Background: Alcohol exposure induces TGFb1 and renders the lung susceptible to injury and disrepair. We determined that TGFb1 regulates myofibroblast differentiation through the loss of Thy-1 expression and consequent induction of a-SMA. TGFb1 is important for T helper 17 (Th17) differentiation and IL-17 secretion, which in turn participates in tissue repair. We hypothesized that alcohol induces Th17 differentiation via TGFb1 and that IL-17 produced by these cells contributes to the development of profibrotic lung myofibroblasts.Methods: Primary lung fibroblasts (PLFs) were treated with alcohol, TGFb1, and IL-17 and then analyzed for Thy-1 expression and cell morphology. Na€ ıve and Th17-polarized CD4 + T cells were exposed to alcohol and assessed for IL-17 expression. CD4 + T cells from alcohol-fed mice were analyzed for Th17 and IL-17 expression. Lungs of control-fed, bleomycin-treated and alcohol-fed, bleomycin-treated mice were analyzed for IL-17 protein expression.Results: Alcohol-treated PLFs expressed lower levels of Thy-1 than untreated cells. TGFb1 or IL-17 exposure suppressed PLF Thy-1 expression. When administered together, TGFb1 and IL-17 additively down-regulated Thy-1 expression. Exposure of na€ ıve and Th17-polarized CD4 + T cells to alcohol induced the Th17 phenotype and augmented their production of IL-17. CD4 + Th17 + levels are elevated in the peripheral compartment but not in the lungs of alcohol-fed animals. Treatment of the PLFs with IL-17 and alcohol induced a-SMA expression. Induction of a-SMA and myofibroblast morphology by IL-17 occurred selectively in a Thy-1 À fibroblast subpopulation. Chronic alcohol ingestion augmented lung-specific IL-17 expression following bleomycin-induced lung injury.Conclusions: Alcohol exposure skews T cells toward a Th17 immune response that in turn primes the lung for fibroproliferative disrepair through loss of Thy-1 expression and induction of myofibroblast differentiation. These effects suggest that IL-17 and TGFb1 contribute to fibroproliferative disrepair in the lung and targeting these proteins could limit morbidity and mortality following lung injury in alcoholic individuals.