Abstract:Objective To dynamically observe the cellular immune function of the patients with multidrug-resistant tuberculosis (MDR-TB) so as to provide supports for clinical diagnosis, treatment and rational drug use and to lay a preliminary foundation for immunotherapy for MDR-TB patients. Methods Drug sensitivity test were performed on 50 MDR-TB patients and 50 drug-susceptible TB (S-TB) patients by the absolute concentration method. 20 healthy controls were selected from the physical examination centre. Lymphocyte subsets (CD4+, CD3+ and CD8+, etc.) were analyzed by flow cytometry. Serum cytokines (IFN-γ, IL-2, IL-4 and IL-10, etc.) were detected by enzyme-linked immunosorbent assay (ELISA). Serological differences were compared among the MDR-TB patients, S-TB patients and healthy controls. Results No statistically significant difference was found in the percentage of CD3+ among the three groups. There were significant differences in the percentages of CD4+, CD8+ and CD4+/CD8+ between any two groups among the MDR-TB group, S-TB group and control group. There were also significant differences in the serum concentrations of IFN-γ, IL-2, IL-4 and IL-10 between the control group and MDR-TB group or S-TB group as well as in the serum concentrations of IL-2, IL-4 and IL-10 between the MDR-TB group and S-TB group. The serum levels of CD4+, IL-2, and CD4+/CD8+ ratio in the MDR-TB group were all significantly lower than those of the S-TB group, while CD8+, IL-4 and IL-10 in the MDR-TB group were all significantly higher than those of S-TB group (P<0.05). Conclusions The cellular immune function of tuberculosis patients is impaired, which manifests as declined percentage of CD4+ lymphocyte, elevated percentage of CD8+ lymphocyte, reduced or even inverted ratio of CD4+/CD8+. As compared with patients with drug-susceptible tuberculosis, the cellular immune function of the patients with multidrug-resistant tuberculosis is further exacerbated and presents more significant indicator changes. Their disease conditions are more complex and increase the difficulty of clinical treatment.
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