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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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Antigen Presentation in the Lung
Kawasaki, T., Ikegawa, M., & Kawai, T. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.860915 · Cited by 78
“Parts of antigen-specific cells differentiate into longlived memory cells, which are divided into three types of population: central memory T (TCM) cells, which are largely found in secondary lymphoid organs; effector memory T (TEF) cells, which systematically circulate, transiently entering peripheral tissue, and res…”
BackgroundMetabolic plasticity and regulation of T cell exhaustion
Li, F., Liu, H., Zhang, D., Ma, Y., & Zhu, B. (2022) · Immunology · doi:10.1111/imm.13575 · Cited by 73
Alberti, A. S., Bivona, A. E., Cerny, N., Schulze, K., Weissmann, S. F., Ebensen, T., Morales, C., Padilla, A. M., Cazorla, S. I., Tarleton, R. L., et al. (2017) · npj Vaccines · doi:10.1038/s41541-017-0010-z · Cited by 71
Beausang, J. F., Wheeler, A. J., Chan, N. H., Hanft, V. R., Dirbas, F. M., Jeffrey, S. S., & Quake, S. R. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1713863114 · Cited by 71
Cytokine-Mediated Regulation of CD8 T-Cell Responses During Acute and Chronic Viral InfectionPreprint
Hashimoto, M., Im, S. J., Araki, K., & Ahmed, R. (2017) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a028464 · Cited by 78
Mechanisms of activation of innate-like intraepithelial T lymphocytes
Vandereyken, M., James, O. J., & Swamy, M. (2020) · Mucosal Immunology · doi:10.1038/s41385-020-0294-6 · Cited by 65
Vincenti, I., Page, N., Steinbach, K., Yermanos, A., Lemeille, S., Nunez, N., Kreutzfeldt, M., Klimek, B., Di Liberto, G., Egervari, K., et al. (2022) · Science Translational Medicine · doi:10.1126/scitranslmed.abl6058 · Cited by 70
“During such infections, TRM proliferate locally, exert cytotoxic effector functions (8, 9), and induce an antiviral state within affected NLTs (10, 11).”
BackgroundMuruganandah, V., Sathkumara, H. D., Navarro, S., & Kupz, A. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.01574 · Cited by 76
“Asian Pac J Trop Biomed (2015) 5(4): 260–7.”
Muthuswamy, R., McGray, A. R., Battaglia, S., He, W., Miliotto, A. J., Eppolito, C., Matsuzaki, J., Tsuji, T., Koya, R. C., Chodon, T., et al. (2021) · Journal for ImmunoTherapy of Cancer · doi:10.1136/jitc-2021-003329 · Cited by 73
“6 7 10 This contrasts with central memory T cells (TCMs) that predominantly circulate within secondary lymphoid organs and effector memory T cells (TEMs), which recirculate mostly in peripheral tissues.”
Rådestad, E., Klynning, C., Stikvoort, A., Mogensen, O. E., Nava, S., Magalhaes, I., & Uhlin, M. (2018) · OncoImmunology · doi:10.1080/2162402x.2018.1535730 · Cited by 71
“To explore this subset further, we included another marker for tissue residency, CD103, a subunit of the αE/β7 integrin which helps to retain expressing cells to epithelium.(19) In the limited sample numbers (n = 8), we found co-expression of CD69 and CD103 to be common among tumor tissuederived CD8+ T-cells (median 4…”
BackgroundChen, X., Zhao, J., Yue, S., Li, Z., Duan, X., Lin, Y., Yang, Y., He, J., Gao, L., Pan, Z., et al. (2024) · Nature Cancer · doi:10.1038/s43018-024-00760-x · Cited by 68
“Further unbiased hierarchical clustering confirmed that P14 T BYS cells are in close proximity with P14 T RM cells and highlighted by cytolytic activity ( Gzmb , Tnf ) and tissue residency ( Cd69 , Nr4a1 ) 26 (Fig.”
