The DOI matches its Crossref record; 37 of the 37 references it cites were found in a registry or an index.
A Role for Mammalian Target of Rapamycin in Regulating T Cell Activation versus Anergy
Abstract
Whether TCR engagement leads to activation or tolerance is determined by the concomitant delivery of multiple accessory signals, cytokines, and environmental cues. In this study, we demonstrate that the mammalian target of rapamycin (mTOR) integrates these signals and determines the outcome of TCR engagement with regard to activation or anergy. In vitro, Ag recognition in the setting of mTOR activation leads to full immune responses, whereas recognition in the setting of mTOR inhibition results in anergy. Full T cell activation is associated with an increase in the phosphorylation of the downstream mTOR target S6 kinase 1 at Thr(421)/Ser(424) and an increase in the mTOR-dependent cell surface expression of transferrin receptor (CD71). Alternatively, the induction of anergy results in markedly less S6 kinase 1 Thr(421)/Ser(424) phosphorylation and CD71 surface expression. Likewise, the reversal of anergy is associated not with proliferation, but rather the specific activation of mTOR. Importantly, T cells engineered to express a rapamycin-resistant mTOR construct are resistant to anergy induction caused by rapamycin. In vivo, mTOR inhibition promotes T cell anergy under conditions that would normally induce priming. Furthermore, by examining CD71 surface expression, we are able to distinguish and differentially isolate anergic and activated T cells in vivo. Overall, our data suggest that by integrating environmental cues, mTOR plays a central role in determining the outcome of Ag recognition.
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
“Moreover, it has been suggested that induction of T cell anergy, a process whereby an activated T cell becomes tolerant and functionally inactive (a desirable effect in cases of hyper T cell activation under autoimmune conditions and undesirable in the tumor microenvironment) involves TFR downregulation (Zheng et al., 2007).”
From The Role of Iron Regulation in Immunometabolism and Immune-Related Disease (2019) · cites this paper as Zheng et al., 2007
In the citing paper
“TfR surface expression has been shown to be different between anergic and activated T cells in vivo, whereby anergic T cells showed decreased TfR levels [143].”
From Iron in immune cell function and host defense (2021) · cites this paper as [143]
Citations
Cites
Upstream and downstream of mTOR
Hay, N., & Sonenberg, N. (2004) · Genes & Development · doi:10.1101/gad.1212704 · Cited by 4,181
Kim, D., Sarbassov, D. D., Ali, S. M., King, J. E., Latek, R. R., Erdjument‐Bromage, H., Tempst, P., & Sabatini, D. M. (2002) · Cell · doi:10.1016/s0092-8674(02)00808-5 · Cited by 3,051
Long-term acceptance of skin and cardiac allografts after blocking CD40 and CD28 pathways
Larsen, C. P., Elwood, E. T., Alexander, D. Z., Ritchie, S. C., Hendrix, R. C., Tucker‐Burden, C., Cho, H. R., Aruffo, A. A., Hollenbaugh, D. L., Linsley, P. S., et al. (1996) · Nature · doi:10.1038/381434a0 · Cited by 1,455
Schwartz, R. H. (1992) · Cell · doi:10.1016/s0092-8674(05)80055-8 · Cited by 1,293
Chung, J., Kuo, C. J., Crabtree, G. R., & Blenis, J. (1992) · Cell · doi:10.1016/0092-8674(92)90643-q · Cited by 1,151
Kim, D., Sarbassov, D. D., Ali, S. M., Latek, R. R., Guntur, K., Erdjument‐Bromage, H., Tempst, P., & Sabatini, D. M. (2003) · Molecular Cell · doi:10.1016/s1097-2765(03)00114-x · Cited by 992
