The pathogenesis of inflammatory bowel disease (IBD) depends on excessive activation of the immune response due to the unbalanced activity of T helper cells and regulatory T cells. The expansion of Th17 cells is promoted by IL-23, and the entire cascade is referred to as the IL-23/IL-17 cytokine axis. Therefore, monoclonal antibodies with immuno-regulatory effects are used in the treatment of a severe form of the disease. Due to their large and unstable structure, difficult production and immunogenic potential, non-immunoglobulin binding proteins are already being developed. Lactic acid bacteria (LAB) can be used as a delivery vehicle to avoid protein digestion, as many of the strains are able to survive the passage through the gastrointestinal tract. Probiotic LAB and delivered therapeutic molecules could have a synergistic effect on the inflammatory response in the intestine. As a part of the master's thesis, we wanted to develop recombinant Lactococcus lactis strains capable of delivering protein blockers (ARS) of the IL-17 receptor (IL-17RA). Gene cloning methods were used to prepare ARS12, ARS14, ARS19 and ARS14CO genetic constructs in plasmid pSDBA3b for either binding to the bacterial surface, or for secretion into the medium. The plasmid contained genes for the Usp45 secretion signal, the Flag-tag, and the cAcmA surface anchor in the case of the surface display. Gene expression was controlled by the addition of nisin and ARS binders were analyzed by SDS-PAGE and western blot, using anti-FLAG antibodies. Only variants anchored to the bacterial wall were detected. Surface display of ARS12, ARS14 and ARS19 proteins was then confirmed by flow cytometry. Furthermore, we wanted to develop dual functionalized L. lactis strains capable of co-expressing IL-17A binders (Fynomers) and IL-17RA binders (ARS14 and ARS19) to achieve a synergistic effect on the immune response. Co-expression was analyzed by SDS-PAGE and western blot, using anti-Flag antibodies for detection of flag-tagged ARS binders, and anti-cMyc antibodies for cMyc-tagged Fynomers. We detected anchor-containing fusion proteins as well as secreted ARS14 protein. In this work we demonstrated the ability of L. lactis bacteria to deliver IL-17A and IL-17RA binders. In the future it is necessary to evaluate their functionality and test them in a mouse model of IBD.
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