Abstract
Inflammatory bowel disease (IBD) is characterized by gastrointestinal inflammation com-prised of Crohn’s disease and ulcerative colitis. Centers for Disease Control and Prevention report that 1.3% of the population of the United States (approximately 3 million people) were affected by the disease in 2015, and the number keeps increasing over time. IBD has a multifactorial etiology, from genetic to environmental factors. Most of the IBD treatments revolve around disease manage-ment, by reducing the inflammatory signals. We previously identified the surface layer protein A (SlpA) of Lactobacillus acidophilus that possesses anti-inflammatory properties to mitigate murine colitis. Herein, we expressed SlpA in a clinically relevant, food-grade Lactococcus lactis to further investigate and characterize the protective mechanisms of the actions of SlpA. Oral administration of SlpA-expressing L. lactis (R110) mitigated the symptoms of murine colitis. Oral delivery of R110 resulted in a higher expression of IL-27 by myeloid cells, with a synchronous increase in IL-10 and cMAF in T cells. Consistent with murine studies, human dendritic cells exposed to R110 showed exquisite differential gene regulation, including IL-27 transcription, suggesting a shared mechanism between the two species, hence positioning R110 as potentially effective at treating colitis in hu-mans.
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Arukha, A. P., Furlan Freguia, C., Mishra, M., Jha, J. K., Kariyawasam, S., Fanger, N. A., … Sahay, B. (2021). Lactococcus lactis delivery of surface layer protein a protects mice from colitis by re-setting host immune repertoire. Biomedicines, 9(9). https://doi.org/10.3390/biomedicines9091098
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