Akt Maintains Cell Size and Survival by Increasing mTOR-dependent Nutrient Uptake
Edinger, A. L., & Thompson, C. B. (2002) · Molecular Biology of the Cell · doi:10.1091/mbc.01-12-0584 · Cited by 592
Chen, J., Zheng, X. F., Brown, E. J., & Schreiber, S. L. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.11.4947 · Cited by 556
Peterson, R., Desai, B. N., Hardwick, J. S., & Schreiber, S. (1999) · Proceedings of the National Academy of Sciences of the United States of America · doi:10.1073/pnas.96.8.4438 · Cited by 496
IL-7 Enhances the Survival and Maintains the Size of Naive T Cells
Rathmell, J. C., Farkash, E. A., Gao, W., & Thompson, C. B. (2001) · The Journal of Immunology · doi:10.4049/jimmunol.167.12.6869 · Cited by 459
Flagged first, then by citations
Research works printed but not linked: 37
- 1992, Cell, 1065
- 2004, Genes Dev., 1926
- 2004, Biochem. Biophys. Res. Commun., 443
- 2004, Curr. Top. Microbiol. Immunol., 245
- 2003, Sci. STKE, re15
- 1999, J. Immunol., 2775
- 2001, J. Immunol., 5636
- 1993, J. Immunol., 1245
- 2001, Eur. J. Immunol., 3737
- 2000, Nat. Med., 290
- 2000, J. Immunol., 2432
- 2002, J. Immunol., 6178
- 2004, J. Immunol., 4797
- 2001, J. Immunol., 952
- 2006, J. Immunol., 2730
- 1992, Cell, 1227
- 2002, Cell, 163
- 2003, Mol. Cell, 895
- 2004, Blood, 3138
- 1994, Science, 1039
- 2001, J. Immunol., 6869
- 1999, Immunity, 525
- 2004, J. Exp. Med., 659
- 2003, Proc. Natl. Acad. Sci. USA, 15113
- 2002, Mol. Biol. Cell, 2276
- 1991, Eur. J. Haematol., 140
- 1995, Proc. Natl. Acad. Sci. USA, 4947
- 1997, Immunol. Rev., 67
- 2005, J. Immunol., 3359
- 2003, Eur. J. Immunol., 3154
- 2005, Front. Biosci., 2856
- 2005, Mol. Cell. Biol., 2558
- 1999, Proc. Natl. Acad. Sci. USA, 4438
- 2000, Immunity, 313
- 1996, Nature, 434
- 1998, Transplantation, 473
- 2005, Transplantation, 1541
Cited by
Sorted by citations
Items 101–200 of 273
Mocholí, E., Dowling, S. D., Botbol, Y. M., Gruber, R. C., Ray, A. K., Vastert, S. J., Shafit‐Zagardo, B., Coffer, P. J., & Macián, F. (2018) · Cell Reports · doi:10.1016/j.celrep.2018.06.065 · Cited by 52
Allergens and Adjuvants in Allergen Immunotherapy for Immune Activation, Tolerance, and Resilience
Jensen‐Jarolim, E., Roth‐Walter, F., Jordakieva, G., & Pali‐Schöll, I. (2021) · The Journal of Allergy and Clinical Immunology In Practice · doi:10.1016/j.jaip.2020.12.008 · Cited by 51
T cell receptor signaling in the differentiation and plasticity of CD4+ T cells
Meitei, H. T., & Lal, G. (2022) · Cytokine & Growth Factor Reviews · doi:10.1016/j.cytogfr.2022.08.001 · Cited by 58
Padilha, C. S., Figueiredo, C., Minuzzi, L. G., Chimin, P., Deminice, R., Krüger, K., Neto, J. C. R., & Lira, F. S. (2021) · Ageing Research Reviews · doi:10.1016/j.arr.2021.101341 · Cited by 54
Collins, D. R., Hitschfel, J., Urbach, J. M., Mylvaganam, G., Ly, N. L., Arshad, U., Racenet, Z. J., Yanez, A. G., Diefenbach, T. J., & Walker, B. D. (2023) · Science Immunology · doi:10.1126/sciimmunol.ade5872 · Cited by 50
Metabolic Regulation of Regulatory T Cell Development and Function
Coe, D., Kishore, M., & Marelli‐Berg, F. M. (2014) · Frontiers in Immunology · doi:10.3389/fimmu.2014.00590 · Cited by 50
Taylor, H. E., Calantone, N., Lichon, D., Hudson, H., Clerc, I., Campbell, E. M., & D’Aquila, R. T. (2020) · Cell Reports · doi:10.1016/j.celrep.2020.107810 · Cited by 48
Protein Kinase CK2 Controls the Fate between Th17 Cell and Regulatory T Cell Differentiation
