FOXO1 promotes HIV Latency by suppressing ER stress in T cells

Vallejo-Gracia, Albert; Chen, Irene P.; Perrone, Rosalba; Besnard, Emilie; Boehm, Daniela; Battivelli, Emilie; Tezil, Tugsan; Krey, Karsten; Raymond, Kyle A.; Hull, Philip A.; Walter, Marius; Habrylo, Ireneusz; Cruz, Andrew; Deeks, Steven; Pillai, Satish; Verdin, Eric; Ott, Melanie

Quiescence is a hallmark of CD4(+) T cells latently infected with HIV-1. While reversing this quiescence is an effective approach to reactivate latent HIV from T cells in culture, it can cause deleterious cytokine dysregulation in patients. As a key regulator of T-cell quiescence, FOXO1 promotes latency and suppresses productive HIV infection. We report that in resting T cells, FOXO1 inhibition impaired autophagy and induced ER stress, thereby activating two associated transcription factors: activating transcription factor 4 (ATF4) and nuclear factor of activated T cells (NFAT). Both factors associate with HIV chromatin and were for HIV reactivation. Indeed, inhibition of PKR-like endoplasmic reticulum kinase (PERK), an ER stress sensor that can mediate the induction of ATF4, and calcineurin, a calcium-dependent regulator of NFAT, synergistically suppressed HIV reactivation induced by FOXO1 inhibition. Thus, our studies uncover a link between FOXO1, ER stress, and HIV infection that could be therapeutically exploited to selectively reverse T-cell quiescence and reduce the size of the latent viral reservoir.