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

Authors :
Qian Zhou
Routy Jean-Pierre
Zhifeng Qiu
Yang Han
Jing Li
Qingren Meng
Jian Wang
Jingfa Xiao
Chu Yanan
Shao Changjun
Jun Yu
Wei Lyu
Taisheng Li
Hua Zhu
Xiaojing Song
Yu Kang
Source :
Computational and Structural Biotechnology Journal, Computational and Structural Biotechnology Journal, Vol 19, Iss, Pp 2928-2937 (2021)
Publication Year :
2021
Publisher :
Elsevier BV, 2021.

Abstract

Graphical abstract<br />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.

Details

ISSN :
20010370
Volume :
19
Database :
OpenAIRE
Journal :
Computational and Structural Biotechnology Journal
Accession number :
edsair.doi.dedup.....02693c6070b4f21e80bb0ba0e08b7405