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À propos de : Cytokine secretion in vivo and ex vivo following chemotherapy of Mycobacterium tuberculosis infection        

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  • Cytokine secretion in vivo and ex vivo following chemotherapy of Mycobacterium tuberculosis infection
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  • Abstract. The human immune response to tuberculosis is partly mediated by the proinflammatory cytokines tumour necrosis factor (TNF), interleukin (IL)-6, and IL-8. We investigated plasma concentrations of these cytokines before and after maximal lipopolysaccharide stimulation ex vivo of whole blood leucocytes from Zambian patients. 32 patients with non-fatal tuberculosis, 25 of whom were seropositive for human immunodeficiency virus (HIV), were followed for 9 months. Patients were assessed at presentation to hospital (visit A), after 2 months' antimycobacterial therapy (visit B), and when chemotherapy was completed (visit C). Between visits A and B, patients regained weight (P = 0·03) and became less anaemic (P = 0·0001). At visit B, haemoglobin concentration remained lower in HIV seropositive patients (P = 0·001) and the erythrocyte sedimentation rate (ESR), initially elevated in all patients, was higher in HIV seropositive patients (100 ± 6 mm vs. 43 ± 11 mm in 1 h in seronegative patients; P = 0·002). Plasma IL-8 concentrations were increased at visit C as was IL-8 secretion ex vivo (P< 0·0001 at all time points). Otherwise plasma cytokine levels and secretion ex vivo remained similar throughout the study. Concurrent HIV infection resulted in persistently decreased IL-6 secretions ex vivo although ESR remained high. In summary, after antibiotic therapy in vivo IL-8 secretion ex vivo increased, which supports other data suggesting that IL-8 has a role in immunity to tuberculosis.
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