Uromune

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Uromune
Vaccine description
TargetBacteria (E. coli, K. pneumoniae, E. faecalis, P. vulgaris)
Vaccine typeInactivated
Clinical data
Trade namesUromune
Other namesMV-140; MV140
Routes of
administration		Sublingual spray
ATC code
  • None

Uromune, also known by its developmental code name MV-140, is a polyvalent bacterial vaccine which is used in the prevention of recurrent urinary tract infections (UTIs).[1][2][3] In clinical studies, it has been found to reduce total number of UTIs (by ~70%), to increase UTI-free rates (from 25% to ~57%), and to increase time to next UTI (from 48 days to 275 days), as well as to reduce UTI symptoms, reduce antibiotic use, and improve quality of life, over a period of 9 months following treatment.[2][4][5][6] The effectiveness of the vaccine appears to wane with time, which may necessitate readministration.[2][5][6][7] Uromune is used as a sublingual spray once daily for 3 months.[2][3][5]

Side effects of Uromune are considered infrequent, minor, and usually not treatment-related.[2] Uromune is an inactivated combination of four major bacteria known to cause recurrent UTIs, including Escherichia coli, Klebsiella pneumoniae, Enterococcus faecalis, and Proteus vulgaris.[2] It is thought to work by increasing adaptive immunity against UTI-causing bacteria and possibly also by increasing trained immunity against these pathogens.[2][8]

Uromune first became available for clinical use in 2010[2] and was first described in the literature by 2012.[9] It was developed and marketed in Spain by Inmunotek S.L.[1][10][9] Uromune has also been approved in Mexico and the Dominican Republic and is currently pending approval in Canada.[2][11][1] The vaccine is under development for use and is available via special-access programs in numerous other countries, including in many European countries, Australia, New Zealand, and Chile, among others.[1][2][11] Development and approval in the United States is expected to take longer than other countries.[6][11] Uromune is also under investigation for other uses besides prevention of uncomplicated recurrent UTIs in adults, as well as readministration following potential waning effectiveness.[2]

Medical uses[edit]

Recurrent urinary tract infections[edit]

Uromune is used in the prevention of uncomplicated recurrent UTIs in adults.[2] It is indicated specifically for prevention of recurrent UTIs, defined as ≥3 UTIs in 12 months or ≥2 UTIs within 6 months.[5][3] The vaccine has been described as highly effective against recurrent UTIs.[10] Uromune is a suspension of selected strains of several whole-cell, heat-killed bacteria, including V121 Escherichia coli (25%), V113 Klebsiella pneumoniae (25%), V125 Enterococcus faecalis (25%), and V127 Proteus vulgaris (25%), in glycerol, sodium chloride, artificial pineapple flavoring, and water.[2][3] These bacteria together are responsible for most cases of UTIs, with E. coli alone responsible for 52 to 80% of recurrent UTIs.[5][3][4] Uromune is thought to increase immunity against these UTI-causing bacteria.[2] The vaccine is self-administered as a sublingual spray with two sprays of 100 μL each given once daily for 3 months.[2][3][5]

A European phase 3 clinical trial, with results published in 2021 and 2022, found that median 0.0 (IQRTooltip interquartile range 0.0–1.0) UTIs occurred with Uromune and median 3.0 UTIs (IQR 0.5–6.0) occurred with placebo during 9 months following a 3- to 6-month Uromune treatment period in 240 women.[2][12][4][13] There were a total of 249 UTIs with placebo, 80 UTIs with 3-month Uromune (−68% relative to placebo), and 70 UTIs (−72% relative to placebo) with 6-month Uromune during the 9-month period.[4] The 9-month UTI-free rate was 55.7% with 3 months of Uromune treatment and 58.0% with 6 months of Uromune treatment versus 25.0% with placebo.[2][12] Hence, the UTI-free rate was more than doubled with Uromune in this trial (increased by ~2.3-fold).[2][12] The median time to first UTI after treatment was 275.0 days with both 3-month and 6-month Uromune relative to 48.0 days with placebo.[2] In subanalyses of the trial, Uromune reduced overall UTI symptoms, resulted in fewer days on antibiotics, and improved total, general, and physical quality of life.[2]

