TCF-1 regulates the stem-like memory potential of HIV-specific CD8+ T cells in elite controllers
Rutishauser, R. L.; Deguit, C. D. T.; Hiatt, J.; Blaeschke, F.; Roth, T. L.; Wang, L.; Raymond, K.; Starke, C. E.; Mudd, J. C.; Chen, W.; Smullin, C.; Matus-Nicodemos, R.; Hoh, R.; Krone, M.; Hecht, F. M.; Pilcher, C. D.; Martin, J. N.; Koup, R. A.; Douek, D. C.; Brenchley, J. M.; Sekaly, R.-P.; Pillai, S. K.; Marson, A.; Deeks, S. G.; McCune, J. M.; Hunt, P. W.
Show 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.
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