bioRxivImmunologyPreprint
TCF-1 regulates the stem-like memory potential of HIV-specific CD8+ T cells in elite controllers
R. L. Rutishauser, C. D. T. Deguit, J. Hiatt, F. Blaeschke, T. L. Roth, L. Wang, K. Raymond, C. E. Starke, J. C. Mudd, W. Chen, C. Smullin, R. Matus-Nicodemos, R. Hoh, M. Krone, F. M. Hecht, C. D. Pilcher, J. N. Martin, R. A. Koup, D. C. Douek, J. M. Brenchley, R.-P. Sekaly, S. K. Pillai, A. Marson, S. G. Deeks, J. M. McCune, P. W. Hunt
Abstract
Although 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.
- organism: human
- organism: non-human primate
- assay: bulk RNA-seq
- research focus: cell type annotation
- research focus: differential expression
- approach: experimental assay
- approach: statistical model
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