7341. Brain 18F-fluorodeoxyglucose positron emission tomography/computed tomography detection of neuropsychiatric lupus with normal cerebral magnetic resonance imaging.
作者: Caroline Soubrier.;Benoit Faucher.;Eric Guedj.;Elsa Kaphan.;Mikael Ebbo.;Benjamin De Sainte Marie.;Nicolas Schleinitz.
来源: Rheumatology (Oxford). 2020年59卷2期457页 7342. ANCA-associated vasculitic neuropathy during treatment with ipilimumab.
作者: Michelle Villarreal-Compagny.;Pablo Iglesias.;Javier Marco-Hernández.;José C Milisenda.;Jordi Casanova-Molla.;José Hernández-Rodríguez.;Susana Puig.;Cristina Carrera.;Sergio Prieto-González.
来源: Rheumatology (Oxford). 2020年59卷1期251-252页 7344. The relationship between patient acceptable symptom state and disease activity in patients with psoriatic arthritis.
作者: Jeanie Z Fei.;Anthony V Perruccio.;Justine Y Ye.;Dafna D Gladman.;Vinod Chandran.
来源: Rheumatology (Oxford). 2020年59卷1期69-76页
The Psoriatic Arthritis Disease Activity Score (PASDAS) and Disease Activity Index for Psoriatic Arthritis (DAPSA) are composite PsA disease activity measures. We sought to identify the PASDAS and DAPSA cut-off points consistent with patient acceptable symptom state (PASS), the threshold of symptoms beyond which patients consider themselves well, and examine PASS across published PASDAS and DAPSA thresholds for low, moderate and high disease activity.
7346. Performance of the Patient-Reported Outcomes Measurement Information System-29 in scleroderma: a Scleroderma Patient-centered Intervention Network Cohort Study.
作者: Linda Kwakkenbos.;Brett D Thombs.;Dinesh Khanna.;Marie-Eve Carrier.;Murray Baron.;Daniel E Furst.;Karen Gottesman.;Frank van den Hoogen.;Vanessa L Malcarne.;Maureen D Mayes.;Luc Mouthon.;Warren R Nielson.;Serge Poiraudeau.;Robert Riggs.;Maureen Sauvé.;Fredrick Wigley.;Marie Hudson.;Susan J Bartlett.
来源: Rheumatology (Oxford). 2023年62卷11期3771页 7347. Infection by Mycobacterium chelonae at the site of administration of sarilumab for rheumatoid arthritis.
作者: Raquel Dos Santos Sobrín.;Nair Pérez Gómez.;Alejandro Souto Vilas.;Manuel Pombo Suárez.;Eva Pérez Pampín.;Jose Ramón Antúnez López.;Antonio Mera Varela.
来源: Rheumatology (Oxford). 2020年59卷1期265页 7350. Calves vasculitis revealing a relapse of polyarteritis nodosa: the gaiters sign.
作者: Jérémy Keraen.;Adrien Bigot.;Anne-Marie Bergemer-Fouquet.;Elisabeth Diot.;Nicole Ferreira-Maldent.;Benoit Erra.;Chloé Giret.;François Maillot.
来源: Rheumatology (Oxford). 2020年59卷1期98页 7351. The relationship between citations, downloads and alternative metrics in rheumatology publications: a bibliometric study.
作者: Winnie M Y Chen.;Marwan Bukhari.;Francesca Cockshull.;James Galloway.
来源: Rheumatology (Oxford). 2020年59卷2期277-280页
Scientific journals and authors are frequently judged on 'impact'. Commonly used traditional metrics are the Impact Factor and H-index. However, both take several years to formulate and have many limitations. Recently, Altmetric-a metric that measures impact in a non-traditional way-has gained popularity. This project aims to describe the relationships between subject matter, citations, downloads and Altmetric within rheumatology.
7352. Treatment of Sjögren's syndrome: current therapy and future directions.
作者: Robert I Fox.;Carla M Fox.;Jacques Eric Gottenberg.;Thomas Dörner.
来源: Rheumatology (Oxford). 2021年60卷5期2066-2074页
SS is usually described as having severe fatigue, dryness, diffuse pain, glandular swelling, and various extraglandular (systemic) manifestations. Clinical trials have generally failed because the vast majority of enrolled patients had no extraglandular manifestations at the time of enrolment but suffered from fatigue, dryness and pain that did not significantly respond to the study medication. A number of hypotheses on the pathogenesis of pSS have been put forward, including disturbances of innate and adaptive immunity as well as abnormalities of the interface between immune disorders and the neuro-endocrine system related to lacrimal and secretory gland dysfunction. Thus, future therapies must be designed for improvement of the symptoms of dry eyes and dry mouth, extraglandular disease, and fatigue and cognitive deficits. Given the inadequacies and limitations of current treatment options, we suggest that innovative directions involving interactions with neuroscientists and neuropsychiatrists together or combined with new immune targeting may be hold promise for better treating pSS.
