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Tissue-Resident Memory T Cells
Open accessAbstract
Tissue-resident memory T (Trm) cells constitute a recently identified lymphocyte lineage that occupies tissues without recirculating. They provide a first response against infections reencountered at body surfaces, where they accelerate pathogen clearance. Because Trm cells are not present within peripheral blood, they have not yet been well characterized, but are transcriptionally, phenotypically, and functionally distinct from recirculating central and effector memory T cells. In this review, we will summarize current knowledge of Trm cell ontogeny, regulation, maintenance, and function and will highlight technical considerations for studying this population.
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“These Trm are specially programmed to persist in their host tissues [249, 250].”
From Guidelines for the use of flow cytometry and cell sorting in immunological studies (third edition) (2021) · cites this paper as [249]
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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 3×
“Much like naive T cells, Tcm cells patrol secondary lymphoid organs (SLOs), which include lymph nodes (LNs) and the white pulp (WP) of spleen (Figure 1) (von Andrian and Mackay, 2000; Sallusto et al., 1999).”
BackgroundLymphocyte Homing and Homeostasis
Butcher, E. C., & Picker, L. J. (1996) · Science · doi:10.1126/science.272.5258.60 · Cited by 2,846 · cited 2×
“Tem cells also lack LN homing receptors (CD62L and CCR7), yet expressed distinct patterns of other homing receptors, and on that basis it was proposed that Tem cells recirculate between blood and nonlymphoid tissues (NLTs) or remain poised to mobilize to sites of inflammation (Butcher and Picker, 1996; Mackay et al.,…”
BackgroundLymphocyte egress from thymus and peripheral lymphoid organs is dependent on S1P receptor 1
Matloubian, M., Lo, C. G., Cinamon, G., Lesneski, M. J., Xu, Y., Brinkmann, V., Allende, M. L., Proia, R. L., & Cyster, J. G. (2004) · Nature · doi:10.1038/nature02284 · Cited by 2,581 · cited 1×
“S1PR1 downregulation is concomitantly associated with cell surface expression of the C-type lectin CD69 (Cyster and Schwab, 2012; Matloubian et al., 2004; Schober et al., 1999; Shiow et al., 2006; Skon et al., 2013).”
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 5×
“Additionally, CD62L cells isolated fromblood and spleen did not recapitulate the panoply of phenotypes expressed by memory T cells isolated from the small intestinal mucosa, lung, and brain (Hawke et al., 1998; Hogan et al., 2001; Kim et al., 1998; Masopust et al., 2001a; van der Most et al., 2003).”
BackgroundResultInfluentialSelf-citationT-Cell Function and Migration — Two Sides of the Same Coin
von Andrian, U. H., & Mackay, C. R. (2000) · New England Journal of Medicine · doi:10.1056/nejm200010053431407 · Cited by 1,429
The 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
Homing and cellular traffic in lymph nodes
von Andrian, U. H., & Mempel, T. R. (2003) · Nature reviews. Immunology · doi:10.1038/nri1222 · Cited by 1,271 · cited 1×
“Naive T cells enter SLOs from blood using a combination of selectins, chemokines, and integrins, and then patrol for 12– 24 hr before leaving to explore other SLOs in their continuous quest for cognate Ag (von Andrian and Mackay, 2000; von Andrian and Mempel, 2003).”
BackgroundHomeostasis of Naive and Memory T Cells
Surh, C. D., & Sprent, J. (2008) · Immunity · doi:10.1016/j.immuni.2008.11.002 · Cited by 1,193 · cited 17×
“Similarly, dendritic cells upregulate CCR7 after activation in tissues, which then acts in concert with S1PR1 to promote migration to downstream SLOs (Braun et al., 2011; Czeloth et al., 2005; Lamana et al., 2011; Ohl et al., 2004; Saeki et al., 1999).”
BackgroundInfluentialCD69 acts downstream of interferon-α/β to inhibit S1P1 and lymphocyte egress from lymphoid organs
Shiow, L. R., Rosen, D. B., Brdičková, N., Xu, Y., An, J., Lanier, L. L., Cyster, J. G., & Matloubian, M. (2006) · Nature · doi:10.1038/nature04606 · Cited by 1,189 · cited 1×
“S1PR1 downregulation is concomitantly associated with cell surface expression of the C-type lectin CD69 (Cyster and Schwab, 2012; Matloubian et al., 2004; Schober et al., 1999; Shiow et al., 2006; Skon et al., 2013).”
