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Quantifying Memory CD8 T Cells Reveals Regionalization of Immunosurveillance
Open accessAbstract
Memory CD8 T cells protect against intracellular pathogens by scanning host cell surfaces; thus, infection detection rates depend on memory cell number and distribution. Population analyses rely on cell isolation from whole organs, and interpretation is predicated on presumptions of near complete cell recovery. Paradigmatically, memory is parsed into central, effector, and resident subsets, ostensibly defined by immunosurveillance patterns but in practice identified by phenotypic markers. Because isolation methods ultimately inform models of memory T cell differentiation, protection, and vaccine translation, we tested their validity via parabiosis and quantitative immunofluorescence microscopy of a mouse memory CD8 T cell population. We report three major findings: lymphocyte isolation fails to recover most cells and biases against certain subsets, residents greatly outnumber recirculating cells within non-lymphoid tissues, and memory subset homing to inflammation does not conform to previously hypothesized migration patterns. These results indicate that most host cells are surveyed for reinfection by segregated residents rather than by recirculating cells that migrate throughout the blood and body.
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“Through parabiosis experiments, it has been shown that both CD69+ and CD69− memory T cells of non-lymphoid tissues, like kidney and liver, are tissue resident [239].”
From Guidelines for the use of flow cytometry and cell sorting in immunological studies (third edition) (2021) · cites this paper as [239]
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“While the majority of Trm cells throughout different tissues constitutively express CD69, parabiosis, and in vivo labeling experiments have highlighted that there are CD69− cells that reside long-term in tissues [239].”
From Guidelines for the use of flow cytometry and cell sorting in immunological studies (third edition) (2021) · cites this paper as [239]
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“They have been defined as independent populations by tissue retention in parabiosis experiments [239, 240], by distinguishing transcriptional profiles [230, 241-245], by exclusive Ag receptor repertoires and specificities [243, 244, 246], and by exclusive persistence in transplanted tissues [247, 248].”
From Guidelines for the use of flow cytometry and cell sorting in immunological studies (third edition) (2021) · cites this paper as [239]
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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×
“Paradigmatically, TEM recirculate through NLT or respond to NLT sites of inflammation, while TCM limit recirculation to SLO (Sallusto et al., 1999).”
BackgroundPhenotypic Analysis of Antigen-Specific T Lymphocytes
Altman, J. D., Moss, P. A. H., Goulder, P. J. R., Barouch, D. H., McHeyzer-Williams, M. G., Bell, J. I., McMichael, A. J., & Davis, M. M. (1996) · Science · doi:10.1126/science.274.5284.94 · Cited by 3,544 · cited 2×
“However, technical innovations, such as the development of MHC I tetramers (Altman et al., 1996), revealed that antigen-specific CD8 T cell responses were 10- to 100-fold bigger than initially thought, precipitating a substantial revision in conceptualization of the immune response (Murali-Krishna et al.”
BackgroundPreferential Localization of Effector Memory Cells in Nonlymphoid Tissue
Masopust, D., Vezys, V., Marzo, A. L., & Lefrançois, L. (2001) · Science · doi:10.1126/science.1058867 · Cited by 1,952 · cited 2×
“…CD8 T cells are broadly distributed throughout the host organism, but the overall magnitude and anatomic apportionment of this population remain unclear and controversial (Ganusov and De Boer, 2007; Masopust et al., 2001; Peaudecerf and Rocha, 2011; Reinhardt et al., 2001; Rocha et al., 1991).”