7354. The role of stroma and epithelial cells in primary Sjögren's syndrome.
作者: Saba Asam.;Georgiana Neag.;Onorina Berardicurti.;David Gardner.;Francesca Barone.
来源: Rheumatology (Oxford). 2021年60卷8期3503-3512页
Primary SS (pSS) is a chronic autoimmune condition characterized by infiltration of the exocrine glands and systemic B cell hyperactivation. This glandular infiltration is associated with loss of glandular function, with pSS patients primarily presenting with severe dryness of the eyes and mouth. Within the affected glands, the infiltrating lymphocytes are organized in tertiary lymphoid structures. Tertiary lymphoid structures subvert normal tissue architecture and impact on organ function, by promoting the activation and maintenance of autoreactive lymphocytes. This review summarizes the current knowledge about the role of stromal cells (including endothelium, epithelium, nerves and fibroblasts) in the pathogenesis of pSS, in particular the interactions taking place between stromal cells and infiltrating lymphocytes. We will provide evidences pointing towards the driving role of stromal cells in the orchestration of the local inflammatory milieu, thus highlighting the need for therapies aimed at targeting this compartment alongside classical immunosuppression in pSS.
7358. Salivary gland ultrasonography in primary Sjögren's syndrome: opportunities and challenges.
作者: Valerie Devauchelle-Pensec.;Alen Zabotti.;Guillermo Carvajal-Alegria.;Nenad Filipovic.;Sandrine Jousse-Joulin.;Salvatore De Vita.
来源: Rheumatology (Oxford). 2021年60卷8期3522-3527页
Salivary gland ultrasonography (SGUS) has an established role in detecting typical structural gland abnormalities in primary Sjögren's Syndrome (pSS). SGUS might be included in pSS classification and could be used as a prognostic and follow-up biomarker, but for this purpose additional efforts, new techniques and larger cohort studies are needed. HarmonicSS, an ongoing Horizon, EU-supported project in pSS, will apply artificial intelligence to SGUS in pSS. Many questions are still unresolved and challenging, but data collected up to now underscore the concept that SGUS will be an important tool for the study of pSS in the near future.
7359. Emerging roles for chemokines and cytokines as orchestrators of immunopathology in Sjögren's syndrome.
作者: Sofie L M Blokland.;Christina-Maria Flessa.;Joel A G van Roon.;Clio P Mavragani.
来源: Rheumatology (Oxford). 2021年60卷7期3072-3087页
In primary SS (pSS), chemokines and cytokines orchestrate immunopathology driven by a complex network of interacting inflammatory cells. In recent years, the importance of chemotactic and non-chemotactic cytokines that control function, movement and placing of all cells within the inflamed exocrine glands and directing immunopathology has become increasingly clear. This paper reviews the current knowledge on chemokines and focuses on the emerging roles of novel chemotactic and non-chemotactic mediators in pSS. It highlights their contribution to pathogenic processes such as B cell hyperactivity and the formation of ectopic lymphoid structures. To this end, the role of acquired (CXCR5/CCR9 Th-cell-mediated) and innate (inflammasome/IL-1/IL-18-mediated) pathways in steering immunopathology is discussed.
7360. Lymphomas complicating primary Sjögren's syndrome: from autoimmunity to lymphoma.
作者: Gaetane Nocturne.;Elena Pontarini.;Michele Bombardieri.;Xavier Mariette.
来源: Rheumatology (Oxford). 2021年60卷8期3513-3521页
Lymphoma development is the most serious complication of SS and the main factor impacting on mortality rate in patients with this condition. Lymphomas in SS are most commonly extranodal non-Hodgkin B-cell lymphomas of the mucosa-associated lymphoid tissue and frequently arise in salivary glands that are the target of a chronic inflammatory autoimmune process. Extensive work on lymphomagenesis in SS has established that the progression towards B-cell lymphoma is a multistep process related to local chronic antigenic stimulation of B cells. These neoplastic B cells in SS frequently derived from autoreactive clones, most commonly RF-producing B cells, which undergo uncontrolled proliferation and malignant escape. In this review, we highlight the most important recent findings that have enhanced our understanding of lymphoma development in SS, with particular reference to the close link between autoimmunity and lymphomagenesis. We also discuss how the identification of key factors involved in B-cell malignancies may impact on our ability to identify at early stages patients at increased risk of lymphoma with potential significant repercussions for the clinical management of SS patients. Finally, we identified the most promising areas of current and further research with the potential to provide novel basic and translational discoveries in the field. The questions of finding new biomarkers, developing a validated score for predicting lymphoma occurrence and assessing if a better control of disease activity will decrease the risk of lymphoma in primary SS will be the enthralling questions of the next few years.
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