Fontanilla C V, Faunce D E, Gregory M S, Messingham K A, Durbin E A, Duffner L A, Kovacs E J
Department of Cell Biology, Neurobiology, and Anatomy, the Burn and Shock Trauma Institute, Loyola University Medical Center, Maywood, Illinois, USA.
Alcohol Clin Exp Res. 2000 Sep;24(9):1392-9.
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.
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.
Burn/ethanol mice exhibited a 91% suppression of the DTH response ( < 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).
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.
本实验室之前的研究报告称,与单独遭受烧伤或急性乙醇暴露相比,在烧伤创伤前急性乙醇暴露后,细胞介导的免疫功能受到抑制,同时白细胞介素(IL)-6的产生增加。本研究的目的是通过迟发型超敏反应(DTH)和丝裂原诱导的脾细胞增殖反应,研究用抗IL-6抗体治疗是否能恢复先前暴露于酒精的烧伤小鼠的免疫能力。
在15%体表面积烧伤前接受旨在使血液酒精水平达到100mg/dl的乙醇处理的小鼠,在受伤后30分钟和24小时用抗IL-6抗体治疗。
与所有其他治疗组相比,烧伤/乙醇处理的小鼠在受伤后48小时,DTH反应受到91%的抑制(<0.01),丝裂原诱导的脾细胞增殖受到76%的抑制(p<0.01),同时循环和脾巨噬细胞衍生的IL-6水平升高。给烧伤/乙醇处理的小鼠注射抗IL-6抗体后,DTH和脾细胞增殖反应分别恢复了25%(p<0.05)和63%(p<0.01)。向从抗IL-6抗体处理的烧伤/乙醇小鼠分离的脾细胞培养物中添加外源性IL-6,导致丝裂原诱导的增殖反应受到70%的抑制(p<0.03)。
这些数据证实了先前的发现,即与单独的任何一种损伤相比,烧伤与急性乙醇暴露相结合会抑制细胞介导的免疫功能。此外,抗IL-6抗体治疗改善烧伤/乙醇组细胞免疫反应的能力表明,阻断这种细胞因子可能对乙醇暴露的热损伤个体有益。