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Updated: Sep 22, 2025

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Tumor Transplantation for Assessing the Dynamics of Tumor-Infiltrating CD8+ T Cells in Mice
Published on: June 12, 2021
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The CD8α-PILRα interaction maintains CD8+ T cell quiescence.
Linghua Zheng1, Xue Han1, Sheng Yao1
1Department of Immunobiology, Yale University School of Medicine, New Haven, CT, USA.
Summary
CD8α maintains T cell quiescence, preventing spontaneous activation and death. The CD8α-PILRα interaction is crucial for regulating peripheral T cell numbers without antigen exposure.
Area of Science:
- Immunology
- Cell Biology
- Molecular Biology
Background:
- T cell quiescence is vital for immune surveillance against diverse antigens.
- The molecular mechanisms governing T cell quiescence are not fully understood.
Purpose of the Study:
- To investigate the role of CD8α in maintaining CD8+ T cell quiescence.
- To identify molecular interactions regulating T cell homeostasis.
Main Methods:
- Inducible deletion of CD8α in mice.
- Analysis of T cell phenotypes and survival.
- Identification of CD8α ligands using co-immunoprecipitation and surface plasmon resonance.
Main Results:
- CD8α deletion led to spontaneous activation and death of naïve and memory CD8+ T cells.
- PILRα was identified as a functional ligand for CD8α in mice and humans.
- Disrupting the CD8α-PILRα interaction abrogated T cell quiescence.
Conclusions:
- CD8α is essential for maintaining CD8+ T cell quiescence in peripheral lymphoid organs.
- The CD8α-PILRα axis actively regulates peripheral T cell pool size independently of antigen exposure.
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