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1.
J Neurol ; 269(3): 1316-1334, 2022 Mar.
Article in English | MEDLINE | ID: covidwho-1703834

ABSTRACT

Multiple sclerosis (MS) is a chronic inflammatory, demyelinating and neurodegenerative disease affecting the central nervous system (CNS), often characterized by the accumulation of irreversible clinical disability over time. During last years, there has been a dramatic evolution in several key concepts of immune pathophysiology of MS and in the treatment of this disease. The demonstration of the strong efficacy and good safety profile of selective B-cell-depleting therapies (such as anti-CD20 monoclonal antibodies) has significantly expanded the therapeutic scenario for both relapsing and progressive MS patients with the identification of a new therapeutic target. The key role of B cells in triggering MS disease has been also pointed out, determining a shift from the traditional view of MS activity as largely being 'T-cell mediated' to the notion that MS-related pathological processes involve bi-directional interactions between several immune cell types, including B cells, both in the periphery and in the CNS. This review provides an updated overview of the involvement of B cells in the immune pathophysiology and pathology of MS. We summarize the rationale regarding the use of anti-CD20 therapies and the results of the main randomized controlled trials and observational studies investigating the efficacy and safety profile of rituximab, ocrelizumab, ofatumumab and ublituximab. Suggestions regarding vaccinations and management of MS patients during COVID-19 pandemic with anti-CD20 therapies are also discussed. Finally, therapies under investigation and future perspectives of anti-CD20 therapies are taken into consideration.


Subject(s)
COVID-19 , Multiple Sclerosis , Neurodegenerative Diseases , Humans , Multiple Sclerosis/drug therapy , Pandemics , SARS-CoV-2
2.
J Neurol ; 268(11): 3975-3979, 2021 Nov.
Article in English | MEDLINE | ID: covidwho-1182249

ABSTRACT

During the COVID-19 pandemic, concerns raised regarding the use of immunosuppressants in multiple sclerosis, even if current data do not support an increased risk of infection. Although fingolimod can be temporarily suspended during COVID-19, the benefit-risk balance of suspension can be challenging. Till now, no adverse events have been described after the resumption of fingolimod, following a previous discontinuation. We report the occurrence of atrioventricular block following fingolimod restart. Fingolimod acts on sphingosine-1-phosphate-axis, a pathway that is altered with COVID-19 and hypoxic conditions. Herein we discuss how these metabolic changes may have influenced fingolimod pharmacology leading to a cardiac event.


Subject(s)
Atrioventricular Block , COVID-19 , Atrioventricular Block/chemically induced , Fingolimod Hydrochloride/adverse effects , Humans , Lysophospholipids , Pandemics , SARS-CoV-2 , Sphingosine/analogs & derivatives
5.
J Neurol ; 267(10): 2790-2796, 2020 Oct.
Article in English | MEDLINE | ID: covidwho-506032

ABSTRACT

The outbreak of a severe acute respiratory syndrome caused by a novel coronavirus (COVID-19), has raised health concerns for patients with multiple sclerosis (MS) who are commonly on long-term immunotherapies. Managing MS during the pandemic remains challenging with little published experience and no evidence-based guidelines. We present five teriflunomide-treated patients with MS who subsequently developed active COVID-19 infection. The patients continued teriflunomide therapy and had self-limiting infection, without relapse of their MS. These observations have implications for the management of MS in the setting of the COVID-19 pandemic.


Subject(s)
Coronavirus Infections/complications , Crotonates/therapeutic use , Immunosuppressive Agents/therapeutic use , Multiple Sclerosis/complications , Multiple Sclerosis/drug therapy , Pneumonia, Viral/complications , Toluidines/therapeutic use , Adult , Aged , Betacoronavirus , COVID-19 , Female , Humans , Hydroxybutyrates , Male , Middle Aged , Nitriles , Pandemics , SARS-CoV-2
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