Exciting research projects and novel therapies

Infections continue to threaten human health as pathogenic organisms outsmart available therapies with remarkable genetic versatility. Fortunately, microbial versatility is matched by the flexibility of the host immune system, which provides a rich source of novel therapeutic concepts.

Our therapeutic strategy is to find and develop substances that strengthen the immune system.

Rather than drugs killing the bacteria directly the patient’s immune system is empowered to deal with the bacteria.

Our goal is to provide a different molecular framework for the treatment of bacterial infections; much needed to combat antibiotic resistance.


IL1-receptor antagonists

IL-1 receptor antagonists to treat acute infections and prevent tissue damage

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A nerve cell receptor antagonist prevents prevents pain and tissue damage during acute infections

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RNA Pol II inhibitors

A small molecule from ”nice bacteria” prevents over-activation of immunity and reduces inflammation

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IRF7 inhibitors

New molecular tools to inhibit ‘’bad’’ inflammation in infected tissue and reduce the risk of sepsis

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Scientific Publications

Immunomodulation therapy offers new molecular strategies to treat UTI

Butler, D. et al. Review Article, Nature Reviews Urology, doi:10.1038/s41585-022-00602-4 (2022).

PDF: NRU 2022

Immunomodulation – a molecular solution to treating patients with severe bladder pain syndrome?

Wullt, B. et al. European Urology Open Science, 31, 49-58, doi:10.1016/j.euros.2021.07.003 (2021).

PDF: Eur Urol Open Sci 2021

Collateral effects of deletion of nlpD on rpoS and rpoS-dependent genes. Reply.

Ambite, I. et al. Letter to the Editor, The Journal of Clinical Investigation 131(18):e153234 doi:10.1172/JCI153234 (2021).

PDF: JCI letter to the Editor 2021

Molecular determinants of disease severity in urinary tract infection

Ambite, I. et al. Review Article, Nature Reviews Urology 18, 468–486, doi:10.1038/s41585-021-00477-x (2021).

PDF: NRU 2021

Active bacterial modification of the host environment through RNA Polymerase II inhibition

Ambite, I. et al. The Journal of Clinical Investigation 131(4), e140333, doi:10.1172/JCI140333 (2021).

PDF: JCI 2021

Neuroepithelial control of mucosal inflammation in acute cystitis

Butler, D.S.C. et al. Scientific Reports 8, 11015, doi:10.1038/s41598-018-28634-0 (2018).

PDF: Sci reports 2018

IRF7 inhibition prevents destructive innate immunity—A target for nonantibiotic therapy of bacterial infections

Puthia, M. et al. Science Translational Medicine 8(336), 336ra59, doi:10.1126/scitranslmed.aaf1156 (2016).

PDF: Sci Trans Med 2016

Molecular basis of acute cystitis reveals susceptibility genes and immunotherapeutic targets.

Ambite, I. et al. PLoS Pathogens 12(10), e1005848, doi:10.1371/journal.ppat.1005848 (2016).

PDF: Plos Pathogens 2016

Bacterial control of host gene expression through RNA polymerase II

Lutay, N. et al. The Journal of Clinical Investigation 123(6), 2366-79, doi:10.1172/JCI6645 (2013).

PDF: JCI 2013