritic cell network | Q42117974 | ||
Intestinal CD103+, but not CX3CR1+, antigen sampling cells migrate in lymph and serve classical dendritic cell functions. | Q42138485 | ||
The liver may act as a firewall mediating mutualism between the host and its gut commensal microbiota | Q42214432 | ||
Gut CD103+ dendritic cells express indoleamine 2,3-dioxygenase which influences T regulatory/T effector cell balance and oral tolerance induction. | Q43081763 | ||
Diabetes and hypercholesterolemia increase blood-brain barrier permeability and brain amyloid deposition: beneficial effects of the LpPLA2 inhibitor darapladib | Q44980018 | ||
Human intestinal epithelial cells promote the differentiation of tolerogenic dendritic cells. | Q45943518 | ||
Colonic inflammation in Parkinson's disease. | Q46015750 | ||
Intestinal epithelial cells promote colitis-protective regulatory T-cell differentiation through dendritic cell conditioning. | Q46040098 | ||
Early retinal and renal abnormalities in diabetes | Q46075141 | ||
The somnogenic T lymphocyte suppressor prostaglandin D2 is selectively elevated in cerebrospinal fluid of advanced sleeping sickness patients. | Q46794773 | ||
Development, maintenance and disruption of the blood-brain barrier | Q26829668 | ||
Oral tolerance to food protein | Q27026259 | ||
Obese-type gut microbiota induce neurobehavioral changes in the absence of obesity | Q27329095 | ||
Size-selective loosening of the blood-brain barrier in claudin-5-deficient mice | Q28203769 | ||
T cell exclusion, immune privilege, and the tumor microenvironment | Q28259872 | ||
Immune cells contribute to the maintenance of neurogenesis and spatial learning abilities in adulthood | Q28292031 | ||
Essential regulation of CNS angiogenesis by the orphan G protein-coupled receptor GPR124. | Q28507603 | ||
GPR124, an orphan G protein-coupled receptor, is required for CNS-specific vascularization and establishment of the blood-brain barrier | Q28509184 | ||
Canonical Wnt signaling regulates organ-specific assembly and differentiation of CNS vasculature | Q28509331 | ||
Wnt/beta-catenin signaling is required for CNS, but not non-CNS, angiogenesis | Q28594356 | ||
Sustained inflammation after pericyte depletion induces irreversible blood-retina barrier breakdown | Q28817495 | ||
Ecological and evolutionary forces shaping microbial diversity in the human intestine | Q29547586 | ||
A functionally specialized population of mucosal CD103+ DCs induces Foxp3+ regulatory T cells via a TGF-beta and retinoic acid-dependent mechanism | Q29614266 | ||
Molecular analysis of commensal host-microbial relationships in the intestine | Q29614776 | ||
Small intestine lamina propria dendritic cells promote de novo generation of Foxp3 T reg cells via retinoic acid | Q29615586 | ||
Pericytes regulate the blood-brain barrier | Q29615840 | ||
Normal gut microbiota modulates brain development and behavior | Q29616855 | ||
Microbiota modulate behavioral and physiological abnormalities associated with neurodevelopmental disorders | Q29617111 | ||
Bifidobacteria can protect from enteropathogenic infection through production of acetate | Q29617592 | ||
Proinflammatory T-cell responses to gut microbiota promote experimental autoimmune encephalomyelitis | Q29619978 | ||
Revisiting the Mechanisms of CNS Immune Privilege | Q30278584 | ||
Developmental regulation of intestinal angiogenesis by indigenous microbes via Paneth cells | Q30476839 | ||
Interleukin-25 expressed by brain capillary endothelial cells maintains blood-brain barrier function in a protein kinase Cepsilon-dependent manner | Q33553749 | ||
Conditional Müllercell ablation causes independent neuronal and vascular pathologies in a novel transgenic model | Q33581991 | ||
Apolipoprotein E controls cerebrovascular integrity via cyclophilin A. | Q33717326 | ||
The treatment-naive microbiome in new-onset Crohn's disease | Q33762817 | ||
Comparison of sensitivity of Th1, Th2, and Th17 cells to Fas-mediated apoptosis | Q33859990 | ||
Enterocolitis induced by autoimmune targeting of enteric glial cells: a possible mechanism in Crohn's disease? | Q33949335 | ||
Anatomical basis of tolerance and immunity to intestinal antigens | Q33965210 | ||
Perivascular microglial cells of the CNS are bone marrow-derived and present antigen in vivo | Q34049368 | ||
Developing nervous tissue induces formation of blood-brain barrier characteristics in invading endothelial cells: a study using quail--chick transplantation chimeras | Q34057185 | ||
The development of blood-retinal barrier during the interaction of astrocytes with vascular wall cells | Q34096257 | ||
