Immunomodulation-A Molecular Solution to Treating Patients with Severe Bladder Pain Syndrome?

Björn Wullt, Daniel S C Butler, Ines Ambite, Julia Kinsolving, Christian Krintel, Catharina Svanborg
Author Information
  1. Björn Wullt: Department of Microbiology, Immunology and Glycobiology, Institute of Laboratory Medicine, Lund University, Lund, Sweden.
  2. Daniel S C Butler: Department of Microbiology, Immunology and Glycobiology, Institute of Laboratory Medicine, Lund University, Lund, Sweden.
  3. Ines Ambite: Department of Microbiology, Immunology and Glycobiology, Institute of Laboratory Medicine, Lund University, Lund, Sweden.
  4. Julia Kinsolving: Department of Microbiology, Immunology and Glycobiology, Institute of Laboratory Medicine, Lund University, Lund, Sweden.
  5. Christian Krintel: Department of Microbiology, Immunology and Glycobiology, Institute of Laboratory Medicine, Lund University, Lund, Sweden.
  6. Catharina Svanborg: Department of Microbiology, Immunology and Glycobiology, Institute of Laboratory Medicine, Lund University, Lund, Sweden.

Abstract

BACKGROUND: Patients with bladder pain syndrome experience debilitating pain and extreme frequency of urination. Numerous therapeutic approaches have been tested, but as the molecular basis of disease has remained unclear, specific therapies are not available.
OBJECTIVE: Recently, a systematic gene deletion strategy identified interleukin-1 (IL-1) hyperactivation as a cause of severe cystitis in a murine model. Treatment with an IL-1 receptor antagonist (IL-1RA) restored health in genetically susceptible mice, linking IL-1-dependent inflammation to pain and pathology in the bladder mucosa. The study objective was to investigate whether IL-1RA treatment might be beneficial in patients with bladder pain syndrome.
DESIGN SETTING AND PARTICIPANTS: Patients diagnosed with bladder pain syndrome were invited to participate and subjected to daily IL-1RA injections for 1 wk, followed by a treatment break. Patients with other urological disorders accompanied by pain were included as controls.
OUTCOME MEASUREMENTS AND STATISTICAL ANALYSIS: When symptoms returned, treatment was resumed and responding patients were maintained on treatment long term, with individualized dosing regimens. Symptom scores were recorded and molecular effects were quantified by neuropeptide and gene expression analysis. DNA samples were subjected to exome genotyping.
RESULTS AND LIMITATIONS: IL-1RA treatment reduced bladder pain and the frequency of urination in 13/17 patients ( < 0.001). Substance P levels in urine were lowered, and responders returned to a more normal lifestyle. Neuroinflammatory-dependent and IL-1-dependent gene networks were inhibited, as well as regulators of innate immunity. Genotyping revealed disease-associated , and DNA sequence variants in the responders. Controls did not benefit from IL-1RA treatment, except for one patent with cystitis cystica.
CONCLUSIONS: In this clinical study, IL-1RA treatment is proposed to reduce chronic bladder pain, immediately and in the long term. Despite the limited number of study patients, the potent acute effect and lasting symptom relief indicate that this therapeutic approach may be worth exploring in controlled clinical trials.
PATIENT SUMMARY: Treatment with an interleukin-1 (IL-1) receptor antagonist is proposed for treating bladder pain syndrome, as it can result in symptom relief and increase quality of life. Reduced neuroinflammation and IL-1 signaling provided molecular evidence of the treatment effects.

