학술논문

Transcriptional down-regulation of ccr5 in a subset of HIV+ controllers and their family members.
Document Type
article
Source
Subject
CD4-Positive T-Lymphocytes
Cells
Cultured
Macrophages
Humans
HIV-1
HIV Infections
Receptors
CCR5
Family
Down-Regulation
Adult
Aged
Middle Aged
HIV Long-Term Survivors
Female
Male
Receptors
CCR2
Young Adult
Viral Tropism
Disease Resistance
HIV
ccr2
ccr5
elite controllers
human
infectious disease
microbiology
transcription
viremic controllers
virus
Cells
Cultured
Receptors
CCR5
CCR2
Biochemistry and Cell Biology
Language
Abstract
HIV +Elite and Viremic controllers (EC/VCs) are able to control virus infection, perhaps because of host genetic determinants. We identified 16% (21 of 131) EC/VCs with CD4 +T cells with resistance specific to R5-tropic HIV, reversed after introduction of ccr5. R5 resistance was not observed in macrophages and depended upon the method of T cell activation. CD4 +T cells of these EC/VCs had lower ccr2 and ccr5 RNA levels, reduced CCR2 and CCR5 cell-surface expression, and decreased levels of secreted chemokines. T cells had no changes in chemokine receptor mRNA half-life but instead had lower levels of active transcription of ccr2 and ccr5, despite having more accessible chromatin by ATAC-seq. Other nearby genes were also down-regulated, over a region of ~500 kb on chromosome 3p21. This same R5 resistance phenotype was observed in family members of an index VC, also associated with ccr2/ccr5 down-regulation, suggesting that the phenotype is heritable.