The DOI matches its Crossref record; 82 of the 82 references it cites were found in a registry or an index.
Metabolism in T cell activation and differentiation
Open accessAbstract
When naïve or memory T cells encounter foreign antigen along with proper co-stimulation they undergo rapid and extensive clonal expansion. In mammals, this type of proliferation is fairly unique to cells of the adaptive immune system and requires a considerable expenditure of energy and cellular resources. While research has often focused on the roles of cytokines, antigenic signals, and co-stimulation in guiding T cell responses, data indicate that, at a fundamental level, it is cellular metabolism that regulates T cell function and differentiation and therefore influences the final outcome of the adaptive immune response. This review will focus on some earlier fundamental observations regarding T cell bioenergetics and its role in regulating cellular function, as well as recent work that suggests that manipulating the immune response by targeting lymphocyte metabolism could prove useful in treatments against infection and cancer.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
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
“In accordance with Treg cell expansion during allograft rejection, there was a substantial increase in serum IL-10—a potent immunomodulatory cytokine produced by protective immune cell subsets, including Treg cells, and known to play a key role in inducing and maintaining allograft tolerance45.”
From Targeting the mTOR pathway uncouples the efficacy and toxicity of PD-1 blockade in renal transplantation (2019) · cites this paper as [45]
In the citing paper
“Regulating energy metabolism may provide a way for T cells to reversibly switch between quiescent and highly proliferative states (12).”
From Fueling Immunity: Insights into Metabolism and Lymphocyte Function (2013) · cites this paper as [12]
In the citing paper
“upon T cell activation, T cells shift from a relatively metabolically quiescent state (characterized primarily by catabolic metabolism) to a highly metabolic phenotype (characterized primarily by anabolic metabolism and the induction of aerobic glycolysis) [106].”
From Hypoxia and hypoxia-inducible factors as regulators of T cell development, differentiation, and function (2013) · cites this paper as [106]
In the citing paper
“there has been an increasing understanding of the central importance of metabolism in regulating T cell function [5, 106, 107].”
From Hypoxia and hypoxia-inducible factors as regulators of T cell development, differentiation, and function (2013) · cites this paper as [106]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Understanding the Warburg Effect: The Metabolic Requirements of Cell Proliferation
Vander Heiden, M. G., Cantley, L. C., & Thompson, C. B. (2009) · Science · doi:10.1126/science.1160809 · Cited by 16,197
Warburg, O. (1956) · Science · doi:10.1126/science.123.3191.309 · Cited by 13,425
The Biology of Cancer: Metabolic Reprogramming Fuels Cell Growth and Proliferation
DeBerardinis, R. J., Lum, J. J., Hatzivassiliou, G., & Thompson, C. B. (2008) · Cell Metabolism · doi:10.1016/j.cmet.2007.10.002 · Cited by 4,088