BackgroundSelf-citationCounting Antigen-Specific CD8 T Cells: A Reevaluation of Bystander Activation during Viral Infection
Murali‐Krishna, K., Altman, J. D., Suresh, M., Sourdive, D. J. D., Zajac, A. J., Miller, J. D., Slansky, J. E., & Ahmed, R. (1998) · Immunity · doi:10.1016/s1074-7613(00)80470-7 · Cited by 1,918
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-citationThe developmental pathway for CD103+CD8+ tissue-resident memory T cells of skin
Mackay, L. K., Rahimpour, A., Ma, J. Z., Collins, N., Stock, A. T., Hafon, M.-L., Vega-Ramos, J., Lauzurica, P., Mueller, S. N., Stefanovic, T., et al. (2013) · Nature Immunology · doi:10.1038/ni.2744 · Cited by 1,331
Gebhardt, T., Wakim, L. M., Eidsmo, L., Reading, P. C., Heath, W. R., & Carbone, F. R. (2009) · Nature Immunology · doi:10.1038/ni.1718 · Cited by 1,157
Visualizing the generation of memory CD4 T cells in the whole body
Reinhardt, R. L., Khoruts, A., Merica, R., Zell, T., & Jenkins, M. K. (2001) · Nature · doi:10.1038/35065111 · Cited by 1,026 · cited 1×
“…CD8 T cells are broadly distributed throughout the host organism, but the overall magnitude and anatomic apportionment of this population remain unclear and controversial (Ganusov and De Boer, 2007; Masopust et al., 2001; Peaudecerf and Rocha, 2011; Reinhardt et al., 2001; Rocha et al., 1991).”
BackgroundHuman memory T cells: generation, compartmentalization and homeostasis
Farber, D. L., Yudanin, N. A., & Restifo, N. P. (2014) · Nature Reviews Immunology · doi:10.1038/nri3567 · Cited by 897
Memory T Cell Subsets, Migration Patterns, and Tissue Residence
Mueller, S. N., Gebhardt, T., Carbone, F., & Heath, W. R. (2012) · Annual Review of Immunology · doi:10.1146/annurev-immunol-032712-095954 · Cited by 884
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Resident memory CD8 T cells persist for years in human small intestine
Bartolomé-Casado, R., Landsverk, O. J. B., Chauhan, S. K., Richter, L., Phung, D., Greiff, V., Risnes, L. F., Yao, Y., Neumann, R. S., Yaqub, S., et al. (2019) · The Journal of Experimental Medicine · doi:10.1084/jem.20190414 · Cited by 155
Tissue-resident CD8 + T cells drive age-associated chronic lung sequelae after viral pneumonia
Goplen, N. P., Wu, Y., Son, Y. M., Li, C., Wang, Z., Cheon, I. S., Jiang, L., Zhu, B., Ayasoufi, K., Chini, E. N., et al. (2020) · Science Immunology · doi:10.1126/sciimmunol.abc4557 · Cited by 148
The spatio-temporal control of effector T cell migration
Fowell, D. J., & Kim, M. (2021) · Nature reviews. Immunology · doi:10.1038/s41577-021-00507-0 · Cited by 154
The evolving role of tissue-resident memory T cells in infections and cancer
Yenyuwadee, S., Lopez, J. L. S.-T., Shah, R., Rosato, P. C., & Boussiotis, V. A. (2022) · Science Advances · doi:10.1126/sciadv.abo5871 · Cited by 162
T RM maintenance is regulated by tissue damage via P2RX7
Stark, R., Wesselink, T. H., Behr, F. M., Kragten, N. A. M., Arens, R., Koch-Nolte, F., van Gisbergen, K. P. J. M., & van Lier, R. A. W. (2018) · Science Immunology · doi:10.1126/sciimmunol.aau1022 · Cited by 141
Emerging concepts in tissue-resident T cells: lessons from humans
Thome, J. J. C., & Färber, D. L. (2015) · Trends in Immunology · doi:10.1016/j.it.2015.05.003 · Cited by 151
Thom, J. T., Weber, T. C., Walton, S. M., Torti, N., & Oxenius, A. (2015) · Cell Reports · doi:10.1016/j.celrep.2015.09.082 · Cited by 148
Pathophysiology of Skin Resident Memory T Cells
