A New in Vitro Human Model to Study MOGAD Physiopathology: The MOGAXON Project
Principal Investigators | Álvaro Cobo-Calvo, MD, PhD and Juan Antonio García León
Institutions | Multiple Sclerosis Center of Catalonia (CEMCAT), Vall d’Hebron and University of Malaga (Spain)
Aim | To establish a new in vitro human model comprising an all-human induced pluripotent stem cells (hiPSC)-derived oligodendrocytes co-cultured with neurons that could serve as the bases to reveal new MOGAD-specific mechanisms, a previous essential step before developing novel therapeutic strategies.
Basic CSF parameters and MRZ reaction help in differentiating MOG antibody-associated autoimmune disease versus multiple sclerosis
Principal Investigators | Benjamin Vlad,Ina Reichen,Stephan Neidhart,Marc Hilty, Dimitra Lekaditi,Christine Heuer, Amanda Eisele, Mario Ziegler, Markus Reindl, Andreas Lutterotti, Axel Regeniter and Ilijas Jelcic
Institution | University Hospital Zurich (Switzerland), University of Zurich (Switzerland), Medizinische Universität Innsbruck (Austria), Neurozentrum Bellevue (Switzerland), and medica Medizinische Laboratorien Dr. F. Kaeppeli (Switzerland)
Grant Type | In 2023, TSF sponsored the publication fees of 12 MOGAD-related articles to be published in Frontiers in Neurology
Delimiting MOGAD as a disease entity using translational imaging
Principal Investigators | Frederike C. Oertel, Maria Hastermann, and Friedemann Paul
Institution | Charité – Universitätsmedizin Berlin (Germany)
Aim | This article reviews suitable animal models for translational MOGAD research and the current state and prospect of translational imaging in MOGAD.
Grant Type | In 2023, TSF sponsored the publication fees of 12 MOGAD-related articles to be published in Frontiers in Neurology
Epidemiology of MOGAD: A review of prevalence and incidence worldwide
Principal Investigators | Jyh Yung Hor and Kazuo Fujihara
Institution | Penang General Hospital (Malaysia), Fukushima Medical University (Japan) and Multiple Sclerosis & Neuromyelitis Optica Center, Southern TOHOKU Research Institute for Neuroscience (Japan)
Grant Type | In 2023, TSF sponsored the publication fees of 12 MOGAD-related articles to be published in Frontiers in Neurology
Helicobacter pylori infection may influence prevalence and disease course in MOGAD similar to MS but not AQP4-IgG associated NMOSD
Principal Investigators | Chaithra Malli, Lekha Pandit, Anita D’Cunha and Akshatha Sudhir
Institution | Nitte University (India)
Aim | To evaluate frequency of Hp IgG among patients with MOGAD, MS, NMOSD and matched controls and its effect on disease course. To ascertain whether childhood socio economic factors were linked to prevalence of Hp infection.
Grant Type | In 2023, TSF sponsored the publication fees of 12 MOGAD-related articles to be published in Frontiers in Neurology
High Level of Agreement in a Fixed vs Live Cell-Based Assay for Antibodies to MOG in a Real-World Clinical Laboratory Setting
Principal Investigators | Tammy L. Smith, Thomas R. Haven, Lauren M. Zuromski, Kyphuong Luong, Stacey L. Clardy and Lisa K. Peterson
Institutions | VA Salt Lake City Health Care System, The University of Utah, ARUP Institute for Clinical and Experimental Pathology and George E. Whalen Department of Veterans Affairs Medical Center (USA)
Grant Type | In 2023, TSF sponsored the publication fees of 12 MOGAD-related articles to be published in Frontiers in Neurology
Hyperreflective Foci (HRF): A New Retinal Marker in NMOSD & MOGAD?
Principal Investigators | Joachim Havla and Jonathan A. Gernert
Institution | Institute for Clinical Neuroimmunology, University Hospital LMU Munich (Germany)
Aim I | To conduct a cross-sectional comparison of the number of HRF in eyes without a history of optic neuritis between patients with NMOSD, MOGAD and other demyelinating diseases.
Aim II | To conduct a longitudinal analysis of the number of HRF between patients with NMOSD, MOGAD and other demyelinating diseases considering clinical and imaging follow-up data.