BackgroundAdhesion between epithelial cells and T lymphocytes mediated by E-cadherin and the αEβ7 integrin
Cepek, K. L., Shaw, S. K., Parker, C. M., Russell, G. J., Morrow, J. S., Rimm, D. L., & Brenner, M. B. (1994) · Nature · doi:10.1038/372190a0 · Cited by 1,178 · cited 4×
“One interpretation is that aeb7 allows CD8+ T cells to physically adhere to E-cadherin expressed on epithelial cells.”
BackgroundInfluential
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Zhang, L., Yu, X., Zheng, L., Zhang, Y., Li, Y., Fang, Q., Gao, R., Kang, B., Zhang, Q., Huang, J. Y., et al. (2018) · Nature · doi:10.1038/s41586-018-0694-x · Cited by 1,505
Human T cell development, localization, and function throughout life
Kumar, B. V., Connors, T. J., & Farber, D. L. (2018) · Immunity · doi:10.1016/j.immuni.2018.01.007 · Cited by 1,257
Kumar, B. V., Ma, W., Miron, M., Granot, T., Guyer, R. S., Carpenter, D. J., Senda, T., Sun, X., Ho, S.-H., Lerner, H., et al. (2017) · Cell Reports · doi:10.1016/j.celrep.2017.08.078 · Cited by 1,068
Normalizing the environment recapitulates adult human immune traits in laboratory mice
Beura, L. K., Hamilton, S. E., Bi, K., Schenkel, J. M., Odumade, O. A., Casey, K. A., Thompson, E. A., Fraser, K. A., Rosato, P. C., Filali-Mouhim, A., et al. (2016) · Nature · doi:10.1038/nature17655 · Cited by 1,072
Self-citationKathleen Cuningham Foundation Consortium for Research into Familial Breast Cancer (kConFab), Savas, P., Virassamy, B., Ye, C., Salim, A., Mintoff, C. P., Caramia, F., Salgado, R., Byrne, D. J., Teo, Z. L., et al. (2018) · Nature Medicine · doi:10.1038/s41591-018-0078-7 · Cited by 992
Tissue-resident memory T cells: local specialists in immune defence
Mueller, S. N., & Mackay, L. K. (2016) · Nature Reviews Immunology · doi:10.1038/nri.2015.3 · Cited by 1,006
Co-expression of CD39 and CD103 identifies tumor-reactive CD8 T cells in human solid tumors
Duhen, T., Duhen, R., Montler, R., Moses, J., Moudgil, T., de Miranda, N. F., Goodall, C. P., Blair, T. C., Fox, B. A., McDermott, J. E., et al. (2018) · Nature Communications · doi:10.1038/s41467-018-05072-0 · Cited by 938
Szabo, P. A., Levitin, H. M., Miron, M., Snyder, M. E., Senda, T., Yuan, J., Cheng, Y. L., Bush, E. C., Dogra, P., Thapa, P., et al. (2019) · Nature Communications · doi:10.1038/s41467-019-12464-3 · Cited by 756
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Jassam, Y. N., Izzy, S., Whalen, M., McGavern, D. B., & El Khoury, J. (2017) · Neuron · doi:10.1016/j.neuron.2017.07.010 · Cited by 799
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Wu, T. D., Madireddi, S., de Almeida, P. E., Banchereau, R., Chen, Y.-J. J., Chitre, A. S., Chiang, E. Y., Iftikhar, H., O’Gorman, W. E., Au-Yeung, A., et al. (2020) · Nature · doi:10.1038/s41586-020-2056-8 · Cited by 770
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CD49a Expression Defines Tissue-Resident CD8 + T Cells Poised for Cytotoxic Function in Human Skin
Cheuk, S., Schlums, H., Gallais Sérézal, I., Martini, E., Chiang, S. C., Marquardt, N., Gibbs, A., Detlofsson, E., Introini, A., Forkel, M., et al. (2017) · Immunity · doi:10.1016/j.immuni.2017.01.009 · Cited by 678
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Self-citationMachado-Santos, J., Saji, E., Tröscher, A. R., Paunovic, M., Liblau, R., Gabriely, G., Bien, C. G., Bauer, J., & Lassmann, H. (2018) · Brain · doi:10.1093/brain/awy151 · Cited by 548
“S1P1 receptor, a key molecule of lymphocyte egress from the tissue was highly expressed on leucocytes within the vascular lumen and moderately expressed in astrocytes and endothelial cells of the brain tissue.”
