scholarly journals Serum level of adiponectin is a surrogate independent biomarker of radiographic disease progression in early rheumatoid arthritis: results from the ESPOIR cohort

2013 ◽  
Vol 15 (6) ◽  
pp. R210 ◽  
Author(s):  
Magali Meyer ◽  
Jérémie Sellam ◽  
Soraya Fellahi ◽  
Salma Kotti ◽  
Jean-Philippe Bastard ◽  
...  
Rheumatology ◽  
2000 ◽  
Vol 39 (9) ◽  
pp. 1009-1013 ◽  
Author(s):  
S. Aman ◽  
L. Paimela ◽  
M. Leirisalo-Repo ◽  
J. Risteli ◽  
H. Kautiainen ◽  
...  

Author(s):  
A. S. Avdeeva ◽  
E. N. Aleksandrova ◽  
D. E. Karateev ◽  
E. L. Luchikhina ◽  
A. A. Novikov ◽  
...  

Rheumatology ◽  
2007 ◽  
Vol 46 (6) ◽  
pp. 931-933 ◽  
Author(s):  
R. B. Mueller ◽  
A. Skapenko ◽  
J. Wendler ◽  
F. Schuch ◽  
J. R. Kalden ◽  
...  

Rheumatology ◽  
2019 ◽  
Vol 58 (8) ◽  
pp. 1331-1343 ◽  
Author(s):  
Irene Di Ceglie ◽  
Nik N L Kruisbergen ◽  
Martijn H J van den Bosch ◽  
Peter L E M van Lent

AbstractBone erosion is one of the central hallmarks of RA and is caused by excessive differentiation and activation of osteoclasts. Presence of autoantibodies in seropositive arthritis is associated with radiographic disease progression. ICs, formed by autoantibodies and their antigens, activate Fcγ-receptor signalling in immune cells, and as such stimulate inflammation-mediated bone erosion. Interestingly, ICs can also directly activate osteoclasts by binding to FcγRs on their surface. Next to autoantibodies, high levels of alarmins, among which is S100A8/A9, are typical for RA and they can further activate the immune system but also directly promote osteoclast function. Therefore, IC-activated FcγRs and S100A8/A9 might act as partners in crime to stimulate inflammation and osteoclasts differentiation and function, thereby stimulating bone erosion. This review discusses the separate roles of ICs, FcγRs and alarmins in bone erosion and sheds new light on the possible interplay between them, which could fuel bone erosion.


1995 ◽  
Vol 14 (5) ◽  
pp. 566-569 ◽  
Author(s):  
J. K. Lacki ◽  
T. Schochat ◽  
K. Klama ◽  
S. H. Mackiewicz ◽  
W. Müller

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