Rapamycin fed late in life extends lifespan in genetically heterogeneous mice
Harrison, D. E., Strong, R., Sharp, Z. D., Nelson, J. F., Astle, C. M., Flurkey, K., Nadon, N. L., Wilkinson, J. E., Frenkel, K., Carter, C. S., et al. (2009) · Nature · doi:10.1038/nature08221 · Cited by 3,766
A C. elegans mutant that lives twice as long as wild type
Kenyon, C., Chang, J., Gensch, E., Rudner, A., & Tabtiang, R. (1993) · Nature · doi:10.1038/366461a0 · Cited by 3,387
Ido expression by dendritic cells: tolerance and tryptophan catabolism
Mellor, A. L., & Munn, D. H. (2004) · Nature Reviews Immunology · doi:10.1038/nri1457 · Cited by 2,341
ATP-citrate lyase links cellular metabolism to histone acetylation
Wellen, K. E., Hatzivassiliou, G., Sachdeva, U. M., Bui, T. V., Cross, J. R., & Thompson, C. B. (2009) · Science · doi:10.1126/science.1164097 · Cited by 2,298
Molecular Signature of CD8+ T Cell Exhaustion during Chronic Viral Infection
Wherry, E. J., Ha, S.-J., Kaech, S. M., Haining, W. N., Sarkar, S., Kalia, V., Subramaniam, S., Blattman, J. N., Barber, D. L., & Ahmed, R. (2007) · Immunity · doi:10.1016/j.immuni.2007.09.006 · Cited by 2,103
Absence of S6K1 protects against age- and diet-induced obesity while enhancing insulin sensitivity
Um, S. H., Frigerio, F., Watanabe, M., Picard, F., Joaquin, M., Sticker, M., Fumagalli, S., Allegrini, P. R., Kozma, S. C., Auwerx, J., et al. (2004) · Nature · doi:10.1038/nature02866 · Cited by 1,677
mTOR regulates memory CD8 T-cell differentiation
Araki, K., Turner, A. P., Shaffer, V. O., Gangappa, S., Keller, S. A., Bachmann, M. F., Larsen, C. P., & Ahmed, R. (2009) · Nature · doi:10.1038/nature08155 · Cited by 1,575
Flagged first, then by citations
Cited by
Sorted by citations
Shi, L. Z., Wang, R., Huang, G., Vogel, P., Neale, G., Green, D. R., & Chi, H. (2011) · Journal of Experimental Medicine · doi:10.1084/jem.20110278 · Cited by 1,803
Metabolic Pathways in Immune Cell Activation and Quiescence
Pearce, E. L., & Pearce, E. J. (2013) · Immunity · doi:10.1016/j.immuni.2013.04.005 · Cited by 1,692
Self-citationTranscriptional control of effector and memory CD8+ T cell differentiation
Kaech, S. M., & Cui, W. (2012) · Nature Reviews Immunology · doi:10.1038/nri3307 · Cited by 1,628
Fueling Immunity: Insights into Metabolism and Lymphocyte Function
Pearce, E. L., Poffenberger, M. C., Chang, C.-H., & Jones, R. G. (2013) · Science · doi:10.1126/science.1242454 · Cited by 1,363
Self-citationSena, L. A., Li, S., Jairaman, A., Prakriya, M., Ezponda, T., Hildeman, D. A., Wang, C.-R., Schumacker, P. T., Licht, J. D., Perlman, H., et al. (2013) · Immunity · doi:10.1016/j.immuni.2012.10.020 · Cited by 1,338
Cell-intrinsic lysosomal lipolysis is essential for alternative activation of macrophages
Huang, S. C., Everts, B., Ivanova, Y., O’Sullivan, D., Nascimento, M., Smith, A. M., Beatty, W. L., Love-Gregory, L. D., Lam, W. Y., O’Neill, C. M., et al. (2014) · Nature Immunology · doi:10.1038/ni.2956 · Cited by 1,256
Self-citationRegulation and function of mTOR signalling in T cell fate decisions
Chi, H. (2012) · Nature Reviews Immunology · doi:10.1038/nri3198 · Cited by 1,035
Regulation of Immune Responses by mTOR
