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Updated: Apr 26, 2026

Transduction and Expansion of Primary T Cells in Nine Days with Maintenance of Central Memory Phenotype
Published on: March 18, 2020
Serial transfer of single-cell-derived immunocompetence reveals stemness of CD8(+) central memory T cells
Patricia Graef1, Veit R Buchholz1, Christian Stemberger2
1Institute for Medical Microbiology, Immunology and Hygiene, Technische Universität München (TUM), Munich 81675, Germany.
Insights
Adult tissue stem cells reside within CD62L(+) central memory T (Tcm) cells. These stem cells possess self-renewal capacity and multipotency, crucial for reconstituting immunocompetence and offering therapeutic potential.
Area of Science:
- Immunology
- Cell Biology
- Stem Cell Research
Background:
- Immunological memory is vital for adaptive immunity.
- The role of stem-cell-like lymphocytes in maintaining memory is hypothesized but not fully established.
- Previous data focused on developmental potential, lacking functional hallmarks of stemness.
Purpose of the Study:
- To investigate the self-renewal capacity and multipotency of individual memory lymphocytes.
- To identify the specific lymphocyte subset acting as adult tissue stem cells.
- To explore the therapeutic potential of identified stem cell populations.
Main Methods:
- In vivo fate mapping of CD8(+) T cells.
- Serial single-cell adoptive transfer across three generations.
- Infection-driven re-expansion using Listeria monocytogenes.
Main Results:
- Immune responses from single naive T (Tn) cells, primary, and secondary central memory T (Tcm) cells showed similar size, diversity, and stochastic variation.
- These responses successfully reconstituted immunocompetence against a lethal bacterial infection.
- The CD62L(+) Tcm cell compartment was identified as the residence of adult tissue stem cells.
Conclusions:
- Adult tissue stem cells are present within the CD62L(+) Tcm cell population.
- These stem cells exhibit self-renewal and multipotency, essential for long-term immune defense.
- The CD62L(+) Tcm cell subset holds significant promise for therapeutic applications in immunology.
Abstract:
Maintenance of immunological memory has been proposed to rely on stem-cell-like lymphocytes. However, data supporting this hypothesis are focused on the developmental potential of lymphocyte populations and are thus insufficient to establish the functional hallmarks of stemness. Here, we investigated self-renewal capacity and multipotency of individual memory lymphocytes by in vivo fate mapping of CD8(+) T cells and their descendants across three generations of serial single-cell adoptive transfer and infection-driven re-expansion. We found that immune responses derived from single naive T (Tn) cells, single primary, and single secondary central memory T (Tcm) cells reached similar size and phenotypic diversity, were subjected to comparable stochastic variation, and could ultimately reconstitute immunocompetence against an otherwise lethal infection with the bacterial pathogen Listeria monocytogenes. These observations establish that adult tissue stem cells reside within the CD62L(+) Tcm cell compartment and highlight the promising therapeutic potential of this immune cell subset.
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