Gut Lactobacillales are associated with higher CD4 and less microbial translocation during HIV infection
CD4-Positive T-Lymphocytes
Male
0301 basic medicine
Biomedical and clinical sciences
gut microbiome
HIV Infections
Medical and Health Sciences
Maraviroc
Placebos
gut-associated lymphoid tissue
Combination/methods Gastrointestinal Tract/*microbiology HIV Infections/*complications/*immunology Humans Lactobacillales/*growth & development Male Maraviroc Middle Aged Placebos/administration & dosage Rectum/microbiology Triazoles/therapeutic use Young Adult
Lactobacillales
Biological Sciences
Middle Aged
Biota
3. Good health
Infectious Diseases
pyrosequencing
Anti-Retroviral Agents
Medical Microbiology
6.1 Pharmaceuticals
Combination
HIV/AIDS
Drug Therapy, Combination
Infection
Adult
microbial translocation
Immunology
Clinical Trials and Supportive Activities
610
immune activation
Young Adult
03 medical and health sciences
Drug Therapy
Double-Blind Method
Clinical Research
Cyclohexanes
Virology
616
Humans
Biomedical and Clinical Sciences
Bacteria
Psychology and Cognitive Sciences
Rectum
Health sciences
Adult Anti-Retroviral Agents/therapeutic use Bacteria/classification/genetics Bacterial Translocation/*immunology Biota CD4 Lymphocyte Count CD4-Positive T-Lymphocytes/*immunology Cyclohexanes/therapeutic use Double-Blind Method Drug Therapy
Triazoles
CD4 Lymphocyte Count
Gastrointestinal Tract
Bacterial Translocation
Sexually Transmitted Infections
Microbiome
DOI:
10.1097/qad.0b013e3283611816
Publication Date:
2013-03-22T22:25:46Z
AUTHORS (12)
ABSTRACT
Early HIV infection is characterized by a dramatic depletion of CD4 T cells in the gastrointestinal tract and translocation of bacterial products from the gut into the blood. In this study, we evaluated if gut bacterial profiles were associated with immune status before and after starting antiretroviral therapy (ART).We evaluated the gut microbiota of men recently infected with HIV (n = 13) who were participating in a randomized, double-blind controlled trial of combination ART and maraviroc versus placebo and who were followed for 48 weeks.To evaluate the gut microbiota of participants, we pyrosequenced the bacterial populations from anal swabs collected before and longitudinally after the initiation of ART. Associations of the gut flora with clinical variables (lymphocyte profiles and viral loads), activation and proliferation markers in peripheral blood mononuclear cells and gut biopsies (measured by flow cytometry) and markers of microbial translocation (lipopolysaccharide and soluble CD14) were performed by regression analyses using R statistical software.Using pyrosequencing, we identified that higher proportions of Lactobacillales in the distal gut of recently HIV-infected individuals were associated with lower markers of microbial translocation, higher CD4% and lower viral loads before ART was started. Similarly, during ART, higher proportions of gut Lactobacillales were associated with higher CD4%, less microbial translocation, less systemic immune activation, less gut T lymphocyte proliferation, and higher CD4% in the gut.Shaping the gut microbiome, especially proportions of Lactobacillales, could help to preserve immune function during HIV infection.
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CITATIONS (109)
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