Powell, J. D., Pollizzi, K. N., Heikamp, E. B., & Horton, M. R. (2012) · Annual Review of Immunology · doi:10.1146/annurev-immunol-020711-075024 · Cited by 836
O’Sullivan, D., van der Windt, G. J. W., Huang, S. C.-C., Curtis, J. D., Chang, C.-H., Buck, M. D., Qiu, J., Smith, A. M., Lam, W. Y., DiPlato, L. M., et al. (2014) · Immunity · doi:10.1016/j.immuni.2014.06.005 · Cited by 790
Self-citationPaths to stemness: building the ultimate antitumour T cell
Gattinoni, L., Klebanoff, C. A., & Restifo, N. P. (2012) · Nature reviews. Cancer · doi:10.1038/nrc3322 · Cited by 616
Metabolic switching and fuel choice during T‐cell differentiation and memory development
van der Windt, G. J. W., & Pearce, E. L. (2012) · Immunological Reviews · doi:10.1111/j.1600-065x.2012.01150.x · Cited by 563
Self-citationHow Tolerogenic Dendritic Cells Induce Regulatory T Cells
Maldonado, R., & von Andrian, U. H. (2010) · Advances in immunology · doi:10.1016/b978-0-12-380995-7.00004-5 · Cited by 568
The Mammalian Target of Rapamycin: Linking T Cell Differentiation, Function, and Metabolism
Powell, J. D., & Delgoffe, G. M. (2010) · Immunity · doi:10.1016/j.immuni.2010.09.002 · Cited by 503
Macrophages and lipid metabolism
Remmerie, A., & Scott, C. L. (2018) · Cellular Immunology · doi:10.1016/j.cellimm.2018.01.020 · Cited by 451
Vitamin D and Immune Regulation: Antibacterial, Antiviral, Anti‐Inflammatory
Bishop, E. L., Ismailova, A., Dimeloe, S., Hewison, M., & White, J. H. (2020) · JBMR Plus · doi:10.1002/jbm4.10405 · Cited by 430
Exhaustion and senescence: two crucial dysfunctional states of T cells in the tumor microenvironment
Zhao, Y., Shao, Q., & Peng, G. (2020) · Cellular & Molecular Immunology · doi:10.1038/s41423-019-0344-8 · Cited by 382
Teriflunomide and Its Mechanism of Action in Multiple Sclerosis
Bar‐Or, A., Pachner, A. R., Menguy-Vacheron, F., Kaplan, J. M., & Wiendl, H. (2014) · Drugs · doi:10.1007/s40265-014-0212-x · Cited by 372
Yang, Z., Fujii, H., Mohan, S. V., Goronzy, J. J., & Weyand, C. M. (2013) · Journal of Experimental Medicine · doi:10.1084/jem.20130252 · Cited by 334
ROS-induced autophagy in cancer cells assists in evasion from determinants of immunogenic cell death
Garg, A. D., Dudek, A. M., Ferreira, G. B., Verfaillie, T., Vandenabeele, P., Krysko, D. V., Mathieu, C., & Agostinis, P. (2013) · Autophagy · doi:10.4161/auto.25399 · Cited by 305
The Role of Iron Regulation in Immunometabolism and Immune-Related Disease
Cronin, S. J. F., Woolf, C. J., Weiss, G., & Penninger, J. M. (2019) · Frontiers in Molecular Biosciences · doi:10.3389/fmolb.2019.00116 · Cited by 299
Yang, K., Neale, G. A. M., Green, D. R., He, W., & Chi, H. (2011) · Nature Immunology · doi:10.1038/ni.2068 · Cited by 302
The burden of obesity on infectious disease
Karlsson, E. A., & Beck, M. A. (2010) · Experimental Biology and Medicine · doi:10.1258/ebm.2010.010227 · Cited by 296
Schenk, U., Frascoli, M., Proietti, M., Geffers, R., Traggiai, E., Buer, J., Ricordi, C., Westendorf, A. M., & Grassi, F. (2011) · Science Signaling · doi:10.1126/scisignal.2001270 · Cited by 303
Beier, U. H., Angelin, A., Akimova, T., Wang, L., Liu, Y., Xiao, H., Koike, M. A., Hancock, S. A., Bhatti, T. R., Han, R., et al. (2015) · The FASEB Journal · doi:10.1096/fj.14-268409 · Cited by 282
