Viral-induced neuroinflammation: Different mechanisms converging to similar exacerbated glial responses
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[1] A. Lophatananon,et al. Investigation of the association between the antibody responses to neurotropic viruses and dementia outcomes in the UK Biobank , 2022, PloS one.
[2] J. Echevarria-Lima,et al. Lessons from the Cerebrospinal Fluid Analysis of HTLV-1-Infected Individuals: Biomarkers of Inflammation for HAM/TSP Development , 2022, Viruses.
[3] C. Ng,et al. Neuronal infection is a major pathogenetic mechanism and cause of fatalities in human acute Nipah virus encephalitis , 2022, Neuropathology and applied neurobiology.
[4] R. Mahieux,et al. Immunoprofiling of fresh HAM/TSP blood samples shows altered innate cell responsiveness , 2021, PLoS neglected tropical diseases.
[5] Marco Antonio de Melo Tavares de Lima,et al. Following the Clues: Usefulness of Biomarkers of Neuroinflammation and Neurodegeneration in the Investigation of HTLV-1-Associated Myelopathy Progression , 2021, Frontiers in Immunology.
[6] N. Dorrello,et al. Molecular Features of the Measles Virus Viral Fusion Complex That Favor Infection and Spread in the Brain , 2021, mBio.
[7] N. Messaddeq,et al. Hamster organotypic modeling of SARS-CoV-2 lung and brainstem infection , 2020, Nature Communications.
[8] M. Santos,et al. Health state utility values in people living with HTLV-1 and in patients with HAM/TSP: The impact of a neglected disease on the quality of life , 2020, PLoS neglected tropical diseases.
[9] K. Tyler,et al. The Role of Microglia during West Nile Virus Infection of the Central Nervous System , 2020, Vaccines.
[10] S. Salinas,et al. Neurocognitive impacts of arbovirus infections , 2020, Journal of Neuroinflammation.
[11] H. Keyvani,et al. The role of human herpesvirus-6 and inflammatory markers in the pathogenesis of multiple sclerosis , 2020, Journal of Neuroimmunology.
[12] R. Mahieux,et al. HTLV-1 infection of myeloid cells: from transmission to immune alterations , 2019, Retrovirology.
[13] B. Horvat,et al. Measles Encephalitis: Towards New Therapeutics , 2019, Viruses.
[14] J. Kuhn,et al. Nipah virus persists in the brains of nonhuman primate survivors. , 2019, JCI insight.
[15] R. Klein,et al. T cells promote microglia-mediated synaptic elimination and cognitive dysfunction during recovery from neuropathogenic flaviviruses , 2019, Nature Neuroscience.
[16] D. Gerlier,et al. Type I Interferon Receptor Signaling Drives Selective Permissiveness of Astrocytes and Microglia to Measles Virus during Brain Infection , 2019, Journal of Virology.
[17] Zhuangzhuang Chen,et al. The role of microglia in viral encephalitis: a review , 2019, Journal of neuroinflammation.
[18] F. Cosset,et al. Sensing of cell-associated HTLV by plasmacytoid dendritic cells is regulated by dense β-galactoside glycosylation , 2019, PLoS pathogens.
[19] W. Löscher,et al. Facets of Theiler’s Murine Encephalomyelitis Virus-Induced Diseases: An Update , 2019, International journal of molecular sciences.
[20] B. Eley,et al. Analysis of a Subacute Sclerosing Panencephalitis Genotype B3 Virus from the 2009-2010 South African Measles Epidemic Shows That Hyperfusogenic F Proteins Contribute to Measles Virus Infection in the Brain , 2018, Journal of Virology.
[21] R. Gallo,et al. Time to eradicate HTLV-1: an open letter to WHO , 2018, The Lancet.
[22] S. Perlman,et al. Microglia are required for protection against lethal coronavirus encephalitis in mice , 2018, The Journal of clinical investigation.