Gibson, S. A., Yang, W., Yan, Z., Liu, Y., Rowse, A. L., Weinmann, A. S., Qin, H., & Benveniste, E. N. (2017) · The Journal of Immunology · doi:10.4049/jimmunol.1601912 · Cited by 47
Bridging angiogenesis and immune evasion in the hypoxic tumor microenvironment
Schito, L. (2018) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00209.2018 · Cited by 49
Lin, J. T., Lineberry, N. B., Kattah, M. G., Su, L., Utz, P. J., Fathman, C. G., & Wu, L. (2009) · The Journal of Immunology · doi:10.4049/jimmunol.0803986 · Cited by 48
Magee, C. N., Murakami, N., Borges, T. J., Shimizu, T., Safa, K., Ohori, S., Cai, S., Uffing, A., Azzi, J. R., Elyaman, W., et al. (2019) · Circulation · doi:10.1161/circulationaha.119.040563 · Cited by 47
Immunometabolism – The Role of Branched-Chain Amino Acids
Yahsi, B., & Günaydın, G. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.886822 · Cited by 51
Zeng, H., Yu, M., Tan, H., Li, Y., Su, W., Shi, H., Dhungana, Y., Guy, C. S., Neale, G. A. M., Cloer, C., et al. (2018) · Science Advances · doi:10.1126/sciadv.aar5701 · Cited by 48
Pedicord, V. A., Cross, J. R., Montalvo-Ortiz, W., Miller, M. L., & Allison, J. P. (2015) · The Journal of Immunology · doi:10.4049/jimmunol.1402390 · Cited by 45
Liu, G., Bi, Y., Wang, R., Yang, H., Zhang, Y., Wang, X. D., Liu, H., Lu, Y., Zhang, Z., Chen, W., et al. (2014) · The Journal of Immunology · doi:10.4049/jimmunol.1301193 · Cited by 45
Specific Gut Commensal Flora Locally Alters T Cell Tuning to Endogenous Ligands
Chappert, P., Bouladoux, N. J., Naik, S., & Schwartz, R. H. (2013) · Immunity · doi:10.1016/j.immuni.2013.06.005 · Cited by 44
Modulation of TSC-mTOR signaling on immune cells in immunity and autoimmunity
Yang, H., Wang, X., Zhang, Y., Liu, H., Liao, J., Shao, K., Chu, Y., & Liu, G. (2013) · Journal of Cellular Physiology · doi:10.1002/jcp.24426 · Cited by 45
Jung, J., Veitch, M., Bridge, J. A., Overgaard, N. H., Cruz, J. L. G., Linedale, R., Franklin, M. E., Saunders, N. A., Simpson, F., Frazer, I. H., et al. (2018) · OncoImmunology · doi:10.1080/2162402x.2018.1479627 · Cited by 43
Cellular Metabolic Regulation in the Differentiation and Function of Regulatory T Cells
Chen, Y., Colello, J., Jarjour, W. N., & Zheng, S. G. (2019) · Cells · doi:10.3390/cells8020188 · Cited by 46
Nencioni, A., Cea, M., Garuti, A., Passalacqua, M., Raffaghello, L., Soncini, D., Morán, E., Zoppoli, G. M., Pistoia, V., Patrone, F., et al. (2010) · PLoS ONE · doi:10.1371/journal.pone.0009024 · Cited by 42
Taylor, H. E., Simmons, G. E., Jr., Mathews, T. P., Khatua, A. K., Popik, W., Lindsley, C. W., D’Aquila, R. T., & Brown, H. A. (2015) · PLoS Pathogens · doi:10.1371/journal.ppat.1004864 · Cited by 43
Xia, Y., Brown, Z. J., Huang, H., & Tsung, A. (2021) · Cancer Medicine · doi:10.1002/cam4.4177 · Cited by 42
Role of intracellular signaling pathways and their inhibitors in the treatment of inflammation
Nailwal, N. P., & Doshi, G. (2021) · Inflammopharmacology · doi:10.1007/s10787-021-00813-y · Cited by 44
Parta, M., Hilligoss, D. M., Kelly, C., Kwatemaa, N., Theobald, N., Malech, H. L., & Kang, E. M. (2015) · Journal of Clinical Immunology · doi:10.1007/s10875-015-0204-y · Cited by 41
Ocular toxicity and distribution of subconjunctival and intravitreal rapamycin in horses
Douglas, L., Yi, N. Y., Davis, J. L., Salmon, J. H., & Gilger, B. C. (2008) · Journal of Veterinary Pharmacology and Therapeutics · doi:10.1111/j.1365-2885.2008.00986.x · Cited by 41
Rapamycin in islet transplantation: friend or foe?