Court, A. C., Le‐Gatt, A., Luz‐Crawford, P., Parra, E., Aliaga‐Tobar, V., Bátiz, L. F., Contreras, R. A., Ortúzar, M. I., Kurte, M., Elizondo‐Vega, R., et al. (2020) · The EMBO Reports · doi:10.15252/embr.201948052 · Cited by 259
Li, L., Liu, X., Sanders, K. L., Edwards, J. L., Ye, J., Si, F., Gao, A., Huang, L., Hsueh, E. C., Ford, D. A., et al. (2018) · Cell Metabolism · doi:10.1016/j.cmet.2018.09.020 · Cited by 248
Temperature Matters! And Why It Should Matter to Tumor Immunologists
Repasky, E. A., Evans, S. S., & Dewhirst, M. W. (2013) · Cancer Immunology Research · doi:10.1158/2326-6066.cir-13-0118 · Cited by 250
Tumor stroma: a complexity dictated by the hypoxic tumor microenvironment
Casazza, A., Conza, G. D., Wenes, M., Finisguerra, V., Deschoemaeker, S., & Mazzone, M. (2013) · Oncogene · doi:10.1038/onc.2013.121 · Cited by 254
Comito, G., Iscaro, A., Bacci, M., Morandi, A., Ippolito, L., Parri, M., Montagnani, I., Raspollini, M. R., Serni, S., Simeoni, L., et al. (2019) · Oncogene · doi:10.1038/s41388-019-0688-7 · Cited by 257
NK cells regulating T cell responses: mechanisms and outcome
Crouse, J., Xu, H. C., Lang, P. A., & Oxenius, A. (2014) · Trends in Immunology · doi:10.1016/j.it.2014.11.001 · Cited by 247
McNamee, E. N., Korns Johnson, D., Homann, D., & Clambey, E. T. (2013) · Immunologic Research · doi:10.1007/s12026-012-8349-8 · Cited by 234
Metabolic control of the Treg/Th17 axis
Barbi, J. J., Pardoll, D. M., & Pan, F. (2013) · Immunological Reviews · doi:10.1111/imr.12029 · Cited by 227
Cytotoxic T-cells mediate exercise-induced reductions in tumor growth
Rundqvist, H., Veliça, P., Barbieri, L., Gameiro, P. A., Bargiela, D., Gojkovic, M., Mijwel, S., Reitzner, S. M., Wulliman, D., Ahlstedt, E., et al. (2020) · eLife · doi:10.7554/elife.59996 · Cited by 216
“Given that metabolism and T-cell differentiation are tightly linked (O’Neill et al., 2016; Pearce, 2010), we next sought to determine whether any of the central carbon metabolites generated during exercise could be a determining factor in the action of CD8+ T cells in this process.”
BackgroundA Tale of Two Glutaminases: Homologous Enzymes with Distinct Roles in Tumorigenesis
Katt, W. P., Lukey, M. J., & Cerione, R. A. (2017) · Future Medicinal Chemistry · doi:10.4155/fmc-2016-0190 · Cited by 179
Metabolic influence on macrophage polarization and pathogenesis
Thapa, B., & Lee, K. (2019) · BMB Reports · doi:10.5483/bmbrep.2019.52.6.140 · Cited by 176
Mitochondrial function, ornamentation, and immunocompetence
Koch, R. E., Josefson, C. C., & Hill, G. E. (2016) · Biological reviews/Biological reviews of the Cambridge Philosophical Society · doi:10.1111/brv.12291 · Cited by 176
Targeting metabolic reprogramming by influenza infection for therapeutic intervention
Smallwood, H. S., Duan, S., Morfouace, M., Rezinciuc, S., Shulkin, B. L., Shelat, A., Zink, E. E., Milasta, S., Bajracharya, R., Oluwaseum, A. J., et al. (2017) · Cell Reports · doi:10.1016/j.celrep.2017.04.039 · Cited by 171
Huang, L., Xu, H., & Peng, G. (2018) · Cellular and Molecular Immunology · doi:10.1038/cmi.2018.4 · Cited by 170
In vivo imaging of nanoparticle-labeled CAR T cells
