Alginates from wound dressings activate human macrophages to secrete tumour necrosis factor-α

被引:185
作者
Thomas, A [1 ]
Harding, KG [1 ]
Moore, K [1 ]
机构
[1] Cardiff Univ, Dept Surg, Wound Healing Res Unit, Cardiff CF14 4SN, S Glam, Wales
关键词
alginate; wound healing; macrophage; activation; TNF alpha; endotoxin;
D O I
10.1016/S0142-9612(00)00072-7
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Alginates are used to manufacture a number of wound dressings. Clinical observations indicate that they may initiate or accelerate healing of chronic wounds after treatment of underlying pathology. Wound granulation tissue contains large numbers of macrophages and they are thought to regulate the healing process. As purified alginates have been demonstrated to activate macrophages this study was initiated to determine whether alginates present within wound dressings may interact with wound macrophages. Alginate fibres taken from four commercially available dressings were co-cultured with the human histiocytic lymphoma cell line U937 following its differentiation with PMA. Activation was assessed by measurement of TNF alpha production. Two of the dressings, Seasorb and Tegagen, had a minimal effect whilst Sorbsan at 1 mg/ml induced 302 + 19 pg/ml TNF alpha. This effect was inhibited by polymyxin B indicating that activation was due to endotoxin contamination. Kaltostat induced production of 839 + 36 pg/ml TNF alpha. This effect was induced both by polymyxin inhibitable endotoxin and a direct interaction with the alginate fibres, These data indicate that some alginate containing dressings have the potential to activate macrophages within the chronic wound bed and generate a pro-inflammatory signal which may initiate a resolving inflammation characteristic of healing wounds. (C) 2000 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:1797 / 1802
页数:6
相关论文
共 26 条
[1]  
Chensue SW, 1990, J LEUKOCYTE BIOL, V48, P412
[2]  
CLARK RAF, 1996, WOUND REPAIR OVERVIE, P3
[3]  
COYNE CP, 1993, AM J VET RES, V54, P305
[4]  
DEVOS P, 1994, TRANSPLANT INT, V7, P264
[5]   ASBESTOS-STIMULATED TUMOR-NECROSIS-FACTOR RELEASE FROM ALVEOLAR MACROPHAGES DEPENDS ON FIBER LENGTH AND OPSONIZATION [J].
DONALDSON, K ;
LI, XY ;
DOGRA, S ;
MILLER, BG ;
BROWN, GM .
JOURNAL OF PATHOLOGY, 1992, 168 (02) :243-248
[6]   COMPARISON OF THE EFFECTS OF MOIST AND DRY CONDITIONS ON DERMAL REPAIR [J].
DYSON, M ;
YOUNG, S ;
PENDLE, CL ;
WEBSTER, DF ;
LANG, SM .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1988, 91 (05) :434-439
[7]   THE INVOLVEMENT OF CD14 IN STIMULATION OF CYTOKINE PRODUCTION BY URONIC-ACID POLYMERS [J].
ESPEVIK, T ;
OTTERLEI, M ;
SKJAKBRAEK, G ;
RYAN, L ;
WRIGHT, SD ;
SUNDAN, A .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1993, 23 (01) :255-261
[8]  
Gensheimer D, 1993, Ostomy Wound Manage, V39, P34
[9]   QUANTITATION OF CYTOKINE LEVELS IN SKIN-GRAFT DONOR SITE WOUND FLUID [J].
GRAYSON, LS ;
HANSBROUGH, JF ;
ZAPATASIRVENT, RL ;
DORE, CA ;
MORGAN, JL ;
NICOLSON, MA .
BURNS, 1993, 19 (05) :401-405
[10]  
GROVES AR, 1986, ANN ROY COLL SURG, V68, P27