Berney, T., & Secchi, A. (2008) · Transplant International · doi:10.1111/j.1432-2277.2008.00743.x · Cited by 44
The sound of silence: modulating anergy in T lymphocytes
Saibil, S. D., Deenick, E. K., & Ohashi, P. S. (2007) · Current Opinion in Immunology · doi:10.1016/j.coi.2007.08.005 · Cited by 39
Immunologic and dose dependent effects of rapamycin and its evolving role in chemoprevention
O’Shea, A. E., Valdera, F. A., Ensley, D. C., Smolinsky, T. R., Cindass, J. L., Bohan, P. M. K., Hickerson, A. T., Carpenter, E. L., McCarthy, P. M., Adams, A. M., et al. (2022) · Clinical Immunology · doi:10.1016/j.clim.2022.109095 · Cited by 40
Iron metabolism in transplantation
Schaefer, B., Effenberger, M., & Zoller, H. (2014) · Transplant International · doi:10.1111/tri.12374 · Cited by 37
Rapamycin Prevents Surgery-Induced Immune Dysfunction in Patients with Bladder Cancer
Svatek, R. S., Ji, N., Leon, E. D., Mukherjee, N. Z., Kabra, A. T., Hurez, V. J., Nicolas, M. M., Michalek, J. E., Javors, M. A., Wheeler, K. M., et al. (2018) · Cancer Immunology Research · doi:10.1158/2326-6066.cir-18-0336 · Cited by 38
Regulatory CD4 T cells: sensing the environment
Matarese, G., Rosa, V. D., & Cava, A. L. (2007) · Trends in Immunology · doi:10.1016/j.it.2007.10.006 · Cited by 37
Delmastro-Greenwood, M. M., Votyakova, T. V., Goetzman, E. S., Marré, M. L., Previte, D. M., Tovmasyan, A. G., Batinic̈‐Haberle, I., Trucco, M., & Piganelli, J. D. (2013) · Antioxidants and Redox Signaling · doi:10.1089/ars.2012.5167 · Cited by 37
Kouidhi, S., Noman, M. Z., Kiéda, C., Elgaaïed, A. B., & Chouaïb, S. (2016) · Frontiers in Immunology · doi:10.3389/fimmu.2016.00114 · Cited by 39
Haploidentical SCT: the mechanisms underlying the crossing of HLA barriers
Chang, Y.-J., & Huang, X.-J. (2014) · Bone Marrow Transplantation · doi:10.1038/bmt.2014.19 · Cited by 35
Fourati, S., Ribeiro, S. P., Lopes, F. B. T. P., Talla, A., Lefebvre, F., Cameron, M. J., Kaewkungwal, J., Pitisuttithum, P., Nitayaphan, S., Rerks‐Ngarm, S., et al. (2019) · Nature Communications · doi:10.1038/s41467-019-08854-2 · Cited by 37
Wüstner, S., Mejías‐Luque, R., Koch, M. F., Rath, E., Vieth, M. W., Sieber, S. A., Haller, D., & Gerhard, M. (2014) · Cellular Microbiology · doi:10.1111/cmi.12335 · Cited by 37
The emerging role of mTOR signalling in antibacterial immunity
Abdel‐Nour, M., Tsalikis, J., Kleinman, D. R., & Girardin, S. E. (2014) · Immunology and Cell Biology · doi:10.1038/icb.2014.3 · Cited by 33
Novel treatment strategies for patients with relapsed classical Hodgkin lymphoma
Jóna, Á., & Younes, A. (2010) · Blood Reviews · doi:10.1016/j.blre.2010.08.003 · Cited by 34
McTernan, P. M., Levitt, D. E., Welsh, D. A., Simon, L., Siggins, R. W., & Molina, P. E. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.839390 · Cited by 35
Enhanced interaction between Hsp90 and raptor regulates mTOR signaling upon T cell activation
Delgoffe, G. M., Kole, T. P., Cotter, R. J., & Powell, J. D. (2009) · Molecular Immunology · doi:10.1016/j.molimm.2009.05.185 · Cited by 34
Ferroptosis of T cell in inflammation and tumour immunity
Xia, X., Wu, H., Chen, Y., Peng, H., & Wang, S. (2025) · Clinical and Translational Medicine · doi:10.1002/ctm2.70253 · Cited by 34
cDC1 coordinate innate and adaptive responses in the omentum required for T cell priming and memory
