Objective To analyze the expression and clinical significance of stimulator of interfer-on genes(STING),C-C motif chemokine ligand 5(CCL5),interferon regulatory factor 3(IRF3)and programmed death ligand-1(PDL1)in squamous cell lung cancer.Methods A total of 56 pa-tients with squamous cell lung cancer were enrolled.Resected tumor tissues and adjacent non-tumor tissues(located more than 5 cm from the tumor margin)were collected.Immunohistochemical staining was performed to detect the expression of STING,CCL5,IRF3 and PDL1.The correlations of STING,CCL5,IRF3 and PDL1 with clinical data were analyzed.The relationship between the expression of STING,CCL5,IRF3 and PDL1 in lung squamous cell carcinoma tissues and prognosis was also evalua-ted.The prognostic factors of patients with lung squamous cell carcinoma were analyzed.Results The positive rate of STING expression in lung squamous cell carcinoma tissues was significantly lower than that in adjacent non-tumor tissues,whereas the positive rates of CCL5,IRF3 and PDL1 were significantly higher(P＜0.05).The expression levels of STING,CCL5,IRF3 and PDL1 were associated with tumor diameter,TNM stage,lymph node metastasis and differentiation degree(P＜0.05).The 3-year survival rate of STING positive expression patients was significantly higher than that of STING negative expression patients(P＜0.05).The 3-year survival rate of CCL5 positive,IRF3 positive and PDL1 positive expression patients was significantly lower than that of CCL5 negative,IRF3 negative and PDL1 negative expression patients(P＜0.05).STING,CCL5,IRF3 and PDL1 were identified as prognostic factors for patients with squamous cell lung cancer(P＜0.05).Conclusion In squamous cell lung cancer tissues,STING is expressed at low levels,while CCL5,IRF3 and PDL1 are ex-pressed at high levels.These findings have significant clinical value in assessing the prognosis of pa-tients with squamous cell lung cancer.

ObjectiveTo investigate the clinical effect of entecavir combined with antituberculosis therapy in patients with tuberculosis complicated by chronic HBV infection. MethodsA total of 108 patients with tuberculosis complicated by chronic HBV infection were divided into entecavir group with 58 patients and control group with 50 patients. The patients in the entecavir group were given entecavir from 1 month before antituberculosis therapy to the end of antituberculosis therapy, and those in the control group were given antitubercular agent alone. The incidence of liver injury and clinical symptoms, time to appearance of abnormal liver function, and time to liver function recovery were compared between the two groups. The two-independent-samples t test was used for comparison of continuous data between groups, and the chi-square test was used for comparison of categorical data between groups. ResultsCompared with the control group, the entecavir group had significantly higher incidence rates of abnormal liver function (29.31% vs 64.00%, χ2=8.475, P＜0.05) and clinical symptoms of liver injury (17.24% vs 28.00%, χ2=5.534, P＜0.05). There were significant differences in the time to appearance of abnormal liver function (25.1±10.2 d vs 20.1±8.9 d, t=2.675, P＜0.05) and time to liver function recovery (26.5±9.8 d vs 32.6±11.2 d, t=3.778, P＜0.05). ConclusionEntecavir can significantly reduce the incidence of liver injury caused by antituberculosis therapy, postpone the time to appearance of liver injury, and accelerate liver function recovery in patients with tuberculosis complicated by chronic HBV infection.