Open AccessJournal Article
Present and novel biologic drugs in primary Sjögren's syndrome.
Serena Fasano,David A. Isenberg +1 more
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TL;DR: Rituximab has been the most frequently used biologic therapy in pSS, but with much less success than in the treatment of patients with rheumatoid arthritis, vasculitis and lupus, however, in the last few years a number of other biologics have been developed and are under investigation.
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Abstract: Primary Sjogren's syndrome (pSS) is a systemic autoimmune disease characterised by xerostomia and xerophthalmia. In at least one-third of patients, the disease may be complicated by extraglandular involvement. Due to the lack of evidence-based recommendations, current therapeutic options for pSS are mainly empirical, often reflecting their use in other autoimmune diseases. Nevertheless, recent advances in the understanding of pathogenic pathways in pSS encourage the belief that blocking them may be of value in the treatment of the disease. Despite failing to demonstrate efficacy in clinical trials, because of the well-established role of B-lymphocytes in the pathogenesis of pSS, rituximab has been the most frequently used to date, but with much less success than in the treatment of patients with rheumatoid arthritis, vasculitis and lupus. However, in the last few years a number of other biologics have been developed and are under investigation. The aim of this article is to review the use of biologic therapies in pSS.
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Citations
•Journal Article
One year in review 2020: comorbidities, diagnosis and treatment of primary Sjogren's syndrome
Valeria Manfrè,Giacomo Cafaro,Ilenia Riccucci,Alen Zabotti,Carlo Perricone,Hendrika Bootsma,S. De Vita,Elena Bartoloni +7 more
TL;DR: A better stratification of patients has important value in the evaluation of mechanisms underlying the risk of lymphoproliferative disorders in these patients and novel targeted therapies may open new possibilities for the application of personalised medicine in pSS.
46
Recent Advances in BTK Inhibitors for the Treatment of Inflammatory and Autoimmune Diseases.
Datong Zhang,He Gong,Fancui Meng +2 more
TL;DR: In this article, a review of the recent development of BTK inhibitors at preclinical and clinical stages in treating these diseases is presented with a focus on their structure, bioactivity and selectivity.
43
Innate Immunity and Biological Therapies for the Treatment of Sjögren's Syndrome.
TL;DR: The role of different immune cells in disease development, therapeutic treatments, and future strategies that are available to target various immune cells to cure the disease are highlighted.
Bruton's Tyrosine Kinase Inhibitors: A New Therapeutic Target for the Treatment of SLE?
Ana Lorenzo-Vizcaya,Serena Fasano,David A. Isenberg +2 more
- 02 Jun 2020
TL;DR: This review will summarize what is known and what has been published so far about the treatment of mouse models of SLE and the human disease, using BTK inhibitors.
T Cells Subsets in the Immunopathology and Treatment of Sjogren's Syndrome.
William de Jesús Ríos-Ríos,Sorely Adelina Sosa-Luis,Honorio Torres-Aguilar +2 more
- 11 Nov 2020
TL;DR: The authors summarize the current knowledge of T cells subsets contribution to the SS immunopathology, focusing on the cellular and biomolecular properties allowing them to infiltrate and to harm target tissues, and that simultaneously make them key therapeutic targets for SS treatment.
References
EULAR Sjögren's Syndrome Patient Reported Index (ESSPRI): development of a consensus patient index for primary Sjögren's syndrome
Raphaèle Seror,Philippe Ravaud,Xavier Mariette,Xavier Mariette,Hendrika Bootsma,Elke Theander,Arne Hansen,Manel Ramos-Casals,Thomas Doerner,Stefano Bombardieri,Eric Hachulla,Johan G. Brun,Aike A. Kruize,Sonja Praprotnik,Matija Tomšič,Jacques-Eric Gottenberg,Valérie Devauchelle,Salvatore deVita,C. Vollenweider,Thomas Mandl,Athanasios G. Tzioufas,Steven E. Carsons,Alain Saraux,Nurhan Sutcliffe,Claudio Vitali,Simon J Bowman +25 more
TL;DR: The EULAR SS Patient Reported Index is a very simple index designed to measure patients' symptoms in primary SS and has good construct validity and is well correlated with SSI and PROFAD.
496
Effectiveness of rituximab treatment in primary Sjögren's syndrome: a randomized, double-blind, placebo-controlled trial.
Jiska Meijer,Petra M. Meiners,Arjan Vissink,Fred K. L. Spijkervet,Wayel H. Abdulahad,N. Kamminga,Elisabeth Brouwer,Cees G. M. Kallenberg,Hendrika Bootsma +8 more
TL;DR: Rituximab treatment is an effective and safe treatment strategy for patients with primary Sjögren's syndrome and significant improvements were found in comparison with baseline values.
489
Inefficacy of infliximab in primary Sjögren's syndrome: results of the randomized, controlled Trial of Remicade in Primary Sjögren's Syndrome (TRIPSS).
Xavier Mariette,Philippe Ravaud,Serge Steinfeld,Gabriel Baron,Joëlle Goetz,Eric Hachulla,Bernard Combe,Xavier Puéchal,Y.L. Pennec,Bernard Sauvezie,Aleth Perdriger,Gilles Hayem,Anne Janin,Jean Sibilia +13 more
TL;DR: This randomized, double-blind, placebo-controlled study of an anti-TNF agent did not show any evidence of efficacy of infliximab in primary SS.
468
Treatment of primary Sjögren syndrome: a systematic review.
TL;DR: Evidence from controlled trials suggests benefits for pilocarpine and cevimeline for sicca features and topical cyclosporine for moderate or severe dry eye in primary Sjögren syndrome.
392
Improvement of Sjögren's syndrome after two infusions of rituximab (anti-CD20).
Valérie Devauchelle-Pensec,Y.L. Pennec,Johanne Morvan,Jacques-Olivier Pers,Capucine Daridon,Sandrine Jousse-Joulin,Anne Roudaut,Christophe Jamin,Yves Renaudineau,Isabelle Quintin Roué,Béatrice Cochener,Pierre Youinou,Alain Saraux +12 more
TL;DR: Low-dose rituximab infusions induced a rapid depletion of B cells in the blood and SG and could improve primary Sjögren's syndrome, and controlled studies are needed.
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