Distinct Effects of Anti-Tumor Necrosis Factor Combined Therapy on TH1/TH2 Balance in Rheumatoid Arthritis Patients

被引:19
作者
Herman, S.
Zurgil, N.
Machlav, S.
Shinberg, A.
Langevitz, P. [2 ]
Ehrenfeld, M. [2 ]
Deutsch, M. [1 ]
机构
[1] Bar Ilan Univ, Biophys Interdisciplinary Schottenstein Ctr Res &, Dept Phys, IL-52900 Ramat Gan, Israel
[2] Sheba Med Ctr, Dept Rheumatol, Tel Hashomer, Israel
关键词
LOW-DOSE METHOTREXATE; T-CELLS; LYMPHOCYTES; APOPTOSIS; INFLIXIMAB; EXPRESSION; COMBINATION; ETANERCEPT; DISEASE; CCR4;
D O I
10.1128/CVI.00061-11
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The immune balance in patients with rheumatoid arthritis (RA), a disease characterized by TH1 dominance, treated by the preferred combined anti-tumor necrosis factor (anti-TNF) and methotrexate (MTX) therapy was evaluated by assessing the chemokine and cytokine receptors as well as apoptosis induction. A meta-analysis of combined therapy by TNF blockers and MTX in 15 RA patients, MTX monotherapy in 20 RA patients, and 11 diagnosed but untreated RA patients was performed by assessing several immune markers in the whole lymphocyte population, as well as in specific CD4 cells, by both flow cytometry and image analysis. A significant downregulation of CXCR3 and IL-12 receptors (both TH1 markers) and a significant increase in the chemokine receptor CCR4 and, to a lesser extent, IL-4R (both TH2 markers) were found; a particularly marked increase was found in patients treated by combined therapy. This phenomenon was pronounced in CD4 cells and was accompanied by a high proportion of apoptotic cells. The therapeutic effect of MTX and TNF blockers may be due to apoptosis induction in lymphocytes infiltrating from the inflammation site and restoring the TH1/TH2 balance.
引用
收藏
页码:1077 / 1082
页数:6
相关论文
共 31 条
[1]   The imbalance in the ratio of Th1 and Th2 helper lymphocytes in uraemia is mediated by an increased apoptosis of Th1 subset [J].
Alvarez-Lara, MA ;
Carracedo, J ;
Ramírez, R ;
Martín-Malo, A ;
Rodríguez, M ;
Madueno, JA ;
Aljama, P .
NEPHROLOGY DIALYSIS TRANSPLANTATION, 2004, 19 (12) :3084-3090
[2]   THE AMERICAN-RHEUMATISM-ASSOCIATION 1987 REVISED CRITERIA FOR THE CLASSIFICATION OF RHEUMATOID-ARTHRITIS [J].
ARNETT, FC ;
EDWORTHY, SM ;
BLOCH, DA ;
MCSHANE, DJ ;
FRIES, JF ;
COOPER, NS ;
HEALEY, LA ;
KAPLAN, SR ;
LIANG, MH ;
LUTHRA, HS ;
MEDSGER, TA ;
MITCHELL, DM ;
NEUSTADT, DH ;
PINALS, RS ;
SCHALLER, JG ;
SHARP, JT ;
WILDER, RL ;
HUNDER, GG .
ARTHRITIS AND RHEUMATISM, 1988, 31 (03) :315-324
[3]   Adalimumab - A review of its use in rheumatoid arthritis [J].
Bang, LM ;
Keating, GM .
BIODRUGS, 2004, 18 (02) :121-139
[4]   Differential Th1/Th2 cytokine patterns in chronic arthritis:: interferon γ is highly expressed in synovium of rheumatoid arthritis compared with seronegative spondyloarthropathies [J].
Cañete, JD ;
Martinez, SE ;
Farrés, J ;
Sanmarti, R ;
Blay, M ;
Gómez, A ;
Salvador, G ;
Muñoz-Gómez, J .
ANNALS OF THE RHEUMATIC DISEASES, 2000, 59 (04) :263-268
[5]  
Chen DY, 2004, J RHEUMATOL, V31, P2189
[6]   Low-dose methotrexate: A mainstay in the treatment of rheumatoid arthritis [J].
Cronstein, BN .
PHARMACOLOGICAL REVIEWS, 2005, 57 (02) :163-172
[7]   Infliximab and the TNF-α system [J].
Ebert, Ellen C. .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 2009, 296 (03) :G612-G620
[8]   Methotrexate inhibits the first committed step of purine biosynthesis in mitogen-stimulated human T-lymphocytes:: a metabolic basis for efficacy in rheumatoid arthritis? [J].
Fairbanks, LD ;
Rückemann, K ;
Qiu, Y ;
Hawrylowicz, CM ;
Richards, DF ;
Swaminathan, R ;
Kirschbaum, B ;
Simmonds, HA .
BIOCHEMICAL JOURNAL, 1999, 342 :143-152
[9]   Immunologic mechanisms in the pathogenesis of rheumatoid arthritis [J].
Firestein, GS .
JCR-JOURNAL OF CLINICAL RHEUMATOLOGY, 2005, 11 (03) :S39-S44
[10]   Immunosuppressive properties of methotrexate: Apoptosis and clonal deletion of activated peripheral T cells [J].
Genestier, L ;
Paillot, R ;
Fournel, S ;
Ferraro, C ;
Miossec, P ;
Revillard, JP .
JOURNAL OF CLINICAL INVESTIGATION, 1998, 102 (02) :322-328