Elena Brambilla

ORCID: 0000-0003-1399-2128
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About
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Research Areas
  • Multiple Sclerosis Research Studies
  • Neurogenesis and neuroplasticity mechanisms
  • Neuroinflammation and Neurodegeneration Mechanisms
  • Systemic Lupus Erythematosus Research
  • Immunotherapy and Immune Responses
  • Nerve injury and regeneration
  • Peripheral Neuropathies and Disorders
  • Mesenchymal stem cell research
  • T-cell and Retrovirus Studies
  • T-cell and B-cell Immunology
  • Immune Cell Function and Interaction
  • Myasthenia Gravis and Thymoma
  • Cytokine Signaling Pathways and Interactions
  • Viral Infections and Immunology Research
  • Eosinophilic Disorders and Syndromes
  • Polyomavirus and related diseases
  • Cytomegalovirus and herpesvirus research
  • Immune Response and Inflammation
  • Chronic Lymphocytic Leukemia Research
  • Tumors and Oncological Cases
  • Monoclonal and Polyclonal Antibodies Research
  • Pluripotent Stem Cells Research
  • Spinal Cord Injury Research
  • Axon Guidance and Neuronal Signaling
  • Immune cells in cancer

Vita-Salute San Raffaele University
2003-2024

Ca' Foncello Hospital
2024

University of Padua
2022-2024

Hôpital Nord
2024

Centre Hospitalier Universitaire Amiens-Picardie
2024

Istituti di Ricovero e Cura a Carattere Scientifico
2019-2023

Istituto di Ricovero e Cura a Carattere Scientifico San Raffaele
2019-2023

San Raffaele University of Rome
1994-2022

Neuroscience Institute
2014-2022

Istituti Clinici Scientifici Maugeri
2022

Recent evidence suggests that neural stem/precursor cells (NPCs) promote recovery in animal models with delayed neuronal death via a number of indirect bystander effects. A comprehensive knowledge how transplanted NPCs exert their therapeutic effects is still lacking. Here, we investigated the transplantation adult syngenic NPCs--injected intravenously 72 h after transient middle cerebral artery occlusion--on neurological recovery, histopathology and gene expression. NPC-transplanted mice...

10.1093/brain/awp174 article EN Brain 2009-07-16

Abstract Innovative pro-regenerative treatment strategies for progressive multiple sclerosis (PMS), combining neuroprotection and immunomodulation, represent an unmet need. Neural precursor cells (NPCs) transplanted in animal models of have shown preclinical efficacy by promoting remyelination releasing molecules sustaining trophic support neural plasticity. Here we present the results STEMS, a prospective, therapeutic exploratory, non-randomized, open-label, single-dose-finding phase 1...

10.1038/s41591-022-02097-3 article EN cc-by Nature Medicine 2023-01-01

Endogenous neural stem/precursor cells (NPCs) are considered a functional reservoir for promoting tissue homeostasis and repair after injury, therefore regenerative strategies that mobilize these have recently been proposed. Despite evidence of increased neurogenesis upon acute inflammatory insults (e.g. ischaemic stroke), the plasticity endogenous brain stem cell compartment in chronic CNS disorders remains poorly characterized. Here we show persistent inflammation, induced by immune...

10.1093/brain/awn198 article EN cc-by-nc Brain 2008-08-30

Transplanted neural stem/precursor cells possess peculiar therapeutic plasticity and can simultaneously instruct several mechanisms in addition to cell replacement. Here, we interrogated the of after their focal implantation severely contused spinal cord. We injected syngeneic at proximal distal ends mouse cord analysed locomotor functions relevant secondary pathological events mice, fate transplanted cells, gene expression inflammatory infiltration injured site. used two different doses...

10.1093/brain/awr339 article EN Brain 2012-01-23

Transplanted neural stem/precursor cells (NPCs) display peculiar therapeutic plasticity in vivo. Although the replacement of was first expected as prime mechanism stem regenerative medicine, it is now clear that transplanted NPCs simultaneously instruct several mechanisms, among which might not necessarily prevail. A comprehensive understanding mechanism(s) by exert their lacking. This study designed a preclinical approach to test feasibility human NPC transplantation an outbreed nonhuman...

10.1002/ana.21745 article EN Annals of Neurology 2009-05-11

The systemic injection of neural stem/precursor cells (NPCs) provides remarkable amelioration the clinico-pathological features experimental autoimmune encephalomyelitis (EAE). This is dependent on capacity transplanted NPCs to engage concurrent mechanisms action within specific microenvironments in vivo. Among a wide range therapeutic actions alternative cell replacement, neuroprotective and immune modulatory capacities have been described. However, lacking detailed understanding by which...

10.1371/journal.pone.0005959 article EN cc-by PLoS ONE 2009-06-18

Abstract The exclusive detrimental role of proinflammatory cytokines in demyelinating diseases the CNS, such as multiple sclerosis, is controversial. Here we show that intrathecal delivery an HSV-1-derived vector engineered with mouse IFN-γ gene leads to persistent (up 4 wk) CNS production and inhibits course a chronic-progressive form experimental autoimmune encephalomyelitis (EAE) induced C57BL/6 mice by myelin oligodendrocyte glycoprotein (MOG)35–55. Mice treated IFN-γ-containing before...

