IMMUNE FUNCTION IN ALCOHOLISM - A CONTROLLED-STUDY

被引:43
作者
KRONFOL, Z [1 ]
NAIR, M [1 ]
HILL, E [1 ]
KROLL, P [1 ]
BROWER, K [1 ]
GREDEN, J [1 ]
机构
[1] UNIV MICHIGAN,ALCOHOL RES CTR,ANN ARBOR,MI 48109
关键词
ALCOHOL; IMMUNITY; LYMPHOCYTE PHENOTYPE; LYMPHOKINE-ACTIVATED KILLER CYTOTOXICITY; NATURAL KILLER CYTOTOXICITY;
D O I
10.1111/j.1530-0277.1993.tb00763.x
中图分类号
R194 [卫生标准、卫生检查、医药管理];
学科分类号
摘要
Several studies have shown an increased risk for infection and cancer in alcoholic patients. The mechanisms for such observations remain largely unknown. In an effort to investigate the possibility of immunological dysfunction in alcoholism, we studied three immune parameters in 47 hospitalized chronic alcoholic patients and 47 age- and sex-matched normal controls. The immune measures were: (1) lymphocyte phenotyping, with estimates of percentages of T cells, B cells, T helpers, T suppressors, natural killer (NK) cells, and cells carrying the activation markers IL2R1 and I2; (2) NK cell activity; and (3) lymphokine-activated killer cell activity. Results indicate a significant increase in the IL2R and I2 lymphocyte markers in alcoholic patients compared with matched controls. We also found a nonsignificant trend for a decrease in the percentage of suppressor T cells in the alcoholic group, as well as a trend for a negative correlation between the percentage of T suppressor cells and age. There were no significant differences in either NK or lymphokine-activated killer cell activities between the two groups. Furthermore, there were no significant associations between duration and intensity of alcohol consumption and any of the immune measures. These results suggest subtle alterations in immune regulation in alcoholic patients that cannot be explained solely on the basis of duration and/or amount of alcohol consumed.
引用
收藏
页码:279 / 283
页数:5
相关论文
共 28 条
[1]  
ABDALLAH RM, 1983, IMMUNOLOGY, V50, P131
[2]   INFECTIONS IN THE ALCOHOLIC [J].
ADAMS, HG ;
JORDAN, C .
MEDICAL CLINICS OF NORTH AMERICA, 1984, 68 (01) :179-200
[3]  
BAGASRA O, 1987, IMMUNOLOGY, V61, P63
[4]   QUANTIFICATION OF NATURAL CYTO-TOXICITY BY HUMAN-LYMPHOCYTE SUBPOPULATIONS ISOLATED BY DENSITY - HETEROGENEITY OF THE EFFECTOR-CELLS [J].
BLOOM, ET ;
KORN, EL .
JOURNAL OF IMMUNOLOGICAL METHODS, 1983, 58 (03) :323-335
[5]  
BOYUM A, 1968, SCAND J CLIN LAB INV, VS 21, P77
[6]  
CHARPENTIER B, 1984, CLIN EXP IMMUNOL, V58, P107
[7]   MECHANISMS OF HOST DEFENSE IN WELL NOURISHED PATIENTS WITH CHRONIC-ALCOHOLISM [J].
ERICSSON, CD ;
KOHL, S ;
PICKERING, LK ;
DAVIS, J ;
GLASS, GS ;
FAILLACE, LA .
ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH, 1980, 4 (03) :261-265
[8]   REDUCED PROLIFERATION IN LYMPHOCYTES-T IN AGED HUMANS IS PREDOMINANTLY IN THE CD8+ SUBSET, AND IS UNRELATED TO DEFECTS IN TRANSMEMBRANE SIGNALING WHICH ARE PREDOMINANTLY IN THE CD4+ SUBSET [J].
GROSSMANN, A ;
LEDBETTER, JA ;
RABINOVITCH, PS .
EXPERIMENTAL CELL RESEARCH, 1989, 180 (02) :367-382
[9]   A RATING SCALE FOR DEPRESSION [J].
HAMILTON, M .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 1960, 23 (01) :56-62
[10]  
HOLMES TH, 1967, J PSYCHOSOM RES, V11, P213, DOI 10.1016/0022-3999(67)90010-4