A 2020 systematic review identified three clinical studies of Uromune, including a prospective cohort study, a retrospective cohort study, and a retrospective observational study, all conducted in the United Kingdom or Spain.[5] For short-term efficacy (≤6 months), the UTI-free rate with Uromune was 63.5 to 81%, relative to 3 to 5.6% for antibiotic therapy.[5] For long-term efficacy (>6 months), the UTI-free rate was 56.6% and 90.3%, with the longest reported outcome being 56.6% at 15 months, whereas almost all patients given daily antibiotic therapy had experienced at least one UTI by 12 and 15 months.[5] UTI recurrence occurred at median 180 days with Uromune and median 19 days with antibiotic prophylaxis.[5] A subsequent 2023 review of five observational studies with over 1,400 women, including the above studies, reported that Uromune was associated with higher UTI-free rates (35–58%) relative to 6-month antibiotic prophylaxis (0%) in two comparative observational studies and was associated with UTI-free rates of 33 to 78% over 9 to 24 months of follow-up in three uncontrolled prospective observational studies.[2][3] Likewise, in the five observational studies with 1,408 women, another 2020 systematic review reported UTI-free rates of 35 to 90% with Uromune in 519 women versus rates of 0–9% with antibiotic prophylaxis in 499 women over 15 months.[3][12]

In a preliminary analysis of the Health Canada-approved first-in-North America observational study, findings were comparable to previous observational studies.[2] In this study, which included 25 patients, the UTI rate was reduced by 82% for the 9-month post-vaccination period, with number of UTIs reducing from mean 11.5 UTIs/month to 2.1 UTIs/month, and the UTI-free rate during this period was 48% (12 of 25).[2] At 12 months, 80% of subjects (20 of 25) reported that they were moderately or markedly improved.[2] The preceding results are from the pre-COVID-19 pandemic cohort and an expanded follow-up with 64 women has been conducted with results published.[2][14][15][16] In the expanded cohort, there were a mean of 6.8 UTIs/year pre-vaccination, the UTI-free rate over the 9-month post-vaccination period was 40.6%, the reduction of infection rate was 75.3% for this period relative to the year prior to vaccination, and 80.3% reported being moderately or markedly improved at 12-month follow-up, with 58.1% considering themselves "mostly satisfied, pleased, or delighted".[14][15][16] Quality of life scored also improved by 1.5 points in the study.[14]

The risk of UTI recurrence with Uromune treatment has been found to increase with time, suggesting that the vaccine gradually wears off.[5][6] In a 2022 long-term prospective observational study with 1,003 patients, Uromune reduced the number of UTIs to 0–2 in 95.5% at 3 months, in 86.8% at 6 months, and in 54.7% at 12 months.[7] On the basis of these findings, readministration may be warranted and may be studied in the future.[5][6][7][2] However, in a 2024 study that was the first long-term study of Uromune, where 60% of individuals had a single course of Uromune and 40% had repeat courses 1 to 2 years after the first course, 54% of 89 women and men remained UTI-free 5 to 9 years after first receiving the vaccine.[17]

As of May 2023, at least eight clinical studies of Uromune, including one phase 3 randomized controlled trial, have been conducted.[2][11][6] These studies have included over 2,200 patients.[2] More than 40,000 patients have received Uromune as of 2023, including at least 22,000 in special-access programs.[18][2][11][6]

Side effects[edit]

Side effects of Uromune are reported to be infrequent and minor.[2] In two comparative studies of Uromune versus antibiotics, no adverse reactions were reported with Uromune.[2] In the United Kingdom prospective study, one serious adverse reaction—an allergic reaction—and seven minor adverse reactions (post-nasal drip, mouth stinging, scar itching, abdomen itching, abdominal pain, mild nausea, and worsening of asthma) were reported.[2] In two other studies of 166 and 784 patients, minor side effects including dry mouth (n=8), gastritis (n=4), general illness (n=3), glossitis (n=2), and flare-up of rheumatoid arthritis not thought to be treatment-related (n=1).[2] In the North American clinical study, there were five non-serious adverse reactions and one serious adverse reaction in 25 individuals, with one mild and self-limited adverse reaction deemed potentially vaccine-related.[2] In safety reports of 22,000 patients receiving the vaccine, there were 15 filed reports of adverse reactions for more than 1.5 million doses.[2]

