作者
Samuel W Kazer, Toby P Aicher, Daniel M Muema, Shaina L Carroll, Jose Ordovas-Montanes, Vincent N Miao, Ang A Tu, Carly GK Ziegler, Sarah K Nyquist, Emily B Wong, Nasreen Ismail, Mary Dong, Amber Moodley, Bonnie Berger, J Christopher Love, Krista L Dong, Alasdair Leslie, Zaza M Ndhlovu, Thumbi Ndung’u, Bruce D Walker, Alex K Shalek
发表日期
2020/4
期刊
Nature medicine
卷号
26
期号
4
页码范围
511-518
出版商
Nature Publishing Group US
简介
Cellular immunity is critical for controlling intracellular pathogens, but individual cellular dynamics and cell–cell cooperativity in evolving human immune responses remain poorly understood. Single-cell RNA-sequencing (scRNA-seq) represents a powerful tool for dissecting complex multicellular behaviors in health and disease, and nominating testable therapeutic targets. Its application to longitudinal samples could afford an opportunity to uncover cellular factors associated with the evolution of disease progression without potentially confounding inter-individual variability. Here, we present an experimental and computational methodology that uses scRNA-seq to characterize dynamic cellular programs and their molecular drivers, and apply it to HIV infection. By performing scRNA-seq on peripheral blood mononuclear cells from four untreated individuals before and longitudinally during acute infection, we were …
引用总数
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