Patients with rheumatold arthritis show a low prevalence of hayfever and suppressed disease activity when hayfever is evident: A role for T1/T2 cell balance

1997 ◽  
Vol 56 ◽  
pp. 484
Author(s):  
C.M. Verhoef ◽  
J.A.G. Van Roon ◽  
C.A.F.M. Brujnzeel-Koomen ◽  
F.P.J.G. Lafeber ◽  
J.W.J. Bijlsma
Lupus ◽  
2019 ◽  
Vol 28 (12) ◽  
pp. 1397-1406 ◽  
Author(s):  
Y Chu ◽  
C Zhao ◽  
B Zhang ◽  
X Wang ◽  
Y Wang ◽  
...  

Objective This study aimed to investigate the effect of rapamycin (RAPA) alone or in combination with all-trans retinoic acid (ATRA) on the T-helper 17 (Th17) cell/regulatory T-cell (Treg) balance in patients with systemic lupus erythematosus (SLE) and to evaluate the clinical efficacy. Methods Seventy patients with SLE were enrolled. They were randomly and equally divided into RAPA and RAPA + ATRA groups. The number of Th17 and Treg cells was measured by flow cytometry before and after treatment for 6, 12 and 24 weeks. The SLE Disease Activity Index (SLEDAI) score and the prednisone dose before and after treatment were used to evaluate the efficacy between the two groups. Results In both groups, at different time points after treatment, the number of Th17 cells ( p = 0.003) and Th17/Treg ratio ( p = 0.044) reduced, while the number of Treg cells ( p = 0.574) tended to increase. The SLEDAI score and the dose of prednisone decreased significantly ( p < 0.001). There was no significant difference in the number of Th17 cells ( p = 0.089), Treg cells ( p = 0.059), Th17/Treg ratio ( p = 0.580), SLEDAI score ( p = 0.127) and the dose of prednisone ( p = 0.329) between the two groups. Conclusion Disease activity in SLE patients reduced with RAPA alone or in conjunction with ATRA, reducing glucocorticoid requirement. One of its mechanisms of action may be regulating the Th17/Treg cell balance, which provides a new model for the pathogenesis and potential treatment of SLE.


Author(s):  
N.V. Bortnyak ◽  
◽  
O.A. Yepanchintseva ◽  
A.V. Khokhlov ◽  
B.M. Todurov ◽  
...  

Takayasu arteritis is a rare form of the vasculitis of large arteries. It is a disease difficult to diagnose and treat, often unpredictable in terms of outcome and life-treatening. Despite its low prevalence, Takayasu arteritis deserves close attention for therapists, cardiologists, rheumatologists and angiosurgeons. This article presents classifications, features of the clinical course of the disease, possibilities of the visualization diagnosis of the lesions of arteries, assessment of the disease activity. The issues of the contemporary drug therapy, interventional and surgical treatment methods and complications of the disease are presented.


Autoimmunity ◽  
2009 ◽  
pp. 1-1
Author(s):  
Jose Miguel Sempere-Ortells ◽  
Vicente Perez-Garcia ◽  
Gema Marin-Alberca ◽  
Alejandra Peris-Pertusa ◽  
Jose Miguel Benito ◽  
...  

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