Amelioration of Murine Colitis by Attenuated Salmonella choleraesuis Encoding Interleukin-19.
Shih-Yao ChenChun-Ting ChuMei-Lin YangJian-Da LinChung-Teng WangChe-Hsin LeeI-Chen LinAi-Li ShiauPin LingChao-Liang WuPublished in: Microorganisms (2023)
The imbalance of mucosal immunity in the lower gastrointestinal tract can lead to chronic inflammatory bowel diseases (IBDs), including Crohn's disease and ulcerative colitis. IBD is a chronic inflammatory disorder that causes small and/or large intestines ulceration. According to previous studies, recombinant interleukin (IL)-10 protein and genetically modified bacteria secreting IL-10 ameliorate dextran sulfate sodium (DSS)-induced colitis in mice. IL-19 is a transcriptional activator of IL-10 and can alter the balance of T helper 1 (Th)1/Th2 cells in favor of Th2. In this study, we aimed to investigate whether the expression of the murine IL-19 gene carried by Salmonella choleraesuis ( S. choleraesuis ) could ameliorate murine IBD. Our results showed that the attenuated S. choleraesuis could carry and express the IL-19 gene-containing plasmid for IBD gene therapy by reducing the mortality and clinical signs in DSS-induced acute colitis mice as compared to the untreated ones. We also found that IL-10 expression was induced in IL-19-treated colitis mice and prevented inflammatory infiltrates and proinflammatory cytokine expression in these mice. We suggest that S. choleraesuis encoding IL-19 provides a new strategy for treating IBD in the future.
Keyphrases
- ulcerative colitis
- poor prognosis
- escherichia coli
- oxidative stress
- high fat diet induced
- binding protein
- copy number
- type diabetes
- metabolic syndrome
- induced apoptosis
- long non coding rna
- immune response
- coronary artery disease
- toll like receptor
- endothelial cells
- wild type
- cell death
- insulin resistance
- nuclear factor
- newly diagnosed