Sarna, V. K., Skodje, G. I., Reims, H. M., Risnes, L. F., Dahal‐Koirala, S., Sollid, L. M., & Lundin, K. E. A. (2017) · Gut · doi:10.1136/gutjnl-2017-314461 · Cited by 69
Liver-resident NK cells and their potential functions
Peng, H. C., & Sun, R. (2017) · Cellular and Molecular Immunology · doi:10.1038/cmi.2017.72 · Cited by 69
Allie, S. R., & Randall, T. D. (2020) · Viral Immunology · doi:10.1089/vim.2019.0141 · Cited by 73
“In addition, many TRM cells, as well as BRM cells, express CD69 (134), which antagonizes S1PR1 signaling (134), further impairing their ability to leave tissues and enter the circulation.”
BackgroundDevelopmental options and functional plasticity of innate lymphoid cells
Lim, A. I., Verrier, T., Vosshenrich, C. A. J., & Santo, J. P. D. (2017) · Current Opinion in Immunology · doi:10.1016/j.coi.2017.03.010 · Cited by 74
Tissue adaptation: Implications for gut immunity and tolerance
Faria, A. M. C., Reis, B. S., & Mucida, D. (2017) · The Journal of Experimental Medicine · doi:10.1084/jem.20162014 · Cited by 69
Groh, J., Feng, R., Yuan, X., Liu, L., Klein, D., Hutahaean, G., Butz, E. S., Wang, Z., Steinbrecher, L., Neher, J. J., et al. (2025) · Nature Neuroscience · doi:10.1038/s41593-025-01955-w · Cited by 81
Herich, S., Schneider‐Hohendorf, T., Rohlmann, A., Ghadiri, M. K., Schulte‐Mecklenbeck, A., Zondler, L., Janoschka, C., Ostkamp, P., Richter, J., Breuer, J., et al. (2019) · Brain · doi:10.1093/brain/awz301 · Cited by 67
Zhou, A. C., Wagar, L. E., Wortzman, M. E., & Watts, T. H. (2017) · Mucosal Immunology · doi:10.1038/mi.2016.124 · Cited by 67
Next Generation Mucosal Vaccine Strategy for Respiratory Pathogens
Dotiwala, F., & Upadhyay, A. (2023) · Vaccines · doi:10.3390/vaccines11101585 · Cited by 72
“Secretory mucosal immunity is more effective than systemic immunity at neutralizing incoming viruses while the T RM cell surveillance rapidly responds to virus-infected mucosal cells [58].”
BackgroundThe emerging role of ECM crosslinking in T cell mobility as a hallmark of immunosenescence in humans
Moreau, J.-F., Pradeu, T., Grignolio, A., Nardini, C., Castiglione, F., Tieri, P., Capri, M., Salvioli, S., Taupin, J.-L., Garagnani, P., et al. (2017) · Ageing Research Reviews · doi:10.1016/j.arr.2016.11.005 · Cited by 67
Bottois, H., Ngollo, M., Hammoudi, N., Courau, T., Bonnereau, J., Chardiny, V., Grand, C., Gergaud, B., Allez, M., & Bourhis, L. L. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.00896 · Cited by 66
Chimeric Antigen Receptor beyond CAR-T Cells
Qin, V. M., D’Souza, C., Neeson, P. J., & Zhu, J. J. (2021) · Cancers · doi:10.3390/cancers13030404 · Cited by 65
Epigenetic Regulation of T Cell Memory: Recalling Therapeutic Implications
Tough, D. F., Rioja, I., Modis, L. K., & Prinjha, R. K. (2019) · Trends in Immunology · doi:10.1016/j.it.2019.11.008 · Cited by 67
Li, L., Tang, W., Zhang, Y., Jia, M., Wang, L., Li, Q., Han, Q., Peng, X., Xie, Y., Wu, J., et al. (2022) · Molecular Therapy · doi:10.1016/j.ymthe.2022.04.024 · Cited by 65
Homing to solid cancers: a vascular checkpoint in adoptive cell therapy using CAR T-cells
Ager, A., Watson, H. A., Wehenkel, S. C., & Mohammed, R. N. (2016) · Biochemical Society Transactions · doi:10.1042/bst20150254 · Cited by 68
Petitdemange, C., Kasturi, S. P., Kozlowski, P. A., Nabi, R., Quarnstrom, C. F., Reddy, P. B. J., Derdeyn, C. A., Spicer, L. M., Patel, P., Legere, T. H., et al. (2019) · JCI Insight · doi:10.1172/jci.insight.126047 · Cited by 64
“The effector functions and tissue localization of memory T cells are thought to be critical for protective immunity (38).”
BackgroundSelf-citationPrasad, S., Hu, S., Sheng, W. S., Chauhan, P., Singh, A. R., & Lokensgard, J. R. (2017) · Journal of Neuroinflammation · doi:10.1186/s12974-017-0860-3 · Cited by 66
Koch, M. R., Gong, R., Friedrich, V., Engelsberger, V., Kretschmer, L., Wanisch, A., Jarosch, S., Ralser, A., Lugen, B., Quante, M., et al. (2022) · Gastroenterology · doi:10.1053/j.gastro.2022.12.016 · Cited by 64
Detection of HIV-1-specific gastrointestinal tissue resident CD8+ T-cells in chronic infection
Kiniry, B. E., Li, S., Ganesh, A., Hunt, P. W., Somsouk, M., Skinner, P. J., Deeks, S. G., & Shacklett, B. L. (2017) · Mucosal Immunology · doi:10.1038/mi.2017.96 · Cited by 58
Ogongo, P., Steyn, A. J. C., Karim, F., Dullabh, K. J., Awala, I., Madansein, R., Leslie, A. J., & Behar, S. M. (2019) · Journal of Clinical Investigation · doi:10.1172/jci130711 · Cited by 61
“The existence of noncirculating tissue-resident memory T cells (Trms) (24) demonstrates that T cell responses in the blood and tissue do not always mirror each other.”
The Roles of CCR7 for the Homing of Memory CD8+ T Cells into Their Survival Niches
Choi, H., Song, H., & Jung, Y. W. (2020) · Immune Network · doi:10.4110/in.2020.20.e20 · Cited by 61
Stojić-Vukanić, Z., Hadžibegović, S., Nicole, O., Nacka-Aleksić, M., Leštarević, S., & Leposavić, G. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.566225 · Cited by 68
Allie, S. R., & Randall, T. D. (2017) · Clinical Science · doi:10.1042/cs20160259 · Cited by 63
Kim, J. H., Han, J. W., Choi, Y. J., Rha, M.-S., Koh, J. Y., Kim, K. H., Kim, C. G., Lee, Y. J., Kim, A. R., Park, J., et al. (2020) · Journal of Hepatology · doi:10.1016/j.jhep.2020.01.010 · Cited by 61
A new therapeutic target: the CD69-Myl9 system in immune responses
Kimura, M. Y., Koyama‐Nasu, R., Yagi, R., & Nakayama, T. (2019) · Seminars in Immunopathology · doi:10.1007/s00281-019-00734-7 · Cited by 58
Li, R., Liu, H., Cao, Y., Wang, J., Chen, Y., Qi, Y., Lv, K., Liu, X., Yu, K., Lin, C., et al. (2020) · British Journal of Cancer · doi:10.1038/s41416-020-0813-y · Cited by 62
Club cells surviving influenza A virus infection induce temporary nonspecific antiviral immunity
Hamilton, J. R., Sachs, D. M., Lim, J. K., Langlois, R. A., Palese, P., & Heaton, N. S. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1522376113 · Cited by 59
da Silva, H. B., Wang, H.-G., Qian, L. J., Hogquist, K., & Jameson, S. (2019) · Journal of Immunology · doi:10.4049/jimmunol.1801613 · Cited by 60
“In nonlymphoid tissues, most memory CD8 T cells are resident (16), and virtually all have been characterized as CD62L(2), based chiefly on flow cytometric analysis (20).”
