scholarly journals IL‐23/IL‐17 axis and soluble receptors isoforms sIL‐23R and sIL‐17RA in patients with rheumatoid arthritis‐presenting periodontitis

Author(s):  
Ruth Rodríguez‐Montaño ◽  
Ana Guilaisne Bernard‐Medina ◽  
Edith Oregon‐Romero ◽  
Vianeth María del Carmen Martínez‐Rodríguez ◽  
María Luisa Pita‐López ◽  
...  
2010 ◽  
Vol 32 (1) ◽  
pp. 199-206 ◽  
Author(s):  
Peter Oelzner ◽  
Sybille Franke ◽  
Gabriele Lehmann ◽  
Thorsten Eidner ◽  
Gert Hein ◽  
...  

2014 ◽  
Vol 2014 ◽  
pp. 1-7 ◽  
Author(s):  
Martin Schulz ◽  
Helmut Dotzlaw ◽  
Gunther Neeck

The effects of the TNF-αblockers infliximab or etanercept on the levels of TNF-α, TNF-receptor 1 (TNF-R1), and TNF-receptor 2 (TNF-R2), as well as the levels of the inflammation markers CRP and IL-6, were measured in ankylosing spondylitis (AS) and rheumatoid arthritis (RA) patients receiving treatment with either compound. We found that RA patients tend to have higher levels of TNF-αthan both healthy individuals and AS patients prior to treatment (P<0.05). We measured greatly increased levels of TNF-αin both the AS and RA etanercept patient groups during the course of treatment, while in the infliximab treated patients, the amount of TNF-αmeasured remained unchanged. Elevated TNF-αin the etanercept treated patients does not appear to be a significant risk factor for the spontaneous development of further autoimmune diseases in our study group. Increased levels of TNF-R1 were determined in both AS (P<0.05) and RA (P<0.001) patients when compared to healthy controls. In AS patients, the levels of TNF-R1 dropped significantly when treated with either infliximab (P<0.01) or etanercept (P<0.001). In contrast, the levels of this receptor remained unchanged in RA patients treated with either compound.


2012 ◽  
Vol 25 (1) ◽  
pp. 281-285 ◽  
Author(s):  
A. Riccio ◽  
L. Postiglione ◽  
P. Sabatini ◽  
M. Linvelli ◽  
I. Soriente ◽  
...  

The high serum levels of Interleukin-6 (IL-6) and its soluble receptors (sIL-6r and sgp 130), described in the course of Rheumatoid Arthritis (RA), have been linked to the enhanced activity of this cytokine in this disorder. In this study, the serum concentrations of IL-6 and its soluble receptors were determined in a group of patients with HCV-related arthritis (HCVrA), a condition resembling RA in several aspects, and then compared to those found in a sample of subjects affected by RA. Twenty-one patients with HCVrA, 24 patients with RA and 20 healthy subjects (control group) were examined. Different ELISA methods were used for determination of serum concentrations of IL-6, sIL-6r and sgp 130. Increased IL-6 serum levels were found in 15 (71%) of the patients with HCVrA and in 16 (62%) of those with RA. Eight (38%) of the patients with HCVrA and 11 (46%) of those with RA denoted high levels of sIL-6r, while sgp 130 levels were elevated in 21 (76%) of the patients with HCVrA and in 16 (69%) of those with RA. A significant difference between the median values of sIL-6r and sgp 130 levels in the two groups of patients versus controls was found. A mild correlation of these parameters with RF levels was detected in the RA group. Furthermore, in HCVrA patients the serum levels of IL-6, sIL-6r and sgpl30 appeared unrelated to HCV viraemia and to levels of transaminases. The enhanced serum levels of IL-6 in HCVra patients indicate an increased synthesis and hyperactivity of this cytokine in HCVrA, and the substantial similarity of the behaviour of IL-6 and its serum receptors in the two groups of patients suggests common mechanisms with RA, in which the function of IL-6 is central.


Rheumatology ◽  
1994 ◽  
Vol 33 (11) ◽  
pp. 1017-1024 ◽  
Author(s):  
P. BARRERA ◽  
A. M. TH. BOERBOOMS ◽  
P. N. M. DEMACKER ◽  
L. B. A. VAN DE PUTTE ◽  
H. GALLATI ◽  
...  

2013 ◽  
Vol 72 (Suppl 3) ◽  
pp. A834.1-A834
Author(s):  
A. A. Alshevskaya ◽  
J. A. Lopatnikova ◽  
F. F. Vasiliev ◽  
S. V. Sennikov ◽  
N. Shkaruba ◽  
...  

2019 ◽  
Vol 10 (2) ◽  
pp. 12-24 ◽  
Author(s):  
L. Matteucci ◽  
M. C. Nucci

Abstract Rheumatoid arthritis is an autoimmune disease of unknown etiology that manifests as a persistent inflammatory synovitis and eventually destroys the joints. The immune system recognizes synovial cells as not self and consequently causes lymphocyte and antibody proliferation that is promoted by the pro-inflammatory cytokines, the most significant being tumor necrosis factor TNF-α. In the treatment of rheumatoid arthritis either monoclonal antibodies or soluble receptors are used to neutralize the TNF-α bioactivity, such as sTNFR2, Etanercept and Infliximab. In [M. Jit et al. Rheumatology 2005;44:323-331] a mathematical model that represents the TNF-α dynamics in the inflamed synovial joint within which locally produced TNF-α can bind to cell-surface receptors was proposed. It consists of four coupled ordinary differential equations, that were integrated numerically assuming a range of estimates of the key parameters. In this paper we complement the previous work by determining the general solution of those equations for specific conditions on the parameters. Then we characterize the behavior of TNF-α in the presence of different inhibitors and also evaluate the inhibitors effectiveness in the treatment of rheumatoid arthritis.


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