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Related Concept Videos

RNA-seq03:21

RNA-seq

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RNA sequencing, or RNA-Seq, is a high-throughput sequencing technology used to study the transcriptome of a cell. Transcriptomics helps to interpret the functional elements of a genome and identify the molecular constituents of an organism. Additionally, it also helps in understanding the development of an organism and the occurrence of diseases. 
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T Cell Activation and Clonal Selection01:22

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T cells are integral to our adaptive immune system, recognizing and effectively responding to foreign antigens. T cell activation and clonal selection are pivotal in orchestrating this immune response. This article elucidates these mechanisms, detailing the roles of cluster of differentiation (CD) markers, major histocompatibility complex (MHC) molecules, costimulatory signals, and the process of clonal selection.
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T Cell Clonal Analysis Using Single-cell RNA Sequencing and Reference Maps.

Massimo Andreatta1,2,3, Paul Gueguen1,2,3, Nicholas Borcherding4

  • 1Ludwig Institute for Cancer Research, Lausanne Branch, and Department of Oncology, CHUV and University of Lausanne, Epalinges, Switzerland.

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|August 28, 2023
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Summary
This summary is machine-generated.

This study introduces a computational workflow for analyzing T-cell states and clonotypes using single-cell RNA sequencing (scRNA-seq) and T-cell receptor (TCR) data. The method links T-cell clonality to their transcriptomic state, revealing relationships between clonal expansion and functional phenotypes.

Keywords:
Reference projectionSingle-cell analysisT-cell cloneT-cell receptorTCRTranscriptomicsscRNA-seqscTCR-seq

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Area of Science:

  • Immunology
  • Computational Biology
  • Bioinformatics

Background:

  • T cells utilize T-cell receptors (TCRs) for antigen recognition, enabling adaptive immune responses.
  • Distinct TCR sequences act as molecular barcodes for tracking T cell clonotypes.
  • Single-cell RNA sequencing (scRNA-seq) offers coupled TCR and transcriptional data for detailed T cell analysis.

Purpose of the Study:

  • To present a computational workflow for integrated T-cell state and clonal analysis from scRNA-seq data.
  • To enable the characterization of T-cell functional states and clonal structures.
  • To link T-cell clonality with transcriptomic profiles for deeper biological insights.

Main Methods:

  • Utilizes R packages Seurat, ProjecTILs, and scRepertoire for data analysis.
  • Employs reference projection with ProjecTILs for automated T-cell state annotation.
  • Integrates scRNA-seq and TCR sequencing data for comprehensive clonotype tracking.

Main Results:

  • The workflow allows for automated annotation of T-cell functional states.
  • Enables detailed tracking of individual T-cell clonotypes, including expansion and proliferation.
  • Facilitates the assessment of clonal overlap between different T-cell subtypes.
  • Links clonal expansion and differentiation states to functional phenotypes.

Conclusions:

  • The presented computational workflow provides a reproducible method for analyzing T-cell states and clonality.
  • This approach enhances the understanding of T-cell responses by integrating transcriptomic and TCR repertoire data.
  • The findings support the use of scRNA-seq and computational tools for dissecting adaptive immunity.