RESUMO
BACKGROUND: Inflammation has long been identified as an essential component of both Type-2 diabetes and tuberculosis. Chemokines are low molecular weight proteins which play an important role in both inflammation (diabetes) and immunity (tuberculosis). METHODS: In this study, we measured the serum levels of IP-10, IL-8 and SDF-1 in subjects with Normal Glucose Tolerance (NGT-TB-â¯=â¯108; NGT-TB+â¯=â¯200), Pre-Diabetes (PDM-TB-â¯=â¯118; PDM-TB+â¯=â¯105), Newly Diagnosed Diabetes (NDM-TB-â¯=â¯105; NDM-TB+â¯=â¯63) and Known Diabetes (KDM-TB-â¯=â¯131; KDM-TB+â¯=â¯108), by ELISA. Along with chemokines pro-inflammatory cytokines TNF-É and IL-6 were also measured in these groups. RESULTS: While IP-10 levels were significantly reduced in TB+ subjects in all the sub-groups, IL-8 levels were significantly reduced in NDM-TB+ and increased in KDM-TB+ subjects. SDF-1 levels were significantly elevated in TB+ subjects in all the subgroups, except for KDM-TB+. CONCLUSION: Altered serum chemokine levels can alter anti-TB immunity in diabetes patients and can fuel DM-TB nexus.