BackgroundMethodStructure and function of the exocrine pancreas in patients with type 1 diabetes
Alexandre‐Heymann, L., Mallone, R., Boîtard, C., Scharfmann, R., & Larger, É. (2019) · Reviews in Endocrine and Metabolic Disorders · doi:10.1007/s11154-019-09501-3 · Cited by 63
Immunological Memory of Psoriatic Lesions
Owczarczyk-Saczonek, A. B., Krajewska–Włodarczyk, M., Kasprowicz‐Furmańczyk, M., & Placek, W. J. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21020625 · Cited by 64
“CD8+ CD49-TRM cells produce IL-17 [20,21].”
BackgroundHan, L., Gao, Q., Zhou, X., Shi, C., Chen, G., Song, Y., Yao, Y., Zhao, Y., Wen, X.-Y., Liu, S., et al. (2020) · Cancer Immunology Immunotherapy · doi:10.1007/s00262-020-02562-3 · Cited by 59
Shields, B. D., Koss, B. S., Taylor, E. M., Storey, A. J., West, K. L., Byrum, S. D., Mackintosh, S. G., Edmondson, R., Mahmoud, F. A., Shalin, S. C., et al. (2019) · Cancer Research · doi:10.1158/0008-5472.can-18-1722 · Cited by 63
TGF-β: Many Paths to CD103+ CD8 T Cell Residency
Qiu, Z., Chu, T. H., & Sheridan, B. S. (2021) · Cells · doi:10.3390/cells10050989 · Cited by 60
The Roles of Tissue-Resident Memory T Cells in Lung Diseases
Yuan, R., Yu, J., Jiao, Z., Li, J., Wu, F., Yan, R., Huang, X., & Chen, C. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.710375 · Cited by 58
Nanotechnologies in Delivery of DNA and mRNA Vaccines to the Nasal and Pulmonary Mucosa
Tang, J., Cai, L., Xu, C., Sun, S., Liu, Y., Rosenecker, J., & Guan, S. (2022) · Nanomaterials · doi:10.3390/nano12020226 · Cited by 54
“Compared with TEM, TRM provides a first line of defense in nonlymphoid tissues against infectious pathogens and limits further spread of infection in the host [83].”
BackgroundA review of HSV pathogenesis, vaccine development, and advanced applications
Bai, L., Xu, J., Zeng, L., Zhang, L., & Zhou, F. (2024) · Molecular Biomedicine · doi:10.1186/s43556-024-00199-7 · Cited by 60
“For example, HSV-2-specific tissue-resident memory CD8 + T cells (TRMs), a subset of CD8 + T cells, are crucial for controlling viral reactivation and act as rapid responders to prevent reinfection or reactivation [142–144].”
BackgroundPosavad, C. M., Zhao, L., Dong, L., Jin, L., Stevens, C. E., Magaret, A., Johnston, C., Wald, A., Zhu, J., Corey, L., et al. (2017) · Mucosal Immunology · doi:10.1038/mi.2016.118 · Cited by 59
Hu, Z., Wong, K., Zhao, H.-M., Wen, H.-L., Ji, P., Ma, H., Wu, K., Lu, S., Li, F., Li, Z.-M., et al. (2017) · Molecular Therapy · doi:10.1016/j.ymthe.2017.02.018 · Cited by 56
Danahy, D. B., Anthony, S. M., Jensen, I. J., Hartwig, S. M., Shan, Q., Xue, H., Harty, J. T., Griffith, T. S., & Badovinac, V. P. (2017) · PLoS Pathogens · doi:10.1371/journal.ppat.1006569 · Cited by 57
Th2-TRMs Maintain Life-Long Allergic Memory in Experimental Asthma in Mice
Bošnjak, B., Kazemi, S., Altenburger, L. M., Mokrović, G., & Epstein, M. M. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.00840 · Cited by 54
Kefalakes, H., Horgan, X. J., Jung, M. K., Amanakis, G., Kapuria, D., Bolte, F. J., Kleiner, D. E., Koh, C., Heller, T., & Rehermann, B. (2021) · Gastroenterology · doi:10.1053/j.gastro.2021.07.027 · Cited by 58
Intestinal helminth infection induces highly functional resident memory CD4+ T cells in mice
Steinfelder, S., Rausch, S., Michael, D., Kühl, A. A., & Hartmann, S. (2016) · European Journal of Immunology · doi:10.1002/eji.201646575 · Cited by 56
TGF-β Controls the Formation of Kidney-Resident T Cells via Promoting Effector T Cell Extravasation
Ma, C., Mishra, S., Demel, E. L., Liu, Y., & Zhang, N. (2016) · The Journal of Immunology · doi:10.4049/jimmunol.1601500 · Cited by 55
Optimal protection against Salmonella infection requires noncirculating memory
Benoun, J. M., Peres, N. G., Wang, N., Pham, O., Rudisill, V. L., Fogassy, Z., Whitney, P. G., Fernandez‐Ruiz, D., Gebhardt, T., Pham, Q.-M., et al. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1808339115 · Cited by 53
“There is considerable heterogeneity within the T cell memory pool (19), and only a fraction of memory cells are accessible by sampling blood and lymphoid organs (20, 21).”
