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Bikash Sahay, LACTOCOCCUS LACTIS DELIVERY OF SURFACE LAYER PROTEIN A PROTECTS MICE FROM COLITIS BY RE-SETTING HOST IMMUNE REPERTOIRE, Inflammatory Bowel Diseases, Volume 28, Issue Supplement_1, February 2022, Page S5, https://doi.org/10.1093/ibd/izac015.009
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Abstract
Inflammatory bowel disease (IBD) is characterized by gastrointestinal inflammation comprised 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 management, 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[1] . 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 humans.
- anti-inflammatory agents
- inflammation
- crohn's disease
- inflammatory bowel disease
- ulcerative colitis
- environmental factors
- administration, oral
- centers for disease control and prevention (u.s.)
- colitis
- obstetric delivery
- dendritic cells
- food
- gene expression regulation
- interleukin-10
- lactobacillus acidophilus
- lactococcus lactis
- myeloid cells
- staphylococcal protein a
- t-lymphocytes
- disease management
- genetics
- mice
- interleukin-27
- causality
- speech-language pathology assistants