Therapeutic Effects of IL-1RA against Acute Bacterial Infections, including Antibiotic-Resistant Strains.
Murphy Lam Yim WanThi Hien TranDaniel S C ButlerMichele CavaleraMurphy Lam Yim WanShahram AhmadiCatharina SvanborgPublished in: Pathogens (Basel, Switzerland) (2023)
Innate immunity is essential for the anti-microbial defense, but excessive immune activation may cause severe disease. In this study, immunotherapy was shown to prevent excessive innate immune activation and restore the anti-bacterial defense. E. coli -infected Asc -/- mice develop severe acute cystitis, defined by IL-1 hyper-activation, high bacterial counts, and extensive tissue pathology. Here, the interleukin-1 receptor antagonist (IL-1RA), which inhibits IL-1 hyper-activation in acute cystitis, was identified as a more potent inhibitor of inflammation and NK1R- and substance P-dependent pain than cefotaxime. Furthermore, IL-1RA treatment inhibited the excessive innate immune activation in the kidneys of infected Irf3 -/- mice and restored tissue integrity. Unexpectedly, IL-1RA also accelerated bacterial clearance from infected bladders and kidneys, including antibiotic-resistant E. coli , where cefotaxime treatment was inefficient. The results suggest that by targeting the IL-1 response, control of the innate immune response to infection may be regained, with highly favorable treatment outcomes, including infections caused by antibiotic-resistant strains.
Keyphrases
- innate immune
- escherichia coli
- rheumatoid arthritis
- liver failure
- oxidative stress
- chronic pain
- ankylosing spondylitis
- type diabetes
- disease activity
- immune response
- early onset
- spinal cord
- physical activity
- microbial community
- high fat diet induced
- combination therapy
- systemic sclerosis
- neuropathic pain
- interstitial lung disease
- aortic dissection
- wild type
- peripheral blood
- replacement therapy