10.4049/jimmunol.167.3.1821 article EN The Journal of Immunology 2001-08-01

Eliciting the in situ accumulation and persistence patterns of stem cells following transplantation would provide critical insight toward human translation cell-based therapies. To this end, we have developed a strategy to track neural stem/precursor (NPCs) vivo using magnetic resonance (MR) imaging. Initially, evaluated three different human-grade superparamagnetic iron oxide particles for labeling NPCs found optimal be achieved with Resovist. Next, carried out experiments monitor...

10.1634/stemcells.2007-0037 article EN Stem Cells 2007-06-28

Abstract Invariant NKT (inv. NKT) cells co‐express an invariant α β T cell receptor and the NK NK1.1 and, upon CD1d‐restricted recognition of glycosphingolipid antigen α‐galactosyl ceramide (αGalCer), secrete large amounts regulatory cytokines. We investigated whether αGalCer‐dependent activation inv. protects from experimental autoimmune encephalomyelitis (EAE), immune‐mediated disease central nervous system mimicking multiple sclerosis, induced in C57BL/6 mice by myelin oligodendrocyte...

10.1002/eji.200323885 article EN European Journal of Immunology 2003-06-02

IL-12 has been shown to be involved in the pathogenesis of Th1-mediated autoimmune diseases, but its role antibody-mediated pathologies is still unclear. We investigated effects exogenous and endogenous experimental myasthenia gravis (EAMG). EAMG an animal model for gravis, a T cell-dependent, autoantibody-mediated disorder neuromuscular transmission caused by antibodies muscle nicotinic acetylcholine receptor (AChR). Administration with Torpedo AChR (ToAChR) C57BL/6 (B6) mice resulted...

10.1002/(sici)1521-4141(199808)28:08<2487::aid-immu2487>3.0.co;2-y article EN European Journal of Immunology 1998-08-01

The functional significance of adult neural stem and progenitor cells in hippocampal-dependent learning memory has been well documented. Although the subventricular zone are known to migrate to, maintain reorganize olfactory bulb, it is less clear whether they functionally required for other processes. Using a conditional transgenic mouse model, selective ablation induced dramatic increase morbidity mortality central nervous system disorders characterized by excitotoxicity-induced cell death...

10.1093/brain/aws194 article EN Brain 2012-09-24

Myelin loss occurring in demyelinating diseases, including multiple sclerosis, is the leading cause of long-lasting neurological disability adults. While endogenous remyelination, driven by resident oligodendrocyte precursor cells (OPCs), might partially compensate myelin early phases disorders, this spontaneous reparative potential fails at later stages. To investigate cellular mechanisms sustaining remyelination we focused our attention on neural (eNPCs) located within subventricular zone...

10.1523/jneurosci.0227-18.2019 article EN cc-by Journal of Neuroscience 2019-05-28

Background There are two generally accepted strategies for treating multiple sclerosis (MS), preventing central nervous system (CNS) damage indirectly through immunomodulatory interventions and/or repairing CNS by promoting remyelination. Both approaches also provide neuroprotection since they can prevent, or directly, axonal damage. Objective Recent experimental and clinical evidence indicates that the novel drug laquinimod exert a neuroprotective role in MS. Whether laquinimod-mediated is...

10.1177/1352458512469698 article EN Multiple Sclerosis Journal 2012-12-11

In multiple sclerosis, the pathological interaction between autoreactive Th cells and mononuclear phagocytes in CNS drives initiation maintenance of chronic neuroinflammation. Here, we found that intrathecal transplantation neural stem/precursor (NPCs) mice with experimental autoimmune encephalomyelitis (EAE) impairs accumulation inflammatory monocyte-derived (MCs) CNS, leading to improved clinical outcome. Secretion IL-23, IL-1, TNF-α, cytokines required for terminal differentiation cells,...

10.1172/jci92387 article EN Journal of Clinical Investigation 2017-09-24

The role of central nervous system (CNS) glia in sustaining self-autonomous inflammation and driving clinical progression multiple sclerosis (MS) is gaining scientific interest. We applied a single transcription factor (SOX10)-based protocol to accelerate oligodendrocyte differentiation from human induced pluripotent stem cell (hiPSC)-derived neural precursor cells, generating self-organizing forebrain organoids. These organoids include neurons, astrocytes, oligodendroglia, hiPSC-derived...

10.1016/j.xcrm.2024.101680 article EN cc-by-nc-nd Cell Reports Medicine 2024-08-01

Human herpesvirus 6 (HHV-6) and HHV-7 are closely related DNA viruses, sharing biologic antigenic properties an overlapping genome organization.1,2 Primary infections with HHV-6 and, in some cases, cause exanthem subitum or fever, without rash.1,2 Major pathologies include reactivation immunocompromised individuals. An association between active infection MS was proposed based on detection of viral antigen oligodendrocytes surrounding plaques,3 sequences sera,4 circulating anti-HHV-6...

10.1212/wnl.53.6.1367-a article EN Neurology 1999-10-01

The role of central nervous system (CNS) glia in sustaining self-autonomous inflammation and driving clinical progression multiple sclerosis (MS) is gaining scientific interest. We applied a single transcription factor (

10.1101/2024.06.20.597748 preprint EN bioRxiv (Cold Spring Harbor Laboratory) 2024-06-24
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