Kiru, L., Zlitni, A., Tousley, A. M., Dalton, G. N., Wu, W. E., Lafortune, F., Liu, A., Cunanan, K. M., Nejadnik, H., Sulchek, T., et al. (2022) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2102363119 · Cited by 152
Glycolysis inhibition as a cancer treatment and its role in an anti-tumour immune response
Gill, K. S., Fernandes, P., O’Donovan, T. R., McKenna, S. L., Doddakula, K., Power, D. G., Soden, D. M., & Forde, P. F. (2016) · Biochimica et Biophysica Acta (BBA) - Reviews on Cancer · doi:10.1016/j.bbcan.2016.06.005 · Cited by 149
Melnik, B. C. (2012) · Dermato-Endocrinology · doi:10.4161/derm.19828 · Cited by 151
Fueling the flame: bioenergy couples metabolism and inflammation
Liu, T. F., Brown, C. M., Gazzar, M. E., McPhail, L. C., Millet, P., Rao, A., Vachharajani, V., Yoza, B. K., & McCall, C. E. (2012) · Journal of Leukocyte Biology · doi:10.1189/jlb.0212078 · Cited by 147
Mandarano, A. H., Maya, J., Giloteaux, L., Peterson, D. L., Maynard, M., Gottschalk, C. G., & Hanson, M. R. (2019) · Journal of Clinical Investigation · doi:10.1172/jci132185 · Cited by 149
Effector T cells require fatty acid metabolism during murine graft-versus-host disease
Byersdorfer, C. A., Tkachev, V., Opipari, A. W., Goodell, S., Swanson, J. B., Sandquist, S., Glick, G. D., & Ferrara, J. L. M. (2013) · Blood · doi:10.1182/blood-2013-04-495515 · Cited by 141
Sun, Y., Tian, T., Gao, J., Liu, X., Hou, H., Cao, R., Li, B., Quan, M., & Guo, L. (2016) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2016.01.014 · Cited by 148
Choi, I. Y., Lee, C., & Longo, V. D. (2017) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2017.01.042 · Cited by 133
Sirtuin deacylases: a molecular link between metabolism and immunity
Preyat, N., & Léo, O. (2013) · Journal of Leukocyte Biology · doi:10.1189/jlb.1112557 · Cited by 134
Induction of T cell anergy: integration of environmental cues and infectious tolerance
Chappert, P., & Schwartz, R. H. (2010) · Current Opinion in Immunology · doi:10.1016/j.coi.2010.08.005 · Cited by 143
Wei, F., Wang, D., Wei, J., Tang, N., Tang, L. M., Xiong, F., Guo, C. J., Zhou, M., Li, X., Li, G., et al. (2020) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-020-03581-0 · Cited by 128
Uncoupling T‐cell expansion from effector differentiation in cell‐based immunotherapy
Crompton, J. G., Sukumar, M., & Restifo, N. P. (2013) · Immunological Reviews · doi:10.1111/imr.12135 · Cited by 123
Hamilton, K. S., Phong, B. L., Corey, C. G., Cheng, J., Gorentla, B. K., Zhong, X., Shiva, S., & Kane, L. (2014) · Science Signaling · doi:10.1126/scisignal.2005169 · Cited by 124
Liu, X., Hoft, D. F., & Peng, G. (2020) · Journal of Clinical Investigation · doi:10.1172/jci133679 · Cited by 116
mTOR and metabolic pathways in T cell quiescence and functional activation
Yang, K., & Chi, H. (2012) · Seminars in Immunology · doi:10.1016/j.smim.2012.12.004 · Cited by 119
Esfahani, K., Al-Aubodah, T.-A., Thebault, P., Lapointe, R., Hudson, M., Johnson, N. A., Baran, D., Bhulaiga, N., Takano, T., Cailhier, J.-F., et al. (2019) · Nature Communications · doi:10.1038/s41467-019-12628-1 · Cited by 109
The Insulin Receptor Plays a Critical Role in T Cell Function and Adaptive Immunity
Fischer, H. J., Sie, C., Schumann, E., Witte, A., Dressel, R., van den Brandt, J., & Reichardt, H. M. (2017) · The Journal of Immunology · doi:10.4049/jimmunol.1601011 · Cited by 111
