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Related Concept Videos

T Cell Activation and Clonal Selection01:22

T Cell Activation and Clonal Selection

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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.
Naive T cells that have not yet encountered an antigen express two primary CD...
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Related Experiment Video

Updated: Sep 8, 2025

Spatial Profiling of Protein and RNA Expression in Tissue: An Approach to Fine-Tune Virtual Microdissection
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Localization of T cell clonotypes using the Visium spatial transcriptomics platform.

William H Hudson1,2, Lisa J Sudmeier3,4

  • 1Emory Vaccine Center, Atlanta, GA, USA.

STAR Protocols
|June 16, 2022
PubMed
Summary
This summary is machine-generated.

We developed a new protocol to map T-cell receptor clones within tissues using spatial transcriptomics. This method precisely locates T-cell clonotypes and gene expression, aiding tumor microenvironment research.

Keywords:
ImmunologyMolecular BiologySequence analysis

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Area of Science:

  • Immunology
  • Genomics
  • Bioinformatics

Background:

  • Understanding the spatial distribution of immune cells is crucial for disease research.
  • Current methods often lack the resolution to pinpoint specific T-cell clones within their tissue microenvironment.

Purpose of the Study:

  • To present a novel protocol for the in situ localization of T-cell receptor (TCR) clones.
  • To enable simultaneous mapping of gene expression and T-cell clonotypes within tissue sections.

Main Methods:

  • Utilized the Visium spatial transcriptomics platform.
  • Integrated T-cell receptor sequencing with spatial gene expression analysis.
  • Validated TCR sequence recapitulation with single-cell sequencing.

Main Results:

  • Successfully localized T-cell receptor clones and gene expression simultaneously within tissue sections.
  • Demonstrated that TCR sequences identified by the protocol are reproducible via single-cell sequencing.
  • Established a method for detailed spatial analysis of the human T-cell repertoire.

Conclusions:

  • The developed protocol allows for precise spatial mapping of T-cell clonotypes.
  • This technique is valuable for studying immune cell infiltration, particularly in the tumor microenvironment.
  • Facilitates in-depth investigations into the spatial organization of immune responses.