eISSN: 1644-4124
ISSN: 1426-3912
Central European Journal of Immunology
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4/2015
vol. 40
 
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abstract:
Clinical immunology

A study on FoxP3 and Tregs in paired samples of peripheral blood and synovium in rheumatoid arthritis

Usha Shalini P.
,
Tanya Debnath
,
Vidyasagar JVS
,
Lakshmi K. Kona
,
Suguna R. Kamaraju
,
Ravindranath Kancherla
,
Lakshmi K. Chelluri

(Cent Eur J Immunol 2015; 40 (4): 431-436)
Online publish date: 2016/01/15
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There is an increasing evidence suggesting the role of fork head boxP3 (FoxP3) in the development and the regulation of CD4+CD25+ Treg cells. T-cell regulatory mechanisms in rheumatoid arthritis patients were evaluated by the contributing factors such as pro-inflammatory cytokines, circulating immune complexes, HLA DR expression, ligand binding biomarkers, FoxP3 expression in paired samples of peripheral blood (PB) and synovial fluid (SF). These cellular responses were further correlated with the humoral immune responses such as anti-cyclic citrullinated peptides IgG (CCP), circulating immune complex-c1q IgG (CIC), immunoglobulin G (IgG) and immunoglobulin M (IgM) of the rheumatoid arthritis factor (RAF). The results suggest a definitive role of Tregs in the homeostatic control because there is an increase in FoxP3 (37%) and HLA-DR (45%) expression in the synovial fluid as compared to PB. Furthermore, humoral responses as a downstream effector mechanism are positively correlated with the pathogenesis of rheumatoid arthritis (RA). A positive relationship exists between quantitative anti-CCP production and the expression of HLA-DR. The study relates an increased and pivotal role of B cell activation in the synovial fluid thereby permitting the need to ablate the targeted B cell immune responses.
keywords:

rheumatoid arthritis, FoxP3, regulatory T cell, circulating immune complex-c1q IgG, anti-cyclic citrullinated peptides IgG, rheumatoid factor IgG, rheumatoid factor IgM

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