TOKURA, Y., Phadungsaksawasdi, P., Kurihara, K., Fujiyama, T., & Honda, T. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2020.618897 · Cited by 148
Tissue resident memory T cells and viral immunity
Rosato, P. C., Beura, L. K., & Masopust, D. (2016) · Current Opinion in Virology · doi:10.1016/j.coviro.2016.11.011 · Cited by 142
Self-citationLocalization, tissue biology and T cell state — implications for cancer immunotherapy
Schenkel, J. M., & Pauken, K. E. (2023) · Nature reviews. Immunology · doi:10.1038/s41577-023-00884-8 · Cited by 144
Self-citationControl of immunity via nutritional interventions
Collins, N., & Belkaid, Y. (2022) · Immunity · doi:10.1016/j.immuni.2022.01.004 · Cited by 131
Niches for the Long-Term Maintenance of Tissue-Resident Memory T Cells
Takamura, S. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.01214 · Cited by 138
Expansible residence decentralizes immune homeostasis
Wijeyesinghe, S., Beura, L. K., Pierson, M. J., Stolley, J. M., Adam, O. A., Ruscher, R., Steinert, E. M., Rosato, P. C., Vezys, V., & Masopust, D. (2021) · Nature · doi:10.1038/s41586-021-03351-3 · Cited by 134
Self-citationHIV-specific CD8+ T cells and HIV eradication
Jones, R. B., & Walker, B. D. (2016) · Journal of Clinical Investigation · doi:10.1172/jci80566 · Cited by 134
Armed and Ready: Transcriptional Regulation of Tissue-Resident Memory CD8 T Cells
Behr, F. M., Chuwonpad, A., Stark, R., & van Gisbergen, K. P. J. M. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.01770 · Cited by 124
Tissue-resident lymphocytes: from adaptive to innate immunity
Sun, H., Sun, C., Xiao, W., & Sun, R. (2019) · Cellular and Molecular Immunology · doi:10.1038/s41423-018-0192-y · Cited by 137
Organ-specific isoform selection of fatty acid–binding proteins in tissue-resident lymphocytes
Frizzell, H., Fonseca, R., Christo, S. N., Evrard, M., Cruz-Gomez, S., Zanluqui, N. G., von Scheidt, B., Freestone, D., Park, S. L., McWilliam, H. E. G., et al. (2020) · Science Immunology · doi:10.1126/sciimmunol.aay9283 · Cited by 141
Metabolic programs of T cell tissue residency empower tumour immunity
Reina-Campos, M., Heeg, M., Kennewick, K., Mathews, I. T., Galletti, G., Luna, V., Nguyen, Q., Huang, H., Milner, J. J., Hu, K. H., et al. (2023) · Nature · doi:10.1038/s41586-023-06483-w · Cited by 132
The Multifaceted Role of Tissue-Resident Memory T Cells
Christo, S. N., Park, S. L., Mueller, S. N., & Mackay, L. K. (2024) · Annual Review of Immunology · doi:10.1146/annurev-immunol-101320-020220 · Cited by 148
da Silva, H. B., Peng, C., Wang, H., Wanhainen, K. M., Ma, C., Lopez, S., Khoruts, A., Zhang, N., & Jameson, S. C. (2020) · Immunity · doi:10.1016/j.immuni.2020.06.010 · Cited by 135
Runx3 drives a CD8+ T cell tissue residency program that is absent in CD4+ T cells
Fonseca, R., Burn, T. N., Gandolfo, L. C., Devi, S., Park, S. L., Obers, A., Evrard, M., Christo, S. N., Buquicchio, F. A., Lareau, C. A., et al. (2022) · Nature Immunology · doi:10.1038/s41590-022-01273-4 · Cited by 131
Reilly, E. C., Emo, K. L., Buckley, P. M., Reilly, N., Smith, I., Chaves, F. A., Yang, H., Oakes, P. W., & Topham, D. J. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1915681117 · Cited by 128
Retrograde migration supplies resident memory T cells to lung-draining LN after influenza infection
