Characterization of KIRCD8 Regulatory T Cells in Humans by scRNA- and TCR-seq.

Methods Mol Biol

Institute of Immunity, Transplantation and Infection, Stanford University School of Medicine, Stanford, CA, USA.

Published: September 2022

Previous studies have demonstrated the regulatory functions of Ly49CD8 T cells toward self-reactive CD4 T cells in mice. Recently, we found KIRCD8 T cells are the equivalent of mouse Ly49CD8 T cells in humans. They are increased in patients with autoimmune or infectious diseases as a negative feedback mechanism to suppress the arising pathogenic cells and maintain peripheral tolerance. Here, we describe the methods on how we characterize the KIRCD8 T cells from different diseases using single-cell RNA and TCR sequencing.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10035765PMC
http://dx.doi.org/10.1007/978-1-0716-2712-9_4DOI Listing

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