The retinal pigment epithelium: something more than a constituent of the blood-retinal barrier--implications for the pathogenesis of diabetic retinopathy. | Q34100527 | ||
Multiple facets of intestinal permeability and epithelial handling of dietary antigens | Q34110996 | ||
SSeCKS regulates angiogenesis and tight junction formation in blood-brain barrier | Q34206194 | ||
Epithelial barrier: an interface for the cross-communication between gut flora and immune system | Q34240555 | ||
Celiac disease and its link to type 1 diabetes mellitus. | Q34274386 | ||
Orchestrated leukocyte recruitment to immune-privileged sites: absolute barriers versus educational gates | Q48151397 | ||
Rejection of fetal neocortical neural transplants by H-2 incompatible mice | Q48201567 | ||
Enteric glia regulate intestinal barrier function and inflammation via release of S-nitrosoglutathione | Q48217613 | ||
Gradual Suppression of Transcytosis Governs Functional Blood-Retinal Barrier Formation | Q48249430 | ||
The role of Müller cells in the formation of the blood-retinal barrier | Q48257006 | ||
Retinal pathology is associated with increased blood-retina barrier permeability in a diabetic and hypercholesterolaemic pig model: Beneficial effects of the LpPLA2 inhibitor Darapladib. | Q48260488 | ||
The fate of allogeneic and xenogeneic neuronal tissue transplanted into the third ventricle of rodents | Q48278859 | ||
CXCL12 limits inflammation by localizing mononuclear infiltrates to the perivascular space during experimental autoimmune encephalomyelitis | Q48365016 | ||
ApoE deficiency leads to a progressive age-dependent blood-brain barrier leakage | Q48461941 | ||
Fulminant jejuno-ileitis following ablation of enteric glia in adult transgenic mice | Q48479409 | ||
The Hedgehog pathway promotes blood-brain barrier integrity and CNS immune quiescence | Q48797548 | ||
Claudin-1, claudin-2 and claudin-11 are present in tight junctions of choroid plexus epithelium of the mouse | Q48828901 | ||
Brain endothelium lack one of two pathways of P-selectin-mediated neutrophil adhesion. | Q48829755 | ||
Dendritic cells permit immune invasion of the CNS in an animal model of multiple sclerosis. | Q49014751 | ||
Alpha-synuclein in colonic submucosa in early untreated Parkinson's disease | Q49037483 | ||
Inhibition of antigen-stimulated effector T cells by human cerebrospinal fluid | Q49068413 | ||
Decreased levels of intrathecal interleukin 1 receptor antagonist in Alzheimer's disease | Q49245290 | ||
Alterations of the intestinal barrier in patients with autism spectrum disorders and in their first-degree relatives. | Q50302739 | ||
Evaluation of Intestinal Function in Children With Autism and Gastrointestinal Symptoms | Q50306071 | ||
Impaired brain angiogenesis and neuronal apoptosis induced by conditional homozygous inactivation of vascular endothelial growth factor. | Q51019927 | ||
Astrocytes induce blood–brain barrier properties in endothelial cells | Q57318253 | ||
Increased intestinal permeability precedes clinical onset of type 1 diabetes | Q79211266 | ||
Retinal and ciliary body pigment epithelium suppress activation of T lymphocytes via transforming growth factor beta | Q80332034 | ||
Oral tolerance can be established via gap junction transfer of fed antigens from CX3CR1⁺ macrophages to CD103⁺ dendritic cells | Q87163156 | ||
Blood-retinal barrier in hypoxic ischaemic conditions: basic concepts, clinical features and management | Q37304800 | ||
Perivascular spaces and the two steps to neuroinflammation | Q37329042 | ||
Immune privilege or privileged immunity? | Q37349741 | ||
Incidence of gastrointestinal symptoms in children with autism: a population-based study | Q37353825 | ||
Tissue factor and PAR1 promote microbiota-induced intestinal vascular remodelling | Q37451950 | ||
Blood-brain barrier and intestinal epithelial barrier alterations in autism spectrum disorders | Q37456857 | ||
The gut immune barrier and the blood-brain barrier: are they so different? | Q37616357 | ||
Immune privilege of the CNS is not the consequence of limited antigen sampling | Q37653497 | ||
Capture, crawl, cross: the T cell code to breach the blood-brain barriers | Q38038445 | ||
Postbiotics: what else? | Q38070062 | ||
Extraintestinal manifestations and complications in IBD. | Q38120146 | ||
Barrier properties of cultured retinal pigment epithelium | Q38204565 | ||
The choroid plexuses and their impact on developmental neurogenesis | Q38266875 | ||
Intestinal mucosal tolerance and impact of gut microbiota to mucosal tolerance | Q38335183 | ||
