The DOI matches its Crossref record; 50 of the 50 references it cites were found in a registry or an index.
Inflammation Directs Memory Precursor and Short-Lived Effector CD8+ T Cell Fates via the Graded Expression of T-bet Transcription Factor
Open accessAbstract
As acute infections resolve, effector CD8(+) T cells differentiate into interleukin-7 receptor(lo) (IL-7R(lo)) short-lived effector cells (SLECs) and IL-7R(hi) memory precursor effector cells (MPECs) capable of generating long-lived memory CD8(+) T cells. By using another SLEC marker, KLRG1, we found that KLRG1(hi) effector cells began appearing early during infection and were committed to downregulating IL-7R. Unlike IL-7R(hi) MPECs, KLRG1(hi) IL-7R(lo) SLECs relied on IL-15, but IL-15 could not sustain their long-term maintenance or homeostatic turnover. The decision between SLEC and MPEC fates was regulated by the amount of inflammatory cytokines (i.e., IL-12) present during T cell priming. According to the amount of inflammation, a gradient of T-bet was created in which high T-bet expression induced SLECs and low expression promoted MPECs. These results elucidate a mechanism by which the innate immune system sets the relative amounts of a lineage-determining transcription factor in activated CD8(+) T cells and, correspondingly, regulates their memory cell potential.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“Ag-specific CD8 T cells derived from the effector phase of a response can express various combinations of CD127 and KLRG1, which define either more short-lived effector cells (SLECs; CD127−KLRG1+), which are lost during the contraction phase of the immune response, or memory precursor effector cells (MPECs; CD127+KLRG1−), which are more likely to persist and contribute to memory populations [224,”
From Guidelines for the use of flow cytometry and cell sorting in immunological studies (third edition) (2021) · cites this paper as [225]
Citations
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 2×
“…on the attribute examined, differ according to their localization, effector functions or potential to become protective memory CD8 T cells (de Bree et al., 2005; Huster et al., 2004; Kaech et al., 2003; Sallusto et al., 1999; Schluns et al., 2000; Voehringer et al., 2001; Wherry et al., 2003).”
BackgroundA Novel Transcription Factor, T-bet, Directs Th1 Lineage Commitment
Szabo, S. J., Kim, S. T., Costa, G. L., Zhang, X., Fathman, C. G., & Glimcher, L. H. (2000) · Cell · doi:10.1016/s0092-8674(00)80702-3 · Cited by 3,589
CpG Motifs in Bacterial DNA and Their Immune Effects
Krieg, A. Μ. (2002) · Annual Review of Immunology · doi:10.1146/annurev.immunol.20.100301.064842 · Cited by 2,598
Lineage relationship and protective immunity of memory CD8 T cell subsets
Wherry, E. J., Teichgräber, V., Becker, T. C., Masopust, D., Kaech, S. M., Antia, R., von Andrian, U. H., & Ahmed, R. (2003) · Nature Immunology · doi:10.1038/ni889 · Cited by 1,864
Self-citationKaech, S. M., Tan, J. T., Wherry, E. J., Konieczny, B. T., Surh, C. D., & Ahmed, R. (2003) · Nature Immunology · doi:10.1038/ni1009 · Cited by 1,830 · cited 12×
“…on the attribute examined, differ according to their localization, effector functions or potential to become protective memory CD8 T cells (de Bree et al., 2005; Huster et al., 2004; Kaech et al., 2003; Sallusto et al., 1999; Schluns et al., 2000; Voehringer et al., 2001; Wherry et al., 2003).”
BackgroundMethodResultInfluentialSelf-citationImmunological memory and protective immunity: understanding their relation
Ahmed, R., & Gray, D. (1996) · Science · doi:10.1126/science.272.5258.54 · Cited by 1,775 · cited 2×
“The “decreasing potential model” for the development of memory CD8 T cells suggests that “memory T cells can only arise under conditions in which the antigenic load is limited and the stimulation of precursors ceases before a point of no return” (Ahmed and Gray, 1996).”
BackgroundInterleukin-7 mediates the homeostasis of naïve and memory CD8 T cells in vivo
Schluns, K. S., Kieper, W. C., Jameson, S. C., & Lefrançois, L. (2000) · Nature Immunology · doi:10.1038/80868 · Cited by 1,619
Th17: An Effector CD4 T Cell Lineage with Regulatory T Cell Ties
Weaver, C. T., Harrington, L. E., Mangan, P. R., Gavrieli, M., & Murphy, K. M. (2006) · Immunity · doi:10.1016/j.immuni.2006.06.002 · Cited by 1,422
Effector and memory CD8+ T cell fate coupled by T-bet and eomesodermin
Intlekofer, A. M., Takemoto, N., Wherry, E. J., Longworth, S. A., Northrup, J. T., Palanivel, V., Mullen, A. C., Gasink, C. R., Kaech, S. M., Miller, J. D., et al. (2005) · Nature Immunology · doi:10.1038/ni1268 · Cited by 1,293
Self-citationKinetics of dendritic cell activation: impact on priming of TH1, TH2 and nonpolarized T cells
Langenkamp, A., Messi, M., Lanzavecchia, A., & Sallusto, F. (2000) · Nature Immunology · doi:10.1038/79758 · Cited by 1,140
Flagged first, then by citations
Cited by
Sorted by citations
Items 301–400 of 1,005
A unified atlas of CD8 T cell dysfunctional states in cancer and infection
Pritykin, Y., van der Veeken, J., Pine, A. R., Zhong, Y., Şahin, M., Mažutis, L., Pe’er, D., Rudensky, A. Y., & Leslie, C. S. (2021) · Molecular Cell · doi:10.1016/j.molcel.2021.03.045 · Cited by 117
Dendritic cells drive memory CD8 T-cell homeostasis via IL-15 transpresentation.
Stonier, S. W., Ma, L. J., Castillo, E. F., & Schluns, K. (2008) · Blood · doi:10.1182/blood-2008-05-156307 · Cited by 133
A central role for Notch in effector CD8+ T cell differentiation
Backer, R. A., Helbig, C., Gentek, R., Kent, A., Laidlaw, B. J., Dominguez, C. X., de Souza, Y., Trierum, S. E. V.-V., van Beek, R., Rimmelzwaan, G. F., et al. (2014) · Nature Immunology · doi:10.1038/ni.3027 · Cited by 120
Self-citationDemento, S. L., Bonafé, N., Cui, W., Kaech, S. M., Caplan, M. J., Fikrig, E., Ledizet, M., & Fahmy, T. M. (2010) · The Journal of Immunology · doi:10.4049/jimmunol.1000768 · Cited by 120
Self-citationCui, W., Joshi, N. S., Jiang, A., & Kaech, S. M. (2009) · Vaccine · doi:10.1016/j.vaccine.2009.01.088 · Cited by 121
Self-citationCurtsinger, J., Agarwal, P., Lins, D. C., & Mescher, M. F. (2012) · The Journal of Immunology · doi:10.4049/jimmunol.1102727 · Cited by 119
Wu, T., Wieland, A., Araki, K., Davis, C. W., Ye, L., Hale, J. S., & Ahmed, R. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1207327109 · Cited by 120
The regulation of lymphocyte activation and proliferation
Heinzel, S., Marchingo, J. M., Horton, M. B., & Hodgkin, P. D. (2018) · Current Opinion in Immunology · doi:10.1016/j.coi.2018.01.002 · Cited by 125
Crompton, J. G., Narayanan, M., Cuddapah, S., Roychoudhuri, R., Ji, Y., Yang, W., Patel, S. J., Sukumar, M., Palmer, D. C., Peng, W., et al. (2015) · Cellular and Molecular Immunology · doi:10.1038/cmi.2015.32 · Cited by 123
Nayar, R., Schutten, E., Bautista, B., Daniels, K. A., Prince, A., Enos, M., Brehm, M. A., Swain, S. L., Welsh, R. M., & Berg, L. J. (2014) · The Journal of Immunology · doi:10.4049/jimmunol.1303187 · Cited by 118
Transcriptional regulatory network for the establishment of CD8+ T cell exhaustion
Seo, W., Jerin, C., & Nishikawa, H. (2021) · Experimental & Molecular Medicine · doi:10.1038/s12276-021-00568-0 · Cited by 125
Chen, R., Bélanger, S., Frederick, M. A., Li, B., Johnston, R. J., Xiao, N., Liu, Y., Sharma, S., Peters, B., Rao, A., et al. (2014) · Immunity · doi:10.1016/j.immuni.2014.08.002 · Cited by 118
