- Gonzalo-Gil, Elena;
- Rapuano, Patrick B;
- Ikediobi, Uchenna;
- Leibowitz, Rebecca;
- Mehta, Sameet;
- Coskun, Ayse K;
- Porterfield, J Zachary;
- Lampkin, Teagan D;
- Marconi, Vincent C;
- Rimland, David;
- Walker, Bruce D;
- Deeks, Steven;
- Sutton, Richard E
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.