Stolley, J. M., Johnston, T. S., Soerens, A. G., Beura, L. K., Rosato, P. C., Joag, V., Wijeyesinghe, S., Langlois, R. A., Osum, K. C., Mitchell, J. S., et al. (2020) · The Journal of Experimental Medicine · doi:10.1084/jem.20192197 · Cited by 126
Self-citationLi, Y., Cao, F., Li, M., Li, P., Yu, Y., Xiang, L., Xu, T., Lei, J., Tai, Y., Zhu, J., et al. (2018) · Journal of Experimental & Clinical Cancer Research · doi:10.1186/s13046-018-0938-5 · Cited by 125
Transcriptional programming of tissue-resident memory CD8+ T cells
Milner, J. J., & Goldrath, A. W. (2018) · Current Opinion in Immunology · doi:10.1016/j.coi.2018.03.017 · Cited by 123
Finding a way out: S1P signaling and immune cell migration
Baeyens, A. A. L., & Schwab, S. R. (2020) · Annual Review of Immunology · doi:10.1146/annurev-immunol-081519-083952 · Cited by 123
CD8αα intraepithelial lymphocytes arise from two main thymic precursors
Ruscher, R., Kummer, R. L., Lee, Y. J., Jameson, S. C., & Hogquist, K. A. (2017) · Nature Immunology · doi:10.1038/ni.3751 · Cited by 120
Hirai, T., Yang, Y., Zenke, Y., Li, H., Chaudhri, V. K., Diaz, J. S. D. L. C., Zhou, P. Y., Nguyen, B. A., Bartholin, L., Workman, C. J., et al. (2020) · Immunity · doi:10.1016/j.immuni.2020.10.022 · Cited by 120
Self-citationOgongo, P., Tezera, L. B., Ardain, A., Nhamoyebonde, S., Ramsuran, D., Singh, A., Ngoepe, A., Karim, F., Naidoo, T., Khan, K., et al. (2021) · Journal of Clinical Investigation · doi:10.1172/jci142014 · Cited by 120
Myelin-specific CD8+ T cells exacerbate brain inflammation in CNS autoimmunity
Wagner, C. A., Roqué, P. J., Mileur, T. R., Liggitt, D., & Goverman, J. M. (2019) · Journal of Clinical Investigation · doi:10.1172/jci132531 · Cited by 112
Harnessing the Power of T Cells: The Promising Hope for a Universal Influenza Vaccine
Clemens, E. B., van de Sandt, C. E., Wong, S., Wakim, L. M., & Valkenburg, S. A. (2018) · Vaccines · doi:10.3390/vaccines6020018 · Cited by 123
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
Prognostic and therapeutic role of tumor-infiltrating lymphocyte subtypes in breast cancer
Nelson, M. A., Ngamcherdtrakul, W., Luoh, S., & Yantasee, W. (2021) · Cancer and Metastasis Reviews · doi:10.1007/s10555-021-09968-0 · Cited by 119
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
Cheng, M. L., Nakib, D., Perciani, C. T., & MacParland, S. A. (2021) · Clinical Science · doi:10.1042/cs20190654 · Cited by 130
Peng, C., Huggins, M. A., Wanhainen, K. M., Knutson, T. P., Lu, H., Georgiev, H., Mittelsteadt, K. L., Jarjour, N. N., Wang, H., Hogquist, K. A., et al. (2021) · Immunity · doi:10.1016/j.immuni.2021.11.017 · Cited by 114
Role of Memory T Cells in Allograft Rejection and Tolerance
Bénichou, G., Gonzalez, B., Marino, J., Ayasoufi, K., & Valujskikh, A. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.00170 · Cited by 119
Human circulating and tissue-resident memory CD8+ T cells
Buggert, M., Price, D. A., Mackay, L. K., & Betts, M. R. (2023) · Nature Immunology · doi:10.1038/s41590-023-01538-6 · Cited by 125
Resident memory CD8+ T cells within cancer islands mediate survival in breast cancer patients
Egelston, C. A., Avalos, C., Tu, T. Y., Rosario, A., Wang, R., Solomon, S. T., Srinivasan, G., Nelson, M. S., Huang, Y., Lim, M. H., et al. (2019) · JCI Insight · doi:10.1172/jci.insight.130000 · Cited by 116
A committed tissue-resident memory T cell precursor within the circulating CD8+ effector T cell pool
