Anti-interleukin-6 Antibody Treatment Restores Cell-mediated Immune Function in Mice with Acute Ethanol Exposure Before Burn Trauma
Overview
Affiliations
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 ( < 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.
Lohade R, Rapp C, Henkels K, Travers J Skin Res Technol. 2024; 30(6):e13743.
PMID: 38881182 PMC: 11180700. DOI: 10.1111/srt.13743.
Recent alcohol intake impacts microbiota in adult burn patients.
Hoisington A, Choy K, Khair S, Dyamenahalli K, Najarro K, Wiktor A Alcohol. 2024; 118:25-35.
PMID: 38604285 PMC: 11179986. DOI: 10.1016/j.alcohol.2024.04.003.
Intestine immune homeostasis after alcohol and burn injury.
Li X, Hammer A, Rendon J, Choudhry M Shock. 2015; 43(6):540-8.
PMID: 25692258 PMC: 4433558. DOI: 10.1097/SHK.0000000000000353.
Zhang Y, Zhang J, Korff S, Ayoob F, Vodovotz Y, Billiar T Shock. 2014; 42(3):218-27.
PMID: 24978887 PMC: 4134434. DOI: 10.1097/SHK.0000000000000211.
Pulmonary inflammation after ethanol exposure and burn injury is attenuated in the absence of IL-6.
Chen M, Bird M, Zahs A, Deburghgraeve C, Posnik B, Davis C Alcohol. 2013; 47(3):223-9.
PMID: 23462222 PMC: 3617054. DOI: 10.1016/j.alcohol.2013.01.004.