Tao, J.-H., Barbi, J. J., & Pan, F. (2015) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00204.2015 · Cited by 104
mTOR and lymphocyte metabolism
Zeng, H., & Chi, H. (2013) · Current Opinion in Immunology · doi:10.1016/j.coi.2013.05.002 · Cited by 101
Ananieva, E. A., Patel, C. H., Drake, C. H., Powell, J. D., & Hutson, S. M. (2014) · Journal of Biological Chemistry · doi:10.1074/jbc.m114.554113 · Cited by 101
Ledderose, C., Bao, Y., Lidicky, M., Zipperle, J., Li, L., Strasser, K., Shapiro, N. I., & JUNGER, W. G. (2014) · Journal of Biological Chemistry · doi:10.1074/jbc.m114.575308 · Cited by 100
Anzengruber, F., Avci, P., de Freitas, L. F., & Hamblin, M. R. (2015) · Photochemical & Photobiological Sciences · doi:10.1039/c4pp00455h · Cited by 97
Previte, D. M., O’Connor, E. C., Novak, E. A., Martins, C. P., Mollen, K. P., & Piganelli, J. D. (2017) · PLoS ONE · doi:10.1371/journal.pone.0175549 · Cited by 96
Cutting Edge: Hypoxia-Inducible Factor 1 Negatively Regulates Th1 Function
Shehade, H., Acolty, V., Moser, M., & Oldenhove, G. (2015) · The Journal of Immunology · doi:10.4049/jimmunol.1402552 · Cited by 98
Wu, H., Huang, H., & Zhao, Y. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1211221 · Cited by 103
Fraser, K. A., Schenkel, J. M., Jameson, S. C., Vezys, V., & Masopust, D. (2013) · Immunity · doi:10.1016/j.immuni.2013.07.003 · Cited by 92
LKB 1 and AMPK : central regulators of lymphocyte metabolism and function
Blagih, J., Krawczyk, C. M., & Jones, R. G. (2012) · Immunological Reviews · doi:10.1111/j.1600-065x.2012.01157.x · Cited by 91
Changing the energy of an immune response.
Delmastro-Greenwood, M. M., & Piganelli, J. D. (2013) · Europe PMC (PubMed Central) · Cited by 84
TCR signaling requirements for activating T cells and for generating memory
Zehn, D., King, C. G., Bevan, M. J., & Palmer, E. (2012) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-012-0965-x · Cited by 86
Vignali, D., Cantarelli, E., Bordignon, C., Canu, A., Citro, A., Annoni, A., Piemonti, L., & Monti, P. (2018) · Diabetes · doi:10.2337/db17-1390 · Cited by 80
Shen, H., Ojo, O. A., Ding, H., Mullen, L. J., Xing, C., Hossain, M. I., Yassin, A., Shi, V. Y., Lewis, Z., Podgórska, E., et al. (2024) · Nature Communications · doi:10.1038/s41467-024-53593-8 · Cited by 90
Primer on tumor immunology and cancer immunotherapy
Harris, T. J., & Drake, C. G. (2013) · Journal for ImmunoTherapy of Cancer · doi:10.1186/2051-1426-1-12 · Cited by 78
STING agonism turns human T cells into interferon‐producing cells but impedes their functionality
Kühl, N., Linder, A., Philipp, N., Nixdorf, D., Fischer, H., Veth, S., Kuut, G., Xu, T. T., Theurich, S., Carell, T., et al. (2023) · EMBO Reports · doi:10.15252/embr.202255536 · Cited by 72
Intestinal Dysbiosis and Tryptophan Metabolism in Autoimmunity
Brown, J., Robusto, B. A., & Morel, L. M. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.01741 · Cited by 68
Glycolysis Inhibition Induces Functional and Metabolic Exhaustion of CD4+ T Cells in Type 1 Diabetes
Martins, C. P., New, L. A., O’Connor, E. C., Previte, D. M., Cargill, K. R., Tse, I., Sims‐Lucas, S., & Piganelli, J. D. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.669456 · Cited by 70
