PROPAGATION OF INFILTRATING LYMPHOCYTES AND GRAFT CORONARY-DISEASE IN CARDIAC TRANSPLANT RECIPIENTS

被引:15
作者
KAUFMAN, CL
ZEEVI, A
KORMOS, RL
ZERBE, TR
KEENAN, RJ
URETSKY, BF
GRIFFITH, BP
HARDESTY, RL
DUQUESNOY, RJ
机构
[1] UNIV PITTSBURGH,DEPT PATHOL,PITTSBURGH,PA 15260
[2] UNIV PITTSBURGH,DEPT SURG,PITTSBURGH,PA 15260
[3] UNIV PITTSBURGH,DEPT CARDIOL,PITTSBURGH,PA 15260
关键词
D O I
10.1016/0198-8859(90)90023-I
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 pattern of lymphocyte growth from endomyocardial biopsies in 55 heart transplant recipients was shown to be correlated with the subsequent development of graft coronary disease. Persistent lymphocyte growth was observed in 39 patients, and 15 of these growers (or 41%) developed graft coronary disease. In contrast, only 1 of 15 patients (or 6%) with nongrower biopsies showed subsequent graft coronary disease. Thus, biopsy growth was associated with a higher incidence of subsequent GCD (p=0.02). A comparison between the group of 15 growers with subsequent graft coronary disease and the 24 growers without subsequent graft coronary disease did not show any differences with respect to patient age, presence of coronary artery disease in the native heart, biopsy histology, donor alloreactivity of biopsy grown lymphocytes, and immunosuppressive drug regimen. On the other hand, the number of treated rejection episodes was significantly lower in the grower group with subsequent graft coronary disease (p=0.04). These data support the concept that graft coronary disease may involve rejection and that more immunosuppression may lower its incidence. This concept is strengthened by findings showing that alloreactive T cells can be propagated from coronary arteries of cardiac allografts with graft coronary disease. © 1990.
引用
收藏
页码:228 / 236
页数:9
相关论文
共 25 条
[1]  
Ahmed-Ansari A, 1988, Am J Cardiovasc Pathol, V2, P193
[2]  
BILLINGHAM M, 1988, TRANSPL P, V21, P3665
[3]  
BILLINGHAM ME, 1981, HEART TRANSPLANT, V1, P25
[4]   A T-CELL RECEPTOR GAMMA-CD3 COMPLEX FOUND ON CLONED FUNCTIONAL LYMPHOCYTES [J].
BORST, J ;
VANDEGRIEND, RJ ;
VANOOSTVEEN, JW ;
ANG, SL ;
MELIEF, CJ ;
SEIDMAN, JG ;
BOLHUIS, RLH .
NATURE, 1987, 325 (6106) :683-688
[5]   IMMUNE INTERFERON ACTIVATES MULTIPLE CLASS-II MAJOR HISTOCOMPATIBILITY COMPLEX GENES AND THE ASSOCIATED INVARIANT CHAIN GENE IN HUMAN-ENDOTHELIAL CELLS AND DERMAL FIBROBLASTS [J].
COLLINS, T ;
KORMAN, AJ ;
WAKE, CT ;
BOSS, JM ;
KAPPES, DJ ;
FIERS, W ;
AULT, KA ;
GIMBRONE, MA ;
STROMINGER, JL ;
POBER, JS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1984, 81 (15) :4917-4921
[6]   CARDIAC TRANSPLANTATION IN THE RAT .1. THE EFFECT OF HISTOCOMPATIBILITY DIFFERENCES ON GRAFT ARTERIOSCLEROSIS [J].
CRAMER, DV ;
QIAN, SQ ;
HARNAHA, J ;
CHAPMAN, FA ;
ESTES, LW ;
STARZL, TE ;
MAKOWKA, L .
TRANSPLANTATION, 1989, 47 (03) :414-419
[7]  
DEMETRIS AJ, 1989, TRANSPLANT P, V21, P3667
[8]   DYNAMICS OF ALLOSPECIFIC LYMPHOCYTE-T INFILTRATION IN VASCULARIZED HUMAN ALLOGRAFTS [J].
FUNG, JJ ;
ZEEVI, A ;
MARKUS, B ;
ZERBE, TR ;
DUQUESNOY, RJ .
IMMUNOLOGIC RESEARCH, 1986, 5 (02) :149-163
[9]   ACCELERATED CORONARY VASCULAR-DISEASE IN THE HEART-TRANSPLANT PATIENT - CORONARY ARTERIOGRAPHIC FINDINGS [J].
GAO, SZ ;
ALDERMAN, EL ;
SCHROEDER, JS ;
SILVERMAN, JF ;
HUNT, SA .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 1988, 12 (02) :334-340
[10]   CYTOMEGALO-VIRUS INFECTION IS ASSOCIATED WITH CARDIAC ALLOGRAFT-REJECTION AND ATHEROSCLEROSIS [J].
GRATTAN, MT ;
MORENOCABRAL, CE ;
STARNES, VA ;
OYER, PE ;
STINSON, EB ;
SHUMWAY, NE .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1989, 261 (24) :3561-3566