RED-CELL ABO INCOMPATIBILITY AND PRODUCTION OF TUMOR-NECROSIS-FACTOR-ALPHA

被引:27
作者
DAVENPORT, RD
STRIETER, RM
KUNKEL, SL
机构
[1] UNIV MICHIGAN,SCH MED,DEPT PATHOL,ANN ARBOR,MI 48104
[2] UNIV MICHIGAN,SCH MED,DEPT INTERNAL MED,ANN ARBOR,MI 48104
关键词
D O I
10.1111/j.1365-2141.1991.tb04485.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Tumour necrosis factor-alpha (TNF) is a major mediator of diverse Pathophysiological events similar to those of haemolytic transfusion reactions (HTR), such as fever, intravascular coagulation and organ failure. However, the possible role of TNF in HTR has not been investigated. We have constructed an in vitro whole blood model of HTR to examine whether TNF may be produced in red cell ABO incompatibility. TNF was observed in plasma, in a dose dependent manner, when ABO incompatible red cells were added, but not with compatible (group O) cells. Plasma TNF levels were maximal at 2 h, and declined to control levels by 24 h. Haemolysis of incompatible red cells was accompanied by TNF production. Immune haemolysis induced TNF gene expression by buffy coat leucocytes, as determined by Northern blot analysis. Heat inactivation of plasma abolished TNF production, whereas prior treatment with interferon-gamma augmented the response. These results demonstrate that a major cytokine is produced in response to red cell incompatibility, and suggest that TNF may play a role in the pathogenesis of haemolytic transfusion reactions.
引用
收藏
页码:540 / 544
页数:5
相关论文
共 23 条
[1]  
BERKOW RL, 1987, J IMMUNOL, V139, P3783
[2]   EFFECT OF GAMMA-INTERFERON ON CACHECTIN EXPRESSION BY MONONUCLEAR PHAGOCYTES - REVERSAL OF THE LPSD (ENDOTOXIN RESISTANCE) PHENOTYPE [J].
BEUTLER, B ;
TKACENKO, V ;
MILSARK, I ;
KROCHIN, N ;
CERAMI, A .
JOURNAL OF EXPERIMENTAL MEDICINE, 1986, 164 (05) :1791-1796
[3]   GAMMA-INTERFERON ENHANCES MACROPHAGE TRANSCRIPTION OF THE TUMOR-NECROSIS-FACTOR CACHECTIN, INTERLEUKIN-1, AND UROKINASE GENES, WHICH ARE CONTROLLED BY SHORT-LIVED REPRESSORS [J].
COLLART, MA ;
BELIN, D ;
VASSALLI, JD ;
DEKOSSODO, S ;
VASSALLI, P .
JOURNAL OF EXPERIMENTAL MEDICINE, 1986, 164 (06) :2113-2118
[4]   A MODIFICATION OF THE BENZIDINE METHOD FOR MEASUREMENT OF HEMOGLOBIN IN PLASMA AND URINE [J].
CROSBY, WH ;
FURTH, FW .
BLOOD, 1956, 11 (04) :380-383
[5]  
DAVENPORT RD, 1990, BLOOD, V76, P2439
[6]   A HIGHLY SENSITIVE CELL-LINE, WEHI-164 CLONE 13, FOR MEASURING CYTOTOXIC FACTOR TUMOR-NECROSIS-FACTOR FROM HUMAN-MONOCYTES [J].
ESPEVIK, T ;
NISSENMEYER, J .
JOURNAL OF IMMUNOLOGICAL METHODS, 1986, 95 (01) :99-105
[7]   ACUTE HEMOLYTIC TRANSFUSION REACTIONS - FRESH LOOK AT PATHOGENESIS AND CONSIDERATIONS REGARDING THERAPY [J].
GOLDFINGER, D .
TRANSFUSION, 1977, 17 (02) :85-98
[8]   PATHOLOGIC STUDY OF INTRAVASCULAR COAGULATION FOLLOWING INCOMPATIBLE BLOOD TRANSFUSION IN DOGS .1. INTRAVENOUS INJECTION OF INCOMPATIBLE BLOOD [J].
HARDAWAY, RM ;
MCKAY, DG ;
WAHLE, GH ;
TARTOCK, DE ;
EDELSTEIN, R .
AMERICAN JOURNAL OF SURGERY, 1956, 91 (01) :24-31
[9]   TUMOR-NECROSIS-FACTOR-ALPHA INDUCES INCREASED HYDROGEN-PEROXIDE PRODUCTION AND FC RECEPTOR EXPRESSION, BUT NOT INCREASED IA-ANTIGEN EXPRESSION BY PERITONEAL-MACROPHAGES [J].
HOFFMAN, M ;
WEINBERG, JB .
JOURNAL OF LEUKOCYTE BIOLOGY, 1987, 42 (06) :704-707
[10]  
KUNKEL SL, 1988, J BIOL CHEM, V263, P5380