Christian, D. A., Adams, T. A., Shallberg, L. A., Phan, A. T., Smith, T. E., Abraha, M., Perry, J. A., Ruthel, G. T., Clark, J. T., Pritchard, G. H., et al. (2022) · Science Immunology · doi:10.1126/sciimmunol.abq7432 · Cited by 33
Mahne, A. E., Klementowicz, J. E., Chou, A. Y., Nguyen, V. Q., & Tang, Q. (2015) · The Journal of Immunology · doi:10.4049/jimmunol.1402739 · Cited by 33
Peripheral tolerance in CD8+ T cells
Srinivasan, M., & Frauwirth, K. A. (2009) · Cytokine · doi:10.1016/j.cyto.2009.01.010 · Cited by 32
REDD1 Is Essential for Optimal T Cell Proliferation and Survival
Reuschel, E. L., Wang, J., Shivers, D. K., Muthumani, K., Weiner, D. B., Ma, Z., & Finkel, T. H. (2015) · PLoS ONE · doi:10.1371/journal.pone.0136323 · Cited by 31
Receptor signaling in immune cell development and function
Zhong, X., Shin, J., Gorentla, B. K., O’Brien, T., Srivatsan, S., Li, X., Chen, Y., Xie, D., & Pan, H. (2010) · Immunologic Research · doi:10.1007/s12026-010-8175-9 · Cited by 31
Eradication of Established Tumors by Chemically Self-Assembled Nanoring Labeled T Cells
Petersburg, J. R., Shen, J., Csizmar, C. M., Murphy, K. A., Spanier, J. A., Gabrielse, K., Griffith, T. S., Fife, B. T., & Wagner, C. R. (2018) · ACS Nano · doi:10.1021/acsnano.8b01308 · Cited by 29
Wu, J., Shin, J., Xie, D., Wang, H., Gao, J., & Zhong, X. (2014) · The Journal of Immunology · doi:10.4049/jimmunol.1302076 · Cited by 28
Borges, T. J., Murakami, N., Lape, I. T., Gassen, R. B., Liu, K., Cai, S., Daccache, J., Safa, K., Shimizu, T., Ohori, S., et al. (2021) · JCI Insight · doi:10.1172/jci.insight.142909 · Cited by 28
Molecular mechanisms of T-cell anergy
Куклина, Е. М. (2013) · Biochemistry (Moscow) · doi:10.1134/s000629791302003x · Cited by 29
Metabolic features of innate lymphoid cells
Yu, H., Jacquelot, N., & Belz, G. T. (2022) · The Journal of Experimental Medicine · doi:10.1084/jem.20221140 · Cited by 31
Gorentla, B. K., Krishna, S., Shin, J., Inoue, M., Shinohara, M. L., Grayson, J. M., Fukunaga, R., & Zhong, X.-P. (2012) · The Journal of Immunology · doi:10.4049/jimmunol.1200026 · Cited by 27
Zarek, P. E., & Powell, J. D. (2007) · Autoimmunity · doi:10.1080/08916930701464939 · Cited by 26
Fu, X., Xu, M., Song, Y., Li, Y., Zhang, H., Zhang, J., & Zhang, C. (2018) · Journal of Biological Chemistry · doi:10.1074/jbc.ra118.003668 · Cited by 26
Regulatory T Cell Stability and Migration Are Dependent on mTOR
Vallion, R., Divoux, J., Glauzy, S., Ronin, É., Lombardi, Y., di Ricco, M. L., Grégoire, S., Nemazanyy, I., Durand, A., Fradin, D., et al. (2020) · The Journal of Immunology · doi:10.4049/jimmunol.1901480 · Cited by 28
Bănică, L. M., Beşliu, A. N., Pistol, G. C., Stăvaru, C., Vlad, V. M., Predețeanu, D., Ionescu, R., Stefănescu, M., & Matache, C. (2014) · International Journal of Rheumatic Diseases · doi:10.1111/1756-185x.12509 · Cited by 25
Rapamycin delays growth of Wnt-1 tumors in spite of suppression of host immunity
Svirshchevskaya, E. V., Mariotti, J., Wright, M. H., Viskova, N. Y., Telford, W. G., Fowler, D. H., & Varticovski, L. (2008) · BMC Cancer · doi:10.1186/1471-2407-8-176 · Cited by 25
Unexpected Roles for Intracellular Complement in the Regulation of Th1 Responses
West, E. E., Afzali, B., & Kemper, C. (2018) · Advances in immunology · doi:10.1016/bs.ai.2018.02.001 · Cited by 27
Sugar, fat, and protein: new insights into what T cells crave