In the phase 3 randomized controlled trial of Uromune versus placebo, there were 76 adverse reactions in the 3-month Uromune group, 48 adverse reactions in the 6-month Uromune group, and 81 adverse reactions in the placebo group.[2] The most frequent adverse reactions, occurring in ≥5% of individuals, were chest infections, candidiasis, and vaginitis.[2] The seven serious adverse reactions, which occurred in five individuals, were not considered not related to Uromune.[2] Of the 205 adverse effects reported in the trial, 9 (4.4%), presenting in five individuals (2.2%), were considered to be study intervention-related.[2] This included two in the placebo group (2.6%), three with 3-month Uromune (3.9%), and zero with 6-month Uromune (0.0%).[2] On the basis of these findings, it has been concluded that Uromune may be considered a very safe medical intervention.[2]

In the 2020 systematic review, Uromune was described as having acceptable safety and minimal adverse effects.[5]

Pharmacology[edit]

The mechanism of action of Uromune is believed to be induction of antibody production and activation of human dendritic cells to generate T helper (Th) 1, Th17, and interleukin-10, in turn resulting in anti-inflammatory T-cell responses in secondary lymphoid organs and locally in the bladder.[2][3][8] It is thought that induction of adaptive immunity following Uromune treatment discontinuation results in lasting clinical protection, although trained immunity may also be involved.[2] Uromune is administered sublingually, which is known to bypass degradation by gastric fluids and gastrointestinal enzymes that occurs with oral administration.[3] Moreover, sublingual administration is thought to have the potential to induce mucosal immune responses in a broad range of tissues, including the genitourinary tract.[3] Accordingly, Uromune has been found to induce immune responses both systemically and in the genitourinary tract.[3]

History[edit]

Uromune was first described in the literature by 2012.[9] The vaccine has been available since 2010 in clinical practice.[2] It was developed and marketed in Spain by the pharmaceutical company Immunotek S.L. in Madrid.[1][10][9] The vaccine has also since been approved in Mexico and the Dominican Republic.[2][11] As of October 2023, Uromune is under development for use in other countries and is in the preregistration phase of development, with approval pending in Canada.[2][1] It is also available for patients through various special-access (compassionate-use) programs in 26 countries.[1][11] Countries where Uromune is under development or available through early-access programs include Australia, Belgium, Canada, Chile, the Czech Republic, Denmark, Finland, France, Germany, Luxembourg, the Netherlands, New Zealand, Norway, Portugal, Romania, Serbia, Slovakia, Slovenia, Sweden, Turkey, and the United Kingdom, among others.[1][2][11] A notable exception among countries is the United States, where more stringent clinical trials are likely to be required before Uromune could be approved or made available.[6][11] Moreover, a United States-based randomized controlled trial may be required for approval in this country.[16] Development of Uromune has been licensed to Red Leaf Medical.[18]

Research[edit]

Clinical development of Uromune for prevention of UTIs in elderly people in long-term care homes, in children with recurrent UTIs, and in adults with complicated recurrent UTIs (e.g., patients with catheters or neurogenic bladder) is in the tentative planning stages.[2][19] Further assessment of Uromune may also include repeated administration following potential long-term loss of immunity and possible combination with vaccines for related infections.[2][20][21]

Several other vaccines for recurrent UTIs, including OM-89/UroVaxom (oral tablet), Solco-Urovac (vaginal suppository/intramuscular injection), and ExPEC4 V (intramuscular injection), are also under development.[3][5]

See also[edit]

References[edit]

