T-cell subsets in rheumatoid arthritis patients on long-term anti-TNF or IL-6 receptor blocker therapy

Data on the impact of biological therapies on the T-cell phenotype in rheumatoid arthritis are limited. Here, we prospectively measured the percentages of 15 circulating T-cell subtypes using flow cytometry. We obtained transversal and longitudinal data in 30 anti-TNF responders, 19 secondary anti-T...

Teljes leírás

Elmentve itt :
Bibliográfiai részletek
Szerzők: Dulic Sonja
Vásárhelyi Zsófia
Sava Florentina
Berta László Gergely
Szalay Balázs
Toldi Gergely
Kovács László
Balog Attila
Dokumentumtípus: Cikk
Megjelent: 2017
Sorozat:MEDIATORS OF INFLAMMATION 2017
doi:10.1155/2017/6894374

mtmt:3288491
Online Access:http://publicatio.bibl.u-szeged.hu/13064
Leíró adatok
Tartalmi kivonat:Data on the impact of biological therapies on the T-cell phenotype in rheumatoid arthritis are limited. Here, we prospectively measured the percentages of 15 circulating T-cell subtypes using flow cytometry. We obtained transversal and longitudinal data in 30 anti-TNF responders, 19 secondary anti-TNF nonresponders, and 43 IL-6R antagonist responders, before, 8 weeks and at least 6 months after biological therapy. Untreated RA patients and healthy controls were also included. The important findings are the following: ( 1) the proportion of regulatory T-cells (Tregs) which are decreased in untreated RA patients becomes normal in all long-term-treated groups; ( 2) in anti-TNF responders as well as in nonresponders, the frequencies of naive CD4+ and CD8+ cells are lower, whereas those of proinflammatory Th1, Th2, and Th17 cells and HLA-DR+-activated cells are higher than those in untreated RA or healthy controls; ( 3) in IL-6R responders, Th1 proportion is decreased, while that of Th2 and Th17 is increased as compared to that in anti-TNF-treated patients and controls; ( 4) pending confirmation, a CD4CD69 ratio <2.43 at baseline, could be useful to predict a good therapeutic response to anti-TNF therapy. This study provides comprehensive information regarding the long-term impacts of those biological therapies on the ecotaxis of T-cells in RA.
Terjedelem/Fizikai jellemzők:Azonosító: 6894374-Terjedelem: 19 p.
ISSN:0962-9351