Department of Microbiology and Immunology, Medical College of Wisconsin, Milwaukee, WI.
Blood Research Institute, Versiti Wisconsin, Milwaukee, WI.
J Exp Med. 2021 Mar 1;218(3). doi: 10.1084/jem.20200650.
Tracking how individual naive T cells from a natural TCR repertoire clonally expand, differentiate, and make lineage choices in response to an infection has not previously been possible. Here, using single-cell sequencing technology to identify clones by their unique TCR sequences, we were able to trace the clonal expansion, differentiation trajectory, and lineage commitment of individual virus-specific CD4 T cells during an acute lymphocytic choriomeningitis virus (LCMV) infection. Notably, we found previously unappreciated clonal diversity and cellular heterogeneity among virus-specific helper T cells. Interestingly, although most naive CD4 T cells gave rise to multiple lineages at the clonal level, ∼28% of naive cells exhibited a preferred lineage choice toward either Th1 or TFH cells. Mechanistically, we found that TCR structure, in particular the CDR3 motif of the TCR α chain, skewed lineage decisions toward the TFH cell fate.
以前,无法跟踪个体天然 TCR 库中的初始 T 细胞如何克隆性扩增、分化并做出谱系选择来响应感染。在这里,我们使用单细胞测序技术通过其独特的 TCR 序列来识别克隆,从而能够追踪个体病毒特异性 CD4 T 细胞在急性淋巴细胞脉络丛脑膜炎病毒 (LCMV) 感染期间的克隆性扩增、分化轨迹和谱系决定。值得注意的是,我们发现了以前未被重视的病毒特异性辅助性 T 细胞中的克隆多样性和细胞异质性。有趣的是,尽管大多数初始 CD4 T 细胞在克隆水平上产生了多个谱系,但约 28%的初始细胞表现出对 Th1 或 TFH 细胞的优先谱系选择。从机制上讲,我们发现 TCR 结构,特别是 TCR α 链的 CDR3 基序,使谱系决策偏向于 TFH 细胞命运。