Cytokines and T cell differentiation in systemic sclerosis

被引:0
作者
Trad, S. [1 ]
Granel, B. [2 ,3 ]
Parizot, C. [4 ]
Dorgham, K. [4 ]
Hanslik, T. [1 ,5 ]
Marie, I. [6 ]
Amoura, Z. [7 ]
机构
[1] CHU Ambroise Pare, AP HP, Serv Med Interne, F-92100 Boulogne, France
[2] Univ Mediterranee, Hop Nord, AP HP, Serv Med Interne, F-13915 Marseille 15, France
[3] Univ Mediterranee, Fac Med Timone, Inserm UMR 906, F-13005 Marseille, France
[4] Univ Paris 06, AP HP, Lab Immunol Tissulaire & Cellulaire, Inserm U945, F-75013 Paris, France
[5] Univ Versailles St Quentin En Yveliness, F-78000 Versailles, France
[6] CHU Rouen, Serv Med Interne, F-76000 Rouen, France
[7] Univ Paris 06, CHU Pitie Salpetriere, AP HP, Serv Med Interne, F-75013 Paris, France
来源
REVUE DE MEDECINE INTERNE | 2011年 / 32卷 / 08期
关键词
Systemic sclerosis; Cytokine; Immunology; Th1; Th2; Th9; Th17; Th22; Treg; T regulatory cells; Lymphocyte; Differentiation; Physiopathology; GROWTH-FACTOR-BETA; NECROSIS-FACTOR-ALPHA; SOLUBLE INTERLEUKIN-2 RECEPTOR; BLOOD MONONUCLEAR-CELLS; BRONCHOALVEOLAR LAVAGE FLUID; HUMAN DERMAL FIBROBLASTS; ELEVATED SERUM-LEVELS; SCLERODERMA FIBROBLASTS; TGF-BETA; TRANSFORMING GROWTH-FACTOR-BETA-1;
D O I
10.1016/j.revmed.2010.07.015
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The physiopathology of systemic sclerosis remains unclear within a complex interaction between vasculopathy, perivascular inflammatory infiltrate, extensive tissue fibrosis and auto-immune manifestations. Chronology between vascular disease and adjacent inflammatory cell infiltration is still not yet clarified. There is growing evidence that T cell activation and its cytokine expression play a key role in vascular impairment occurrence and collagen dysregulation. Nevertheless, cytokine descriptions are mainly limited to blood and tissue measurement and the T cells differentiation analysis restricted to the Th1/Th2 balance. The purpose of this review is to establish an exhaustive cartography of cytokines involved in T cell differentiation, regarding the recent advance in T lymphocyte differentiation, including Th9, Th17, Th22 and regulatory T cells (Treg) pathways. This review will focus on Th17, Th22 and Treg differentiation, corresponding to the equilibrium between inflammation and tolerance. Finally, regarding published results in systemic sclerosis, T cells participation appears to be more a Th1/Th2 co-expression than an exclusive Th1 or Th2 polarization. Also, a possible Th22/Treg imbalance is suggested, leading to a Th22 overexpression and likely to tissue inflammation genesis. (C) 2010 Societe nationale francaise de medecine interne (SNFMI). Published by Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:472 / 485
页数:14
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