  1. ^ a b c d e f g h "MV 140". Adis Insight. Springer Nature Switzerland AG. Retrieved 15 February 2024.
  2. ^ a b c d e f g h i j k l m n o p q r s t u v w x y z aa ab ac ad ae af ag ah ai aj ak al am an ao ap aq ar as at au av aw Nickel JC, Doiron RC (February 2023). "An Effective Sublingual Vaccine, MV140, Safely Reduces Risk of Recurrent Urinary Tract Infection in Women". Pathogens. 12 (3): 359. doi:10.3390/pathogens12030359. PMC 10052183. PMID 36986281.
  3. ^ a b c d e f g h i j k l m Nickel JC, Saz-Leal P, Doiron RC (August 2020). "Could sublingual vaccination be a viable option for the prevention of recurrent urinary tract infection in Canada? A systematic review of the current literature and plans for the future". Can Urol Assoc J. 14 (8): 281–287. doi:10.5489/cuaj.6690. PMC 7402698. PMID 33626320.
  4. ^ a b c d Lorenzo-Gómez MF, Foley S, Nickel JC, García-Cenador MB, Padilla-Fernández BY, González-Casado I, Martínez-Huélamo M, Yang B, Blick C, Ferreira F, Caballero R, Saz-Leal P, Casanovas M (April 2022). "Sublingual MV140 for Prevention of Recurrent Urinary Tract Infections". NEJM Evid. 1 (4): EVIDoa2100018. doi:10.1056/EVIDoa2100018. PMID 38319200. S2CID 246177950.
  5. ^ a b c d e f g h i j k l m n Prattley S, Geraghty R, Moore M, Somani BK (May 2020). "Role of Vaccines for Recurrent Urinary Tract Infections: A Systematic Review". Eur Urol Focus. 6 (3): 593–604. doi:10.1016/j.euf.2019.11.002. PMID 31806578. S2CID 208743752.
  6. ^ a b c d e f g h Hart, Janelle (September 16, 2021). "Novel vaccine MV140 effective at treating recurrent UTIs". Vol 49 No 12. 49 – via www.urologytimes.com. {{cite journal}}: Cite journal requires |journal= (help)
  7. ^ a b c Ramírez Sevilla C, Gómez Lanza E, Llopis Manzanera J, Cetina Herrando A, Puyol Pallàs JM (November 2022). "A Focus on Long-Term Follow-Up of Immunoprophylaxis to Recurrent Urinary Tract Infections: 10 Years of Experience with MV140 Vaccine in a Cohort of 1003 Patients Support High Efficacy and Safety". Arch Esp Urol. 75 (9): 753–757. doi:10.56434/j.arch.esp.urol.20227509.110. PMID 36472057. S2CID 254274602.
  8. ^ a b Benito-Villalvilla C, Cirauqui C, Diez-Rivero CM, Casanovas M, Subiza JL, Palomares O (July 2017). "MV140, a sublingual polyvalent bacterial preparation to treat recurrent urinary tract infections, licenses human dendritic cells for generating Th1, Th17, and IL-10 responses via Syk and MyD88". Mucosal Immunol. 10 (4): 924–935. doi:10.1038/mi.2016.112. PMID 27966556.
  9. ^ a b c d Lorenzo-Gómez MF, Padilla-Fernández B, García-Criado FJ, Mirón-Canelo JA, Gil-Vicente A, Nieto-Huertos A, Silva-Abuin JM (January 2013). "Evaluation of a therapeutic vaccine for the prevention of recurrent urinary tract infections versus prophylactic treatment with antibiotics". Int Urogynecol J. 24 (1): 127–34. doi:10.1007/s00192-012-1853-5. PMC 3536982. PMID 22806485.
  10. ^ a b c Mba IE, Sharndama HC, Anyaegbunam ZK, Anekpo CC, Amadi BC, Morumda D, Doowuese Y, Ihezuo UJ, Chukwukelu JU, Okeke OP (April 2023). "Vaccine development for bacterial pathogens: Advances, challenges and prospects". Trop Med Int Health. 28 (4): 275–299. doi:10.1111/tmi.13865. PMID 36861882. Uromune, developed by Inmunotek, a Spanish-based pharmaceutical company, is also currently in phase III clinical trial. This vaccine, Uromune, administered as a spray, has proven to be highly effective against chronic or recurrent UTIs. It contains inactivated E. coli, Proteus vulgaris, K. pneumoniae and Enterococcus faecalis (https://Clinicaltrials.gov).
  11. ^ a b c d e f g h i "Sublingual Vaccine Shows Efficacy in Preventing Recurrent UTIs, Helping to Eliminate Need for Antibiotics". 25 May 2023. Retrieved 15 February 2024.
  12. ^ a b c d Nickel, J. Curtis; Lorenzo-Gómez, María Fernanda; Foley, Stephen; Saz-Leal, Paula (2021). "PLLBA-02 A novel sublingual vaccine will dramatically alter the clinical management of recurrent urinary tract infections in women". Journal of Urology. 206 (Supplement 3). doi:10.1097/JU.0000000000002150.02. ISSN 0022-5347.
