Uridine and pyruvate protect T cells’ proliferative capacity from mitochondrial toxic antibiotics: a clinical pilot study

Abstract Antibiotics that inhibit bacterial protein or nucleic acid synthesis and function can exert an off-target action on mitochondria (mitotoxic antibiotics), making actively dividing mammalian cells dependent on uridine and pyruvate supplementation. Based on this rationale, we carried out, for...

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Autores principales: Stefano Battaglia, Stefania De Santis, Monica Rutigliano, Fabio Sallustio, Angela Picerno, Maria Antonia Frassanito, Ingo Schaefer, Angelo Vacca, Antonio Moschetta, Peter Seibel, Michele Battaglia, Gaetano Villani
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Publicado: Nature Portfolio 2021
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Acceso en línea:https://doaj.org/article/175fce9d945345579c3dc0579ab7593b
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spelling oai:doaj.org-article:175fce9d945345579c3dc0579ab7593b2021-12-02T17:13:27ZUridine and pyruvate protect T cells’ proliferative capacity from mitochondrial toxic antibiotics: a clinical pilot study10.1038/s41598-021-91559-82045-2322https://doaj.org/article/175fce9d945345579c3dc0579ab7593b2021-06-01T00:00:00Zhttps://doi.org/10.1038/s41598-021-91559-8https://doaj.org/toc/2045-2322Abstract Antibiotics that inhibit bacterial protein or nucleic acid synthesis and function can exert an off-target action on mitochondria (mitotoxic antibiotics), making actively dividing mammalian cells dependent on uridine and pyruvate supplementation. Based on this rationale, we carried out, for the first time, a randomized pilot study in 55 patients with asymptomatic bacteriuria or positive sperm culture, each treated with a single mitotoxic antibiotic with or without oral supplementation of uridine + pyruvate (Uripyr, Mitobiotix, Italy). The in vivo and ex vivo data show a a 3.4-fold higher value in the differential (before and after the antibiotic treatment) lymphocytes count and a 3.7-fold increase in the percentage of dividing T cells, respectively, in the Uripyr vs the control group. Our findings lay the groundwork to enhance the synergy between antibiotics and the immune system in order to optimize the administration protocols and widen the application potentials of antibiotic therapies as well as to re-evaluate old “forgotten” molecules to fight bacterial infections in the antibiotics resistance era.Stefano BattagliaStefania De SantisMonica RutiglianoFabio SallustioAngela PicernoMaria Antonia FrassanitoIngo SchaeferAngelo VaccaAntonio MoschettaPeter SeibelMichele BattagliaGaetano VillaniNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 11, Iss 1, Pp 1-9 (2021)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Stefano Battaglia
Stefania De Santis
Monica Rutigliano
Fabio Sallustio
Angela Picerno
Maria Antonia Frassanito
Ingo Schaefer
Angelo Vacca
Antonio Moschetta
Peter Seibel
Michele Battaglia
Gaetano Villani
Uridine and pyruvate protect T cells’ proliferative capacity from mitochondrial toxic antibiotics: a clinical pilot study
description Abstract Antibiotics that inhibit bacterial protein or nucleic acid synthesis and function can exert an off-target action on mitochondria (mitotoxic antibiotics), making actively dividing mammalian cells dependent on uridine and pyruvate supplementation. Based on this rationale, we carried out, for the first time, a randomized pilot study in 55 patients with asymptomatic bacteriuria or positive sperm culture, each treated with a single mitotoxic antibiotic with or without oral supplementation of uridine + pyruvate (Uripyr, Mitobiotix, Italy). The in vivo and ex vivo data show a a 3.4-fold higher value in the differential (before and after the antibiotic treatment) lymphocytes count and a 3.7-fold increase in the percentage of dividing T cells, respectively, in the Uripyr vs the control group. Our findings lay the groundwork to enhance the synergy between antibiotics and the immune system in order to optimize the administration protocols and widen the application potentials of antibiotic therapies as well as to re-evaluate old “forgotten” molecules to fight bacterial infections in the antibiotics resistance era.
format article
author Stefano Battaglia
Stefania De Santis
Monica Rutigliano
Fabio Sallustio
Angela Picerno
Maria Antonia Frassanito
Ingo Schaefer
Angelo Vacca
Antonio Moschetta
Peter Seibel
Michele Battaglia
Gaetano Villani
author_facet Stefano Battaglia
Stefania De Santis
Monica Rutigliano
Fabio Sallustio
Angela Picerno
Maria Antonia Frassanito
Ingo Schaefer
Angelo Vacca
Antonio Moschetta
Peter Seibel
Michele Battaglia
Gaetano Villani
author_sort Stefano Battaglia
title Uridine and pyruvate protect T cells’ proliferative capacity from mitochondrial toxic antibiotics: a clinical pilot study
title_short Uridine and pyruvate protect T cells’ proliferative capacity from mitochondrial toxic antibiotics: a clinical pilot study
title_full Uridine and pyruvate protect T cells’ proliferative capacity from mitochondrial toxic antibiotics: a clinical pilot study
title_fullStr Uridine and pyruvate protect T cells’ proliferative capacity from mitochondrial toxic antibiotics: a clinical pilot study
title_full_unstemmed Uridine and pyruvate protect T cells’ proliferative capacity from mitochondrial toxic antibiotics: a clinical pilot study
title_sort uridine and pyruvate protect t cells’ proliferative capacity from mitochondrial toxic antibiotics: a clinical pilot study
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/175fce9d945345579c3dc0579ab7593b
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