Sikora, A. G., Jaffarzad, N., Hailemichael, Y., Gelbard, A. H., Stonier, S. W., Schluns, K. S., Frasca, L., Lou, Y., Liu, C., Andersson, H. A., et al. (2009) · The Journal of Immunology · doi:10.4049/jimmunol.0802982 · Cited by 118
Delineation of a molecularly distinct terminally differentiated memory CD8 T cell population
Milner, J. J., Nguyen, H., Omilusik, K. D., Reina‐Campos, M., Tsai, M. S., Toma, C., Delpoux, A., Boland, B. S., Hedrick, S. Μ., Chang, J. T., et al. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2008571117 · Cited by 115
Li, Y., Cong, Y., Jia, M., He, Q., Zhong, H., Zhao, Y., Li, H., Yan, M., You, J., Liu, J., et al. (2021) · Nature Communications · doi:10.1038/s41467-021-21241-0 · Cited by 117
Vaccine adjuvants: Tailoring innate recognition to send the right message
Lavelle, E. C., & McEntee, C. P. (2024) · Immunity · doi:10.1016/j.immuni.2024.03.015 · Cited by 124
Dissecting the human immunologic memory for pathogens
Zielinski, C. E., Corti, D., Mele, F., Pinto, D., Lanzavecchia, A., & Sallusto, F. (2011) · Immunological Reviews · doi:10.1111/j.1600-065x.2010.01000.x · Cited by 118
Memory-T-Cell-Derived Interferon-γ Instructs Potent Innate Cell Activation for Protective Immunity
Soudja, S. M., Chandrabos, C., Yakob, E., Veenstra, M., Palliser, D., & Lauvau, G. S. (2014) · Immunity · doi:10.1016/j.immuni.2014.05.005 · Cited by 122
van der Waart, A. B., van de Weem, N. M. P., Maas, F., Kramer, C. S. M., Kester, M. G. D., Falkenburg, J. H. F., Schaap, N. P., Jansen, J. H., van der Voort, R., Gattinoni, L., et al. (2014) · Blood · doi:10.1182/blood-2014-05-578583 · Cited by 116
Sallin, M. A., Sakai, S., Kauffman, K. D., Young, H. A., Zhu, J., & Barber, D. L. (2017) · Cell Reports · doi:10.1016/j.celrep.2017.03.007 · Cited by 116
Sercan-Alp, Ö., Durlanik, S., Schulz, D., McGrath, M., Grün, J. R., Bardua, M., Ikuta, K., Sgouroudis, E., Riedel, R., Zehentmeier, S., et al. (2015) · European Journal of Immunology · doi:10.1002/eji.201445295 · Cited by 122
Li, Y., Hofmann, M., Wang, Q., Teng, L., Chlewicki, L. K., Pircher, H., & Mariuzza, R. A. (2009) · Immunity · doi:10.1016/j.immuni.2009.04.019 · Cited by 114
Kurktschiev, P., Raziorrouh, B., Schraut, W., Backmund, M., Wächtler, M., Wendtner, C., Bengsch, B., Thimme, R., Denk, G., Zachoval, R., et al. (2014) · The Journal of Experimental Medicine · doi:10.1084/jem.20131333 · Cited by 115
Evrard, M., Wynne-Jones, E., Peng, C., Kato, Y., Christo, S. N., Fonseca, R., Park, S. L., Burn, T. N., Osman, M., Devi, S., et al. (2021) · The Journal of Experimental Medicine · doi:10.1084/jem.20210116 · Cited by 117
Blimp‐1 homolog Hobit identifies effector‐type lymphocytes in humans
Braga, F. A. V., Hertoghs, K. M. L., Kragten, N. A. M., Doody, G. M., Barnes, N. A., Remmerswaal, E. B. M., Hsiao, C., Moerland, P. D., Wouters, D., Derks, I. A. M., et al. (2015) · European Journal of Immunology · doi:10.1002/eji.201545650 · Cited by 114
Wieten, R. W., Jonker, E. F. F., van Leeuwen, E. M. M., Remmerswaal, E. B. M., ten Berge, I. J. M., de Visser, A. W., van Genderen, P. J. J., Goorhuis, A., Visser, L. G., Grobusch, M. P., et al. (2016) · PLoS ONE · doi:10.1371/journal.pone.0149871 · Cited by 119
Type 1 Treg cells promote the generation of CD8+ tissue-resident memory T cells
Ferreira, C., Barros, L., Baptista, M., Blankenhaus, B., Barros, A., Figueiredo‐Campos, P., Konjar, Š., Lainé, A., Kamenjarin, N., Stojanovic, A., et al. (2020) · Nature Immunology · doi:10.1038/s41590-020-0674-9 · Cited by 110
Kuroda, S., Yamazaki, M., Abe, M., Sakimura, K., Takayanagi, H., & Iwai, Y. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1105133108 · Cited by 114
Mechanisms of CD8 + T cell‐mediated suppression of HIV/SIV replication
McBrien, J. B., Kumar, N., & Silvestri, G. (2018) · European Journal of Immunology · doi:10.1002/eji.201747172 · Cited by 111
Duckworth, B. C., Lafouresse, F., Wimmer, V. C., Broomfield, B. J., Dalit, L., Alexandre, Y. O., Sheikh, A. A., Qin, R. Z., Alvarado, C., Mielke, L. A., et al. (2021) · Nature Immunology · doi:10.1038/s41590-021-00878-5 · Cited by 113
Makedonas, G., Hutnick, N. A., Haney, D., Amick, A. C., Gardner, J. S., Cosma, G. L., Hersperger, A. R., Dolfi, D. V., Wherry, E. J., Ferrari, G., et al. (2010) · PLoS Pathogens · doi:10.1371/journal.ppat.1000798 · Cited by 112
Duration of Antigen Availability Influences the Expansion and Memory Differentiation of T Cells
Blair, D. A., Turner, D., Bose, T. O., Pham, Q.-M., Bouchard, K. R., Williams, K., McAleer, J. P., Cauley, L. S., Vella, A. T., & Lefrançois, L. (2011) · The Journal of Immunology · doi:10.4049/jimmunol.1100363 · Cited by 111
Jung, Y. W., Rutishauser, R. L., Joshi, N. S., Haberman, A. M., & Kaech, S. M. (2010) · The Journal of Immunology · doi:10.4049/jimmunol.1001948 · Cited by 111
Self-citationQuinn, K. M., Costa, A. D. S., Yamamoto, A., Berry, D., Lindsay, R. W. B., Darrah, P. A., Wang, L., Cheng, C., Kong, W., Gall, J. G. D., et al. (2013) · The Journal of Immunology · doi:10.4049/jimmunol.1202861 · Cited by 109
Kalia, V., Penny, L. A., Yuzefpolskiy, Y., Baumann, F. M., & Sarkar, S. (2015) · Immunity · doi:10.1016/j.immuni.2015.05.023 · Cited by 111
CTLs heterogeneity and plasticity: implications for cancer immunotherapy
Peng, S., Lin, A., Jiang, A., Zhang, C., Zhang, J., Cheng, Q., Luo, P., & Bai, Y. (2024) · Molecular Cancer · doi:10.1186/s12943-024-01972-6 · Cited by 114
Nutrient-driven histone code determines exhausted CD8 + T cell fates
Ma, S., Dahabieh, M. S., Mann, T. H., Zhao, S., McDonald, B., Song, W., Chung, H., Farsakoglu, Y., Garcia-Rivera, L., Hoffmann, F. A., et al. (2024) · Science · doi:10.1126/science.adj3020 · Cited by 118
Self-citationExpanding Roles for CD4 T Cells and Their Subpopulations in Tumor Immunity and Therapy
Dobrzanski, M. J. (2013) · Frontiers in Oncology · doi:10.3389/fonc.2013.00063 · Cited by 116
Nanjappa, S. G., Héninger, E., Wüthrich, M., Gasper, D. J., & Klein, B. S. (2012) · PLoS Pathogens · doi:10.1371/journal.ppat.1002771 · Cited by 110
Molecular signatures of T-cell inhibition in HIV-1 infection
Larsson, M., Shankar, E. M., Che, K. F., Saeidi, A., Ellegård, R., Barathan, M., Velu, V., & Kamarulzaman, A. (2013) · Retrovirology · doi:10.1186/1742-4690-10-31 · Cited by 110
Reduced generation of lung tissue–resident memory T cells during infancy
Zens, K. D., Chen, J. K., Guyer, R. S., Wu, F. L., Cvetkovski, F., Miron, M., & Färber, D. L. (2017) · The Journal of Experimental Medicine · doi:10.1084/jem.20170521 · Cited by 101
Stem, Effector, and Hybrid States of Memory CD8+ T Cells
Lugli, E., Galletti, G., Boi, S. K., & Youngblood, B. (2019) · Trends in Immunology · doi:10.1016/j.it.2019.11.004 · Cited by 107
Combined Inhibition of SHP2 and CXCR1/2 Promotes Antitumor T-cell Response in NSCLC
Tang, K. H., Li, S., Khodadadi-Jamayran, A., Jen, J., Han, H., Guidry, K., Chen, T., Hao, Y., Fedele, C., Zebala, J. A., et al. (2022) · Cancer Discovery · doi:10.1158/2159-8290.cd-21-0369 · Cited by 105
The Aryl Hydrocarbon Receptor Promotes IL-10 Production by NK Cells
Wagage, S., John, B., Krock, B. L., Hall, A. O., Randall, L. M., Karp, C. L., Simon, M. C., & Hunter, C. A. (2014) · The Journal of Immunology · doi:10.4049/jimmunol.1300497 · Cited by 112