BackgroundInfluenza infection fortifies local lymph nodes to promote lung-resident heterosubtypic immunity
Paik, D. H., & Färber, D. L. (2020) · The Journal of Experimental Medicine · doi:10.1084/jem.20200218 · Cited by 56
Nasal vaccines: solutions for respiratory infectious diseases
Nakahashi-Ouchida, R., Fujihashi, K., Kurashima, Y., Yuki, Y., & Kiyono, H. (2022) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2022.10.009 · Cited by 54
du Halgouet, A., Bruder, K., Peltokangas, N., Darbois, A., Obwegs, D., Salou, M., Thimme, R., Hofmann, M., Lantz, O. J., & Sagar (2024) · Nature Immunology · doi:10.1038/s41590-023-01710-y · Cited by 55
Tissue-Resident T Cells as the Central Paradigm of Chlamydia Immunity
Johnson, R. M., & Brunham, R. C. (2016) · Infection and Immunity · doi:10.1128/iai.01378-15 · Cited by 55
Ayasoufi, K., Wolf, D. M., Namen, S. L., Jin, F., Tritz, Z. P., Pfaller, C. K., Zheng, J., Goddery, E. N., Fain, C. E., Gulbicki, L. R., et al. (2022) · SSRN Electronic Journal · doi:10.1016/j.bbi.2023.05.009 · Cited by 54
Ju, Y.-J., Lee, S., Kye, Y.-C., Lee, G.-W., Kim, H.-O., Yun, C., & Cho, J.-H. (2021) · Nature Communications · doi:10.1038/s41467-021-26351-3 · Cited by 53
Nanoplatform Based Intranasal Vaccines: Current Progress and Clinical Challenges
Bai, Z., Wan, D., Lan, T., Hong, W., Dong, H., Wei, Y., & Wei, X. (2024) · ACS Nano · doi:10.1021/acsnano.3c10797 · Cited by 58
“50,51 In the upper respiratory tract, T RM B cells are found in the adenoids and tonsils of humans, 52 NALT of mice, 53 and the submucosa of the nasal cavity and trachea of most mammals.”
BackgroundChemokines: Critical Regulators of Memory T Cell Development, Maintenance, and Function
Rahimi, R. A., & Luster, A. D. (2018) · Advances in immunology · doi:10.1016/bs.ai.2018.02.002 · Cited by 55
Flórido, M., Muflihah, H., Lin, L. C. W., Xia, Y.-J., Sierro, F., Palendira, M., Feng, C. G., Bertolino, P., Stambas, J., Triccas, J., et al. (2018) · Mucosal Immunology · doi:10.1038/s41385-018-0065-9 · Cited by 53
“The presence of TRM in tissues has been associated with protection against several pathogens, and the high number of TRM found in mucosal sites support the concept that these cells represent a first line of defense against pathogens.(8) Most studies have focused on CD8 TRM cells in the context of viral infections and…”
BackgroundInfluentialNikolić, T., Suwandi, J. S., Wesselius, J., Laban, S., Joosten, A. M., Sonneveld, P., Mul, D., Aanstoot, H., Kaddis, J. S., Zwaginga, J. J., et al. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.1054968 · Cited by 52
“(C) Frequency in time of total Treg and Treg subclusters, shows significant increase of eTregs (subcluster 6.4) 1 month after tolDC treatment (*p=0.035). frontiersin.org Frontiers in Immunology 10 therapy was also followed by a transient increase of Trm CD4+ T-cells expressing CD103 (30).”