[23] A. Crawshaw,et al. Human T-cell lymphotropic virus (HTLV)-associated encephalopathy: an under-recognised cause of acute encephalitis? Case series and literature review , 2018, Journal of Neurology.
[24] G. Khan,et al. Epstein-Barr virus is present in the brain of most cases of multiple sclerosis and may engage more than just B cells , 2018, PloS one.
[25] S. Harakeh,et al. HTLV-1 Associated Neurological Disorders. , 2017, Current topics in medicinal chemistry.
[26] Christopher M. Bland,et al. Management of Viral Central Nervous System Infections: A Primer for Clinicians , 2017, Journal of central nervous system disease.
[27] Y. Yamano,et al. HTLV-1 induces a Th1-like state in CD4+ CCR4+ T cells that produces an inflammatory positive feedback loop via astrocytes in HAM/TSP , 2017, Journal of Neuroimmunology.
[28] M. Azarpazhooh,et al. Altered expression of CXCR3 and CCR6 and their ligands in HTLV‐1 carriers and HAM/TSP patients , 2017, Journal of medical virology.
[29] H. Feldmann,et al. Identifying Early Target Cells of Nipah Virus Infection in Syrian Hamsters , 2016, PLoS neglected tropical diseases.
[30] Roger N Gunn,et al. Evidence of Brain Inflammation in Patients with Human T-Lymphotropic Virus Type 1–Associated Myelopathy (HAM): A Pilot, Multimodal Imaging Study Using 11C-PBR28 PET, MR T1-Weighted, and Diffusion-Weighted Imaging , 2016, The Journal of Nuclear Medicine.
[31] Toshihide Yamashita,et al. Microglia in central nervous system repair after injury. , 2016, Journal of biochemistry.
[32] Peixiang Ni,et al. Detection of virus in CSF from the cases with meningoencephalitis by next-generation sequencing , 2016, Journal of NeuroVirology.
[33] I. Marriott,et al. RIG‐I is required for VSV‐induced cytokine production by murine glia and acts in combination with DAI to initiate responses to HSV‐1 , 2015, Glia.
[34] R. Leak,et al. Demyelination as a rational therapeutic target for ischemic or traumatic brain injury , 2015, Experimental Neurology.
[35] L. Enquist,et al. Axonal spread of neuroinvasive viral infections. , 2015, Trends in microbiology.
[36] I. Lizasoain,et al. Rational modulation of the innate immune system for neuroprotection in ischemic stroke , 2015, Front. Neurosci..
[37] F. Cosset,et al. Heparan Sulfate-Dependent Enhancement of Henipavirus Infection , 2015, mBio.
[38] B. Horvat,et al. Henipavirus pathogenesis and antiviral approaches , 2015, Expert review of anti-infective therapy.
[39] M. Yoneyama,et al. Viral RNA detection by RIG-I-like receptors. , 2015, Current opinion in immunology.
[40] Yuetsu Tanaka,et al. Visualization of HTLV-1–Specific Cytotoxic T Lymphocytes in the Spinal Cords of Patients With HTLV-1–Associated Myelopathy/Tropical Spastic Paraparesis , 2015, Journal of neuropathology and experimental neurology.
[41] G. Barton,et al. Emerging principles governing signal transduction by pattern-recognition receptors. , 2015, Cold Spring Harbor perspectives in biology.
[42] Suhailah Abdullah,et al. Henipavirus encephalitis. , 2014, Handbook of clinical neurology.
[43] D. Sulzer,et al. MHC-I expression renders catecholaminergic neurons susceptible to T-cell-mediated degeneration , 2014, Nature Communications.
[44] J. Brady,et al. Gem-Induced Cytoskeleton Remodeling Increases Cellular Migration of HTLV-1-Infected Cells, Formation of Infected-to-Target T-Cell Conjugates and Viral Transmission , 2014, PLoS pathogens.
[45] A. Utsunomiya,et al. Positive feedback loop via astrocytes causes chronic inflammation in virus-associated myelopathy. , 2013, Brain : a journal of neurology.
