CD14+CD16+ monocytes in coronary artery disease and their relationship to serum TNF-α levels

被引:247
作者
Schlitt, A [1 ]
Heine, GH
Blankenberg, S
Espinola-Klein, C
Dopheide, JF
Bickel, C
Lackner, KJ
Iz, M
Meyer, J
Darius, H
Rupprecht, HJ
机构
[1] Univ Mainz, Dept Med 2, D-55101 Mainz, Germany
[2] Univ Mainz, Inst Clin Chem & Lab Med, D-55101 Mainz, Germany
[3] Univ Saarland, Dept Med 4, Homburg, Germany
关键词
CD14+CD16+monocytes; TNF-alpha; coronary artery disease;
D O I
10.1160/TH04-02-0095
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Monocytes play a central role in the inflammatory disease atherosclerosis. CD14+CD16+ monocytes are considered proinflammatory monocytes, as they have an increased capacity to produce proinflammatory cytokines, such as TNF-alpha, and are elevated in various inflammatory diseases. We hypothesized that :patients with coronary artery disease (CAD) have increased levels of CD14+CD16+ monocytes, and that CD14+CD16+ monocytes are associated with inflammation markiers.We investigated CD14+CD16+ monocytes in 247 Patients with CAD and 61 control subjects using flow cytometry. In addition serum concentrations of TNF-alpha IL-6, and Hs-CRP w ere assessed. Patients with CAD had higher levels of CD 14+CD 16+ monocytes than controls (13.6% versus 11.4%; p<0.001). Logistic regression analysis including quartiles of CD 14+CD 16+ monocytes showed that CD 14+CD 16+ monocytes were associated with prevalence of CAD (OR 4.9,95% Cl 2.5-19.1, for subjects in the fourth quartile in comparison to subjects in the first quartile). The association between CD14+CD16+ monocytes and CAD remained independently significant after adjustment for most potential confounders (OR 5.0, 95% Cl 1.2-20.0). Serum concentrations of TNF-alpha were elevated in subjects within the highest cluartiles of CD 14+CD 16+ monocytes (p=0.018). Our study showed that increased numbers of CD 14+CD 16+ monocytes are associated with coronary atherosclerosis and TNF-alpha. In accordance, recent animal studies suggest a possibly important role of these monocytes in the development of atherosclerosis.
引用
收藏
页码:419 / 424
页数:6
相关论文
共 27 条
[1]   Fractalkine preferentially mediates arrest and migration of CD16+ monocytes [J].
Ancuta, P ;
Rao, R ;
Moses, A ;
Mehle, A ;
Shaw, SK ;
Luscinskas, FW ;
Gabuzda, D .
JOURNAL OF EXPERIMENTAL MEDICINE, 2003, 197 (12) :1701-1707
[2]   A new class of membrane-bound chemokine with a CX(3)C motif [J].
Bazan, JF ;
Bacon, KB ;
Hardiman, G ;
Wang, W ;
Soo, K ;
Rossi, D ;
Greaves, DR ;
Zlotnik, A ;
Schall, TJ .
NATURE, 1997, 385 (6617) :640-644
[3]   The proinflammatory CD14+CD16+DR++ monocytes are a major source of TNF [J].
Belge, KU ;
Dayyani, F ;
Horelt, A ;
Siedlar, M ;
Frankenberger, M ;
Frankenberger, B ;
Espevik, T ;
Ziegler-Heitbrock, L .
JOURNAL OF IMMUNOLOGY, 2002, 168 (07) :3536-3542
[4]   Decreased atherosclerotic lesion formation in CX3CR1/apolipoprotein E double knockout mice [J].
Combadière, C ;
Potteaux, S ;
Gao, JL ;
Esposito, B ;
Casanova, S ;
Lee, EJ ;
Debré, P ;
Tedgui, A ;
Murphy, PM ;
Mallat, Z .
CIRCULATION, 2003, 107 (07) :1009-1016
[5]  
FINGERLE G, 1993, BLOOD, V82, P3170
[6]   Fractalkine and CX3CR1 mediate a novel mechanism of leukocyte capture, firm adhesion, and activation under physiologic flow [J].
Fong, AM ;
Robinson, LA ;
Steeber, DA ;
Tedder, TF ;
Yoshie, O ;
Imai, T ;
Patel, DD .
JOURNAL OF EXPERIMENTAL MEDICINE, 1998, 188 (08) :1413-1419
[7]  
Frankenberger M, 1996, BLOOD, V87, P373
[8]   Humoral immune responses in uremia and the role of IL-10 [J].
Girndt, M .
BLOOD PURIFICATION, 2002, 20 (05) :485-488
[9]   C-reactive protein, fibrinogen, interleukin-6 and tumour necrosis factor-α in the prognostic classification of unstable angina pectoris [J].
Koukkunen, H ;
Penttilä, K ;
Kemppainen, A ;
Halinen, M ;
Penttilä, I ;
Rantanen, T ;
Pyörälä, K .
ANNALS OF MEDICINE, 2001, 33 (01) :37-47
[10]   Decreased atherosclerosis in CX3CR1-/- mice reveals a role for fractalkine in atherogenesis [J].
Lesnik, P ;
Haskell, CA ;
Charo, IF .
JOURNAL OF CLINICAL INVESTIGATION, 2003, 111 (03) :333-340