Author:
Rutishauser Rachel L.,Deguit Christian Deo T.,Hiatt Joseph,Blaeschke Franziska,Roth Theodore L.,Wang Lynn,Raymond Kyle,Starke Carly E.,Mudd Joseph C.,Chen Wenxuan,Smullin Carolyn,Matus-Nicodemos Rodrigo,Hoh Rebecca,Krone Melissa,Hecht Frederick M.,Pilcher Christopher D.,Martin Jeffrey N.,Koup Richard A.,Douek Daniel C.,Brenchley Jason M.,Sékaly Rafick-Pierre,Pillai Satish K.,Marson Alexander,Deeks Steven G.,McCune Joseph M.,Hunt Peter W.
Abstract
AbstractAlthough many HIV cure strategies seek to expand HIV-specific CD8+ T cells to control the virus, all are likely to fail if cellular exhaustion is not prevented. A loss in stem-like memory properties (i.e., the ability to proliferate and generate secondary effector cells) is a key feature of exhaustion; little is known, however, about how these properties are regulated in human virus-specific CD8+ T cells. We found that virus-specific CD8+ T cells from humans and non-human primates naturally controlling HIV/SIV infection express more of the transcription factor, TCF-1, than non-controllers. HIV-specific CD8+ T cell TCF-1 expression correlated with memory marker expression and proliferative capacity and declined with antigenic stimulation. CRISPR-Cas9 editing of TCF-1 in human primary T cells demonstrated a direct role in regulating expansion capacity. Collectively, these data suggest that TCF-1 controls the stem-like memory properties of HIV-specific CD8+ T cells and provides a rationale for enhancing this pathway in T cell-based therapeutic strategies for HIV.One Sentence SummaryTCF-1 is highly expressed in HIV-specific CD8+ T cells from elite controllers and directly regulates human CD8+ T cell expansion capacity in response to T cell receptor stimulation.
Publisher
Cold Spring Harbor Laboratory
Cited by
3 articles.
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