@inbook{0dbe512430bc4c45828dce0c394ed663,
title = "An In Vitro System to Model the Establishment and Reactivation of HIV-1 Latency in Primary Human CD4+ T Cells",
abstract = "HIV-1 establishes latency primarily by infecting activated CD4+ T cells that later return to quiescence as memory cells. Latency allows HIV-1 to evade immune responses and to persist during antiretroviral therapy, which represents an important problem in clinical practice. Here we describe both the original and a simplified version of HIV-1 latency models that mimics this process using replication competent viruses. Our model allows generation of large numbers of latently infected CD4+ T cell to dissect molecular mechanisms of HIV latency and reactivation.",
keywords = "CD4+ T cells, HIV-1, Latency, Monocyte-derived dendritic cells",
author = "Rui Li and Fabio Romerio",
note = "Funding Information: This work was supported by the National Institute of Health grants R21AI084711 and R21AI106508 (to F.R.). The authors would like to thank Zahra Gholizadeh for helpful discussion. Publisher Copyright: {\textcopyright} 2022, Springer Science+Business Media, LLC, part of Springer Nature.",
year = "2022",
doi = "10.1007/978-1-0716-1871-4_3",
language = "English (US)",
series = "Methods in Molecular Biology",
publisher = "Humana Press Inc.",
pages = "31--43",
booktitle = "Methods in Molecular Biology",
}