Meyran, D., Zhu, J. J., Butler, J., Tantalo, D. G. M., Macdonald, S., Nguyen, T. N., Wang, M., Thio, N., D’Souza, C., Qin, V. M., et al. (2023) · Science Translational Medicine · doi:10.1126/scitranslmed.abk1900 · Cited by 108
Exploring regulatory mechanisms of CD8 + T cell contraction
Prlic, M., & Bevan, M. J. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0808997105 · Cited by 110
Intraepithelial Lymphocytes: To Serve and Protect
Sheridan, B., & Lefrançois, L. (2010) · Current Gastroenterology Reports · doi:10.1007/s11894-010-0148-6 · Cited by 118
Schouppe, E., Mommer, C., Movahedi, K., Laoui, D., Morias, Y., Gysemans, C. A., Luyckx, A., BAETSELIER, P. D., & Ginderachter, J. A. V. (2013) · European Journal of Immunology · doi:10.1002/eji.201343349 · Cited by 110
Chronic Bystander Infections and Immunity to Unrelated Antigens
Stelekati, E., & Wherry, E. J. (2012) · Cell Host & Microbe · doi:10.1016/j.chom.2012.10.001 · Cited by 103
Chiang, E. Y., de Almeida, P. E., Nagata, D. D. A., Bowles, K. H., Du, X., Chitre, A. S., Banta, K. L., Kwon, Y. C., McKenzie, B. S., Mittman, S., et al. (2020) · European Journal of Immunology · doi:10.1002/eji.201948405 · Cited by 107
Wang, S., Zhang, Q., Hui, H., Agrawal, K., Karris, M., & Rana, T. M. (2020) · Emerging Microbes & Infections · doi:10.1080/22221751.2020.1826361 · Cited by 103
Reductive carboxylation epigenetically instructs T cell differentiation
Jaccard, A., Wyss, T., Maldonado‐Pérez, N., Rath, J. A., Bevilacqua, A., Peng, J.-J., Lepez, A., Gunten, C. V., Franco, F., Kao, K., et al. (2023) · Nature · doi:10.1038/s41586-023-06546-y · Cited by 105
The importance of regulatory T‐cell heterogeneity in maintaining self‐tolerance
Yuan, X., Cheng, G., & Malek, T. R. (2014) · Immunological Reviews · doi:10.1111/imr.12163 · Cited by 101
Regulatory T Cells Selectively Control CD8+ T Cell Effector Pool Size via IL-2 Restriction
Kastenmüller, W., Gasteiger, G., Subramanian, N., Sparwasser, T. D., Busch, D. H., Belkaid, Y., Drexler, I., & Germain, R. N. (2011) · The Journal of Immunology · doi:10.4049/jimmunol.1101649 · Cited by 99
Iraolagoitia, X. L. R., Spallanzani, R. G., Torres, N. I., Araya, R. E., Ziblat, A., Domaica, C. I., Sierra, J. M., Núñez, S. Y., Secchiari, F., Gajewski, T. F., et al. (2016) · The Journal of Immunology · doi:10.4049/jimmunol.1502291 · Cited by 105
Bcl-2 Allows Effector and Memory CD8+ T Cells To Tolerate Higher Expression of Bim
Kurtuluş, S., Tripathi, P., Moreno‐Fernandez, M. E., Sholl, A., Katz, J. D., Grimes, H. L., & Hildeman, D. A. (2011) · The Journal of Immunology · doi:10.4049/jimmunol.1100102 · Cited by 102
Memory T-Cell Heterogeneity and TerminologyPreprint
Muroyama, Y., & Wherry, E. J. (2021) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a037929 · Cited by 104
Control of Lymphocyte Fate, Infection, and Tumor Immunity by TCF-1
Raghu, D., Xue, H., & Mielke, L. A. (2019) · Trends in Immunology · doi:10.1016/j.it.2019.10.006 · Cited by 98
KLRG1+ Memory CD8 T Cells Combine Properties of Short-Lived Effectors and Long-Lived Memory
Renkema, K. R., Huggins, M. A., da Silva, H. B., Knutson, T. P., Henzler, C. M., & Hamilton, S. E. (2020) · The Journal of Immunology · doi:10.4049/jimmunol.1901512 · Cited by 102
FoxO1 Controls Effector-to-Memory Transition and Maintenance of Functional CD8 T Cell Memory
Tejera, M. M., Kim, E. H., Sullivan, J. A., Plisch, E. H., & Suresh, M. (2013) · The Journal of Immunology · doi:10.4049/jimmunol.1300331 · Cited by 101
Gray, S. M., Kaech, S. M., & Staron, M. M. (2014) · Immunological Reviews · doi:10.1111/imr.12205 · Cited by 105
Self-citationImmune mechanisms of protection: can adjuvants rise to the challenge?
