Anti-inflammatory cytokines IL-27, IL-10, IL-1Ra and TGF-β in subjects with increasing grades of glucose intolerence (DM-LTB-2)

•High serum levels of anti-inflammatory cytokines was seen in the LTB-PDM, compared to LTB-NGT group.•Increased IL-27 and IL-10 levels were seen in the LTB-NDM, compared to LTB-NGT group.•TB antigen induced secretion of IL-1Ra was absent in LTB+KDM group.•Both glucose intolerance and LTBI modulated...

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Published inCytokine (Philadelphia, Pa.) Vol. 137; p. 155333
Main Authors Bobhate, Anup, Viswanathan, Vijay, Aravindhan, Vivekanandhan
Format Journal Article
LanguageEnglish
Published England Elsevier Ltd 01.01.2021
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Summary:•High serum levels of anti-inflammatory cytokines was seen in the LTB-PDM, compared to LTB-NGT group.•Increased IL-27 and IL-10 levels were seen in the LTB-NDM, compared to LTB-NGT group.•TB antigen induced secretion of IL-1Ra was absent in LTB+KDM group.•Both glucose intolerance and LTBI modulated systemic levels and in vitro secretion of anti-inflammatory cytokine. Anti-inflammatory cytokines act as double edged swords- they can dampen inflammation but can also suppress immunity. The role played by these cytokines in latent TB infected (LTBI) subjects, with various grades of glucose intolerance was studied. Both serum levels and recall-secretion of IL-27, IL-10, IL-1Ra and TGF-β in Normal Glucose Tolerance (NGT), Pre-Diabetes (PDM), Newly diagnosed Diabetes (NDM) and Known Diabetes (KDM) subjects, both with and without LTBI (n = 382), were quantified by ELISA. All the subjects were screened for LTBI by QuantiFERON-TB Gold test. Serum levels of IL-27, IL-10 and IL-1Ra were significantly elevated in the LTB-PDM, compared to LTB-NGT group. Increased IL-27 and IL-10 levels and decreased levels of TGF-β were seen in the LTB−NDM, compared to LTB−NGT group. Decreased serum levels of IL-27 and increased levels of IL-1Ra and TGF-β were seen in the LTB−KDM, compared to LTB−NGT group. TB antigens induced the secretion of IL-1Ra in LTB+ subjects in the NGT, PDM and NDM groups, but not in the KDM group. Co-morbidity with LTBI brought about (diabetic) stage-specific modulation, in these cytokine levels. Major defects in the circulating levels and recall secretion of anti-inflammatory cytokines, as seen in LTB+KDM subjects, could fuel DM-TB synergy.
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ISSN:1043-4666
1096-0023
1096-0023
DOI:10.1016/j.cyto.2020.155333