| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
(Circulation. 1995;92:2876-2885.)
© 1995 American Heart Association, Inc.
Articles |
From the Second Department of Surgery (C.H., M.I., A.Z., E.W.) and Department of Urology (A.S., C.R., G.K., G.S.), University of Vienna, Austria.
Correspondence to Dr Christoph Holzinger, Allgemeines Krankenhaus Wien, Abteilung Herz- und Thoraxchirurgie, Währinger Gürtel 18-20, A-1090 Vienna, Austria.
Background Immunological factors in the pathogenesis of idiopathic dilated cardiomyopathy (IDC) were suggested previously on the basis of the demonstration of mononuclear cell infiltrates and autoantibodies against the myocardium. The present study investigated whether tissue leukocyte subpopulations isolated from hearts with IDC (n=6) differ in phenotype from those of tissues without IDC (n=7).
Methods and Results Leukocytes were quantified as reactive cells
per square millimeter in perivascular, interstitial, and
parenchymal tissue sections. Freshly isolated heart-tissue T cells
and peripheral-blood T cells from the same patients
were analyzed by triple staining and flow cytometry to identify
T-cell subpopulations as well as their states of differentiation
(expression of CD45RA and Leu-8 versus CD45RO) and activation (IL-2R,
IL-7R, very late antigen1, HLA-DR). All types of infiltrating cells
(T cells, B cells, macrophages, granulocytes) are increased in
hearts with IDC compared with normal hearts, but only CD8+
T cells and macrophages are increased relative to the other
leukocyte subpopulations.
CD45RO+/CD45RA-/Leu-8-
cells constitute the majority of heart-tissue T cells in both
normal hearts and hearts with IDC. Strikingly, hearts with IDC are
infiltrated by eightfold greater numbers of perivascularly located
IL-2R+ (26% of all T cells) and
CD45RO+activated memory T cells; moreover, in
contrast to normal heart,
40% of both CD4+ and
CD8+ heart-tissue T cells express activation
markers.
Conclusions Both normal hearts and hearts with IDC are populated by leukocytes. The quantitative increase in IDC, associated with a dramatically altered activation status of heart-tissue T cells, suggests a direct role of infiltrating leukocytes in the pathogenesis of IDC.
Key Words: cardiomyopathy lymphocytes genes cells
This article has been cited by other articles:
![]() |
L. Codarri, L. Vallotton, D. Ciuffreda, J.-P. Venetz, M. Garcia, K. Hadaya, L. Buhler, S. Rotman, M. Pascual, and G. Pantaleo Expansion and tissue infiltration of an allospecific CD4+CD25+CD45RO+IL-7R{alpha}high cell population in solid organ transplant recipients J. Exp. Med., July 9, 2007; 204(7): 1533 - 1541. [Abstract] [Full Text] [PDF] |
||||
![]() |
L. Agnoletti, S. Curello, F. Malacarne, P. Airò, A. Cargnoni, M. Valgimigli, and R. Ferrari Immune activation in severe heart failure: Does etiology play a role? Eur. Heart J. Suppl., November 1, 2004; 6(suppl_F): F22 - F29. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Hayashidani, H. Tsutsui, T. Shiomi, M. Ikeuchi, H. Matsusaka, N. Suematsu, J. Wen, K. Egashira, and A. Takeshita Anti-Monocyte Chemoattractant Protein-1 Gene Therapy Attenuates Left Ventricular Remodeling and Failure After Experimental Myocardial Infarction Circulation, October 28, 2003; 108(17): 2134 - 2140. [Abstract] [Full Text] [PDF] |
||||
![]() |
A Angelini, M Crosato, G M Boffa, F Calabrese, V Calzolari, R Chioin, L Daliento, and G Thiene Active versus borderline myocarditis: clinicopathological correlates and prognostic implications Heart, March 1, 2002; 87(3): 210 - 215. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Staudt, F. Schaper, V. Stangl, A. Plagemann, M. Bohm, K. Merkel, G. Wallukat, K. D. Wernecke, K. Stangl, G. Baumann, et al. Immunohistological Changes in Dilated Cardiomyopathy Induced by Immunoadsorption Therapy and Subsequent Immunoglobulin Substitution Circulation, June 5, 2001; 103(22): 2681 - 2686. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. Shioi, A. Matsumori, Y. Kihara, M. Inoko, K. Ono, Y. Iwanaga, T. Yamada, A. Iwasaki, K. Matsushima, and S. Sasayama Increased Expression of Interleukin-1ß and Monocyte Chemotactic and Activating Factor/Monocyte Chemoattractant Protein-1 in the Hypertrophied and Failing Heart With Pressure Overload Circ. Res., November 19, 1997; 81(5): 664 - 671. [Abstract] [Full Text] |
||||
![]() |
H. Funakoshi, T. Kubota, Y. Machida, N. Kawamura, A. M. Feldman, H. Tsutsui, H. Shimokawa, and A. Takeshita Involvement of inducible nitric oxide synthase in cardiac dysfunction with tumor necrosis factor-alpha Am J Physiol Heart Circ Physiol, June 1, 2002; 282(6): H2159 - H2166. [Abstract] [Full Text] [PDF] |
||||
|
Circulation Home | Subscriptions | Archives | Feedback | Authors | Help | AHA Journals Home | Search Copyright © 1995 American Heart Association, Inc. All rights reserved. Unauthorized use prohibited. |