| Literature DB >> 31239514 |
John P Thornhill1,2, Matthew Pace1, Genevieve E Martin1, Jonathan Hoare2, Simon Peake2, Carolina Herrera2, Chan Phetsouphanh1, Jodi Meyerowitz1, Emily Hopkins1, Helen Brown1, Polly Dunn1, Natalia Olejniczak1, Christian Willberg1,3, Paul Klenerman1, Rob Goldin2, Julie Fox4, Sarah Fidler2,5, John Frater6,7.
Abstract
Gut-associated lymphoid tissue (GALT) is a key location for the HIV reservoir. The observation that B-cell-T-cell doublets are enriched for CD32a (a low-affinity IgG receptor) in peripheral blood raises interesting questions, especially as these cells have been associated with HIV DNA in some studies. We sought to determine if similar doublets were present in GALT, the significance of these doublets, and their implications for the HIV reservoir. Given the importance of GALT as a reservoir for HIV, we looked for expression of CD32 on gut CD4 T cells and for evidence of doublets, and any relationship with HIV DNA in HIV + individuals initiated on antiretroviral therapy (ART) during primary HIV infection (PHI). Tonsil tissue was also available for one individual. As previously shown for blood, CD32high CD4 cells were mainly doublets of CD4 T cells and B cells, with T-cell expression of ICOS in tonsil and gut tissue. CD4 T cells associated with CD32 (compared with 'CD32-' CD4 cells) had higher expression of follicular markers CXCR5, PD-1, ICOS, and Bcl-6 consistent with a T follicular helper (TFH) phenotype. There was a significant correlation between rectal HIV DNA levels and CD32 expression on TFH cells. Together, these data suggest that CD32high doublets are primarily composed of TFH cells, a subset known to be preferentially infected by HIV.Entities:
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Year: 2019 PMID: 31239514 DOI: 10.1038/s41385-019-0180-2
Source DB: PubMed Journal: Mucosal Immunol ISSN: 1933-0219 Impact factor: 7.313