Objective To investigate the therapeutic effect of Ejiao ( colla coni asini) on the imbalance of Thl7/Treg subsets in the lung tissues of mice with smoking-induced airway inflammation. Methods Twenty-four male C57BL/6 mice were randomly divided into the control group, model group, and Ejiao (colla corii asini) group (Ejiao group). Mice in the model group and Ejiao group were exposed to cigarette smoking. Mice in the model group were administered 0.2 mL PBS daily, mice in the Ejiao group were administered 0.2 mL Ejiao ( colla corii asini) solution (0.2g/ml) daily, and mice in the control group were fed normally. Twenty-four weeks later, the histopathological condition of lung in mice of each group was observed. The proportion of helper T cell 17 subsets (Thl7) and regulatory T cell subsets (Treg) in the lung tissues were detected by flow cytometry. The expression of IL-6. IL-17A, and Eoxp3 mRNA in the lung tissues was detected by reverse transcription polymerase chain reaction (RT-PCR) , and the serum levels of IL-6, IL-17A, and Eoxp3 were detected by enzyme-linked immunosorbent assay. Results Compared with the control group, the lung tissues of mice in the model group were infiltrated with large number of inflammatory cells, alveoli ruptured and fused, the proportion of Thl7 cells and Treg cells in the lung tissue increased, and the levels of IL-17A, IL-6, Eoxp3 in the serum, and IL-17A, Eoxp3, and IL-6 mRNA in the lung tissues increased (all P <0. 05). Compared with the model group, the inflammation of the lung tissues of mice in the Ejiao group wras significantly improved, the proportion of Thl7 cells and Treg cells in the lung tissues decreased, and the levels of serum IL-17A, IL-6. and Eoxp3, and IL-17A, Eoxp3, and IL-mRNA in the lung tissues decreased (all P <0.05). Conclusions Smoke can induce the increased proportion of Thl7 and Treg subsets and up-regulate the expression of 1L-6 . IL-17A, and Foxp3 cytokines in the lung tissues of mice with airway inflammation. Ejiao (colla corii asini) can reduce the lung inflammation in mice by reducing the proportion of Thl7 and Treg subsets and expression of IL-6 and IL-17A, and Foxp3. [ABSTRACT FROM AUTHOR]