| Literature DB >> 27689749 |
Jun-Ai Zhang1, Gan-Bin Liu2, Bi-Ying Zheng3, Yuan-Bin Lu1, Yu-Chi Gao1, Xiao-Zhen Cai4, You-Chao Dai1, Shi-Yan Yu1, Yan Jia1, Chen Chen1, Ze-Gang Zhuang1, Xin Wang1, Wan-Dang Wang5, Xiao-Xia Fu3, Lai-Long Yi2, Ling Shen6, Zheng W Chen6, Jun-Fa Xu7.
Abstract
Roles of human IL-37 in infections remain poorly characterized. Although plasma IL-37 is elevated in patients with tuberculosis (TB), IL-37 source and immune correlate in TB have not been investigated. It is also unknown whether and how TB can influence the ability of immune cells to mount innate responses of IL-37 and pre-inflammatory cytokines. Here, we demonstrated that IL-37b-producing monocytes coincided with a source of elevated plasma IL-37b in TB patients. While IL-37b production in TB was associated with prolonged/complicated TB, TB burdens and inflammatory reactions, it negatively correlated with immune responses of pro-inflammatory cytokines IL-1β, IL-6 and TNF-α or IL-10. Interestingly, mycobacterial re-infection of monocytes from TB patients, but not healthy BCG-vaccinated controls, enhanced or sustained IL-37b production by cultured monocytes. TB-sensitized monocytes from TB patients mounted more robust immune responses of IL-37b than those of pre-inflammatory cytokines during mycobacterial re-infection in culture. Our data represent new findings in terms of IL-37b responses, immune correlates and potential mechanisms in TB patients. Copyright ÂEntities:
Keywords: Active tuberculosis; Cytokines; IL-37b; Innate immunity; Monocytes
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Year: 2016 PMID: 27689749 PMCID: PMC5760171 DOI: 10.1016/j.molimm.2016.09.018
Source DB: PubMed Journal: Mol Immunol ISSN: 0161-5890 Impact factor: 4.407