Delgoffe, G. M., & Powell, J. D. (2015) · Current Opinion in Immunology · doi:10.1016/j.coi.2015.01.015 · Cited by 27
T cell metabolism and susceptibility to autoimmune diseases
Galgani, M., Rosa, V. D., & Matarese, G. (2015) · Molecular Immunology · doi:10.1016/j.molimm.2015.07.035 · Cited by 27
Arshad, Z., Rezapour-Firouzi, S., Ebrahimifar, M., Mosavi-Jarrahi, A., & Mohammadian, M. (2019) · Asian Pacific Journal of Cancer Prevention · doi:10.31557/apjcp.2019.20.4.1005 · Cited by 22
Pleiotropic effects of antibiotics on T cell metabolism and T cell-mediated immunity
Franz, T. J., Negele, J., Bruno, P., Böttcher, M., Mitchell-Flack, M., Reemts, L., Krone, A., Mougiakakos, D., Müller, A. J., Zautner, A. E., et al. (2022) · Frontiers in Microbiology · doi:10.3389/fmicb.2022.975436 · Cited by 24
mTOR and its tight regulation for iNKT cell development and effector function
Yang, W., Gorentla, B. K., Zhong, X., & Shin, J. (2015) · Molecular Immunology · doi:10.1016/j.molimm.2015.07.022 · Cited by 23
Pidala, J., Kim, J., Alsina, M., Ayala, E. S. I., Betts, B. C., Fernandez, H. F., Field, T. L., Jim, H., Kharfan‐Dabaja, M. A., Locke, F. L., et al. (2015) · Haematologica · doi:10.3324/haematol.2015.123588 · Cited by 23
Cytometric evaluation of transferrin receptor 1 (CD71) in childhood acute lymphoblastic leukemia
Płoszyńska, A., Rückemann-Dziurdzińska, K., Jóźwik, A., Mikosik, A., Lisowska, K. A., Balcerska, A., & Witkowski, J. M. (2012) · Folia Histochemica et Cytobiologica · doi:10.5603/fhc.2012.0040 · Cited by 23
Morel, L. M., & Scindia, Y. M. (2024) · Clinical Immunology · doi:10.1016/j.clim.2024.110181 · Cited by 21
Metabolic Mysteries of the Inflammatory Response: T Cell Polarization and Plasticity
Fracchia, K. M., & Walsh, C. M. (2014) · International Reviews of Immunology · doi:10.3109/08830185.2014.974748 · Cited by 23
The Role and Regulation of mTOR in T-Lymphocyte Function
O’Brien, T. F., & Zhong, X. (2012) · Archivum Immunologiae et Therapiae Experimentalis · doi:10.1007/s00005-012-0171-4 · Cited by 22
Zhang, R., Zhang, N., & Mueller, D. L. (2008) · The Journal of Immunology · doi:10.4049/jimmunol.181.8.5331 · Cited by 21
Practical strategies for suppressing hypoxia-inducible factor activity in cancer therapy
McCarty, M. F., Barroso-Aranda, J., & Contreras, F. (2010) · Medical Hypotheses · doi:10.1016/j.mehy.2009.12.022 · Cited by 21
Wang, Y., Lifshitz, L. M., Silverstein, N. J., Mintzer, E., Luk, K., StLouis, P., Brehm, M. A., Wolfe, S. A., Deeks, S. G., & Luban, J. (2023) · The EMBO Journal · doi:10.15252/embj.2023114153 · Cited by 16
Decoding the crosstalk between mevalonate metabolism and T cell function
Kennewick, K. T., & Bensinger, S. J. (2023) · Immunological Reviews · doi:10.1111/imr.13200 · Cited by 20
Allgäuer, A., Schreiner, E., Ferrazzi, F., Ekici, A. B., Gerbitz, A., Mackensen, A., & Völkl, S. (2015) · The Journal of Immunology · doi:10.4049/jimmunol.1501389 · Cited by 19
New Developments in T Cell Immunometabolism and Implications for Cancer Immunotherapy
Oberholtzer, N. P., Quinn, K. M., Chakraborty, P., & Mehrotra, S. (2022) · Cells · doi:10.3390/cells11040708 · Cited by 19
Wu, Q., Lv, Q., Liu, X., Ye, X., Cao, L., Wang, M., Li, J., Yang, Y., Li, L., & Wang, S. (2023) · Frontiers in Pharmacology · doi:10.3389/fphar.2023.1083875 · Cited by 21
TSC2 regulates tumor susceptibility to TRAIL‐mediated T‐cell killing by orchestrating mTOR signaling
Lin, C., Traets, J. J. H., Vredevoogd, D. W., Visser, N. L., & Peeper, D. S. (2023) · The EMBO Journal · doi:10.15252/embj.2022111614 · Cited by 19
Immunosuppressive Treatment of Non-infectious Uveitis: History and Current Choices
Zhao, C., & Zhang, M. (2017) · Chinese Medical Sciences Journal · doi:10.24920/j1001-9242.2007.007 · Cited by 18
Lin, J. T., Stein, E. A., Wong, M. T., Kalpathy, K. J., Su, L., Utz, P. J., Robinson, W. H., & Fathman, C. G. (2011) · Clinical Immunology · doi:10.1016/j.clim.2011.09.008 · Cited by 17
Pestina, T. I., Hargrove, P. W., Zhao, H., Mead, P. E., Smeltzer, M. P., Weiss, M. J., Wilber, A. C., & Persons, D. A. (2015) · Molecular Therapy — Methods & Clinical Development · doi:10.1038/mtm.2015.45 · Cited by 18
Engineering metabolism to modulate immunity
Kapnick, S. M., Martin, C. A., & Jewell, C. M. (2023) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2023.115122 · Cited by 18
Mechanism and effects of Zearalenone on mouse T lymphocytes activation in vitro
Cai, G., Sun, K., Wang, T., Zou, H., Gu, J., Yuan, Y., Liu, X., Liu, Z., & Bian, J. (2018) · Ecotoxicology and Environmental Safety · doi:10.1016/j.ecoenv.2018.06.055 · Cited by 17
An Integrative Network Modeling Approach to T CD4 Cell Activation
Martínez-Méndez, D., Villarreal, C., Mendoza, L., & Huerta, L. (2020) · Frontiers in Physiology · doi:10.3389/fphys.2020.00380 · Cited by 16
Walsh, Z. H., Frangieh, C. J., Kothapalli, N., Levy, J. A., Heck, C., Melms, J. C., Gejman, R. S., Shah, P., Pollard, J. M., Naik, A., et al. (2025) · Cell · doi:10.1016/j.cell.2025.05.037 · Cited by 16
The E3 ubiquitin ligase Itch restricts antigen-driven B cell responses
Moser, E. K., Roof, J., Dybas, J. M., Spruce, L. A., Seeholzer, S. H., Cancro, M. P., & Oliver, P. M. (2019) · The Journal of Experimental Medicine · doi:10.1084/jem.20181953 · Cited by 17
Ionic Regulation of T-Cell Function and Anti-Tumour Immunity
Ginefra, P., Hope, H. C., Spagna, M., Zecchillo, A., & Vannini, N. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms222413668 · Cited by 17
Dekter, H., Romijn, F. P. H. T. M., Temmink, W. P. M., PELT, J. V., de Fijter, J. W., & Smit, N. P. M. (2010) · Analytical Biochemistry · doi:10.1016/j.ab.2010.04.022 · Cited by 16
Clinical value of high expression level of CD71 in acute myeloid leukemia
Wu, B., SHI, N., Li, S., & LIU, L. (2016) · Neoplasma · doi:10.4149/neo_2016_519 · Cited by 16
SNX27 links DGKζ to the control of transcriptional and metabolic programs in T lymphocytes
Tello‐Lafoz, M., Rodríguez‐Rodríguez, C., Kinna, G., Loo, L. S., Hong, W., Collins, B. M., Teasdale, R. D., & Mérida, I. (2017) · Scientific Reports · doi:10.1038/s41598-017-16370-w · Cited by 17
Continuous Modeling of T CD4 Lymphocyte Activation and Function
Martínez-Méndez, D., Mendoza, L., Villarreal, C., & Huerta, L. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.743559 · Cited by 17
Cellular Immunobiology and Molecular Mechanisms in Alloimmunity—Pathways of Immunosuppression
Schrezenmeier, E. V., Dörner, T., Halleck, F., & Budde, K. (2023) · Transplantation · doi:10.1097/tp.0000000000004646 · Cited by 16
Effect of Inhibiting the Signal of Mammalian Target of Rapamycin on Memory T Cells
Chen, S., Liu, D., Wu, J., Xu, B., Lu, K., Zhu, W., & Chen, M. (2014) · Transplantation Proceedings · doi:10.1016/j.transproceed.2013.10.063 · Cited by 15
