The DOI matches its Crossref record; 14 of the 14 references it cites were found in a registry or an index.
Lineage relationship of effector and memory T cells
Open accessAbstract
Adaptive immunity is characterized by the ability to form long-lived immunological memory. Upon re-exposure to antigen, memory T cells respond more rapidly and robustly than naïve T cells, providing better clearance of pathogens. Recent reviews have reinforced the text-book view that memory T cells arise from effector cells. Although this notion is teleologically appealing, emerging data is more consistent with a model where naïve cells directly develop into memory cells without transitioning through an effector stage. A clear understanding of the lineage relationships between memory and effector cells has profound implications for the design of vaccines and for the development of effective T cell-based therapies.
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Cites
Two subsets of memory T lymphocytes with distinct homing potentials and effector functions
Sallusto, F., Lenig, D., Förster, R., Lipp, M., & Lanzavecchia, A. (1999) · Nature · doi:10.1038/44385 · Cited by 5,846 · cited 1×
“This view, however, is at odds with the findings that length of telomeres [23–25] and activity of telomerase [25] are both reduced in effector compared to memory cells.”
ResultCentral Memory and Effector Memory T Cell Subsets: Function, Generation, and Maintenance
Sallusto, F., Geginat, J., & Lanzavecchia, A. (2004) · Annual Review of Immunology · doi:10.1146/annurev.immunol.22.012703.104702 · Cited by 3,067
A human memory T cell subset with stem cell–like properties
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Self-citationLineage relationship and protective immunity of memory CD8 T cell subsets
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Metabolic Pathways in Immune Cell Activation and Quiescence
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Adoptive immunotherapy for cancer: harnessing the T cell response
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Self-citationEnhancing CD8 T-cell memory by modulating fatty acid metabolism
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Inhibiting glycolytic metabolism enhances CD8+ T cell memory and antitumor function
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Cited by
Saxena, M., van der Burg, S. H., Melief, C. J. M., & Bhardwaj, N. (2021) · Nature reviews. Cancer · doi:10.1038/s41568-021-00346-0 · Cited by 1,581
T memory stem cells in health and disease
Gattinoni, L., Speiser, D. E., Lichterfeld, M., & Bonini, C. (2017) · Nature Medicine · doi:10.1038/nm.4241 · Cited by 620
Self-citationSpatial map of human T cell compartmentalization and maintenance over decades of life
Thome, J. J. C., Yudanin, N., Ohmura, Y., Kubota, M., Grinshpun, B., Sathaliyawala, T., Kato, T., Lerner, H., Shen, Y., & Farber, D. L. (2014) · Cell · doi:10.1016/j.cell.2014.10.026 · Cited by 587
T cell stemness and dysfunction in tumors are triggered by a common mechanism
Vodnala, S. K., Eil, R., Kishton, R. J., Sukumar, M., Yamamoto, T. N., Ha, N.-H., Lee, P.-H., Shin, M., Patel, S. J., Yu, Z., et al. (2019) · Science · doi:10.1126/science.aau0135 · Cited by 552
Self-citationMetabolic Regulation of T Cell Longevity and Function in Tumor Immunotherapy
Kishton, R. J., Sukumar, M., & Restifo, N. P. (2017) · Cell Metabolism · doi:10.1016/j.cmet.2017.06.016 · Cited by 548
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Metadata
- Authors
- Restifo, N. P., & Gattinoni, L.
- Venue
- Current Opinion in Immunology
- Publisher
- Elsevier BV
- Published
- 2013-10
- Volume
- 25
- Issue
- 5
- Pages
- 556-563
- ISSN
- 0952-7915 (ISSN-L)
- OpenAlex
- W1966047059
- Cited by
- 228
- References
- 14
- FWCI
- 0.94
- Type
- journal article
- Language
- en
- Open access
- green
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