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Cossarizza, A., Chang, H., Radbruch, A., Abrignani, S., Addo, R., Akdis, M., Andrä, I., Andreata, F., Annunziato, F., Arranz, E., et al. (2021) · European Journal of Immunology · doi:10.1002/eji.202170126 · Cited by 531
T cell responses to cytomegalovirus
Klenerman, P., & Oxenius, A. (2016) · Nature Reviews Immunology · doi:10.1038/nri.2016.38 · Cited by 483
Pal, B., Chen, Y., Vaillant, F., Capaldo, B. D., Joyce, R., Song, X., Bryant, V. L., Penington, J. S., Stefano, L. D., Ribera, N. T., et al. (2021) · The EMBO Journal · doi:10.15252/embj.2020107333 · Cited by 478
“Cells resembling tissue-resident memory T (T RM ) cells (Schenkel & Masopust, 2014) were apparent in TNBC and HER2 + but not in ER + cancers (Fig EV4A).”
Non-classical Immunity Controls Microbiota Impact on Skin Immunity and Tissue Repair
Linehan, J. L., Harrison, O. J., Han, S.-J., Byrd, A. L., Vujkovic-Cvijin, I., Villarino, A. V., Sen, S. K., Shaik, J., Smelkinson, M., Tamoutounour, S., et al. (2018) · Cell · doi:10.1016/j.cell.2017.12.033 · Cited by 456
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IL-2high tissue-resident T cells in the human liver: Sentinels for hepatotropic infection
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BackgroundHan, S., Zaretsky, A. G., Andrade‐Oliveira, V., Collins, N., Dzutsev, A. H., Shaik, J. S., da Fonseca, D. M., Harrison, O. J., Tamoutounour, S., Byrd, A. L., et al. (2017) · Immunity · doi:10.1016/j.immuni.2017.11.009 · Cited by 250
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Carrasco, E., Heras, M. M. G. D. L., Gabandé‐Rodríguez, E., Desdín-Micó, G., Aranda, J. F., & Mittelbrunn, M. (2021) · Nature reviews. Immunology · doi:10.1038/s41577-021-00557-4 · Cited by 250
Takamura, S., Yagi, H., Hakata, Y., Motozono, C., McMaster, S. R., Masumoto, T., Fujisawa, M., Chikaishi, T., Komeda, J., Itoh, J., et al. (2016) · The Journal of Experimental Medicine · doi:10.1084/jem.20160938 · Cited by 243
Zundler, S., Becker, E., Spocinska, M., Slawik, M., Vidal, L. P., Stark, R., Wiendl, M., Atreya, R. N., Räth, T., Leppkes, M., et al. (2019) · Nature Immunology · doi:10.1038/s41590-018-0298-5 · Cited by 241
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He, S., Wang, L.-H., Liu, Y., Li, Y., Chen, H.-T., Xu, J.-H., Peng, W., Lin, G.-W., Wei, P.-P., Li, B., et al. (2020) · Genome biology · doi:10.1186/s13059-020-02210-0 · Cited by 237
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BackgroundInfluentialTissue-resident memory T cells in tumor immunity and immunotherapy
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The Regulation of Inflammation by Innate and Adaptive Lymphocytes
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Jóźwik, A., Habibi, M. S., Paras, A., Zhu, J., Guvenel, A., Dhariwal, J., Almond, M., Wong, E., Sykes, A., Maybeno, M., et al. (2016) · Nature Communications · doi:10.1038/ncomms11011 · Cited by 223
Mohammed, J., Beura, L. K., Bobr, A., Astry, B., Chicoine, B., Kashem, S. W., Welty, N. E., Igyártó, B. Z., Wijeyesinghe, S., Thompson, E. A., et al. (2016) · Nature Immunology · doi:10.1038/ni.3396 · Cited by 231
Self-citationMemory CD8+ T cell responses to cancer
Han, J., Khatwani, N., Searles, T. G., Turk, M. J., & Angeles, C. V. (2020) · Seminars in Immunology · doi:10.1016/j.smim.2020.101435 · Cited by 236
TGF-β in T Cell Biology: Implications for Cancer Immunotherapy
Dahmani, A., & Delisle, J. (2018) · Cancers · doi:10.3390/cancers10060194 · Cited by 222
“These long-lived T cells infiltrate tissues and are retained peripherally to mediate rapid responses to invading pathogens [134].”
BackgroundBrain-resident memory T cells represent an autonomous cytotoxic barrier to viral infection
Steinbach, K., Vincenti, I., Kreutzfeldt, M., Pagé, N., Muschaweckh, A., Wagner, I., Drexler, I., Pinschewer, D. D., Korn, T., & Merkler, D. (2016) · The Journal of Experimental Medicine · doi:10.1084/jem.20151916 · Cited by 212
Khan, T. N., Mooster, J. L., Kilgore, A. M., Osborn, J. F., & Nolz, J. C. (2016) · The Journal of Experimental Medicine · doi:10.1084/jem.20151855 · Cited by 218
Son, Y. M., Cheon, I. S., Wu, Y., Li, C., Wang, Z., Gao, X., Chen, Y., Takahashi, Y., Fu, Y., Dent, A. L., et al. (2021) · Science Immunology · doi:10.1126/sciimmunol.abb6852 · Cited by 218
Salou, M., Legoux, F. P., Gilet, J., Darbois, A., du Halgouet, A., Alonso, R., Richer, W., Goubet, A., Daviaud, C., Menger, L., et al. (2018) · The Journal of Experimental Medicine · doi:10.1084/jem.20181483 · Cited by 207
“TRM T cells have been implicated in tissue homeostasis and defense against pathogens, mostly in the context of CD8+ T cell antiviral responses (Wakim et al., 2008; Schenkel and Masopust, 2014; Fan and Rudensky, 2016; Mackay et al., 2016; Milner et al., 2017).”
BackgroundInfluentialCD4+ resident memory T cells dominate immunosurveillance and orchestrate local recall responses
Beura, L. K., Fares-Frederickson, N. J., Steinert, E. M., Scott, M. C., Thompson, E. A., Fraser, K. A., Schenkel, J. M., Vezys, V., & Masopust, D. (2019) · Journal of Experimental Medicine · doi:10.1084/jem.20181365 · Cited by 190
Self-citationMatejuk, A. (2017) · Archivum Immunologiae et Therapiae Experimentalis · doi:10.1007/s00005-017-0477-3 · Cited by 233
Skin Wound Healing: Of Players, Patterns, and Processes
Sorg, H., & Sorg, C. G. G. (2022) · European Surgical Research · doi:10.1159/000528271 · Cited by 225
Morens, D. M., Taubenberger, J. K., & Fauci, A. S. (2023) · Cell Host & Microbe · doi:10.1016/j.chom.2022.11.016 · Cited by 208
Cohen, M., Giladi, A., Barboy, O., Hamon, P., Li, B., Zada, M., Gurevich‐Shapiro, A., Beccaría, C. G., David, E., Maier, B. B., et al. (2022) · Nature Cancer · doi:10.1038/s43018-022-00338-5 · Cited by 204
Durek, P., Nordström, K. J. V., Gasparoni, G., Salhab, A., Kressler, C., de Almeida, M., Bassler, K. E., Ulas, T., Schmidt, F., Xiong, J., et al. (2016) · Immunity · doi:10.1016/j.immuni.2016.10.022 · Cited by 200
Tissue resident memory T cells in the respiratory tract
Zheng, M. Z. M., & Wakim, L. M. (2021) · Mucosal Immunology · doi:10.1038/s41385-021-00461-z · Cited by 192
Tissue-resident immune cells in humans
Gray, J. I., & Farber, D. L. (2022) · Annual Review of Immunology · doi:10.1146/annurev-immunol-093019-112809 · Cited by 181
Single-cell RNA sequencing identifies inflammatory tissue T cells in eosinophilic esophagitis
Wen, T., Aronow, B. J., Rochman, Y., Rochman, M., Kiran, K. C., Dexheimer, P. J., Putnam, P. E., Mukkada, V. A., Foote, H. L., Rehn, K., et al. (2019) · Journal of Clinical Investigation · doi:10.1172/jci125917 · Cited by 187
“%) being able to be recovered (54), which draws into question their representability.”