[46] V. Perry,et al. Microglia and macrophages of the central nervous system: the contribution of microglia priming and systemic inflammation to chronic neurodegeneration , 2013, Seminars in Immunopathology.
[47] V. Borisevich,et al. Pathogenesis of Hendra and Nipah virus infection in humans. , 2013, Journal of infection in developing countries.
[48] H. Feldmann,et al. Rapid Nipah virus entry into the central nervous system of hamsters via the olfactory route , 2012, Scientific Reports.
[49] C. Richardson,et al. Nectin 4 is the epithelial cell receptor for measles virus. , 2012, Trends in microbiology.
[50] P. Kubes,et al. Immune surveillance in the central nervous system , 2012, Nature Neuroscience.
[51] M. Prevost,et al. Transcytosis of HTLV-1 across a tight human epithelial barrier and infection of subepithelial dendritic cells. , 2012, Blood.
[52] I. Marriott,et al. Viral CNS infections: role of glial pattern recognition receptors in neuroinflammation , 2012, Front. Microbio..
[53] N. Beeching,et al. Management of suspected viral encephalitis in adults--Association of British Neurologists and British Infection Association National Guidelines. , 2012, The Journal of infection.
[54] V. Guillaume,et al. Lethal Nipah Virus Infection Induces Rapid Overexpression of CXCL10 , 2012, PloS one.
[55] H. Weingartl,et al. Nipah Virus Infects Specific Subsets of Porcine Peripheral Blood Mononuclear Cells , 2012, PloS one.
[56] M. David,et al. Immunomodulatory functions of type I interferons , 2012, Nature Reviews Immunology.
[57] Joshua A. Smith,et al. Role of pro-inflammatory cytokines released from microglia in neurodegenerative diseases , 2012, Brain Research Bulletin.
[58] P. Chan,et al. Neuroprotection by Interleukin-6 Is Mediated by Signal Transducer and Activator of Transcription 3 and Antioxidative Signaling in Ischemic Stroke , 2011, Stroke.
[59] K. Cichutek,et al. Adherens junction protein nectin-4 (PVRL4) is the epithelial receptor for measles virus , 2011, Nature.
[60] R. Giffard,et al. Astrocytes: targets for neuroprotection in stroke. , 2011, Central nervous system agents in medicinal chemistry.
[61] F. Cosset,et al. Nipah Virus Uses Leukocytes for Efficient Dissemination within a Host , 2011, Journal of Virology.
[62] A. Tolkovsky,et al. Inhibition of Microglial Phagocytosis Is Sufficient To Prevent Inflammatory Neuronal Death , 2011, The Journal of Immunology.
[63] M. Nagai,et al. Human T-cell lymphotropic virus type I and neurological diseases , 2003, Journal of NeuroVirology.
[64] H. Neumann,et al. Protective effects of microglia in multiple sclerosis , 2010, Experimental Neurology.
[65] V. Grdzelishvili,et al. Vesicular stomatitis virus infects resident cells of the central nervous system and induces replication-dependent inflammatory responses. , 2010, Virology.
[66] Richard M. Page,et al. Microglial Cx3cr1 knockout prevents neuron loss in a mouse model of Alzheimer's disease , 2010, Nature Neuroscience.
[67] C. Long-Smith,et al. The influence of microglia on the pathogenesis of Parkinson's disease , 2009, Progress in Neurobiology.
[68] A. Pol. Viral Infection Leading to Brain Dysfunction: More Prevalent Than Appreciated? , 2009, Neuron.
[69] A. Becker,et al. CD8+ T-cell clones dominate brain infiltrates in Rasmussen encephalitis and persist in the periphery. , 2009, Brain : a journal of neurology.
[70] Aidan MacNamara,et al. The Avidity and Lytic Efficiency of the CTL Response to HTLV-11 , 2009, The Journal of Immunology.