Ligons, D. L., Hwang, S., Waickman, A. T., Park, J., Luckey, M. A., & Park, J.-H. (2018) · Science Signaling · doi:10.1126/scisignal.aam8939 · Cited by 13
Wu, C.-E., Yu, C.-W., Chang, K., Chou, W.-H., Lu, C.-Y., Ghelfi, E., Wu, F.-C., Jan, P.-S., Huang, M.-C., Allard, P., et al. (2017) · Experimental & Molecular Medicine · doi:10.1038/emm.2017.134 · Cited by 14
Lan, T., Zeng, Q., Zhu, Y., Zheng, G., Chen, K., Jiang, W., & Lu, W. (2023) · Journal of Traditional and Complementary Medicine · doi:10.1016/j.jtcme.2023.03.009 · Cited by 13
Iron capture through CD71 drives perinatal and tumor-associated Treg expansion
Pacella, I., Grimaldos, A. P., Rossi, A., Tucci, G., Zagaglioni, M., Potenza, E., Pinna, V., Rotella, I., Cammarata, I., Cancila, V., et al. (2024) · JCI Insight · doi:10.1172/jci.insight.167967 · Cited by 15
Current treatment strategies in Hodgkin lymphomas
Copeland, A. R. M., & Younes, A. (2012) · Current Opinion in Oncology · doi:10.1097/cco.0b013e32835689a3 · Cited by 13
Tracking and treating activated T cells
Kim, N., Nadithe, V., El-Sayed, M., & Merkel, O. M. (2013) · Journal of Drug Delivery Science and Technology · doi:10.1016/s1773-2247(13)50002-5 · Cited by 13
Bex, A., Etto, T. L., Vyth‐Dreese, F. A., Blank, C. U., & Griffioen, A. W. (2012) · Current Oncology Reports · doi:10.1007/s11912-012-0229-9 · Cited by 12
Wagle, M. V., Marchingo, J. M., Howitt, J. A., Tan, S., Goodnow, C. C., & Parish, I. A. (2018) · Cell Reports · doi:10.1016/j.celrep.2018.06.060 · Cited by 12
Li, T., Yang, C.-L., Du, T., Zhang, P., Zhou, Y., Li, X.-L., Wang, C., Liu, Y., Li, H., Zhang, M., et al. (2022) · Clinical Immunology · doi:10.1016/j.clim.2022.109141 · Cited by 11
Metadata
- Authors
- Zheng, Y., Collins, S. L., Lutz, M. A., Allen, A. N., Kole, T. P., Zarek, P. E., & Powell, J. D.
- Affiliations
- Johns Hopkins University (US)
- Venue
- The Journal of Immunology
- Publisher
- Oxford University Press (OUP)
- Published
- 2007-02
- Volume
- 178
- Issue
- 4
- Pages
- 2163-2170
- ISSN
- 0022-1767 (ISSN-L)
- 1550-6606
- OpenAlex
- W1944331591
- Cited by
- 274
- References
- 37
- Citations by year
- 2026: 2 · 2025: 5 · 2024: 5 · 2023: 14 · 2022: 18 · 2021: 12 · 2020: 12 · 2019: 15 · 2018: 20 · 2017: 18 · 2016: 14 · 2015: 18 · 2014: 23 · 2013: 21 · 2012: 18
- FWCI
- 5.71
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- The Journal of Immunology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Johns Hopkins University
- National Institutes of Health (1k22ai001773-01)
- National Cancer Institute (R01CA098109, R01CA98109)
- National Institute of Allergy and Infectious Diseases (5K22AI1773)
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › PI3K/AKT/mTOR signaling in cancer
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Signaling Pathways in Disease
- Keywords
- mTOR, T cell anergy, T cell activation, T cell receptor signaling, transferrin receptor, rapamycin resistance, T cell tolerance, antigen recognition, T cell proliferation
- MeSH terms
- Animals, Gene Expression Regulation, Humans, Immunosuppressive Agents, Lymphocyte Activation, Protein Kinases, Receptors, Transferrin, T-Lymphocytes, Antigens, CD, Clonal Anergy, Antigen Presentation, Jurkat Cells, Ribosomal Protein S6 Kinases, Sirolimus, Mice, TOR Serine-Threonine Kinases
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