BackgroundInfluentialCharacterization of CD45RO+ memory T lymphocytes in keloid disease
Chen, Z., Zhou, L., Won, T., Gao, Z., Wu, X., & Lu, L. (2017) · British Journal of Dermatology · doi:10.1111/bjd.16173 · Cited by 55
The Role of TRM Cells in the Pathogenesis of Vitiligo—A Review of the Current State-Of-The-Art
Frączek, A., Owczarczyk-Saczonek, A. B., & Placek, W. J. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21103552 · Cited by 54
“CD 103+ Participation in binding TRM cells to E-cadherin to promote retention within epithelial tissues [72]”
BackgroundTissue-resident memory CD8+ T cells in cancer immunology and immunotherapy
Wang, T., Shen, Y., Luyten, S., Yang, Y., & Jiang, X. (2020) · Pharmacological Research · doi:10.1016/j.phrs.2020.104876 · Cited by 53
Bošnjak, B., Odak, I., Barros‐Martins, J., Sandrock, I., Hammerschmidt, S. I., Permanyer, M., Patzer, G. E., Georgiev, H., Jauregui, R. G., Tscherne, A., et al. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.772240 · Cited by 50
“boosting led to a massive accumulation of spike-specific CD8 T cells expressing CD103 and CD69, markers for tissue residency in the lungs (71).”
BackgroundLong-distance microbial mechanisms impacting cancer immunosurveillance
Zitvogel, L., Fidelle, M., & Kroemer, G. (2024) · Immunity · doi:10.1016/j.immuni.2024.07.020 · Cited by 56
Jeyanathan, M., Afkhami, S., Khera, A., Mandur, T. S., Damjanovic, D., Yao, Y., Lai, R., Haddadi, S., Dvorkin-Gheva, A., Jordana, M., et al. (2017) · Journal of Immunology · doi:10.4049/jimmunol.1700382 · Cited by 51
Aim2-mediated/IFN-β–independent regulation of gastric metaplastic lesions via CD8+ T cells
Zaatari, M. E., Bishu, S., Zhang, M., Grasberger, H., Hou, G., Haley, H. R., Humphries, B. A., Syu, L.-J., Dlugosz, A. A., Luker, K., et al. (2020) · JCI Insight · doi:10.1172/jci.insight.94035 · Cited by 50
Immune cell composition in normal human kidneys
Park, J.-G., Na, M., Kim, M.-G., Park, S. H., Lee, H. J., Kim, D. K., Kwak, C. H., Kim, Y. S., Chang, S., Moon, K. C., et al. (2020) · Scientific Reports · doi:10.1038/s41598-020-72821-x · Cited by 51
The contribution of neuropathology to multiple sclerosis research
Lassmann, H. (2022) · European Journal of Neurology · doi:10.1111/ene.15360 · Cited by 55
Functional heterogeneity of human tissue-resident memory T cells based on dye efflux capacities
Kumar, B. V., Kratchmarov, R., Miron, M., Carpenter, D. J., Senda, T., Lerner, H., Friedman, A. L., Reiner, S. L., & Färber, D. L. (2018) · JCI Insight · doi:10.1172/jci.insight.123568 · Cited by 52
“Strikingly, expression of CD103, a canonical CD8+ TRM marker (29), was enriched within the efflux(+) compared with efflux(–) fraction in both spleen and lung, with some interdonor variability for the lung (Figure 2C).”