Investigating the association between neoplasms & MOGAD
Principal Investigators | Milena Trentinaglia, Alessandro Dinoto, Sara Carta, Vanessa Chiodega, Sergio Ferrari, Vincenzo Andreone, Giorgia Teresa Maniscalco and Sara Mariotto
Institutions | University of Verona, Neurological Clinic and Stroke Unit – Naples and Multiple Sclerosis Center – Naples (Italy)
Aim | To investigate the occurrence of tumors in a cohort of patients with MOGAD and to describe their clinical features, in addition to previously reported cases.
Grant Type | In 2023, TSF sponsored the publication fees of 12 MOGAD-related articles to be published in Frontiers in Neurology
Institutions | Clínica Alemana de Santiago (Chile) & Hospital Ramos Mejia (Argentina)
Aim | To develop a consensus on the use of disease-modifying treatments in NMOSD patients and write guidelines for Latin America of treatment for NMOSD (aquaporin-4 positive and negative patients).
Latin American Consensus Recommendations for Management & Treatment of Adult MOGAD Patients in Clinical Practice
Latin American Consensus Recommendations for Management & Treatment of Adult MOGAD Patients in Clinical Practice
Principal Investigator | Edgar Carnero Contentti
Institution | Hospital Alemán (Argentina)
Aim | To review how adult patients living with MOGAD should be managed and treated in Latin America in order to improve long-term outcomes and to optimize resources in these populations.
Funds Awarded | $5,000
Grant Type | SPARK Grant – This grant was made possible with support from Terry & Greg Clark of The Dorchester Foundation
NMOSD and MOGAD in Montenegro: Clinical Aspects, Pain, and Community Impact
Principal Investigator | Sanja Gluscevic
Institution | Clinical Centre of Montenegro, Neurology Clinic, University of Montenegro
Aim | To provide a comprehensive understanding of NMOSD and MOGAD in Montenegro, with a focus on clinical aspects, pain, and the impact on the community. The findings of this study can potentially contribute to the development of better strategies for diagnosis, treatment, and support for patients with NMOSD and MOGAD in the country.
Funds Awarded | $5,000
Grant Type | SPARK Grant – This grant was made possible with support from Terry & Greg Clark of The Dorchester Foundation
Pediatric MOGAD in southern China: analysis of 93 cases
Principal Investigators | Xiaojing Li, Wenlin Wu, Chi Hou, Yiru Zeng, Wenxiao Wu, Lianfeng Chen, Yinting Liao, Haixia Zhu, Yang Tian, Bingwei Peng, Kelu Zheng, Kaili Shi, Ying Li, Yuanyuan Gao, Yani Zhang, Haisheng Lin and Wen-Xiong Chen
Institution | Guangzhou Medical University, Guangzhou (China)
Aim | To study the clinical features of children diagnosed with myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD) in southern China.
Grant Type | In 2023, TSF sponsored the publication fees of 12 MOGAD-related articles to be published in Frontiers in Neurology
Thymic Negative Selection in T-cell Repertoire Development in MOG CNS Autoimmunity
Principal Investigator | Scott Zamvil
Institution | University of California, San Francisco (United States)
Aim I | To evaluate the role of thymic MOG expression in development of the pathogenic T-cell repertoire in MOG-targeted CNS autoimmunity
Aim II | To breed our new MOGfl/fl mice with Foxn1-cre mice to generate mice deficient in thymic expression of MOG (Foxn1-cre-MOGfl/fl) and to confirm selective thymic deficiency.
Principal Investigators | Elena Grebenciucova, Gina S. Perez Giraldo and Natalia Gonzalez Caldito
Institution | Northwestern University (USA)
Aim | To empower physicians to recognize diagnostic challenges of transverse myelitis associated with MOGAD, such as low predictive value of low titers of MOG antibodies for the diagnosis of MOGAD, importance of both clinical and radiological characteristics, exclusion of other causes, discussing risk of recurrence, and administering acute treatment as well as communicating the rationale of whether chronic treatments are necessary to reduce the risk of relapse after the first relapse.
