Chemokines in stored platelet concentrates

被引:96
作者
Bubel, S
Wilhelm, D
Entelmann, M
Kirchner, H
Kluter, H
机构
[1] UNIV LUBECK,SCH MED,INST IMMUNOL & TRANSFUS MED,D-23538 LUBECK,GERMANY
[2] INST APPL DERMATOL RES,SCHENEFELD HAMBURG,GERMANY
关键词
D O I
10.1046/j.1537-2995.1996.36596282589.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Platelets contain several mediators, belonging to a family of proinflammatory cytokines named chemokines, that are stored in the organelles. Release and accumulation of these chemokines during storage of platelet concentrates (PCs) might be responsible for nonhemolytic transfusion reactions. Study Design and Methods: Analysis was done of pH and the levels of platelet factor 4, beta-thromboglobulin, interleukin 8, RANTES, macrophage-inflammatory protein-1 alpha, lactate dehydrogenase, and serotonin in the supernatant of stored PCs on Days 1, 3, 5, and 8. PCs were prepared by apheresis or from pools of four buffy coats. Puffy coat PCs were filtered before storage. Results: Nonfiltered apheresis PCs, which had a higher white cell contamination (p<0.01), contained significantly more platelets than did buffy coat PCs (p = 0.02). The pH decreased significantly in apheresis PCs (p = 0.01), whereas there was a significant increase in lactate dehydrogenase (p<0.001). In buffy coat PCs, pH remained stable and lactate dehydrogenase increased moderately. Concentrations of platelet factor 4 and beta-thromboglobulin increased steadily in both preparations over the storage period (p<0.001). Macrophage-inflammatory protein-1 alpha was hardly detectable in the supernatant of both PCs, while RANTES levels increased significantly with storage time (p<0.001). Interleukin 8 was not found in the supernatant of any PCs, with the exception of one apheresis PC with high white cell contamination (>10(9)/L). Serotonin levels were higher in apheresis PCs (p = 0.01), but the levels did not correlate with storage time. Conclusion: Platelet factor 4, beta-thromboglobulin, and RANTES were released from platelets during storage and accumulated over time in the PCs. These chemokines might play a causative role in nonhemolytic transfusion reactions because of their inflammatory potential, but the clinical effects of the transfusion of PCs with high chemokine contents remain to be investigated.
引用
收藏
页码:445 / 449
页数:5
相关论文
共 23 条
[1]   MACROPHAGE INFLAMMATORY PROTEIN-1-ALPHA ACTIVATES BASOPHILS AND MAST-CELLS [J].
ALAM, R ;
FORSYTHE, PA ;
STAFFORD, S ;
LETTBROWN, MA ;
GRANT, JA .
JOURNAL OF EXPERIMENTAL MEDICINE, 1992, 176 (03) :781-786
[2]  
ALAM R, 1993, J IMMUNOL, V150, P3442
[3]   EFFECT OF FILTRATION OF PLATELET CONCENTRATES ON THE ACCUMULATION OF CYTOKINES AND PLATELET-RELEASE FACTORS DURING STORAGE [J].
AYE, MT ;
PALMER, DS ;
GIULIVI, A ;
HASHEMI, S .
TRANSFUSION, 1995, 35 (02) :117-124
[4]   NEUTROPHIL-ACTIVATING PEPTIDE-1 INTERLEUKIN-8, A NOVEL CYTOKINE THAT ACTIVATES NEUTROPHILS [J].
BAGGIOLINI, M ;
WALZ, A ;
KUNKEL, SL .
JOURNAL OF CLINICAL INVESTIGATION, 1989, 84 (04) :1045-1049
[5]   CC-CHEMOKINES IN ALLERGIC INFLAMMATION [J].
BAGGIOLINI, M ;
DAHINDEN, CA .
IMMUNOLOGY TODAY, 1994, 15 (03) :127-133
[6]   RANTES AND RELATED CHEMOKINES ACTIVATE HUMAN BASOPHIL GRANULOCYTES THROUGH DIFFERENT G-PROTEIN-COUPLED RECEPTORS [J].
BISCHOFF, SC ;
KRIEGER, M ;
BRUNNER, T ;
ROT, A ;
VONTSCHARNER, V ;
BAGGIOLINI, M ;
DAHINDEN, CA .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1993, 23 (03) :761-767
[7]   THE FEBRILE PLATELET TRANSFUSION REACTION - A CYTOKINE SHOWER [J].
FERRARA, JLM .
TRANSFUSION, 1995, 35 (02) :89-90
[8]   PREVALENCE OF PLATELET TRANSFUSION REACTIONS BEFORE AND AFTER IMPLEMENTATION OF LEUKOCYTE-DEPLETED PLATELET CONCENTRATES BY FILTRATION [J].
GOODNOUGH, LT ;
RIDDELL, J ;
LAZARUS, H ;
CHAFEL, TL ;
PRINCE, G ;
HENDRIX, D ;
YOMTOVIAN, R .
VOX SANGUINIS, 1993, 65 (02) :103-107
[9]   THE ROLE OF THE PLASMA FROM PLATELET CONCENTRATES IN TRANSFUSION REACTIONS [J].
HEDDLE, NM ;
KLAMA, L ;
SINGER, J ;
RICHARDS, C ;
FEDAK, P ;
WALKER, I ;
KELTON, JG .
NEW ENGLAND JOURNAL OF MEDICINE, 1994, 331 (10) :625-628
[10]  
HERVIG T, 1990, CLIN CHEM, V36, P28