BackgroundComeau, K., Paradis, P., & Schiffrin, E. L. (2020) · Cellular Immunology · doi:10.1016/j.cellimm.2020.104217 · Cited by 53
“TRM are thought to be derived from precursors that entered the tissues during the effector phase of the immune response, which remain positioned in the periphery [28].”
BackgroundCurrent Vaccine Platforms in Enhancing T-Cell Response
Ura, T., Takeuchi, M., Kawagoe, T., Mizuki, N., Okuda, K., & Shimada, M. (2022) · Vaccines · doi:10.3390/vaccines10081367 · Cited by 56
Mao, X., Chen, Y., Lu, X., Jin, S., Jiang, P., Deng, Z., Zhu, X., Cai, Q., Wu, C. Y., & Kang, S. (2023) · Journal of Cancer · doi:10.7150/jca.83615 · Cited by 50
Yeon, S.-M., Halim, L., Chandele, A., Perry, C. J., Kim, S. H., Kim, S.-U., Byun, Y., Yuk, S. H., Kaech, S. M., & Jung, Y. W. (2017) · Scientific Reports · doi:10.1038/s41598-017-11492-7 · Cited by 50
Lassmann, H. (2019) · Current Opinion in Neurology · doi:10.1097/wco.0000000000000685 · Cited by 50
Hassert, M. A., & Harty, J. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.1039194 · Cited by 47
Cancer-specific tissue-resident memory T-cells express ZNF683 in colorectal cancer
Kitakaze, M., Uemura, M., Hara, T., Chijimatsu, R., Motooka, D., Hirai, T., Konno, M., Okuzaki, D., Sekido, Y., Hata, T., et al. (2023) · British Journal of Cancer · doi:10.1038/s41416-023-02202-4 · Cited by 49
“Trm cells remain in peripheral tissues for a long time [7].”
BackgroundMcDonald, B., Chick, B. Y., Ahmed, N. S., Burns, M. J., Ma, S., Casillas, E., Chen, D., Mann, T. H., O’Connor, C., Hah, N., et al. (2023) · Immunity · doi:10.1016/j.immuni.2023.05.005 · Cited by 51
Immune correlates of protection as a game changer in tuberculosis vaccine development
Wang, J., Fan, X., & Hu, Z. (2024) · npj Vaccines · doi:10.1038/s41541-024-01004-w · Cited by 51
“T RM represents a distinct subset of memory lymphocyte lineage that colo-nizestissuesindependentlyofnewrecruitmentofTcellsfromthebloodandprovidesarapidresponseagainstreencounteredinfections 69,70 .”
BackgroundThe spatial landscape of glial pathology and T cell response in Parkinson’s disease substantia nigra
Ma, M., Paryani, F., Jakubiak, K. A., Xia, S., Antoku, S., Kannan, A., Lee, J., Madden, N., Kumar, S. S., Li, J., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-62478-3 · Cited by 61
Martin, M. D., Kim, M. T., Shan, Q., Sompallae, R. R., Xue, H., Harty, J. T., & Badovinac, V. P. (2015) · PLoS Pathogens · doi:10.1371/journal.ppat.1005219 · Cited by 52
Tissue-Resident Lymphocytes Across Innate and Adaptive Lineages
Chou, C., & Li, M. O. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.02104 · Cited by 53
“This restricted migratory pattern of tissue-resident lymphocytes is often associated with their lack of lymphoid tissue homing chemokine receptors and elevated expressions of several adhesion molecules (7, 12).”
