生物
恒河猴
T细胞受体
剧目
免疫系统
吞吐量
计算生物学
T细胞
遗传学
计算机科学
物理
电信
无线
声学
作者
Evan Walsh,Tammy Tollison,Hayden Brochu,Brian I. Shaw,Kayleigh Diveley,Hsuan Chou,G. Lynn Law,Allan D. Kirk,Michael Gale,Xinxia Peng
出处
期刊:Journal of Immunology
[American Association of Immunologists]
日期:2022-01-05
卷期号:208 (3): 762-771
被引量:12
标识
DOI:10.4049/jimmunol.2100824
摘要
Recent advancements in microfluidics and high-throughput sequencing technologies have enabled recovery of paired H and L chains of Igs and VDJ and VJ chains of TCRs from thousands of single cells simultaneously in humans and mice. Despite rhesus macaques being one of the most well-studied model organisms for the human adaptive immune response, high-throughput single-cell immune repertoire sequencing assays are not yet available due to the complexity of these polyclonal receptors. We used custom primers that capture all known rhesus macaque Ig and TCR isotypes and chains that are fully compatible with a commercial solution for single-cell immune repertoire profiling. Using these rhesus-specific assays, we sequenced Ig and TCR repertoires in >60,000 cells from cryopreserved rhesus PBMCs, splenocytes, and FACS-sorted B and T cells. We were able to recover every Ig isotype and TCR chain, measure clonal expansion in proliferating T cells, and pair Ig and TCR repertoires with gene expression profiles of the same single cells. Our results establish the ability to perform high-throughput immune repertoire analysis in rhesus macaques at the single-cell level.
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