Modulation of Phenylalanine and Tyrosine Metabolism in HIV-1 Infected Patients with Neurocognitive Impairment: Results from a Clinical Trial

To investigate the effects of oral bacteriotherapy on intestinal phenylalanine and tyrosine metabolism, in this longitudinal, double-arm trial, 15 virally suppressed HIV+ individuals underwent blood and fecal sample collection at baseline and after 6 months of oral bacteriotherapy. A baseline fecal...

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Bibliographic Details
Main Authors: Giuseppe P. Innocenti, Letizia Santinelli, Luca Laghi, Cristian Borrazzo, Claudia Pinacchio, Mariangela Fratino, Luigi Celani, Eugenio N. Cavallari, Carolina Scagnolari, Federica Frasca, Guido Antonelli, Claudio M. Mastroianni, Gabriella d’Ettorre, Giancarlo Ceccarelli
Format: Article
Language:English
Published: MDPI AG 2020-07-01
Series:Metabolites
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Online Access:https://www.mdpi.com/2218-1989/10/7/274
Description
Summary:To investigate the effects of oral bacteriotherapy on intestinal phenylalanine and tyrosine metabolism, in this longitudinal, double-arm trial, 15 virally suppressed HIV+ individuals underwent blood and fecal sample collection at baseline and after 6 months of oral bacteriotherapy. A baseline fecal sample was collected from 15 healthy individuals and served as control group for the baseline levels of fecal phenylalanine and tyrosine. CD4 and CD8 immune activation (CD38<sup>+</sup>) was evaluated by flow cytometry. Amino acid evaluation on fecal samples was conducted by Proton Nuclear Magnetic Resonance. Results showed that HIV+ participants displayed higher baseline phenylalanine/tyrosine ratio values than healthy volunteers. A significand reduction in phenylalanine/tyrosine ratio and peripheral CD4<sup>+</sup> CD38<sup>+</sup> activation was observed at the end of oral bacteriotherapy. In conclusion, probiotics beneficially affect the immune activation of HIV+ individuals. Therefore, the restoration of intestinal amino acid metabolism could represent the mechanisms through which probiotics exert these desirable effects.
ISSN:2218-1989