McKee, A. S., MacLeod, M. K. L., Kappler, J. W., & Marrack, P. (2010) · BMC Biology · doi:10.1186/1741-7007-8-37 · Cited by 102
Sprent, J., Cho, J., Boyman, O., & Surh, C. D. (2008) · Immunology and Cell Biology · doi:10.1038/icb.2008.12 · Cited by 99
Dissecting T Cell Contraction In Vivo Using a Genetically Encoded Reporter of Apoptosis
Garrod, K. R., Moreau, H. D., Garcia, Z., Lemaı̂tre, F., Bouvier, I., Albert, M. L., & Bousso, P. (2012) · Cell Reports · doi:10.1016/j.celrep.2012.10.015 · Cited by 99
Cytotoxic CD4 T Cells: Differentiation, Function, and Application to Dengue Virus Infection
Tian, Y., Sette, A., & Weiskopf, D. (2016) · Frontiers in Immunology · doi:10.3389/fimmu.2016.00531 · Cited by 99
CCR8 Expression Defines Tissue-Resident Memory T Cells in Human Skin
McCully, M. L., Ladell, K., Andrews, R., Jones, R. E., Miners, K. L., Roger, L., Baird, D. M., Cameron, M. J., Jessop, Z. M., Whitaker, I. S., et al. (2018) · The Journal of Immunology · doi:10.4049/jimmunol.1701377 · Cited by 103
Chung, H. K., McDonald, B., & Kaech, S. M. (2021) · The Journal of Experimental Medicine · doi:10.1084/jem.20201730 · Cited by 105
Self-citationKeppler, S. J., Rosenits, K., Kögl, T., Vucikuja, S., & Aichele, P. (2012) · PLoS ONE · doi:10.1371/journal.pone.0040865 · Cited by 99
He, B., Xing, S., Chen, C., Gao, P., Li, T., Shan, Q., Gullicksrud, J. A., Martin, M. D., Yu, S., Harty, J. T., et al. (2016) · Immunity · doi:10.1016/j.immuni.2016.11.009 · Cited by 99
Raczkowski, F., Ritter, J., Heesch, K., Schumacher, V., Guralnik, A., Höcker, L., Raifer, H., Klein, M., Bopp, T., Harb, H., et al. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1309378110 · Cited by 98
Cellular and molecular mechanisms of CD8(+) T cell differentiation, dysfunction and exhaustion
Verdon, D. J., Mulazzani, M., & Jenkins, M. R. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21197357 · Cited by 98
Baeza Garcia, A., Siu, E., Sun, T., Exler, V., Brito, L., Hekele, A., Otten, G., Augustijn, K., Janse, C. J., Ulmer, J. B., et al. (2018) · Nature Communications · doi:10.1038/s41467-018-05041-7 · Cited by 97
Homeostatic maintenance of T cells and natural killer cells
Boyman, O., Krieg, C., Homann, D., & Sprent, J. (2012) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-012-0968-7 · Cited by 99
Bystander Chronic Infection Negatively Impacts Development of CD8+ T Cell Memory
Stelekati, E., Shin, H., Doering, T. A., Dolfi, D. V., Ziegler, C. G. K., Beiting, D. P., Dawson, L. A., Liboon, J., Wolski, D., Ali, M.-A., et al. (2014) · Immunity · doi:10.1016/j.immuni.2014.04.010 · Cited by 101
Xia, L., Zheng, Z., Liu, J., Chen, Y., Ding, J., Xia, N., Luo, W., & Liu, W. (2020) · Clinical & Translational Immunology · doi:10.1002/cti2.1135 · Cited by 100
Hobit identifies tissue-resident memory T cell precursors that are regulated by Eomes
Vidal, L. P., Behr, F. M., Kragten, N. A. M., Nota, B., Wesselink, T. H., Kavazović, I., Covill, L., Schuller, M. B. P., Bryceson, Y. T., Wensveen, F. M., et al. (2021) · Science Immunology · doi:10.1126/sciimmunol.abg3533 · Cited by 101
Pham, N., Badovinac, V. P., & Harty, J. T. (2009) · The Journal of Immunology · doi:10.4049/jimmunol.0901203 · Cited by 97
Wilson, D. C., Grotenbreg, G. M., Liu, K., Zhao, Y., Frickel, E., Gubbels, M., Ploegh, H. L., & Yap, G. S. (2010) · PLoS Pathogens · doi:10.1371/journal.ppat.1000815 · Cited by 96
