circVDJ-seq for T cell clonotype detection in single-cell and spatial multi-omics
Authors
- Izabela Plumbom
- Benedikt Obermayer
- Raphael Raspe
- Anna Pascual-Reguant
- Ilan Theurillat
- Tancredi Massimo Pentimalli
- Yu-Hsin Hsieh
- Marine Gil
- Carola Dietrich
- Michaela Seeger-Zografakis
- Claudia Quedenau
- Jeannine Wilde
- Caroline Braeuning
- Cornelius Fischer
- Markus Schuelke
- Volkhard Seitz
- Leif S. Ludwig
- Angelika Eggert
- Nikolaus Rajewsky
- Tatiana Borodina
- Dieter Beule
- Janine Altmueller
- Helena Radbruch
- Anja Erika Hauser
- Thomas Conrad
Journal
- Genome Medicine
Citation
- Genome Med 18 (1): 84
Abstract
Monitoring T cell repertoires in human tissues provides important insights into immune response mechanisms in cancer, infectious diseases, and autoimmunity. However, retrieving VDJ information from single-cell and spatial transcriptomics workflows with 3’-barcoding of cDNA remains resource-intensive or requires specialized sequencing equipment. Here, we introduce circVDJ-seq for simplified and cost-efficient T cell receptor (TCR) profiling from 3’-directed workflows like single-cell or single-nucleus RNA sequencing, ATAC + RNA multi-omics, and spatial transcriptomics. Application of circVDJ-seq to freshly resected neuroblastomas and postmortem lymph nodes affected by pneumonia or COVID-19 reveals distinct immune microenvironments and T cell clonality patterns, highlighting broad utility across diverse clinical contexts.