Claudin-1, -2 and -3 Are Selectively Expressed in the Epithelia of the Choroid Plexus of the Mouse from Early Development and into Adulthood While Claudin-5 is Restricted to Endothelial Cells | Q38582363 | ||
Intestinal Dysbiosis, Gut Hyperpermeability and Bacterial Translocation: Missing Links Between Depression, Obesity and Type 2 Diabetes. | Q38964759 | ||
Gut Microbiota, Bacterial Translocation, and Interactions with Diet: Pathophysiological Links between Major Depressive Disorder and Non-Communicable Medical Comorbidities. | Q39018851 | ||
The movers and shapers in immune privilege of the CNS. | Q39090554 | ||
Impaired Amino Acid Transport at the Blood Brain Barrier Is a Cause of Autism Spectrum Disorder | Q39135788 | ||
Gastrointestinal problems in children with autism, developmental delays or typical development | Q34382693 | ||
Central nervous system perivascular cells are immunoregulatory cells that connect the CNS with the peripheral immune system | Q34398632 | ||
Pre-eclampsia and pregnancy-induced hypertension are associated with severe diabetic retinopathy in type 1 diabetes later in life | Q34407459 | ||
Host microbiota constantly control maturation and function of microglia in the CNS. | Q34478756 | ||
Zonulin upregulation is associated with increased gut permeability in subjects with type 1 diabetes and their relatives. | Q34518641 | ||
Angiogenic sprouting into neural tissue requires Gpr124, an orphan G protein-coupled receptor. | Q34582564 | ||
The mucus and mucins of the goblet cells and enterocytes provide the first defense line of the gastrointestinal tract and interact with the immune system | Q34798439 | ||
Immunological Markers for PML Prediction in MS Patients Treated with Natalizumab | Q34818048 | ||
Immunity to homologous grafted skin; the fate of skin homografts transplanted to the brain, to subcutaneous tissue, and to the anterior chamber of the eye. | Q34853757 | ||
Autistic disorder and gastrointestinal disease | Q34916579 | ||
Microbiota controls the homeostasis of glial cells in the gut lamina propria | Q35013616 | ||
Development of the choroid plexus and blood-CSF barrier | Q35140713 | ||
Human cerebrospinal fluid central memory CD4+ T cells: evidence for trafficking through choroid plexus and meninges via P-selectin. | Q35168188 | ||
The gut microbiota and developmental programming of the testis in mice | Q35223991 | ||
Direct evidence of Parkinson pathology spread from the gastrointestinal tract to the brain in rats | Q35313910 | ||
The gut microbiota influences blood-brain barrier permeability in mice | Q35413892 | ||
A review of the influence of aqueous humor on immunity | Q35620171 | ||
Role of the gastrointestinal ecosystem in the development of type 1 diabetes. | Q35624584 | ||
Chronic low level complement activation within the eye is controlled by intraocular complement regulatory proteins. | Q35750345 | ||
A gut-vascular barrier controls the systemic dissemination of bacteria. | Q35840463 | ||
ApoE deficiency compromises the blood brain barrier especially after injury. | Q35944147 | ||
The Central Nervous System and the Gut Microbiome. | Q36182979 | ||
Gut microbiota influences pathological angiogenesis in obesity-driven choroidal neovascularization | Q36196897 | ||
Gut Microbiota Regulate Motor Deficits and Neuroinflammation in a Model of Parkinson's Disease | Q36212145 | ||
Gut microbial metabolites limit the frequency of autoimmune T cells and protect against type 1 diabetes | Q36323689 | ||
Complexity and developmental changes in the expression pattern of claudins at the blood-CSF barrier. | Q36353414 | ||
See no evil, hear no evil, do no evil: the lessons of immune privilege | Q36426813 | ||
Plasmacytoid dendritic cells mediate oral tolerance | Q36534744 | ||
Ocular autoimmunity: the price of privilege? | Q36593726 | ||
Immune privilege in the gut: the establishment and maintenance of non-responsiveness to dietary antigens and commensal flora | Q36593729 | ||
Fecal microbiota composition differs between children with β-cell autoimmunity and those without | Q36720600 | ||
Commensal microbiota is fundamental for the development of inflammatory pain. | Q36883155 | ||
Wnt/beta-catenin signaling controls development of the blood-brain barrier | Q36955697 | ||
P433 | issue | 12 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | cooperation | Q380962 |
P304 | page(s) | 761-773 | |
P577 | publication date | 2017-09-04 | |
P1433 | published in | Nature Reviews Immunology | Q43355 |
P1476 | title | Organ-specific protection mediated by cooperation between vascular and epithelial barriers | |
P478 | volume | 17 |
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