Riccardo Cassiani Ingoni

Summary

Affiliation: National Institutes of Health
Country: USA

Publications

  1. ncbi Disease progression after bone marrow transplantation in a model of multiple sclerosis is associated with chronic microglial and glial progenitor response
    Riccardo Cassiani-Ingoni
    Neuroimmunology Branch, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD, USA
    J Neuropathol Exp Neurol 66:637-49. 2007
  2. ncbi Borrelia burgdorferi Induces TLR1 and TLR2 in human microglia and peripheral blood monocytes but differentially regulates HLA-class II expression
    Riccardo Cassiani-Ingoni
    Cellular Immunology Section, Neuroimmunology Branch, National Institute of Neurological Disorders and Stroke, Bethesda, MD 20892, USA
    J Neuropathol Exp Neurol 65:540-8. 2006
  3. ncbi Cytoplasmic translocation of Olig2 in adult glial progenitors marks the generation of reactive astrocytes following autoimmune inflammation
    Riccardo Cassiani-Ingoni
    Cellular Immunology Section, Neuroimmunology Branch, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD 20892, USA
    Exp Neurol 201:349-58. 2006
  4. ncbi Thymic output generates a new and diverse TCR repertoire after autologous stem cell transplantation in multiple sclerosis patients
    Paolo A Muraro
    Neuroimmunology Branch, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD 20892, USA
    J Exp Med 201:805-16. 2005
  5. ncbi Evidence that nucleocytoplasmic Olig2 translocation mediates brain-injury-induced differentiation of glial precursors to astrocytes
    Tim Magnus
    Laboratory of Neurosciences, National Institute on Aging Intramural Research Program, National Institutes of Health, Baltimore, Maryland 21224, USA
    J Neurosci Res 85:2126-37. 2007
  6. ncbi Clonotypic analysis of cerebrospinal fluid T cells during disease exacerbation and remission in a patient with multiple sclerosis
    Paolo A Muraro
    Neuroimmunology Branch, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bldg 10, Room 5B16, 10 Center Dr MSC1400 Bethesda, MD 20892 1400, USA
    J Neuroimmunol 171:177-83. 2006
  7. ncbi CD45-positive blood cells give rise to uterine epithelial cells in mice
    Andras Bratincsak
    National Institute of Mental Health, Bethesda, Maryland, USA
    Stem Cells 25:2820-6. 2007
  8. ncbi CD46 on glial cells can function as a receptor for viral glycoprotein-mediated cell-cell fusion
    Riccardo Cassiani-Ingoni
    Neuroimmunology Branch, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD 20892, USA
    Glia 52:252-8. 2005
  9. ncbi Hematopoietic stem cell transplantation for multiple sclerosis: current status and future challenges
    Paolo A Muraro
    Neuroimmunology Branch, National Institute of Neurological Diseases and Stroke, National Institutes of Health, MSC1400 Bethesda, MD 20892-1400, USA
    Curr Opin Neurol 16:299-305. 2003
  10. ncbi Variant-specific tropism of human herpesvirus 6 in human astrocytes
    Donatella Donati
    Viral Immunology Section, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD 20892, USA
    J Virol 79:9439-48. 2005

