[Treatment of primary Sjögren syndrome]

Autor: Valérie Devauchelle-Pensec, Jacques-Olivier Pers, Alain Saraux
Přispěvatelé: Service de Rhumatologie [CHU de la Cavale-Blanche], Hôpital de la Cavale Blanche - CHRU Brest (CHU - BREST ), Immunologie et Pathologie (EA2216), Université de Brest (UBO)-IFR148, Michel, Geneviève, CHRU Brest - Service de Rhumatologie (CHU - BREST - Rhumato), Centre Hospitalier Régional Universitaire de Brest (CHRU Brest)
Jazyk: francouzština
Rok vydání: 2012
Předmět:
0301 basic medicine
MESH: Fatigue
Lung Diseases
Pathology
medicine.medical_treatment
Sialic Acid Binding Ig-like Lectin 2
Severity of Illness Index
law.invention
0302 clinical medicine
Randomized controlled trial
law
Interferon
Epidemiology
B-Cell Activating Factor
Molecular Targeted Therapy
Fatigue
MESH: Polyneuropathies
Arthralgia
3. Good health
Biological Therapy
Artificial tears
Sjogren's Syndrome
Cryoglobulinemia
MESH: Sialic Acid Binding Ig-like Lectin 2
[SDV.IMM]Life Sciences [q-bio]/Immunology
Dry Eye Syndromes
MESH: Pain
Nephritis
MESH: Pain Management
medicine.drug
medicine.medical_specialty
[SDV.IMM] Life Sciences [q-bio]/Immunology
education
Pain
Salivary Gland Diseases
Skin Diseases
Xerostomia
Proinflammatory cytokine
03 medical and health sciences
Polyneuropathies
Rheumatology
MESH: Salivary Gland Diseases
Muscular Diseases
Internal medicine
Severity of illness
medicine
Humans
Pain Management
MESH: B-Cell Activating Factor
030203 arthritis & rheumatology
Autoimmune disease
MESH: Humans
business.industry
Tumor Necrosis Factor-alpha
Arthritis
medicine.disease
030104 developmental biology
MESH: Sjogren's Syndrome
MESH: Tumor Necrosis Factor-alpha
Nephritis
Interstitial

Nervous System Diseases
business
Zdroj: Nature Reviews Rheumatology
Nature Reviews Rheumatology, Nature Publishing Group, 2016, 12 (8), pp.456-71
Revue du Praticien (La)
Revue du Praticien (La), J B Bailliere et Fils, 2012, 62 (2), pp.234-8
ISSN: 0035-2640
1759-4804
Popis: International audience; Primary Sjögren syndrome (pSS) is a progressive autoimmune disease characterized by sicca and systemic manifestations. In this Review, we summarize the available data on topical and systemic medications, according to clinical signs and disease activity, and we describe the ongoing studies using biologic drugs in the treatment of pSS. Expanding knowledge about the epidemiology, classification criteria, systemic activity scoring (ESSDAI) and patient-reported outcomes (ESSPRI) is driving active research. Treatment decisions are based on the evaluation of symptoms and extraglandular manifestations. Symptomatic treatment is usually appropriate, whereas systemic treatment is reserved for systemic manifestations. Sicca is managed by education, environment modification, elimination of contingent offending drugs, artificial tears, secretagogues and treatments for complications. Mild systemic signs such as fatigue are treated by exercise. Pain can require short-term moderate-dose glucocorticoid therapy and, in some cases, disease-modifying drugs. Severe and acute systemic manifestations indicate treatment with glucocorticoids and/or immunosuppressant drugs. The role for biologic agents is promising, but no double-blind randomized controlled trials (RCTs) proving the efficacy of these drugs are available. Targets for new treatments directed against the immunopathological mechanisms of pSS include epithelial cells, T cells, B-cell overactivity, the interferon signature, proinflammatory cytokines, ectopic germinal centre formation, chemokines involved in lymphoid cell homing, and epigenetic modifications.
Databáze: OpenAIRE