[71] G. Zoppo. Inflammation and the neurovascular unit in the setting of focal cerebral ischemia , 2009, Neuroscience.
[72] P. Couraud,et al. Alteration of Blood–Brain Barrier Integrity by Retroviral Infection , 2008, PLoS pathogens.
[73] R. Garg. Subacute sclerosing panencephalitis , 2008, Journal of Neurology.
[74] Charles R. M. Bangham. HTLV-1 infection: role of CTL efficiency , 2008, Blood.
[75] M. Ekstrand,et al. The alpha-herpesviruses: molecular pathfinders in nervous system circuits. , 2008, Trends in molecular medicine.
[76] S. Miller,et al. Glial toll-like receptor signaling in central nervous system infection and autoimmunity , 2008, Brain, Behavior, and Immunity.
[77] R. Diefenbach,et al. Transport and egress of herpes simplex virus in neurons , 2008, Reviews in medical virology.
[78] J. Oliveira-Filho,et al. Brain magnetic resonance imaging white matter lesions are frequent in HTLV-I carriers and do not discriminate from HAM/TSP. , 2007, AIDS research and human retroviruses.
[79] Tom Solomon,et al. Viral encephalitis: a clinician’s guide , 2007, Practical Neurology.
[80] J. Sejvar. The long-term outcomes of human West Nile virus infection. , 2007, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.
[81] J. Hiscott. Triggering the Innate Antiviral Response through IRF-3 Activation* , 2007, Journal of Biological Chemistry.
[82] Benhur Lee. Envelope–Receptor Interactions in Nipah Virus Pathobiology , 2007, Annals of the New York Academy of Sciences.
[83] S. Jacobson,et al. Differentiation of HAM/TSP from patients with multiple sclerosis infected with HTLV-I , 2007, Neurology.
[84] T. Kielian. Toll‐like receptors in central nervous system glial inflammation and homeostasis , 2006, Journal of neuroscience research.
[85] P. Monk,et al. Microglia as potential contributors to motor neuron injury in amyotrophic lateral sclerosis , 2005, Glia.
[86] Y. Berhane,et al. Invasion of the Central Nervous System in a Porcine Host by Nipah Virus , 2005, Journal of Virology.
[87] T. Hökfelt,et al. A role for MHC class I molecules in synaptic plasticity and regeneration of neurons after axotomy. , 2004, Proceedings of the National Academy of Sciences of the United States of America.
[88] R. Howard,et al. Factors influencing PCR detection of viruses in cerebrospinal fluid of patients with suspected CNS infections , 2004, Journal of Neurology, Neurosurgery & Psychiatry.
[89] C. Lim,et al. Neuropsychiatric sequelae of Nipah virus encephalitis. , 2004, The Journal of neuropsychiatry and clinical neurosciences.
[90] F. Mostashari,et al. Long-Term Prognosis for Clinical West Nile Virus Infection , 2004, Emerging infectious diseases.
[91] P. Spano,et al. Prevention of neuron and oligodendrocyte degeneration by interleukin-6 (IL-6) and IL-6 receptor/IL-6 fusion protein in organotypic hippocampal slices , 2004, Molecular and Cellular Neuroscience.
[92] S. Sato,et al. Detection of human herpesvirus-6 in mesial temporal lobe epilepsy surgical brain resections , 2003, Neurology.
[93] P. Loth,et al. A golden hamster model for human acute Nipah virus infection. , 2003, The American journal of pathology.
[94] B. Anlar,et al. Acute Disseminated Encephalomyelitis in Children: Outcome and Prognosis , 2003, Neuropediatrics.
[95] K. Wong,et al. Nipah encephalitis outbreak in Malaysia. , 2003, Annals of the Academy of Medicine, Singapore.
[96] J. Guarner,et al. Nipah virus infection: pathology and pathogenesis of an emerging paramyxoviral zoonosis. , 2002, The American journal of pathology.
[97] R. Ravid,et al. Broad Expression of Toll‐Like Receptors in the Human Central Nervous System , 2002, Journal of neuropathology and experimental neurology.