Interleukin-2 shapes the cytotoxic T cell proteome and immune environment–sensing programs
Rollings, C. M., Sinclair, L. V., Brady, H. J. M., Cantrell, D. A., & Ross, S. H. (2018) · Science Signaling · doi:10.1126/scisignal.aap8112 · Cited by 99
Regulation of CD8+ T memory and exhaustion by the mTOR signals
Chen, Y., Xu, Z., Sun, H., Ouyang, X., Han, Y., Yu, H., Wu, N., Xie, Y., & Su, B. (2023) · Cellular and Molecular Immunology · doi:10.1038/s41423-023-01064-3 · Cited by 101
Generating diversity: transcriptional regulation of effector and memory CD8+ T‐cell differentiation
Rutishauser, R. L., & Kaech, S. M. (2010) · Immunological Reviews · doi:10.1111/j.0105-2896.2010.00901.x · Cited by 97
Self-citationRole of TCF‐1 in differentiation, exhaustion, and memory of CD8 + T cells: A review
Zhang, J., Lyu, T., Cao, Y., & Feng, H. (2021) · The FASEB Journal · doi:10.1096/fj.202002566r · Cited by 109
Reprogramming the tumor microenvironment by genome editing for precision cancer therapy
Liu, K., Cui, J., Zhan, Y., Ouyang, Q., Lu, Q., Yang, D., Li, X., & Yin, J. (2022) · Molecular Cancer · doi:10.1186/s12943-022-01561-5 · Cited by 100
Yang, J., Xing, X., Luo, L., Zhou, X., Feng, J.-X., Huang, K., Liu, H., Jin, S., Liu, Y.-N., Zhang, S.-H., et al. (2023) · Science Immunology · doi:10.1126/sciimmunol.abq2424 · Cited by 101
Khan, A. A., Penny, L. A., Yuzefpolskiy, Y., Sarkar, S., & Kalia, V. (2013) · Blood · doi:10.1182/blood-2012-06-435412 · Cited by 94
Modulation of let-7 miRNAs controls the differentiation of effector CD8 T cells
Wells, A. C., Daniels, K. A., Angelou, C. C., Fagerberg, E., Burnside, A., Markstein, M., Alfandari, D., Welsh, R. M., Pobezinskaya, E. L., & Pobezinsky, L. A. (2017) · eLife · doi:10.7554/elife.26398 · Cited by 93
Oh, J., Barve, M. A., Matthews, C. M., Koon, E. C., Heffernan, T. P., Fine, B. A., Grosen, E. A., Bergman, M. K., Fleming, E. L., DeMars, L. R., et al. (2016) · Gynecologic Oncology · doi:10.1016/j.ygyno.2016.09.018 · Cited by 94
Wensveen, F. M., van Gisbergen, K. P. J. M., Derks, I. A. M., Gerlach, C., Schumacher, T. N., van Lier, R. A. W., & Eldering, E. (2010) · Immunity · doi:10.1016/j.immuni.2010.06.005 · Cited by 93
Memory CD4 T Cells in Influenza
Zens, K. D., & Färber, D. L. (2014) · Current topics in microbiology and immunology · doi:10.1007/82_2014_401 · Cited by 95
Blimp‐1 induces and Hobit maintains the cytotoxic mediator granzyme B in CD8 T cells
Kragten, N. A. M., Behr, F. M., Vieira Braga, F. A., Remmerswaal, E. B. M., Wesselink, T. H., Oja, A. E., Hombrink, P., Kallies, A., van Lier, R. A. W., Stark, R., et al. (2018) · European Journal of Immunology · doi:10.1002/eji.201847771 · Cited by 91
Increased T-bet is associated with senescence of influenza virus-specific CD8 T cells in aged humans
Dolfi, D. V., Mansfield, K. D., Polley, A. M., Doyle, S. A., Freeman, G. J., Pircher, H., Schmader, K. E., & Wherry, E. J. (2013) · Journal of Leukocyte Biology · doi:10.1189/jlb.0912438 · Cited by 93
The contextual role of TNFR family members in CD 8+ T‐cell control of viral infections
Wortzman, M. E., Clouthier, D., McPherson, A. J., Lin, G. H. Y., & Watts, T. H. (2013) · Immunological Reviews · doi:10.1111/imr.12086 · Cited by 99
MicroRNA-directed program of cytotoxic CD8 + T-cell differentiation
Trifari, S., Pipkin, M. E., Bandukwala, H. S., Äijö, T., Bassein, J. A., Chen, R., Martínez, G., & Rao, A. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1317191110 · Cited by 92
