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Gut lactate-producing bacteria promote CD4 T cell recovery on Anti-retroviral therapy in HIV-infected patients

Anti-retroviral therapy (ART) effectively suppresses viral replication in HIV-infected patients, however CD4 + cell restoration to normal value is not achieved by 15–20% of patients who are called immune non-responders. Gut microbiota composition has been shown to influence host immunity. Herein, to...

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Autores principales: Lyu, Wei, Meng, Qingren, Xiao, Jingfa, Li, Jing, Wang, Jian, Qiu, Zhifeng, Song, Xiaojing, Zhu, Hua, Shao, Changjun, Chu, Yanan, Zhou, Qian, Li, Taisheng, Jean-Pierre, Routy, Yu, Jun, Han, Yang, Kang, Yu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Research Network of Computational and Structural Biotechnology 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8191414/
https://www.ncbi.nlm.nih.gov/pubmed/34141131
http://dx.doi.org/10.1016/j.csbj.2021.05.021
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author Lyu, Wei
Meng, Qingren
Xiao, Jingfa
Li, Jing
Wang, Jian
Qiu, Zhifeng
Song, Xiaojing
Zhu, Hua
Shao, Changjun
Chu, Yanan
Zhou, Qian
Li, Taisheng
Jean-Pierre, Routy
Yu, Jun
Han, Yang
Kang, Yu
author_facet Lyu, Wei
Meng, Qingren
Xiao, Jingfa
Li, Jing
Wang, Jian
Qiu, Zhifeng
Song, Xiaojing
Zhu, Hua
Shao, Changjun
Chu, Yanan
Zhou, Qian
Li, Taisheng
Jean-Pierre, Routy
Yu, Jun
Han, Yang
Kang, Yu
author_sort Lyu, Wei
collection PubMed
description Anti-retroviral therapy (ART) effectively suppresses viral replication in HIV-infected patients, however CD4 + cell restoration to normal value is not achieved by 15–20% of patients who are called immune non-responders. Gut microbiota composition has been shown to influence host immunity. Herein, to identify intestinal microbial agents that may influence the CD4 recovery in HIV-infected patients, we utilized a “Quasi-paired cohort” method to analyze intestinal metagenome data from immunological responders (IRs) and immunological non-responders (INRs). This method identified significant enrichment for Streptococcus sp. and related lactate-producing bacteria (LAB) in IRs. In a validation cohort, positive correlations between the abundance of these LAB and the post-ART CD4 + recovery was observed, and a prediction model based on these LAB performed well in predicting immune recovery. Finally, experiments using a germ-free mouse model of antibody-induced CD4 + cell depletion showed that supplementation with a lactate-producing commensal Streptococcus thermophilus strongly promoted CD4 recovery. In conclusion, our study identified a group of LAB that was associated with enhanced immune recovery in post-ART HIV-infected patients and promotes CD4 + cell restoration in a mouse model. These findings favour supplementation of LAB commensal as a therapeutic strategy for CD4 + cell count improvement in HIV-infected patients.
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spelling pubmed-81914142021-06-16 Gut lactate-producing bacteria promote CD4 T cell recovery on Anti-retroviral therapy in HIV-infected patients Lyu, Wei Meng, Qingren Xiao, Jingfa Li, Jing Wang, Jian Qiu, Zhifeng Song, Xiaojing Zhu, Hua Shao, Changjun Chu, Yanan Zhou, Qian Li, Taisheng Jean-Pierre, Routy Yu, Jun Han, Yang Kang, Yu Comput Struct Biotechnol J Research Article Anti-retroviral therapy (ART) effectively suppresses viral replication in HIV-infected patients, however CD4 + cell restoration to normal value is not achieved by 15–20% of patients who are called immune non-responders. Gut microbiota composition has been shown to influence host immunity. Herein, to identify intestinal microbial agents that may influence the CD4 recovery in HIV-infected patients, we utilized a “Quasi-paired cohort” method to analyze intestinal metagenome data from immunological responders (IRs) and immunological non-responders (INRs). This method identified significant enrichment for Streptococcus sp. and related lactate-producing bacteria (LAB) in IRs. In a validation cohort, positive correlations between the abundance of these LAB and the post-ART CD4 + recovery was observed, and a prediction model based on these LAB performed well in predicting immune recovery. Finally, experiments using a germ-free mouse model of antibody-induced CD4 + cell depletion showed that supplementation with a lactate-producing commensal Streptococcus thermophilus strongly promoted CD4 recovery. In conclusion, our study identified a group of LAB that was associated with enhanced immune recovery in post-ART HIV-infected patients and promotes CD4 + cell restoration in a mouse model. These findings favour supplementation of LAB commensal as a therapeutic strategy for CD4 + cell count improvement in HIV-infected patients. Research Network of Computational and Structural Biotechnology 2021-05-11 /pmc/articles/PMC8191414/ /pubmed/34141131 http://dx.doi.org/10.1016/j.csbj.2021.05.021 Text en © 2021 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research Article
Lyu, Wei
Meng, Qingren
Xiao, Jingfa
Li, Jing
Wang, Jian
Qiu, Zhifeng
Song, Xiaojing
Zhu, Hua
Shao, Changjun
Chu, Yanan
Zhou, Qian
Li, Taisheng
Jean-Pierre, Routy
Yu, Jun
Han, Yang
Kang, Yu
Gut lactate-producing bacteria promote CD4 T cell recovery on Anti-retroviral therapy in HIV-infected patients
title Gut lactate-producing bacteria promote CD4 T cell recovery on Anti-retroviral therapy in HIV-infected patients
title_full Gut lactate-producing bacteria promote CD4 T cell recovery on Anti-retroviral therapy in HIV-infected patients
title_fullStr Gut lactate-producing bacteria promote CD4 T cell recovery on Anti-retroviral therapy in HIV-infected patients
title_full_unstemmed Gut lactate-producing bacteria promote CD4 T cell recovery on Anti-retroviral therapy in HIV-infected patients
title_short Gut lactate-producing bacteria promote CD4 T cell recovery on Anti-retroviral therapy in HIV-infected patients
title_sort gut lactate-producing bacteria promote cd4 t cell recovery on anti-retroviral therapy in hiv-infected patients
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8191414/
https://www.ncbi.nlm.nih.gov/pubmed/34141131
http://dx.doi.org/10.1016/j.csbj.2021.05.021
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