Kok, L., Dijkgraaf, F. E., Urbanus, J. H. M., Bresser, K., Vredevoogd, D. W., Cardoso, R. F., Perié, L., Beltman, J. B., & Schumacher, T. N. (2020) · The Journal of Experimental Medicine · doi:10.1084/jem.20191711 · Cited by 120
Strobl, J., Pandey, R. V., Krausgruber, T., Bayer, N., Kleißl, L., Reininger, B., Vieyra-Garcia, P. A., Wolf, P., Jentus, M. M., Mitterbauer, M., et al. (2020) · Science Translational Medicine · doi:10.1126/scitranslmed.abb7028 · Cited by 117
Local heroes or villains: tissue-resident memory T cells in human health and disease
Sasson, S. C., Gordon, C. L., Christo, S. N., Klenerman, P., & Mackay, L. K. (2020) · Cellular & Molecular Immunology · doi:10.1038/s41423-019-0359-1 · Cited by 111
Checkpoint inhibitor immunotherapy diminishes oocyte number and quality in mice
Winship, A., Alesi, L. R., Sant, S. A., Stringer, J. M., Cantavenera, A., Hegarty, T., Requesens, C. L., Liew, S. H., Sarma, U. C., Griffiths, M. J., et al. (2022) · Nature Cancer · doi:10.1038/s43018-022-00413-x · Cited by 110
Leal, J. M., Huang, J. Y., Kohli, K., Stoltzfus, C. R., Lyons‐Cohen, M. R., Olin, B. E., Gale, M., & Gerner, M. Y. (2021) · Science Immunology · doi:10.1126/sciimmunol.abb9435 · Cited by 109
ABC transporters and NR4A1 identify a quiescent subset of tissue-resident memory T cells
Boddupalli, C. S., Nair, S., Gray, S. M., Nowyhed, H. N., Verma, R., Gibson, J. A., Abraham, C., Narayan, D., Vasquez, J. C., Hedrick, C. C., et al. (2016) · Journal of Clinical Investigation · doi:10.1172/jci85329 · Cited by 110
Stelma, F., Niet, A. D., Sinnige, M. J., van Dort, K. A., van Gisbergen, K. P. J. M., Verheij, J., van Leeuwen, E. M. M., Kootstra, N. A., & Reesink, H. W. (2017) · Scientific Reports · doi:10.1038/s41598-017-06352-3 · Cited by 110
Holz, L. E., Prier, J. E., Freestone, D., Steiner, T. M., English, K., Johnson, D. N., Mollard, V., Cozijnsen, A. J., Davey, G. M., Godfrey, D. I., et al. (2018) · Cell Reports · doi:10.1016/j.celrep.2018.08.094 · Cited by 109
Tissue Resident CD8 Memory T Cell Responses in Cancer and Autoimmunity
Molodtsov, A. K., & Turk, M. J. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.02810 · Cited by 111
Tan, H.-X., Juno, J., Esterbauer, R., Kelly, H. G., Wragg, K. M., Konstandopoulos, P., Alcântara, S., Alvarado, C., Jones, R., Starkey, G., et al. (2022) · Science immunology · doi:10.1126/sciimmunol.abf5314 · Cited by 98
Self-citationKidney tissue hypoxia dictates T cell–mediated injury in murine lupus nephritis
Chen, P.-M., Wilson, P. C., Shyer, J. A., Veselits, M., Steach, H. R., Cui, C., Moeckel, G. W., Clark, M. R., & Craft, J. E. (2020) · Science Translational Medicine · doi:10.1126/scitranslmed.aay1620 · Cited by 103
Blimp-1 Rather Than Hobit Drives the Formation of Tissue-Resident Memory CD8+ T Cells in the Lungs
Behr, F. M., Kragten, N. A. M., Wesselink, T. H., Nota, B., van Lier, R. A. W., Amsen, D., Stark, R., Hombrink, P., & van Gisbergen, K. P. J. M. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.00400 · Cited by 103
Tissue-resident memory CD8 T cell diversity is spatiotemporally imprinted
Reina‐Campos, M., Monell, A., Ferry, A., Luna, V., Cheung, K. P., Galletti, G., Scharping, N. E., Takehara, K. K., Quon, S., Challita, P. P., et al. (2025) · Nature · doi:10.1038/s41586-024-08466-x · Cited by 111
Morabito, K. M., Ruckwardt, T., Redwood, A., Moin, S., Price, D., & Graham, B. (2016) · Mucosal Immunology · doi:10.1038/mi.2016.48 · Cited by 102
The Identity of Human Tissue-Emigrant CD8+ T Cells
Buggert, M., Vella, L. A., Nguyen, S., Wu, V. H., Chen, Z., Sekine, T., Perez‐Potti, A., Maldini, C. R., Manne, S., Darko, S. W., et al. (2020) · Cell · doi:10.1016/j.cell.2020.11.019 · Cited by 105
Inhibitory checkpoint receptors control CD8+ resident memory T cells to prevent skin allergy
Gamradt, P., Laoubi, L., Nosbaum, A., Mutez, V., Lenief, V., Grande, S., Redoules, D., Schmitt, A.-M., Nicolas, J., & Vocanson, M. (2019) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2018.11.048 · Cited by 104
Woon, H. G., Braun, A., Li, J., Smith, C., Edwards, J., Sierro, F., Feng, C. G., Khanna, R., Elliot, M., Bell, A., et al. (2016) · PLOS Pathogens · doi:10.1371/journal.ppat.1005799 · Cited by 97
T Cell Immunity to Bacterial Pathogens: Mechanisms of Immune Control and Bacterial Evasion
Shepherd, F. R., & McLaren, J. E. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21176144 · Cited by 101
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
Torcellan, T., Friedrich, C., Doucet-Ladevèze, R., Ossner, T., Solé, V. V., Riedmann, S., Ugur, M., Imdahl, F., Rosshart, S. P., Arnold, S. J., et al. (2023) · Immunity · doi:10.1016/j.immuni.2023.11.018 · Cited by 103
Mechanisms of Mixed Chimerism-Based Transplant Tolerance
Zuber, J., & Sykes, M. (2017) · Trends in Immunology · doi:10.1016/j.it.2017.07.008 · Cited by 98
Burbach, B. J., O’Flanagan, S. D., Shao, Q., Young, K. M., Slaughter, J. R., Rollins, M. R., Street, T. J. L., Granger, V., Beura, L. K., Azarin, S. M., et al. (2021) · Nature Communications · doi:10.1038/s41467-021-24132-6 · Cited by 103
Self-citationImmunology of the Uterine and Vaginal Mucosae
Zhou, J., Way, S. S., & Chen, K. (2018) · Trends in Immunology · doi:10.1016/j.it.2018.01.007 · Cited by 95
TGFβ restricts expansion, survival, and function of T cells within the tuberculous granuloma
Gern, B. H., Adams, K. N., Plumlee, C. R., Stoltzfus, C. R., Shehata, L., Moguche, A. O., Busman‐Sahay, K., Hansen, S. G., Axthelm, M. K., Picker, L. J., et al. (2021) · Cell Host & Microbe · doi:10.1016/j.chom.2021.02.005 · Cited by 92
Distribution and storage of inflammatory memory in barrier tissues
Ordovás-Montañés, J., Beyaz, S., Rakoff-Nahoum, S., & Shalek, A. K. (2020) · Nature reviews. Immunology · doi:10.1038/s41577-019-0263-z · Cited by 94
Zimmer, C. L., von Seth, E., Buggert, M., Strauss, O., Hertwig, L., Nguyen, S., Wong, A. Y. W., Zotter, C., Berglin, L., Michaëlsson, J., et al. (2021) · Science Translational Medicine · doi:10.1126/scitranslmed.abb3107 · Cited by 90
Niessl, J., Sekine, T., Lange, J., Kónya, V., Forkel, M., Marić, J., Rao, A., Mazzurana, L., Kokkinou, E., Weigel, W., et al. (2021) · Science Immunology · doi:10.1126/sciimmunol.abk0894 · Cited by 94
Burrack, A. L., Spartz, E. J., Raynor, J. F., Wang, I., Olson, M. A., & Stromnes, I. M. (2019) · Cell Reports · doi:10.1016/j.celrep.2019.07.059 · Cited by 89
Phenotypically distinct neutrophils patrol uninfected human and mouse lymph nodes
Lok, L. S. C., Dennison, T. W., Mahbubani, K., Saeb‐Parsy, K., Chilvers, E. R., & Clatworthy, M. R. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1905054116 · Cited by 89
Delpoux, A., Michelini, R. H., Verma, S., Lai, C.-Y., Omilusik, K. D., Utzschneider, D. T., Redwood, A., Goldrath, A. W., Benedict, C. A., & Hedrick, S. Μ. (2017) · The Journal of Experimental Medicine · doi:10.1084/jem.20170697 · Cited by 91