IL-21 Promotes CD8+ CTL Activity via the Transcription Factor T-bet
Sutherland, A. P. R., Joller, N., Michaud, M., Liu, S. M., Kuchroo, V. K., & Grusby, M. J. (2013) · The Journal of Immunology · doi:10.4049/jimmunol.1201730 · Cited by 95
Zwijnenburg, A. J., Pokharel, J., Varnaitė, R., Zheng, W., Hoffer, E., Shryki, I., Comet, N. R., Ehrström, M., Gredmark‐Russ, S., Eidsmo, L., et al. (2023) · Immunity · doi:10.1016/j.immuni.2023.06.025 · Cited by 92
Tim-3 Directly Enhances CD8 T Cell Responses to Acute Listeria monocytogenes Infection
Gorman, J. V., Starbeck-Miller, G. R., Pham, N., Traver, G. L., Rothman, P. B., Harty, J. T., & Colgan, J. D. (2014) · The Journal of Immunology · doi:10.4049/jimmunol.1302290 · Cited by 91
Reprogramming T cell differentiation and exhaustion in CAR-T cell therapy
Bulliard, Y., Andersson, B. S., Baysal, M. A., Damiano, J. S., & Tsimberidou, A. M. (2023) · Journal of Hematology & Oncology · doi:10.1186/s13045-023-01504-7 · Cited by 98
Cui, X., Liu, S., He, S., Xu, J., & Sun, Y. (2025) · Molecular Cancer · doi:10.1186/s12943-025-02287-w · Cited by 105
IL-15 Regulates Both Quantitative and Qualitative Features of the Memory CD8 T Cell Pool
Sandau, M. M., Kohlmeier, J. E., Woodland, D. L., & Jameson, S. C. (2009) · The Journal of Immunology · doi:10.4049/jimmunol.0803355 · Cited by 91
Type‐I IFN drives the differentiation of short‐lived effector CD8+ T cells in vivo
Wiesel, M., Crouse, J., Bedenikovic, G., Sutherland, A. P. R., Joller, N., & Oxenius, A. (2011) · European Journal of Immunology · doi:10.1002/eji.201142091 · Cited by 91
Metadata
- Authors
- Joshi, N. S., Cui, W., Chandele, A., Lee, H. K., Urso, D. R., Hagman, J., Gapin, L., & Kaech, S. M.
- Affiliations
- Yale University (US)
- National Jewish Health (US)
- Corresponding author
- Kaech, Susan M.
- ORCID
- Venue
- Immunity
- Publisher
- Elsevier BV
- Published
- 2007-08
- Volume
- 27
- Issue
- 2
- Pages
- 281-295
- ISSN
- 1074-7613 (ISSN-L)
- PMC
- PMC2034442
- OpenAlex
- W1985294654
- Cited by
- 1,861
- References
- 50
- Citations by year
- 2026: 77 · 2025: 99 · 2024: 94 · 2023: 112 · 2022: 108 · 2021: 137 · 2020: 125 · 2019: 105 · 2018: 99 · 2017: 73 · 2016: 105 · 2015: 110 · 2014: 106 · 2013: 117 · 2012: 102
- FWCI
- 25.67
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Immunity (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- Wellcome Trust
- National Institute of Allergy and Infectious Diseases (P01AI022295, R01AI057485, R01AI054661, P01 AI22295, T32AI055403, R01AI056322, R01AI066232)
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
- Life Sciences › Immunology and Microbiology › Immunology › Immunotherapy and Immune Responses
- Life Sciences › Immunology and Microbiology › Immunology › Psoriasis: Treatment and Pathogenesis
- Keywords
- CD8+ T cells, short-lived effector cells, memory precursor effector cells, T-bet, IL-7 receptor, KLRG1, IL-15, IL-12, inflammation, T cell differentiation, memory T cell generation, innate immune regulation
- MeSH terms
- T-bet Transcription Factor, Animals, Immunologic Memory, Infections, Inflammation, Interferon-gamma, Mice, Mutant Strains, Receptors, Immunologic, Biomarkers, Cytokines, CD8-Positive T-Lymphocytes, Interleukin-12, Interleukin-15, Receptors, Interleukin-7, T-Box Domain Proteins, Lectins, C-Type, Mice
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review