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Cited by 428

The DOI matches its Crossref record; 14 of the 14 references it cites were found in a registry or an index.

Cutting Edge: The Transcription Factor Eomesodermin Enables CD8+ T Cells To Compete for the Memory Cell Niche

Open access
Banerjee, Arnob, Gordon, Scott M, Intlekofer, Andrew M, Paley, Michael A, Mooney, Erin C, Lindsten, Tulia, Wherry, E John, Reiner, Steven L·2010·The Journal of Immunology

Abstract

CD8+ T cells responding to intracellular infection give rise to cellular progeny that become terminally differentiated effector cells and self-renewing memory cells. T-bet and eomesodermin (Eomes) are key transcription factors of cytotoxic lymphocyte lineages. We show in this study that CD8+ T cells lacking Eomes compete poorly in contributing to the pool of Ag-specific central memory cells. Eomes-deficient CD8+ T cells undergo primary clonal expansion but are defective in long-term survival, populating the bone marrow niche and re-expanding postrechallenge. The phenotype of Eomes-deficient CD8+ T cells supports the hypothesis that T-bet and Eomes can act redundantly to induce effector functions, but can also act to reciprocally promote terminal differentiation versus self-renewal of Ag-specific memory cells.

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Crossref · 10.4049/jimmunol.1002042

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Metadata

Authors
Banerjee, A., Gordon, S. M., Intlekofer, A. M., Paley, M. A., Mooney, E. C., Lindsten, T., Wherry, E. J., & Reiner, S. L.
Venue
The Journal of Immunology
Published
2010-11-01
Volume
185
Issue
9
Pages
4988-4992
ISSN
  • 0022-1767 (ISSN-L)
  • 1550-6606
OpenAlex
W2106166533
Cited by
428
References
14
FWCI
9.72
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: Cutting Edge: The Transcription Factor Eomesodermin Enables CD8+ T Cells To Compete for the Memory Cell Niche. https://app.cochat.ai/papers/10.4049/jimmunol.1002042
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Banerjee, A., Gordon, S. M., Intlekofer, A. M., Paley, M. A., Mooney, E. C., Lindsten, T., Wherry, E. J., & Reiner, S. L. (2010). Cutting Edge: The Transcription Factor Eomesodermin Enables CD8+ T Cells To Compete for the Memory Cell Niche. The Journal of Immunology. https://doi.org/10.4049/jimmunol.1002042

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