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Wu, H., Liao, W., Li, Q., Long, H., Yin, H., Zhao, M., Chan, V. S. F., Lau, C.-S., & Lu, Q. (2018) · Autoimmunity Reviews · doi:10.1016/j.autrev.2018.03.014 · Cited by 93
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Gill, U. S., Pallett, L. J., Thomas, N., Burton, A. R., Patel, A. A., Yona, S., Kennedy, P. T. F., & Maini, M. K. (2019) · Gut · doi:10.1136/gutjnl-2018-317071 · Cited by 87
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Kadoki, M., Patil, A., Thaiss, C. C., Brooks, D., Pandey, S., Deep, D., Álvarez, D., von Andrian, U. H., Wagers, A. J., Nakai, K., et al. (2017) · Cell · doi:10.1016/j.cell.2017.08.024 · Cited by 85
Hirai, T., Zenke, Y., Yang, Y., Bartholin, L., Beura, L. K., Masopust, D., & Kaplan, D. H. (2019) · Immunity · doi:10.1016/j.immuni.2019.03.002 · Cited by 91
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Gavil, N. V., Cheng, K., & Masopust, D. (2024) · Immunity · doi:10.1016/j.immuni.2024.06.017 · Cited by 104
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Turner, J., Becker, M., Mittrücker, H., & Panzer, U. (2017) · Journal of the American Society of Nephrology · doi:10.1681/asn.2017060599 · Cited by 89
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Takamura, S., Kato, S., Motozono, C., Shimaoka, T., Ueha, S., Matsuo, K., Miyauchi, K., Masumoto, T., Katsushima, A., Nakayama, T., et al. (2019) · Journal of Experimental Medicine · doi:10.1084/jem.20190557 · Cited by 70
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Tieu, R., Zeng, Q., Zhao, D., Zhang, G., Feizi, N., Manandhar, P., Williams, A. L., Popp, B. A., Wood, M. A., Demetris, A. J., et al. (2023) · Science Immunology · doi:10.1126/sciimmunol.add8454 · Cited by 88
Dean, J. W., Helm, E. Y., Fu, Z., Xiong, L., Sun, N., Oliff, K. N., Muehlbauer, M., Avram, D., & Zhou, L. (2023) · Cell Reports · doi:10.1016/j.celrep.2022.111963 · Cited by 79
Morgan, S. B., Hemmink, J. D., Porter, E., Harley, R., Shelton, H. A., Aramouni, M., Everett, H., Brookes, S. M., Bailey, M., Townsend, A., et al. (2016) · The Journal of Immunology · doi:10.4049/jimmunol.1502632 · Cited by 81
Künzli, M., O’Flanagan, S. D., LaRue, M., Talukder, P., Dileepan, T., Stolley, J. M., Soerens, A. G., Quarnstrom, C. F., Wijeyesinghe, S., Ye, Y., et al. (2022) · Science Immunology · doi:10.1126/sciimmunol.add3075 · Cited by 80
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Stolp, B., Thelen, F., Ficht, X., Altenburger, L. M., Ruef, N., Inavalli, V. V. G. K., Germann, P., Pagé, N., Moalli, F., Raimondi, A., et al. (2020) · Science Immunology · doi:10.1126/sciimmunol.aaz4371 · Cited by 78
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Shaw, T. N., Stewart-Hutchinson, P. J., Strangward, P., Dandamudi, D. B., Coles, J. A., Villegas-Méndez, A., Gallego‐Delgado, J., van Rooijen, N., Zindy, E., Rodrı́guez, A., et al. (2015) · PLoS Pathogens · doi:10.1371/journal.ppat.1005210 · Cited by 79
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Valencia-Hernandez, A., Ng, W.-Y., Ghazanfari, N., Ghilas, S., de Menezes, M. N., Holz, L. E., Huang, C., English, K., Naung, M. T., Tan, P., et al. (2020) · Cell Host and Microbe · doi:10.1016/j.chom.2020.04.010 · Cited by 71
Gilchuk, P., Hill, T. M., Guy, C. S., McMaster, S. R., Boyd, K. L., Rabacal, W., Wang, L., Shyr, Y., Kohlmeier, J. E., Sebzda, E., et al. (2016) · Cell Reports · doi:10.1016/j.celrep.2016.07.037 · Cited by 77
