Anti-interleukin-6 antibody treatment restores cell-mediated immune function in mice with acute ethanol exposure before burn trauma

被引:33
作者
Fontanilla, CV
Faunce, DE
Gregory, MS
Messingham, KAN
Durbin, EA
Duffner, LA
Kovacs, EJ
机构
[1] Loyola Univ, Med Ctr, Burn & Shock Trauma Inst, Dept Cell Biol Neurobiol & Anat, Maywood, IL 60153 USA
[2] Loyola Univ, Med Ctr, Dept Surg, Maywood, IL 60153 USA
[3] Loyola Univ, Med Ctr, Immunol & Aging Program, Maywood, IL 60153 USA
关键词
macrophage; immunosuppression; alcohol; interleukin-6; thermal injury;
D O I
10.1097/00000374-200009000-00010
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
Background: Previous studies from this laboratory reported that suppression of cell-mediated immune function was coincident with elevated interleukin (IL)-6 production after acute ethanol exposure before burn trauma, compared with either insult alone. The goal of this study was to investigate whether treatment with an anti-IL-6 antibody could restore immunocompetence in mice subjected to burn trauma with previous exposure to alcohol, as assessed by delayed-type hypersensitivity (DTH) and mitogen-induced splenocyte proliferative responses. Methods: Mice given an ethanol treatment designed to reach a blood alcohol level of 100 mg/dl before a 15% total body surface area burn injury were treated with an anti-IL-6 antibody at 30 min and 24 hr postinjury. Results: Burn/ethanol mice exhibited a 91% suppression of the DTH response (p < 0.01) and a 76% suppression of mitogen-induced splenocyte proliferation (p < 0.01) at 48 hr postinjury, along with increased levels of circulating and splenic macrophage-derived IL-6, compared with all other treatment groups. After anti-IL-6 antibody administration to burn/ethanol mice, there was a 25% (p < 0.05) and 63% (p < 0.01) recovery of the DTH and splenocyte proliferative responses, respectively. Addition of exogenous IL-6 to splenocyte cultures isolated from anti-IL-6 antibody-treated burn/ethanol mice resulted in a 70% inhibition of mitogen-induced proliferative responses (p < 0.03). Conclusions: These data confirm previous findings that burn in combination with acute ethanol exposure suppresses cell-mediated immune function compared with either insult alone. Furthermore, the ability of the anti-IL-6 antibody treatment to improve cellular immune responses in the burn/ethanol group suggests that blocking this cytokine may be beneficial for the ethanol-exposed, thermally injured individual.
引用
收藏
页码:1392 / 1399
页数:8
相关论文
共 55 条
[1]   BIOLOGY OF MULTIFUNCTIONAL CYTOKINES - IL-6 AND RELATED MOLECULES (IL-1 AND TNF) [J].
AKIRA, S ;
HIRANO, T ;
TAGA, T ;
KISHIMOTO, T .
FASEB JOURNAL, 1990, 4 (11) :2860-2867
[2]  
Brezel B S, 1988, J Burn Care Rehabil, V9, P169, DOI 10.1097/00004630-198803000-00009
[3]  
Casson P, 1966, Surg Forum, V17, P268
[4]  
CHOUDRY MA, 2000, IN PRESS ALCOHOL
[5]   Dose-dependent effect of ethanol on hepatic oxidative stress and interleukin-6 production after burn injury in the mouse [J].
Colantoni, A ;
Duffner, LA ;
De Maria, N ;
Fontanilla, CV ;
Messingham, KAN ;
Van Thiel, DH ;
Kovacs, EJ .
ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH, 2000, 24 (09) :1443-1448
[6]   PLASMA CYTOKINES FOLLOWING THERMAL-INJURY AND THEIR RELATIONSHIP WITH PATIENT MORTALITY, BURN SIZE, AND TIME POSTBURN [J].
DROST, AC ;
BURLESON, DG ;
CIOFFI, WG ;
JORDAN, BS ;
MASON, AD ;
PRUITT, BA .
JOURNAL OF TRAUMA-INJURY INFECTION AND CRITICAL CARE, 1993, 35 (03) :335-339
[7]   DEFECTIVE INFLAMMATORY RESPONSE IN INTERLEUKIN 6-DEFICIENT MICE [J].
FATTORI, E ;
CAPPELLETTI, M ;
COSTA, P ;
SELLITTO, C ;
CANTONI, L ;
CARELLI, M ;
FAGGIONI, R ;
FANTUZZI, G ;
GHEZZI, P ;
POLI, V .
JOURNAL OF EXPERIMENTAL MEDICINE, 1994, 180 (04) :1243-1250
[8]   Acute ethanol exposure prior to thermal injury results in decreased T-cell responses mediated in part by increased production of IL-6 [J].
Faunce, DE ;
Gregory, MS ;
Kovacs, EJ .
SHOCK, 1998, 10 (02) :135-140
[9]   Effects of acute ethanol exposure on cellular immune responses in a murine model of thermal injury [J].
Faunce, DE ;
Gregory, MS ;
Kovacs, EJ .
JOURNAL OF LEUKOCYTE BIOLOGY, 1997, 62 (06) :733-740
[10]  
FAUNCE DE, 1998, J LEUKOCYTE BIOL, V64, P1