Publications by authors named "Faissner S"

A substantial proportion of patients suffer from Post-COVID Syndrome (PCS) with fatigue and impairment of memory and concentration being the most important symptoms. We here set out to perform in-depth neuropsychological assessment of PCS patients referred to the Neurologic PCS clinic compared to patients without sequelae after COVID-19 (non-PCS) and healthy controls (HC) to decipher the most prevalent cognitive deficits. We included n = 60 PCS patients with neurologic symptoms, n = 15 non-PCS patients and n = 15 healthy controls.

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  • - The study investigates the effects of siponimod, a medication for progressive multiple sclerosis, on immune cells and the central nervous system, specifically its relationship with the neurotrophin BDNF.
  • - Researchers used mice models with and without BDNF to evaluate siponimod's impact on disease activity and neurotoxicity in experimental autoimmune encephalomyelitis (EAE), finding that siponimod reduced disease severity and inflammation regardless of BDNF expression.
  • - Siponimod demonstrated both anti-inflammatory and neuroprotective effects, suggesting its effectiveness in treating the progression of multiple sclerosis may partially relate to BDNF levels in immune cells.
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Introduction: Ofatumumab (Kesimpta) is a subcutaneous CD20-targeting antibody approved in Germany in 2021 for the treatment of relapsing multiple sclerosis (RMS). After careful instruction, patients can administer the treatment themselves. We previously reported data of 101 patients (Klimas et al.

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  • Autologous chimeric antigen receptor (CAR) T cell therapy has shown promise in treating neuroimmunological disorders like myasthenia gravis, and this study details a case of its successful application for stiff-person syndrome (SPS).
  • A 69-year-old woman with severe, treatment-resistant SPS underwent an infusion of anti-CD19 CAR T cells, leading to significant improvements in her symptoms, including reduced leg stiffness and increased walking capacity.
  • The treatment was well tolerated with minimal side effects, encouraging further exploration of CAR T cell therapy for SPS and other autoimmune disorders involving B cells.
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Background: Pregnancy in patients with multiple sclerosis (MS) is accompanied by a decline of relapse activity with increased risk of relapses 3 months post-partum, for unknown reasons. Eomesodermin T-helper cells (Eomes Th cells) are known to mediate neuroinflammation and disease progression in MS and are induced by prolactin-secreting cells.

Objectives: Here, investigated immune cell alterations and the pathophysiological role of Eomes Th cells for disease activity during pregnancy and post-partum in MS.

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The recent success of anti-CD20 monoclonal antibody therapies in the treatment of multiple sclerosis (MS) has highlighted the role of B cells in the pathogenesis of MS. In people with MS, the inflammatory characteristics of B-cell activity are elevated, leading to increased pro-inflammatory cytokine release, diminished anti-inflammatory cytokine production and an accumulation of pathogenic B cells in the cerebrospinal fluid. Rituximab, ocrelizumab, ofatumumab, ublituximab and BCD-132 are anti-CD20 therapies that are either undergoing clinical development, or have been approved, for the treatment of MS.

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Background: While substantial progress has been made in the development of disease-modifying medications for multiple sclerosis (MS), a high percentage of treated patients still show progression and persistent inflammatory activity. Autologous haematopoietic stem cell transplantation (AHSCT) aims at eliminating a pathogenic immune repertoire through intense short-term immunosuppression that enables subsequent regeneration of a new and healthy immune system to re-establish immune tolerance for a long period of time. A number of mostly open-label, uncontrolled studies conducted over the past 20 years collected about 4000 cases.

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Introduction: Ofatumumab (Kesimpta™) is a s.c. applicable anti-CD20 antibody, which has been used in Germany since 2021 for the treatment of relapsing multiple sclerosis (RMS).

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Glatiramer acetate (GA) is a well-established treatment option for patients with clinically isolated syndrome and relapsing-remitting multiple sclerosis (MS) with few side effects. The double transgenic mouse model spontaneous opticospinal encephalomyelitis (OSE), based on recombinant myelin oligodendrocyte glycoprotein reactive T and B cells, mimicks features of chronic inflammation and degeneration in MS and related disorders. Here, we investigated the effects of prophylactic GA treatment on the clinical course, histological alterations and peripheral immune cells in OSE.

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Background: Data on the humoral vaccine response in patients on anti-interleukin-6 (IL-6) receptor therapy remain scarce.

Objective: The main objective of our study was to investigate the humoral response after vaccination against SARS-CoV-2 in neuromyelitis optica spectrum disorder (NMOSD)/myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD) patients treated with anti-IL-6 receptor therapy. Secondarily, we analyzed relapse activity timely associated with vaccination.

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Although the understanding of secondary progressive multiple sclerosis (SPMS) is evolving, early detection of relapse-independent progression remains difficult. This is further complicated by superimposed relapses and compensatory mechanisms that allow for silent progression. The term relapsing multiple sclerosis (RMS) subsumes relapsing-remitting multiple sclerosis (RRMS) and SPMS with relapses.

