Abstract

BackgroundCD4+ T cell counts in certain human immunodeficiency virus (HIV)-infected patients called immunological non-responders (INRs) could not return to a normal level even with sustained antiretroviral therapy (ART) because of persistent immune activation, which is associated with pro-inflammatory cytokines production and an altered intestinal microbiome profile. Changes in gut bacterial composition have been linked to low CD4+ T cell counts in HIV-infected individuals. However, the association between CD4+ T cell counts and gut microbiota community composition and cytokines levels in INRs (CD4+ T cell counts < 500 cells/μL) from Yunnan Province, China, has not been previously investigated.MethodsTo address this issue, we carried out a cross-sectional study of 34 HIV-infected INRs. The patients were divided into CD4 count > 200 cells/μL group and CD4 count < 200 cells/μL group. The gut microbiota composition of each subject was analyzed by 16S rRNA gene sequencing. We also compared CD8+ T cell counts, pro-inflammatory cytokines levels, and nutritional status between the two groups.ResultsCompared to INRs with CD4 count > 200 cells/μL, those with CD4 count < 200 cells/μL had a lower CD4/CD8 ratio, lower nutritional status and higher serum levels of tumor necrosis factor (TNF)-α, interferon-γ-inducible protein (IP)-10 and interleukin (IL)-1α. Ruminococcaceae was less abundant in the CD4 count < 200 cells/μL group than in the CD4 count > 200 cells/μL group, and difference in alpha diversity was observed between the two groups. Moreover, CD4+ T cell counts were negatively associated with TNF-α and IL-1α levels and positively associated with the relative abundance of Ruminococcaceae.ConclusionsOur study demonstrated that lower CD4+ T cell counts in INRs are associated with a reduced abundance of Ruminococcaceae in the gut and elevated serum pro-inflammatory cytokines levels. Thus, interventions targeting gut microbiota to increase CD4+ T cell counts are a potential strategy for promoting immune reconstitution in HIV-infected INRs.

Highlights

  • CD4+ T cell counts in certain human immunodeficiency virus (HIV)-infected patients called immu‐ nological non-responders (INRs) could not return to a normal level even with sustained antiretroviral therapy (ART) because of persistent immune activation, which is associated with pro-inflammatory cytokines production and an altered intestinal microbiome profile

  • This study investigated the association between C­ D4+ T cell counts, gut microbiota community composition and abundance, and serum cytokines levels in HIV-infected INRs in Yunnan

  • By Principal coordinates analysis (PCoA) and nonmetric multidimensional scaling (NMDS) analysis based on unweighted UniFrac distances, we found that bacterial community structure differed to a certain extent between the two groups; Analysis of Similarities (ANOSIM) analysis of the distance matrices showed that these differences were not statistically significant (PCoA: P = 0.111; Additional file 1: Fig. S1A; NMDS: P = 0.101, Additional file 1: Fig. S1B)

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Summary

Introduction

CD4+ T cell counts in certain human immunodeficiency virus (HIV)-infected patients called immu‐ nological non-responders (INRs) could not return to a normal level even with sustained antiretroviral therapy (ART) because of persistent immune activation, which is associated with pro-inflammatory cytokines production and an altered intestinal microbiome profile. Plasma viral load declines to undetectable levels after initiation of antiretroviral therapy (ART), immune reconstitution may not occur; about 10–40% of HIV-infected individuals fail to normalize ­CD4+ T cell counts. These patients, known as immunological non-responders (INRs), have severe immune dysfunction with C­ D4+ T cell counts < 500 or < 350 cells/μL, or in extreme cases, < 200 cells/μL [3, 4]. It was reported that ARTtreated HIV patients with poor ­CD4+ T cell and CD4/ CD8 ratio recovery have increased microbial translocation and elevated levels of pro-inflammatory cytokines [16]

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