| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1937444 | Biochemical and Biophysical Research Communications | 2007 | 6 Pages |
Despite of encountering a robust immune response, Mycobacterium tuberculosis (MTB) successfully survives and persists in the human host. We investigated the early regulation of MTB 85B gene by allicin in MTB-infected human monocytes. During the first 24 h of infection, levels of both MTB 85B intracellular mRNA and secreted protein were significantly down-regulated by allicin in a dose-dependent manner, which was mediated by inhibition of glutathione and NF-κB pathway. Allicin-induced MTB 85B suppression correlated with suppression of TNF-α released from infected monocytes. The allicin-induced up-regulation of glutathione and IFN-γ with simultaneous decrease in TNF-α supports the anti-inflammatory property of allicin by elicitation of protective immune response. Thus, allicin may prove to be valuable in the containment of MTB and therefore be useful as an adjunct in treatment of tuberculosis.
