Inflammatory Manifestations of Systemic Diseases in the Central Nervous System

التفاصيل البيبلوغرافية
العنوان: Inflammatory Manifestations of Systemic Diseases in the Central Nervous System
المؤلفون: David A. Lapides, Mark McDonald
المصدر: Current Treatment Options in Neurology
سنة النشر: 2020
مصطلحات موضوعية: IgG-4 related disease, Disease, medicine.disease_cause, Autoimmunity, Immune checkpoint inhibitors, 03 medical and health sciences, chemistry.chemical_compound, Systemic lupus erythematosus, 0302 clinical medicine, Natalizumab, Tocilizumab, medicine, Demyelinating disease, Neurobehcet’s disease, Immunodeficiency, Autoimmune encephalitis, business.industry, Common variable immune deficiency, Immune dysregulation, medicine.disease, Neurologic Manifestations of Systemic Disease (D Lapides, Section Editor), chemistry, 030220 oncology & carcinogenesis, Immunology, Sjogren’s syndrome, Neurology (clinical), business, 030217 neurology & neurosurgery, medicine.drug
الوصف: Purpose of Review This review presents the current recommended therapeutic interventions for inflammatory disease in the central nervous system (CNS) secondary to systemic diseases of immune dysregulation. Treatment recommendations for CNS inflammation associated with rheumatologic conditions, immune-related adverse effects from immune checkpoint inhibitors (ICIs), and demyelinating disease from tumor necrosis factor-α (anti-TNFs) are explored. Additional therapeutic options for inflammation related to postviral syndromes and genetic immunodeficiencies are also discussed. Recent Findings In addition to treatment of mild, moderate, and severe CNS rheumatologic disease as guided by the European League Against Rheumatism (EULAR), early consideration of rituximab for severe IgG4-related disease and induction with anti-TNF therapy for severe neurosarcoidosis should be considered. Although often not first line, treatment options for CNS inflammatory diseases based on disease mechanism are emerging, including tocilizumab for Behcet’s disease, natalizumab for ICI associated autoimmune encephalitis, and abatacept for treatment of infiltrative disease secondary to CTLA-4 deficiency. Hematopoietic stem cell treatments represent highly efficacious but risky options for autoimmunity related to genetic immunodeficiency. Summary While early high dose steroids remains first line therapy for most CNS inflammatory conditions, a rapidly expanding arsenal of immune targeted therapies offers clinicians tailored disease specific options for treatment.
تدمد: 1092-8480
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b3645924e734a5ecc24a1af769308196Test
https://pubmed.ncbi.nlm.nih.gov/32834714Test
حقوق: OPEN
رقم الانضمام: edsair.doi.dedup.....b3645924e734a5ecc24a1af769308196
قاعدة البيانات: OpenAIRE