Tissue-resident memory CD8+ T cells shape local and systemic secondary T cell responses
Behr, F. M., Parga-Vidal, L., Kragten, N. A. M., van Dam, T. J. P., Wesselink, T. H., Sheridan, B. S., Arens, R., van Lier, R. A. W., Stark, R., & van Gisbergen, K. P. J. M. (2020) · Nature Immunology · doi:10.1038/s41590-020-0723-4 · Cited by 184
Collins, N., Jiang, X., Zaid, A., Macleod, B. L., Li, J., Park, C. O., Haque, A., Bedoui, S., Heath, W. R., Mueller, S. N., et al. (2016) · Nature Communications · doi:10.1038/ncomms11514 · Cited by 187
Human memory T cells with a naive phenotype accumulate with aging and respond to persistent viruses
Pulko, V., Davies, J. S., Martinez, C., Lanteri, M. C., Busch, M. P., Diamond, M. S., Knox, K., Bush, E. C., Sims, P. A., Sinari, S., et al. (2016) · Nature Immunology · doi:10.1038/ni.3483 · Cited by 175
Phenotypic signatures of immune selection in HIV-1 reservoir cells
Sun, W., Gao, C., Hartana, C. A., Osborn, M. R., Einkauf, K. B., Lian, X., Bone, B., Bonheur, N., Chun, T., Rosenberg, E. S., et al. (2023) · Nature · doi:10.1038/s41586-022-05538-8 · Cited by 181
Hallmarks of the aging T‐cell system
Zhang, H., Weyand, C. M., & Goronzy, J. J. (2021) · FEBS Journal · doi:10.1111/febs.15770 · Cited by 181
Vesely, M. C. A., Pallis, P., Bielecki, P., Low, J. S., Zhao, J., Harman, C. C. D., Kroehling, L., Jackson, R. P., Bailis, W., Licona-Limón, P., et al. (2019) · Cell · doi:10.1016/j.cell.2019.07.032 · Cited by 166
Memory B cells and plasma cells: The differentiative continuum of humoral immunity
Cancro, M. P., & Tomayko, M. M. (2021) · Immunological Reviews · doi:10.1111/imr.13016 · Cited by 189
Exit Strategies: S1P Signaling and T Cell Migration
Baeyens, A., Fang, V., Chen, C., & Schwab, S. R. (2015) · Trends in Immunology · doi:10.1016/j.it.2015.10.005 · Cited by 174
Long-term maintenance of human naive T cells through in situ homeostasis in lymphoid tissue sites
Thome, J. J. C., Grinshpun, B., Kumar, B. V., Kubota, M., Ohmura, Y., Lerner, H., Sempowski, G. D., Shen, Y., & Farber, D. L. (2016) · Science Immunology · doi:10.1126/sciimmunol.aah6506 · Cited by 162
Myocardial aging as a T-cell–mediated phenomenon
Ramos, G. C., van den Berg, A., Nunes-Silva, V., Weirather, J., Peters, L., Burkard, M., Friedrich, M., Pinnecker, J., Abeßer, M., Heinze, K. G., et al. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1621047114 · Cited by 168
van Nierop, G. P., van Luijn, M. M., Michels, S. S., Melief, M.-J., Janssen, M., Langerak, A. W., Ouwendijk, W. J. D., Hintzen, R. Q., & Verjans, G. M. G. M. (2017) · Acta Neuropathologica · doi:10.1007/s00401-017-1744-4 · Cited by 174
Buggert, M., Nguyen, S., de Oca, G. S. M., Bengsch, B., Darko, S. W., Ransier, A., Roberts, E. R., Alcazar, D. D., Brody, I. B., Vella, L. A., et al. (2018) · Science Immunology · doi:10.1126/sciimmunol.aar4526 · Cited by 165
“CD69+ CD8+ T cells show enriched traits of residency in LTs Although CD69 is classically associated with activation, it also marks noncirculating TRMs in NLTs (32).”