Keywords

References

  1. Urology. 2009 Feb;73(2):258-62 [PMID: 19036420]
  2. Arthritis Rheum. 2004 Jun;50(6):1752-60 [PMID: 15188350]
  3. Urology. 1997 May;49(5A Suppl):58-63 [PMID: 9146003]
  4. Sci Transl Med. 2016 Apr 27;8(336):336ra59 [PMID: 27122612]
  5. Eur Urol. 2008 Jan;53(1):60-7 [PMID: 17900797]
  6. Front Pharmacol. 2018 Nov 06;9:1157 [PMID: 30459597]
  7. Urology. 2014 Aug;84(2):321-6 [PMID: 24958479]
  8. Urology. 1997 May;49(5A Suppl):2-9 [PMID: 9145997]
  9. Hum Mol Genet. 2011 Oct 15;20(20):4056-68 [PMID: 21768215]
  10. PLoS Pathog. 2016 Oct 12;12(10):e1005848 [PMID: 27732661]
  11. Nat Rev Immunol. 2013 Mar;13(3):176-89 [PMID: 23411799]
  12. Curr Opin Microbiol. 1999 Feb;2(1):99-105 [PMID: 10047563]
  13. Neurourol Urodyn. 2019 Dec;38 Suppl 5:S71-S81 [PMID: 31821630]
  14. Immunol Rev. 2018 Jan;281(1):8-27 [PMID: 29247995]
  15. Rheumatology (Oxford). 2016 Aug;55(8):1499-506 [PMID: 27143789]
  16. Int Urogynecol J. 2016 May;27(5):697-708 [PMID: 26272202]
  17. Bioinformatics. 2011 Mar 1;27(5):718-9 [PMID: 21208982]
  18. PLoS One. 2011;6(12):e28632 [PMID: 22174851]
  19. Brain. 2008 Nov;131(Pt 11):2812-23 [PMID: 18567924]
  20. J Urol. 2007 Feb;177(2):450-6 [PMID: 17222607]
  21. Urology. 2008 Jun;71(6):1085-90 [PMID: 18538691]
  22. J Urol. 2005 Dec;174(6):2231-4 [PMID: 16280776]
  23. Lancet. 2008 Mar 22;371(9617):998-1006 [PMID: 18358927]
  24. Int J Urol. 2019 Jun;26 Suppl 1:26-34 [PMID: 31144757]
  25. Bioinformatics. 2009 Aug 15;25(16):2078-9 [PMID: 19505943]
  26. Sci Rep. 2018 Jul 20;8(1):11015 [PMID: 30030504]
  27. Nat Rev Immunol. 2016 Jul;16(7):407-20 [PMID: 27291964]

Word Cloud

Created with Highcharts 10.0.0paintreatmentbladderIL-1RAsyndromePatientsIL-1patientsmoleculargenecystitisreceptorantagoniststudyANDfrequencyurinationtherapeuticinterleukin-1TreatmentIL-1-dependentsubjectedreturnedlongtermeffectsDNArespondersclinicalproposedsymptomreliefBACKGROUND:experiencedebilitatingextremeNumerousapproachestestedbasisdiseaseremainedunclearspecifictherapiesavailableOBJECTIVE:RecentlysystematicdeletionstrategyidentifiedhyperactivationcauseseveremurinemodelrestoredhealthgeneticallysusceptiblemicelinkinginflammationpathologymucosaobjectiveinvestigatewhethermightbeneficialDESIGNSETTINGPARTICIPANTS:diagnosedinvitedparticipatedailyinjections1wkfollowedbreakurologicaldisordersaccompaniedincludedcontrolsOUTCOMEMEASUREMENTSSTATISTICALANALYSIS:symptomsresumedrespondingmaintainedindividualizeddosingregimensSymptomscoresrecordedquantifiedneuropeptideexpressionanalysissamplesexomegenotypingRESULTSLIMITATIONS:reduced13/17<0001SubstancePlevelsurinelowerednormallifestyleNeuroinflammatory-dependentnetworksinhibitedwellregulatorsinnateimmunityGenotypingrevealeddisease-associatedsequencevariantsControlsbenefitexceptonepatentcysticaCONCLUSIONS:reducechronicimmediatelyDespitelimitednumberpotentacuteeffectlastingindicateapproachmayworthexploringcontrolledtrialsPATIENTSUMMARY:treatingcanresultincreasequalitylifeReducedneuroinflammationsignalingprovidedevidenceImmunomodulation-AMolecularSolutionTreatingSevereBladderPainSyndrome?BladderImmunotherapyInterleukin-1Interstitial

Similar Articles

Cited By (6)