Collaborators

Detail Information

Publications11

  1. ncbi Disease progression after bone marrow transplantation in a model of multiple sclerosis is associated with chronic microglial and glial progenitor response
    Riccardo Cassiani-Ingoni
    Neuroimmunology Branch, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD, USA
    J Neuropathol Exp Neurol 66:637-49. 2007
    ..Our data indicate that reactivation of a local inflammatory process after BMT is sustained predominantly by endogenous microglia/macrophages...
  2. ncbi Borrelia burgdorferi Induces TLR1 and TLR2 in human microglia and peripheral blood monocytes but differentially regulates HLA-class II expression
    Riccardo Cassiani-Ingoni
    Cellular Immunology Section, Neuroimmunology Branch, National Institute of Neurological Disorders and Stroke, Bethesda, MD 20892, USA
    J Neuropathol Exp Neurol 65:540-8. 2006
    ..burgdorferi can elicit opposite immunoregulatory effects in blood and in brain immune cells, which could play a role in the different susceptibility of these compartments to infection...
  3. ncbi Cytoplasmic translocation of Olig2 in adult glial progenitors marks the generation of reactive astrocytes following autoimmune inflammation
    Riccardo Cassiani-Ingoni
    Cellular Immunology Section, Neuroimmunology Branch, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD 20892, USA
    Exp Neurol 201:349-58. 2006
    ..Together, these data ascribe a pivotal role to Olig2+ glial precursor cells in the adult CNS, linking autoimmune inflammation and glial scar formation...
  4. ncbi Thymic output generates a new and diverse TCR repertoire after autologous stem cell transplantation in multiple sclerosis patients
    Paolo A Muraro
    Neuroimmunology Branch, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD 20892, USA
    J Exp Med 201:805-16. 2005
    ....
  5. ncbi Evidence that nucleocytoplasmic Olig2 translocation mediates brain-injury-induced differentiation of glial precursors to astrocytes
    Tim Magnus
    Laboratory of Neurosciences, National Institute on Aging Intramural Research Program, National Institutes of Health, Baltimore, Maryland 21224, USA
    J Neurosci Res 85:2126-37. 2007
    ..In contrast, neural stem cells and neuronal progenitor cells appear to play only a minor role in the injured adult CNS...
  6. ncbi Clonotypic analysis of cerebrospinal fluid T cells during disease exacerbation and remission in a patient with multiple sclerosis
    Paolo A Muraro
    Neuroimmunology Branch, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bldg 10, Room 5B16, 10 Center Dr MSC1400 Bethesda, MD 20892 1400, USA
    J Neuroimmunol 171:177-83. 2006
    ..CDR3 spectratyping is a valuable approach to identify disease-associated T cells in the CNS...
  7. ncbi CD45-positive blood cells give rise to uterine epithelial cells in mice
    Andras Bratincsak
    National Institute of Mental Health, Bethesda, Maryland, USA
    Stem Cells 25:2820-6. 2007
    ....
  8. ncbi CD46 on glial cells can function as a receptor for viral glycoprotein-mediated cell-cell fusion
    Riccardo Cassiani-Ingoni
    Neuroimmunology Branch, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD 20892, USA
    Glia 52:252-8. 2005
    ..These data suggest a mechanism that involves cell-cell fusion by which certain viruses could spread the infection from the periphery to the cells in the nervous system...
  9. ncbi Hematopoietic stem cell transplantation for multiple sclerosis: current status and future challenges
    Paolo A Muraro
    Neuroimmunology Branch, National Institute of Neurological Diseases and Stroke, National Institutes of Health, MSC1400 Bethesda, MD 20892-1400, USA
    Curr Opin Neurol 16:299-305. 2003
    ..Recent advances on the migratory potential and on the differentiation plasticity of hematopoietic stem cells have opened new opportunities for remyelination and axonal repair strategies for multiple sclerosis...
  10. ncbi Variant-specific tropism of human herpesvirus 6 in human astrocytes
    Donatella Donati
    Viral Immunology Section, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD 20892, USA
    J Virol 79:9439-48. 2005
    ..Astrocytes may be an important reservoir for this virus in which differential tropism of HHV-6A and HHV-6B may be associated with different disease outcomes...
  11. ncbi Revisiting the astrocyte-oligodendrocyte relationship in the adult CNS
    Jessica Carmen
    Laboratory of Neurosciences, National Institute on Aging Intramural Research Program, NIH, Baltimore, MD 21224, USA
    Prog Neurobiol 82:151-62. 2007
    ..Ideally, better understanding the origin of new glial cells in the injured CNS will facilitate the development of therapeutics targeted to alter the glial response in a beneficial way...