Kimura, M. Y., Hayashizaki, K., Tokoyoda, K., Takamura, S., Motohashi, S., & Nakayama, T. (2017) · Immunological Reviews · doi:10.1111/imr.12559 · Cited by 82
Lin, Y. H., Duong, H. G., Limary, A. E., Kim, E. S., Hsu, P. W., Patel, S. A., Wong, W. H., Indralingam, C. S., Liu, Y. C., Yao, P., et al. (2022) · Immunity · doi:10.1016/j.immuni.2022.12.007 · Cited by 76
Gao, C., Yao, Y., Li, L., Yang, S., Chu, H., Tsuneyama, K., Li, X., Gershwin, M. E., & Lian, Z. (2018) · Arthritis & Rheumatology · doi:10.1002/art.40676 · Cited by 75
Evrard, M., Becht, É., Fonseca, R., Obers, A., Park, S. L., Zanluqui, N. G., Schröder, J., Christo, S. N., Schienstock, D., Lai, J., et al. (2023) · Immunity · doi:10.1016/j.immuni.2023.06.005 · Cited by 76
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Halkias, J., Rackaityte, E., Hillman, S. L., Aran, D., Mendoza, V. F., Marshall, L. R., MacKenzie, T. C., & Burt, T. D. (2019) · Journal of Clinical Investigation · doi:10.1172/jci125957 · Cited by 71
Tissue-specific differentiation of CD8+ resident memory T cells
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Maintenance of PD‐1 on brain‐resident memory CD8 T cells is antigen independent
Shwetank, Abdelsamed, H. A., Frost, E. L., Schmitz, H. M., Mockus, T. E., Youngblood, B., & Lukacher, A. E. (2017) · Immunology and Cell Biology · doi:10.1038/icb.2017.62 · Cited by 73
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Gola, A., Silman, D., Walters, A. A., Sridhar, S., Uderhardt, S., Salman, A. M., Halbroth, B. R., Bellamy, D. G., Bowyer, G., Powlson, J., et al. (2018) · Science Translational Medicine · doi:10.1126/scitranslmed.aap9128 · Cited by 73
Metadata
- Authors
- Steinert, E. M., Schenkel, J. M., Fraser, K. A., Beura, L. K., Manlove, L. S., Igyártó, B. Z., Southern, P. J., & Masopust, D.
- Affiliations
- University of Minnesota (US)
- Corresponding author
- Masopust, David
- ORCID
- Venue
- Cell
- Publisher
- Elsevier BV
- Published
- 2015-05
- Volume
- 161
- Issue
- 4
- Pages
- 737-749
- ISSN
- 0092-8674 (ISSN-L)
- PMC
- PMC4426972
- OpenAlex
- W1632859538
- Cited by
- 685
- References
- 46
- Citations by year
- 2026: 29 · 2025: 46 · 2024: 46 · 2023: 50 · 2022: 62 · 2021: 76 · 2020: 74 · 2019: 79 · 2018: 91 · 2017: 60 · 2016: 57 · 2015: 15
- FWCI
- 36.57
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Cell (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Cancer Institute (F31CA183226, P30CA077598)
- National Institute of Allergy and Infectious Diseases (R01AI084913, R01AI111671, R37AI084913, T32AI083196)
- National Institute of Diabetes and Digestive and Kidney Diseases (F30DK100159, F30-DK100159-02)
- 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 › Immune responses and vaccinations
- Keywords
- memory CD8+ T cells, immune surveillance, parabiosis, lymphocyte isolation, tissue-resident memory T cells, effector memory T cells, central memory T cells, T cell migration, tissue inflammation, T cell differentiation, non-lymphoid tissues
- MeSH terms
- CD69 Antigens, Animals, Antigens, Differentiation, T-Lymphocyte, Arenaviridae Infections, Cell Movement, Immunologic Memory, Inflammation, Lymphocytic choriomeningitis virus, Mice, Inbred C57BL, Monitoring, Immunologic, Antigens, CD, T-Lymphocyte Subsets, CD8-Positive T-Lymphocytes, Lectins, C-Type, Mice
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