BackgroundInfluentialSelf-citationWalsh, D., da Silva, H. B., Beura, L. K., Peng, C., Hamilton, S. E., Masopust, D., & Jameson, S. C. (2019) · The Journal of Immunology · doi:10.4049/jimmunol.1900052 · Cited by 174
Self-citationThe known unknowns of T cell immunity to COVID-19
Karlsson, A. C., Humbert, M., & Buggert, M. (2020) · Science Immunology · doi:10.1126/sciimmunol.abe8063 · Cited by 165
“tinels mediating rapid protection from reinfection (35).”
Hunter, S., Willcox, C. R., Davey, M. S., Kasatskaya, S. A., Jeffery, H. C., Chudakov, D. M., Oo, Y. H., & Willcox, B. E. (2018) · Journal of Hepatology · doi:10.1016/j.jhep.2018.05.007 · Cited by 170
Bergsbaken, T., Bevan, M. J., & Fink, P. J. (2017) · Cell Reports · doi:10.1016/j.celrep.2017.03.031 · Cited by 163
McMaster, S. R., Wein, A. N., Dunbar, P. R., Hayward, S. L., Cartwright, E. K., Denning, T. L., & Kohlmeier, J. E. (2018) · Mucosal Immunology · doi:10.1038/s41385-018-0003-x · Cited by 160
Human T Cell Response to Dengue Virus Infection
Tian, Y., Grifoni, A., Sette, A., & Weiskopf, D. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.02125 · Cited by 160
Integrin αvβ6: Structure, function and role in health and disease
Koivisto, L., Bi, J., Häkkinen, L., & Larjava, H. (2018) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2018.04.013 · Cited by 159
Transcriptional and Epigenetic Regulation of Effector and Memory CD8 T Cell Differentiation
Chen, Y., Zander, R., Khatun, A., Schauder, D., & Cui, W. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.02826 · Cited by 156
“Other studies have further identified that exposure to IL-15 helps skew CD8T cells along a memory pathway (60–62), whereas IL-2 signaling is implicated in promoting the differentiation of short-lived effector T cells (63, 64).”
BackgroundInfluential
Metadata
- Authors
- Schenkel, J. M., & Masopust, D.
- Affiliations
- University of Minnesota (US)
- Corresponding author
- Masopust, David
- Venue
- Immunity
- Publisher
- Elsevier BV
- Published
- 2014-12
- Volume
- 41
- Issue
- 6
- Pages
- 886-897
- ISSN
- 1074-7613 (ISSN-L)
- PMC
- PMC4276131
- OpenAlex
- W2046700010
- Cited by
- 1,059
- References
- 135
- Citations by year
- 2026: 74 · 2025: 84 · 2024: 88 · 2023: 92 · 2022: 108 · 2021: 113 · 2020: 103 · 2019: 102 · 2018: 96 · 2017: 81 · 2016: 71 · 2015: 45 · 2014: 1
- FWCI
- 6.44
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Immunity (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institute of Allergy and Infectious Diseases (R01AI084913, R01AI111671, R37AI084913, T32AI007313)
- National Institute of Diabetes and Digestive and Kidney Diseases (F30DK100159)
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
- Life Sciences › Immunology and Microbiology › Immunology › Psoriasis: Treatment and Pathogenesis
- Life Sciences › Immunology and Microbiology › Immunology › Immunotherapy and Immune Responses
- Keywords
- tissue-resident memory T cells, mucosal immunity, memory T cell differentiation
- MeSH terms
- Animals, Cell Differentiation, Cell Movement, Humans, Immunity, Immunologic Memory, T-Lymphocytes, T-Lymphocyte Subsets
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