Clinical Efficacy of a Combination of Thymopentin and Antituberculosis Drugs in Treating Drug-Resistant Pulmonary Tuberculosis: Meta Analysis

OBJECTIVE: To make a systematic evaluation of the clinical efficacy of thymopentin combined with antituberculous drugs in treating drug-resistant pulmonary TB (PTB). METHODS: Relevant studies were retrieved from PubMed, Embase, Cochrane Library, Chinese Biomedical Literature Database, CNKI, and Wanfang Database. STATA software was used to evaluate the differences in focal absorption rate, the time to cough symptom remission, sputum culture-negative rate, CD3(+) T, CD4(+) T, and CD8(+) T cell levels after treatment. RESULTS: A total of 23 randomized controlled trials literature involving 2031 cases were included. Meta-analysis revealed that compared with conventional therapy, the sputum culture-negative rate was significantly increased after 2–3 months and 6–9 months of treatment and the whole course of combined thymopentin treatment. The risk ratio (RR, 95% CI) was 1.44 (1.26–1.64), 1.47 (1.21–1.78), and 1.27 (1.18–1.36), respectively. In the combined thymopentin treatment group, the focal absorption rate was higher, with RR (95% CI) = 1.36 (1.25–1.47), the time of cough remission was shortened, with WMD (95% CI) =−9.46d (−10.36,−8.57) and the differences were all statistically significant. Combined thymopentin therapy could effectively improve the levels of CD3(+) T and CD4(+) T lymphocytes in patients with drug-resistant PTB after 2–3 months, 6–9 months of treatment. The WMD (95% CI) were 9.96% (7.84, 12.08), 4.68% (2.90, 6.47) and 10.26% (7.81, 12.71), 7.21% (6.28, 8.15), respectively, and could also reduce the level of CD8(+) T lymphocytes after 2–3 months and 6–9 months of treatment. The WMD (95% CI) were −4.06% (−4.96, −3.13), −3.52%, (−4.07,−2.98), respectively, and the differences were all statistically significant. CONCLUSION: Thymopentin adjuvant treatment for drug-resistant PTB can promote the therapeutic effect and improve the immune indexes in patients with drug-resistant PTB.