Biological Therapy in Primary Sjogren's Syndrome: Effect on Salivary Gland Function and Inflammation

被引:12
作者
Chowdhury, Farzana [1 ,2 ]
Tappuni, Anwar [2 ]
Bombardieri, Michele [1 ]
机构
[1] William Harvey Res Inst, Ctr Expt Med & Rheumatol, London, England
[2] Barts & London Queen Marys Sch Med & Dent, Inst Dent, London, England
基金
英国医学研究理事会;
关键词
B cell depletion; secretory function; salivary gland histopathology; salivary gland ultrasound; B/T cell co-stimulation; ANTI-CD20; MONOCLONAL-ANTIBODY; B-CELL HYPERACTIVITY; DOUBLE-BLIND; ABATACEPT TREATMENT; RITUXIMAB TREATMENT; DISEASE-ACTIVITY; LOW-GRADE; BAFF; EFFICACY; BELIMUMAB;
D O I
10.3389/fmed.2021.707104
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Primary Sjogren's syndrome (pSS) is a chronic, systemic autoimmune disease. It is the second most common rheumatic autoimmune disorder, affecting 0.7% of European Americans and up to 1% of people globally. pSS is characterized by the impaired secretory function of exocrine glands, including salivary and lachrymal glands. A lymphocytic infiltration of these organs leads to the common and debilitating symptoms of oral and ocular dryness, majorly affecting the quality of life of these patients. Currently, no disease-modifying drug has been approved for the treatment of pSS, with therapies largely aimed at relieving symptoms of dry mouth and dry eyes. In particular, management of oral dryness still represents a major unmet clinical need in pSS and a significant burden for patients with this condition. Recently, several randomized clinical trials in pSS with biological therapies targeting specific mechanistic pathways implicated in the disease pathogenesis, including B-cell hyperactivity, T-cell co-stimulation and the aberrant role of cytokines, have been completed with mixed results. In this review, we summarize evidence from recent clinical trials investigating biological therapy in pSS, specifically highlighting efficacy, or lack thereof, in modulating local inflammation and improving salivary gland function.
引用
收藏
页数:10
相关论文
共 77 条
[1]   Evaluation of Histologic, Serologic, and Clinical Changes in Response to Abatacept Treatment of Primary Sjogren's Syndrome: A Pilot Study [J].
Adler, Sabine ;
Koerner, Meike ;
Foerger, Frauke ;
Huscher, Doerte ;
Caversaccio, Marco-Domenico ;
Villiger, Peter M. .
ARTHRITIS CARE & RESEARCH, 2013, 65 (11) :1862-1868
[2]  
[Anonymous], 2018, EUCTR201600355834ESE
[3]  
Arends S., 2020, ANN RHEUM DIS, V79, P1026, DOI [10.1136/annrheumdis-2020-eular.4500, DOI 10.1136/ANNRHEUMDIS-2020-EULAR.4500]
[4]   Efficacy and safety of abatacept in active primary Sjogren's syndrome: results of a phase III, randomised, placebo-controlled trial [J].
Baer, Alan N. ;
Gottenberg, Jacques-Eric ;
St Clair, E. William ;
Sumida, Takayuki ;
Takeuchi, Tsutomu ;
Seror, Raphaele ;
Foulks, Gary ;
Nys, Marleen ;
Mukherjee, Sumanta ;
Wong, Robert ;
Ray, Neelanjana ;
Bootsma, Hendrika .
ANNALS OF THE RHEUMATIC DISEASES, 2021, 80 (03) :339-348
[5]   The value of histopathological examination of salivary gland biopsies in diagnosis, prognosis and treatment of Sjogren's Syndrome [J].
Barone, Francesca ;
Campos, Joana ;
Bowman, Simon ;
Fisher, Benjamin A. .
SWISS MEDICAL WEEKLY, 2015, 145
[6]   Environmental factors in the pathogenesis of primary Sjogren's syndrome [J].
Bjork, A. ;
Mofors, J. ;
Wahren-Herlenius, M. .
JOURNAL OF INTERNAL MEDICINE, 2020, 287 (05) :475-492
[7]   Randomized Controlled Trial of Rituximab and Cost-Effectiveness Analysis in Treating Fatigue and Oral Dryness in Primary Sjogren's Syndrome [J].
Bowman, Simon J. ;
Everett, Colin C. ;
O'Dwyer, John L. ;
Emery, Paul ;
Pitzalis, Costantino ;
Ng, Wan-Fai ;
Pease, Colin T. ;
Price, Elizabeth J. ;
Sutcliffe, Nurhan ;
Gendi, Nagui S. T. ;
Hall, Frances C. ;
Ruddock, Sharon P. ;
Fernandez, Catherine ;
Reynolds, Catherine ;
Hulme, Claire T. ;
Davies, Kevin A. ;
Edwards, Christopher J. ;
Lanyon, Peter C. ;
Moots, Robert J. ;
Roussou, Euthalia ;
Giles, Ian P. ;
Sharples, Linda D. ;
Bombardieri, Michele .
ARTHRITIS & RHEUMATOLOGY, 2017, 69 (07) :1440-1450
[8]   Sjogren syndrome [J].
Brito-Zeron, Pilar ;
Baldini, Chiara ;
Bootsma, Hendrika ;
Bowman, Simon J. ;
Jonsson, Roland ;
Mariette, Xavier ;
Sivils, Kathy ;
Theander, Elke ;
Tzioufas, Athanasios ;
Ramos-Casals, Manuel .
NATURE REVIEWS DISEASE PRIMERS, 2016, 2
[9]   Prevalence of interferon type I signature in CD14 monocytes of patients with Sjogren's syndrome and association with disease activity and BAFF gene expression [J].
Brkic, Zana ;
Maria, Naomi I. ;
van Helden-Meeuwsen, Cornelia G. ;
van de Merwe, Joop P. ;
van Daele, Paul L. ;
Dalm, Virgil A. ;
Wildenberg, Manon E. ;
Beumer, Wouter ;
Drexhage, Hemmo A. ;
Versnel, Marjan A. .
ANNALS OF THE RHEUMATIC DISEASES, 2013, 72 (05) :728-735
[10]   The TRACTISS Protocol: a randomised double blind placebo controlled clinical TRial of Anti-B-Cell Therapy In patients with primary Sjogren's Syndrome [J].
Brown, Sarah ;
Coy, Nuria Navarro ;
Pitzalis, Costantino ;
Emery, Paul ;
Pavitt, Sue ;
Gray, Janine ;
Hulme, Claire ;
Hall, Frances ;
Busch, Robert ;
Smith, Pete ;
Dawson, Luke ;
Bombardieri, Michele ;
Wan-fai, Ng ;
Pease, Colin ;
Price, Elizabeth ;
Sutcliffe, Nurhan ;
Woods, Clodagh ;
Ruddock, Sharon ;
Everett, Colin ;
Reynolds, Catherine ;
Skinner, Emma ;
Poveda-Gallego, Ana ;
Rout, John ;
Macleod, Iain ;
Rauz, Saaeha ;
Bowman, Simon .
BMC MUSCULOSKELETAL DISORDERS, 2014, 15