Publication: Immunomodulatory tetracyclines shape the intestinal inflammatory response inducing mucosal healing and resolution.
dc.contributor.author | Garrido-Mesa, J | |
dc.contributor.author | Rodríguez-Nogales, A | |
dc.contributor.author | Algieri, F | |
dc.contributor.author | Vezza, T | |
dc.contributor.author | Hidalgo-Garcia, L | |
dc.contributor.author | Garrido-Barros, M | |
dc.contributor.author | Utrilla, M P | |
dc.contributor.author | Garcia, F | |
dc.contributor.author | Chueca, N | |
dc.contributor.author | Rodriguez-Cabezas, M E | |
dc.contributor.author | Garrido-Mesa, N | |
dc.contributor.author | Gálvez, J | |
dc.date.accessioned | 2023-01-25T10:21:52Z | |
dc.date.available | 2023-01-25T10:21:52Z | |
dc.date.issued | 2018-10-15 | |
dc.description.abstract | Immunomodulatory tetracyclines are well-characterized drugs with a pharmacological potential beyond their antibiotic properties. Specifically, minocycline and doxycycline have shown beneficial effects in experimental colitis, although pro-inflammatory actions have also been described in macrophages. Therefore, we aimed to characterize the mechanism behind their effect in acute intestinal inflammation. A comparative pharmacological study was initially used to elucidate the most relevant actions of immunomodulatory tetracyclines: doxycycline, minocycline and tigecycline; other antibiotic or immunomodulatory drugs were assessed in bone marrow-derived macrophages and in dextran sodium sulfate (DSS)-induced mouse colitis, where different barrier markers, inflammatory mediators, microRNAs, TLRs, and the gut microbiota composition were evaluated. The sequential immune events that mediate the intestinal anti-inflammatory effect of minocycline in DSS-colitis were then characterized. Novel immunomodulatory activity of tetracyclines was identifed; they potentiated the innate immune response and enhanced resolution of inflammation. This is also the first report describing the intestinal anti-inflammatory effect of tigecycline. A minor therapeutic benefit seems to derive from their antibiotic properties. Conversely, immunomodulatory tetracyclines potentiated macrophage cytokine release in vitro, and while improving mucosal recovery in colitic mice, they up-regulated Ccl2, miR-142, miR-375 and Tlr4. In particular, minocycline initially enhanced IL-1β, IL-6, IL-22, GM-CSF and IL-4 colonic production and monocyte recruitment to the intestine, subsequently increasing Ly6C- MHCII+ macrophages, Tregs and type 2 intestinal immune responses. Immunomodulatory tetracyclines potentiate protective immune pathways leading to mucosal healing and resolution, representing a promising drug reposition strategy for the treatment of intestinal inflammation. | |
dc.identifier.doi | 10.1111/bph.14494 | |
dc.identifier.essn | 1476-5381 | |
dc.identifier.pmc | PMC6240124 | |
dc.identifier.pmid | 30184260 | |
dc.identifier.pubmedURL | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6240124/pdf | |
dc.identifier.unpaywallURL | https://bpspubs.onlinelibrary.wiley.com/doi/pdfdirect/10.1111/bph.14494 | |
dc.identifier.uri | http://hdl.handle.net/10668/12909 | |
dc.issue.number | 23 | |
dc.journal.title | British journal of pharmacology | |
dc.journal.titleabbreviation | Br J Pharmacol | |
dc.language.iso | en | |
dc.organization | Hospital Universitario San Cecilio | |
dc.organization | Hospital Universitario San Cecilio | |
dc.page.number | 4353-4370 | |
dc.pubmedtype | Journal Article | |
dc.pubmedtype | Research Support, Non-U.S. Gov't | |
dc.rights.accessRights | open access | |
dc.subject.mesh | Animals | |
dc.subject.mesh | Anti-Inflammatory Agents, Non-Steroidal | |
dc.subject.mesh | Colitis | |
dc.subject.mesh | Dextran Sulfate | |
dc.subject.mesh | Immunologic Factors | |
dc.subject.mesh | Inflammation | |
dc.subject.mesh | Intestines | |
dc.subject.mesh | Mice | |
dc.subject.mesh | Mucous Membrane | |
dc.subject.mesh | RAW 264.7 Cells | |
dc.subject.mesh | Tetracyclines | |
dc.title | Immunomodulatory tetracyclines shape the intestinal inflammatory response inducing mucosal healing and resolution. | |
dc.type | research article | |
dc.type.hasVersion | VoR | |
dc.volume.number | 175 | |
dspace.entity.type | Publication |