Stimulation of TLR7 prior to polymicrobial sepsis improves the immune control of the inflammatory response in adult mice
- PMID: 20953969
- DOI: 10.1007/s00011-010-0265-6
Stimulation of TLR7 prior to polymicrobial sepsis improves the immune control of the inflammatory response in adult mice
Abstract
Objective: The role of Toll-like receptor 7 (TLR7), so far regarded as a receptor for viral RNA, was evaluated in a murine sepsis model.
Material: We used the colon ascendens stent peritonitis model (CASP) in female C57B/6 mice. R-848 (1.5 μg/g body weight) was injected intravenously prior to sepsis induction.
Methods: We determined levels of cytokines by CBA detection kit. Different cell populations were isolated from the spleen by magnetic cell separation and the expression of TLR7 was visualized by immunofluorescence staining. Bacterial load of organs was quantified by incubating suspensions on agar in colony forming units.
Results: R-848 application per se led to elevated cytokine levels in serum, spleen and peritoneal cavity. Expression of TLR7 on splenocytes was upregulated following CASP. Bacterial clearance in polymicrobial sepsis was significantly increased in spleen and peritoneum of mice pre-treated with the TLR7-agonist. Cytokine release was regulated in the peritoneum and spleen. Furthermore, apoptosis in thymus and spleen during polymicrobial sepsis was significantly decreased following TLR7 agonist application.
Conclusions: TLR7 seems to be essential for pathogen defence not only in viral but also in bacterial infections. Pharmacological stimulation of this receptor prior to induction of sepsis improves the host's capacity to cope with pathogens.
Similar articles
-
Persistent Toll-like receptor 7 stimulation induces behavioral and molecular innate immune tolerance.Brain Behav Immun. 2019 Nov;82:338-353. doi: 10.1016/j.bbi.2019.09.004. Epub 2019 Sep 6. Brain Behav Immun. 2019. PMID: 31499172 Free PMC article.
-
Tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) improves the innate immune response and enhances survival in murine polymicrobial sepsis.Crit Care Med. 2010 Nov;38(11):2169-74. doi: 10.1097/CCM.0b013e3181eedaa8. Crit Care Med. 2010. PMID: 20657274
-
B cell autophagy mediates TLR7-dependent autoimmunity and inflammation.Autophagy. 2015;11(7):1010-24. doi: 10.1080/15548627.2015.1052206. Autophagy. 2015. PMID: 26120731 Free PMC article.
-
Triggering TLR7 in mice induces immune activation and lymphoid system disruption, resembling HIV-mediated pathology.Blood. 2009 Jan 8;113(2):377-88. doi: 10.1182/blood-2008-04-151712. Epub 2008 Sep 29. Blood. 2009. PMID: 18824599
-
Toll-like receptors 7 and 9 in myasthenia gravis thymus: amplifiers of autoimmunity?Ann N Y Acad Sci. 2018 Feb;1413(1):11-24. doi: 10.1111/nyas.13534. Epub 2018 Jan 24. Ann N Y Acad Sci. 2018. PMID: 29363775 Review.
Cited by
-
Lipopolysaccharide inhibits Sindbis virus-induced IP-10 release in human peripheral blood mononuclear cells.Viral Immunol. 2011 Jun;24(3):237-43. doi: 10.1089/vim.2010.0120. Viral Immunol. 2011. PMID: 21668365 Free PMC article.
-
Toll-like Receptor 7 Contributes to Inflammation, Organ Injury, and Mortality in Murine Sepsis.Anesthesiology. 2019 Jul;131(1):105-118. doi: 10.1097/ALN.0000000000002706. Anesthesiology. 2019. PMID: 31045897 Free PMC article.
-
Increased MDSC accumulation and Th2 biased response to influenza A virus infection in the absence of TLR7 in mice.PLoS One. 2011;6(9):e25242. doi: 10.1371/journal.pone.0025242. Epub 2011 Sep 23. PLoS One. 2011. PMID: 21966467 Free PMC article.
-
Single stranded (ss)RNA-mediated antiviral response against infectious laryngotracheitis virus infection.BMC Microbiol. 2019 Feb 8;19(1):34. doi: 10.1186/s12866-019-1398-6. BMC Microbiol. 2019. PMID: 30736730 Free PMC article.
-
Targeting toll-like receptors: promising therapeutic strategies for the management of sepsis-associated pathology and infectious diseases.Front Immunol. 2013 Nov 18;4:387. doi: 10.3389/fimmu.2013.00387. Front Immunol. 2013. PMID: 24302927 Free PMC article. Review.
References
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical