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Induction of memory-like CD8+ T cells and CD4+ T cells from human naive T cells in culture.
- Source :
- Clinical & Experimental Immunology; Jan2022, Vol. 207 Issue 1, p95-103, 9p
- Publication Year :
- 2022
-
Abstract
- Memory T cells are crucial players in vertebrate adaptive immunity but their development is incompletely understood. Here, we describe a method to produce human memory-like T cells from naive human T cells in culture. Using commercially available human T-cell differentiation kits, both purified naive CD8<superscript>+</superscript> T cells and purified naive CD4<superscript>+</superscript> T cells were activated via T-cell receptor signaling and appropriate cytokines for several days in culture. All the T-cell activators were then removed from the medium and the cultures were continued in hypoxic condition (1% O<subscript>2</subscript> atmosphere) for several more days; during this period, most of the cells died, but some survived in a quiescent state for a month. The survivors had small round cell bodies, expressed differentiation markers characteristic of memory T cells and restarted proliferation when the T-cell activators were added back. We could also induce memory-like T cells from naive human T cells without hypoxia, if we froze the activated T cells or prepared the naive T cells from chilled filter buffy coats. Pre-activated human naïve CD4<superscript>+</superscript> or CD8<superscript>+</superscript> T cells were cultured in activator-free medium to induce cell death for 5 to 10 days. Although no cell survived in normal oxygen condition (20% O2), 2 to 30% of the activated T cells could survive in hypoxia (1% O2) and became memory-like T cells. We named this simple procedure as 'the Death Assay'. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 00099104
- Volume :
- 207
- Issue :
- 1
- Database :
- Complementary Index
- Journal :
- Clinical & Experimental Immunology
- Publication Type :
- Academic Journal
- Accession number :
- 158572311
- Full Text :
- https://doi.org/10.1093/cei/uxab012