  13. ^ Werneburg GT (2022). "Catheter-Associated Urinary Tract Infections: Current Challenges and Future Prospects". Res Rep Urol. 14: 109–133. doi:10.2147/RRU.S273663. PMC 8992741. PMID 35402319. MV-140 (Uromune, Syner-Med Ltd UK; Immunotek S.L. Spain), a sublingual spray, has been evaluated for safety and efficacy.128 The MV-140 vaccine is composed of inactivated cell lysates of common uropathogens. Specifically, it contains lysates of E. coli, Klebsiella pneumonia, Proteus vulgaris, and Enterococcus faecalis. In a prospective study that included 77 women with recurrent UTI (each had 3 or more UTI episodes in the preceding 12 months), the vaccine was administered for 3 months, and 78% of the population was UTI-free over the 12-month follow-up period.128 In this study, one patient experienced rash and thus had to stop treatment. The first phase III, randomized, placebo-controlled, double-blind clinical trial was recently reported.129 The trial included 240 women with recurrent UTI, randomized to either MV140 (for 3 or 6 months) or placebo. The median number of UTIs in the 9 months post-vaccination was 3.0 in the placebo compared to 0.0 in the MV-140 treatment groups. There was a greater UTI-free rate in the MV-140 groups. Five subjects reported adverse reactions, all of which were non-serious (3 in the treatment groups, 2 in the placebo group). While these remarkable findings open new prevention avenues for this patient cohort, whether or not they are generalizable to a population with indwelling urethral catheters remains to be determined.
  14. ^ a b c Nickel JC, Kelly KL, Griffin A, Elterman S, Clark-Pereira J, Doiron RC (February 2024). "MV140 sublingual vaccine reduces recurrent urinary tract infection in women Results from the first North American clinical experience study". Can Urol Assoc J. 18 (2): 25–31. doi:10.5489/cuaj.8455. PMC 10841562. PMID 37931282.
  15. ^ a b Hickling D (February 2024). "MV140 sublingual vaccine proves promising in fighting recurrent urinary tract infections in women". Can Urol Assoc J. 18 (2): 32. doi:10.5489/cuaj.8716. PMC 10841568. PMID 38315548.
  16. ^ a b c "Vaccine for recurrent UTIs reduces infection rate by 74.8%". www.healio.com.
  17. ^ Kanabar, S.; Foley, S.; Yang, B. (2024). "Assessing the long-term efficacy and safety of MV140 sublingual bacterial vaccine in the initial cohort: A 9-year study in the UK for treating recurrent urinary tract infections in men and women". European Urology. 85 (Suppl 1): S1037–S1037. doi:10.1016/S0302-2838(24)00833-9.
  18. ^ a b https://redleafmedical.com/redleaf-medical-solutions/infectious-disease/uromune/
  19. ^ Kovacic J, Canagasingham A, Zhong W, Lockhart K, Dhar A, Shepherd A, Chung A (December 2023). "Evaluation of MV140 in preventing recurrent urinary tract infections: a multicentre double-blind randomized controlled trial protocol". BJU Int. doi:10.1111/bju.16247. PMID 38060333. S2CID 266147428.
  20. ^ Martin-Cruz L, Sevilla-Ortega C, Benito-Villalvilla C, Diez-Rivero CM, Sanchez-Ramón S, Subiza JL, Palomares O (2020). "A Combination of Polybacterial MV140 and Candida albicans V132 as a Potential Novel Trained Immunity-Based Vaccine for Genitourinary Tract Infections". Front Immunol. 11: 612269. doi:10.3389/fimmu.2020.612269. PMC 7858650. PMID 33552074.
  21. ^ Martín-Cruz L, Angelina A, Baydemir I, Bulut Ö, Subiza JL, Netea MG, Domínguez-Andrés J, Palomares O (2022). "Candida albicans V132 induces trained immunity and enhances the responses triggered by the polybacterial vaccine MV140 for genitourinary tract infections". Front Immunol. 13: 1066383. doi:10.3389/fimmu.2022.1066383. PMC 9729253. PMID 36505433.

External links[edit]


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