[98] M. Kitajima,et al. Central nervous system lesions in adult T-cell leukaemia: MRI and pathology , 2002, Neuroradiology.
[99] K. Tan,et al. Relapsed and late‐onset Nipah encephalitis , 2002, Annals of neurology.
[100] L. Enquist,et al. Directional spread of an α-herpesvirus in the nervous system , 2002 .
[101] E. Benveniste,et al. Immune function of astrocytes , 2001, Glia.
[102] M. Wong,et al. Late presentation of Nipah virus encephalitis and kinetics of the humoral immune response , 2001, Journal of neurology, neurosurgery, and psychiatry.
[103] U. Parashar,et al. Nipah virus among military personnel involved in pig culling during an outbreak of encephalitis in Malaysia, 1998-1999. , 2001, Emerging infectious diseases.
[104] M. Dailey,et al. Dynamics of microglial activation: A confocal time‐lapse analysis in hippocampal slices , 2001, Glia.
[105] S. Jacobson,et al. Viruses and multiple sclerosis. , 2012, Viral immunology.
[106] K. Chua,et al. Clinical features of Nipah virus encephalitis among pig farmers in Malaysia. , 2000, The New England journal of medicine.
[107] W. Bellini,et al. Measles inclusion-body encephalitis caused by the vaccine strain of measles virus. , 1999, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.
[108] Y. Itoyama,et al. [A case of encephalomyeloneuritis and HTLV-I infection]. , 1999, No to shinkei = Brain and nerve.
[109] E. Castaños-Vélez,et al. Measles virus antigen in macrophage/microglial cells and astrocytes of subacute sclerosing panencephalitis , 1998, APMIS : acta pathologica, microbiologica, et immunologica Scandinavica.
[110] J. Durkin,et al. Stimulation of glutamate uptake and Na, K‐ATPase activity in rat astrocytes exposed to ischemia‐like insults , 1997, Glia.
[111] L. Lampson. Interpreting MHC class I expression and class I/class II reciprocity in the CNS: Reconciling divergent findings , 1995, Microscopy research and technique.
[112] P. A. Schad,et al. Plaque-associated expression of human herpesvirus 6 in multiple sclerosis. , 1995, Proceedings of the National Academy of Sciences of the United States of America.
[113] R. Jacobson,et al. Failure to reach the goal of measles elimination. Apparent paradox of measles infections in immunized persons. , 1994, Archives of internal medicine.
[114] N. Tachi,et al. Acute disseminated encephalomyelitis following HTLV-I associated myelopathy , 1992, Journal of the Neurological Sciences.
[115] S. Izumo,et al. Neuropathology of HTLV‐I‐Associated Myelopathy—A Report of Two Autopsy Cases— , 1992, Acta paediatrica Japonica : Overseas edition.
[116] L. Samkoff,et al. Recurrent encephalopathy and seizures in a US native with HTLV‐I‐associated myelopathy/tropical spastic paraparesis , 1992, Neurology.
[117] F. Fonnum,et al. Persistent changes in behaviour and brain serotonin during ageing in rats subjected to infant nasal virus infection , 1992, Neurobiology of Aging.
[118] A. Fauci,et al. Circulating CD8+ cytotoxic T lymphocytes specific for HTLV-I pX in patients with HTLV-I associated neurological disease , 1990, Nature.
[119] S. Araga,et al. Subacute meningoencephalitis associated with human T‐lymphotrophic virus Type I (HTLV‐I) Report of a case , 1989, Acta neurologica Scandinavica.
[120] J. Hess,et al. Immune Responses in the Central Nervous System , 1987, Toxicologic pathology.
[121] F. Barin,et al. ANTIBODIES TO HUMAN T-LYMPHOTROPIC VIRUS TYPE-I IN PATIENTS WITH TROPICAL SPASTIC PARAPARESIS , 1985, The Lancet.