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The mechanisms that preserve memory cells are poorly understood. Fate mapping of the transcriptional repressor GFI1 identified that GFI1 was differentially regulated in virus-specific CD8\n                    <jats:sup>+<\/jats:sup>\n                    T\u2009cells and was selectively expressed in stem cell memory and central memory cells. Deletion of GFI1 led to reduced proliferation and progressive loss of memory T\u2009cells, which in turn resulted in failure to maintain antigen-specific CD8\n                    <jats:sup>+<\/jats:sup>\n                    T\u2009cell populations following infection with chronic lymphocytic choriomeningitis virus or murine cytomegalovirus. Ablation of GFI1 resulted in downregulation of the transcription factors EOMES and BCL-2 in memory CD8\n                    <jats:sup>+<\/jats:sup>\n                    T\u2009cells. Ectopic expression of EOMES rescued the expression of BCL-2, but the persistence of memory CD8\n                    <jats:sup>+<\/jats:sup>\n                    T\u2009cells was only partially rescued. These findings highlight the critical role of GFI1 in the long-term maintenance of memory CD8\n                    <jats:sup>+<\/jats:sup>\n                    T\u2009cells in persistent infections by sustaining their proliferative potential.\n                  <\/jats:p>","DOI":"10.1038\/s41590-025-02151-5","type":"journal-article","created":{"date-parts":[[2025,5,15]],"date-time":"2025-05-15T05:01:50Z","timestamp":1747285310000},"page":"894-907","update-policy":"https:\/\/doi.org\/10.1007\/springer_crossmark_policy","source":"Crossref","is-referenced-by-count":9,"title":["GFI1-driven transcriptional and epigenetic programs maintain CD8+ T\u2009cell stemness and persistence"],"prefix":"10.1038","volume":"26","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-1372-4257","authenticated-orcid":false,"given":"M. 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