Grant Type | In 2023, TSF sponsored the publication fees of 12 MOGAD-related articles to be published in Frontiers in Neurology
Two case reports and systematic review of the literature of adult cerebral cortical encephalitis with anti-myelin oligodendrocyte glycoprotein antibody
Principal Investigators | Xu M. Hui, Ma Chi, Ming Dong, Liu Yue and Wang Xu
Institution | The First Hospital of Jilin University (China)
Aim | To further characterize the clinical symptoms, magnetic resonance imaging (MRI) findings, and prognosis of CCE with anti-MOG antibody.
Grant Type | In 2023, TSF sponsored the publication fees of 12 MOGAD-related articles to be published in Frontiers in Neurology
Validating the TRIPS-A Scoring Tool for Relapse Prediction in MOGAD
Validating the TRIPS-A Scoring Tool for Relapse Prediction in MOGAD
Principal Investigator | Ahmed Obeidat
Institution | Medical College of Wisconsin (United States)
Aim I | To develop and apply a scoring tool to predict subsequent relapses after an initial attack in people with myelin oligodendrocyte glycoprotein antibody disease.
Aim II | To compare serum levels of neurofilament light (NfL), a marker of neuroaxonal damage, cross-sectionally, between patients falling into the high score category (potentially relapsing) versus those falling into the lower score category (potentially monophasic).
Aim I | Determine the frequency of misdiagnosis of NMOSD patients as MS, and the point prevalence of misdiagnosis in different geographic census regions
Aim II | Identify the frequency of utilization of FDA-approved MS therapies in misdiagnosed NMOSD patients
Aim III | Understand the cost of misdiagnosis of NMOSD patients
Institution | Charité – Universitätsmedizin Berlin (Germany)
Aim I | To investigate the involvement of inflammasome in NMOSD, by detecting pyroptosis and the inflammasome effector cytokine IL1β in microglia-mediated astrocytic damage by AQP4-IgG
Aim II | To study whether inhibition of inflammasome and its effectors may protect astrocytes from inflammasome-mediated damage
Aim | To better understand the interplay of genetics, metabolics, and other non-genetic factors that relate to NMOSD/MOGAD patient outcomes, including quality of life.
Aim I | To compare retinal vascular plexus densities between eyes with a history of optic neuritis from people with NMOSD, MOGAD, MS and controls
Aim II | To compare retinal vascular plexus densities between eyes without a history of optic neuritis from patients with NMOSD, MOGAD, MS and controls
Aim III | To assess correlations of retinal vascular plexus densities with visual function in NMOSD, MOGAD and MS eyes
Aim | To depict the impact of neuromyelitis optica spectrum disorder (NMOSD) on employment, job loss, and work hours in a multi-country prospective survey-based study of people living with NMOSD
Aim I | Develop longitudinal database and biorepository for MOG Antibody Disease (MOGAD) patients at the Stanford Neuroimmunology Center, including multi-center collaboration. Demographic, clinical outcomes, biochemical (including MOG-IgG serial titers, presence of co-neuronal antibodies), neuroimaging and neuropsychological outcomes, when available.
Aim II | To determine if MOG IgG positivity or titer predicts index event severity or relapse
Aim III | To correlate MOG IgG serostatus with serum and cerebrospinal fluid (CSF) immune profiles (pleocytosis, oligoclonal bands, paired serum/CSF IL-6, TNF-alpha, T and B lymphocyte profiles) to inform immunopathogenesis and treatment
Aim | The overall goals of this study are to better understand the effects of the SARS-CoV-2 pandemic and COVID-19 in our population of patients with NMOSD.
Aim I | To describe the epidemiologic characteristics of all patients who carry a diagnosis of NMOSD within the Department of Defense/Defense Medical Surveillance System (DMSS).
Aim II | To confirm the presence of Aquaporin-4 and MOG autoantibodies in pre-symptomatic NMO samples.
Aim | To pilot a novel point-of-care dry blood spot diagnostic test for patients with aquaporin 4-antibody (AQP4) seropositive neuromyelitis optica spectrum disorder (NMOSD).
Aim | To evaluate the effect of different disease modifying treatments on attack and disability prevention in children with neuromyelitis optica spectrum disorder.