BackgroundAgeing, immune fitness and cancer
Dolan, M., Libby, K. A., Ringel, A. E., van Galen, P., & McAllister, S. S. (2025) · Nature reviews. Cancer · doi:10.1038/s41568-025-00858-z · Cited by 55
Natural Killer Cell Integrins and Their Functions in Tissue Residency
Shannon, M. J., & Mace, E. M. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.647358 · Cited by 53
Metabolic Reprogramming in the Tumor Microenvironment With Immunocytes and Immune Checkpoints
Xu, Y., He, L., Fu, Q., & Hu, J. (2021) · Frontiers in Oncology · doi:10.3389/fonc.2021.759015 · Cited by 51
Bangert, C., Villazala‐Merino, S., Fahrenberger, M., Krausgruber, T., Bauer, W. M., Stanek, V., Campion, N. J., Bartosik, T. J., Quint, T., Regelsberger, G., et al. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.850494 · Cited by 47
“org 9 resident memory T-cells (TRM) based on CD69 and integrin subunit alpha E ITGAE (CD103) or integrin subunit alpha 4 ITGA4 (CD49d) expression (Figures 6D–F) (35, 36).”
BackgroundSnyder, M. E., Moghbeli, K., Bondonese, A., Craig, A., Popescu, I., Fan, L., Tabib, T., Lafyatis, R., Chen, K., Bittar, H. E. T., et al. (2022) · The Journal of Experimental Medicine · doi:10.1084/jem.20212059 · Cited by 49
“TRM cells are memory T cells that persist in either lymphoid or mucosal organs, do not recirculate, and are poised to have a rapid effector response in the setting of secondary challenge to pathogen (Schenkel and Masopust, 2014; Thome et al., 2014).”
BackgroundLei, H., Alu, A., Yang, J., He, X., He, C., Ren, W., Chen, Z., Hong, W., Chen, L., He, X., et al. (2023) · Nature Communications · doi:10.1038/s41467-023-38066-8 · Cited by 49
“Respiratory T RM cells are essential components of fi rst-line defense against viral infection at local sites without recirculating 49 – 51 .”
Shwetank, Frost, E. L., Mockus, T. E., Ren, H. M., Toprak, M., Lauver, M. D., Netherby, C. S., Jin, G., Cosby, J., Evavold, B. D., et al. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.00783 · Cited by 47
“Tissue-resident memory CD8 T cells are an essential component of the first line of defense against re-infection in non-lymphoid tissues (24) (25) (26) .”
BackgroundRissiek, B., Lukowiak, M., Raczkowski, F., Magnus, T., Mittrücker, H.-W., & Koch-Nolte, F. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.01580 · Cited by 45
“Tissue-resident memory T cells (Trm) comprise a population of T cells, which stays in peripheral tissues after an immune response against invading pathogens, forming a rapid first-line defense against recurring infection (18).”
BackgroundSkin-Resident Memory T Cells: Pathogenesis and Implication for the Treatment of Psoriasis
Vu, T. T., Koguchi‐Yoshioka, H., & Watanabe, R. (2021) · Journal of Clinical Medicine · doi:10.3390/jcm10173822 · Cited by 52
Influence of Age on Functional Memory T Cell Diversity
Fang, F., Cao, W., Zhu, W., Lam, N., Li, L., Gaddam, S., Wang, Y., Kim, C., Lambert, S., Zhang, H., et al. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.109981 · Cited by 47
Accumulation of γδ T cells in visceral fat with aging promotes chronic inflammation
Bruno, M. E. C., Mukherjee, S., Powell, W. L., Mori, S. F., Wallace, F. K., Balasuriya, B. K., Su, L. C., Stromberg, A. J., Cohen, D. A., & Starr, M. E. (2022) · GeroScience · doi:10.1007/s11357-022-00572-w · Cited by 47
Sharma, D., Sharma, S., Akojwar, N., Dondulkar, A., Yenorkar, N. Y., Pandita, D., Prasad, S. K., & Dhobi, M. (2023) · Vaccines · doi:10.3390/vaccines11020206 · Cited by 45
“In addition, CD8+ TRM, a subtype of memory lymphocyte that dwells in non-lymphoid tissues [77], has been shown to activate the adaptive immune response in HSV-1 infection [78] via IFN-Y and granzyme B effectors.”
BackgroundDevelopment and Function of Protective and Pathologic Memory CD4 T Cells
Jaigirdar, S. A., & MacLeod, M. K. L. (2015) · Frontiers in Immunology · doi:10.3389/fimmu.2015.00456 · Cited by 49
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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