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Despite the development of vaccines, which protect healthy people from severe and life-threatening Covid-19, the immunological responses of people with secondary immunodeficiencies to these vaccines remain incompletely understood. Here, we investigated the humoral and cellular immune responses elicited by mRNA-based SARS-CoV-2 vaccines in a cohort of people living with HIV (PLWH) receiving anti-retroviral therapy. While antibody responses in PLWH increased progressively after each vaccination, they were significantly reduced compared to the HIV-negative control group.

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Background: The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) pandemic has tremendous implications for the management of patients with autoimmune conditions such as multiple sclerosis (MS) under immune therapies targeting CD20 B cells (aCD20).

Objectives: Here, we investigated humoral and cellular immune responses, including anti-spike titers, neutralization against SARS-CoV-2 wild-type (WT), delta, and omicron variant and T cell responses of aCD20-treated relapsing-remitting MS patients following SARS-CoV-2 vaccination compared with healthy controls.

Methods: Blood samples were collected within 4-8 weeks following the second vaccination against SARS-CoV-2.

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Article Synopsis
  • This study explores post-COVID syndrome, focusing on the pathogenesis, clinical signs, and factors affecting patients, particularly regarding gender differences in symptoms and fatigue.
  • Researchers analyzed 101 patients at a specialized clinic, revealing that most experienced severe fatigue, impaired concentration and memory, with notable differences in symptom severity between genders.
  • The findings suggest that female patients are at a higher risk for severe fatigue, while males exhibit more depressive symptoms, emphasizing the need for tailored interdisciplinary treatment approaches for long-COVID patients.
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Objective: The pandemic induced by SARS-CoV-2 has huge implications for patients with immunosuppression that is caused by disorders or specific treatments. Especially approaches targeting B cells anti-CD20 therapy are associated with impaired humoral immune response but sustained cellular immunity. Ofatumumab is a human anti-CD20 directed antibody applied in low dosages subcutaneously, recently licensed for Multiple Sclerosis (MS).

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Background: The role of neuroinflammation and autoimmune processes in neurodegenerative diseases is not fully understood. Activation of microglia with expression of proinflammatory cytokines supports the hypothesis that immune processes may play an important role in the pathophysiology of Huntington's disease (HD) and thus, immunomodulating therapies might have potential neuroprotective properties. Until now, no disease-modifying therapy (DMT) is available for HD.

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  • Significant advancements in multiple sclerosis (MS) treatment over the past two decades have introduced new therapies with tailored mechanisms and reduced side effects.
  • Second-generation therapies like diroximel fumarate and selective sphingosine-1-phosphate receptor modulators (siponimod, ozanimod, ponesimod) offer improved safety profiles and more convenient oral administration.
  • Innovative treatments such as B-cell-targeted therapies (ocrelizumab, ofatumumab) and upcoming oral Bruton's tyrosine kinase inhibitors are expected to enhance personalized care for MS patients, improving relapse rates and daily functioning.
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γδ T cells are unconventional T cells, distinguished from αβ T cells in a number of functional properties. Being small in number compared to αβ T cells, γδ T cells have surprised us with their pleiotropic roles in various diseases. γδ T cells are ambiguous in nature as they can produce a number of cytokines depending on the (micro) environmental cues and engage different immune response mechanisms, mainly due to their epigenetic plasticity.

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The phosphodiesterase-5 inhibitor sildenafil was postulated to reduce the risk for Alzheimer's Disease. Since preclinical data revealed beneficial effects in Huntington's Disease (HD), we now for the first time investigated effects of sildenafil in HD patients using the database ENROLL-HD. We demonstrate beneficial effects on motoric, functional and cognitive capacities in cross-sectional data.

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Objective: Long coronavirus disease (Long-COVID) syndrome is a hitherto poorly understood phenomenon with a broad spectrum of symptoms, including depression and anxiety. Depressive symptoms have been associated with brainstem raphe (BR) alterations in transcranial sonography (TCS) that might reflect dysfunction of the serotonergic system. The primary aim was to investigate the connection of BR alterations with depressive and anxiety symptoms in patients with Long-COVID syndrome.

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  • * A study using double-transgenic mice (2D2/Th) with spontaneous opticospinal encephalomyelitis (OSE) showed that these mice developed retinal thinning and impaired photoreceptor function, indicating visual system degeneration.
  • * Findings revealed increased inflammation in the optic nerves and retinas, including higher levels of immune cells and upregulation of the complement system, highlighting both inflammatory and degenerative processes in the visual system of OSE mice
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Background: Since the coronavirus disease 2019 (COVID-19) has risen, several risk factors have been identified, predicting a worse outcome. It has been speculated that patients with Multiple sclerosis (MS) have an increased risk for a severe course of COVID-19 due to a suspected higher vulnerability. Therefore, we aimed to analyze the impact of comorbid MS on the outcome of patients with COVID-19 in Germany.

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  • The COVID-19 pandemic significantly impacted hospitalizations for patients with multiple sclerosis (MS) and neuromyelitis optica spectrum disorder (NMOSD) in Germany, with a notable decline observed during the first wave of the pandemic.
  • A nationwide study analyzed data from 1463 hospitals, showing a decrease in hospital admissions for various types of MS and NMOSD, with some groups experiencing reductions as high as 48.9%.
  • Conversely, the study found an increase in the application of plasmapheresis therapy for these patients during 2020 compared to 2019, particularly noticeable during the initial wave of COVID-19.
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