Mu, P., Huo, J., Li, X., Li, W., Li, X., Ao, J., & Chen, X. (2022) · The Journal of Immunology · doi:10.4049/jimmunol.2100764 · Cited by 69
Targeting cancer metabolic pathways for improving chemotherapy and immunotherapy
Luo, Z., Eichinger, K. M., Zhang, A., & Li, S. (2023) · Cancer Letters · doi:10.1016/j.canlet.2023.216396 · Cited by 71
Metabolic regulation of TH17 cells
Shen, H., & Shi, L. Z. (2019) · Molecular Immunology · doi:10.1016/j.molimm.2019.03.005 · Cited by 72
Cellular Metabolism on T-Cell Development and Function
Chen, H., Yang, T., Zhu, L., & Zhao, Y. X. (2014) · International Reviews of Immunology · doi:10.3109/08830185.2014.902452 · Cited by 68
Palmer, C. S., Duette, G., Wagner, M. C. E., Henstridge, D. C., Saleh, S., Pereira, C. F., Zhou, J., Simar, D., Lewin, S. R., Ostrowski, M., et al. (2017) · FEBS Letters · doi:10.1002/1873-3468.12843 · Cited by 72
IL-7 Restores T Lymphocyte Immunometabolic Failure in Septic Shock Patients through mTOR Activation
Venet, F., Demaret, J., Blaise, B. J., Rouget, C., Girardot, T., Idealisoa, E., Rimmele, T. R., Mallet, F., Lepape, A., Textoris, J., et al. (2017) · The Journal of Immunology · doi:10.4049/jimmunol.1700127 · Cited by 76
Mitochondria in monocytes and macrophages-implications for translational and basic research
Ravi, S., Mitchell, T., Kramer, P. A., Chacko, B. K., & Darley-Usmar, V. M. (2014) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2014.05.019 · Cited by 69
Oxygen regulation of TET enzymes
Matulevičiūtė, R., Cunha, P. P., Johnson, R. S., & Foskolou, I. P. (2021) · FEBS Journal · doi:10.1111/febs.15695 · Cited by 69
Hegedus, A., Williamson, M. K., Khan, M. B., Zeidler, J. D., Poian, A. T. D., El‐Bacha, T., Struys, E. A., & Huthoff, H. (2017) · AIDS Research and Human Retroviruses · doi:10.1089/aid.2017.0165 · Cited by 65
Waickman, A. T., & Powell, J. D. (2012) · The Journal of Immunology · doi:10.4049/jimmunol.1103143 · Cited by 64
Metabolic Adaptations of CD4+ T Cells in Inflammatory Disease
Dumitru, C., Kabat, A. M., & Maloy, K. J. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.00540 · Cited by 65
T Cell Co-inhibitory Receptors-Functions and Signalling Mechanisms
Thaventhiran, T. (2013) · Journal of Clinical & Cellular Immunology · doi:10.4172/2155-9899.s12-005 · Cited by 64
Adipose tissue at the nexus of systemic and cellular immunometabolism
Kohlgruber, A. C., LaMarche, N. M., & Lynch, L. (2016) · Seminars in Immunology · doi:10.1016/j.smim.2016.09.005 · Cited by 60
Engineering self-assembled materials to study and direct immune function
Tostanoski, L. H., & Jewell, C. M. (2017) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2017.03.005 · Cited by 60
Braga, F. A. V., Hertoghs, K. M. L., van Lier, R. A. W., & van Gisbergen, K. P. J. M. (2015) · European Journal of Immunology · doi:10.1002/eji.201545495 · Cited by 56
The effect of immunosuppressive molecules on T-cell metabolic reprogramming
Fernández-Ramos, A. A., Poindessous, V., Marchetti, C., Pallet, N., & Loriot, M. (2016) · Biochimie · doi:10.1016/j.biochi.2016.04.016 · Cited by 53
Sun, C., Liang, H., Zhao, Y., Li, S., Li, X., Yuan, X., Cheng, G., Zhang, Y., Liu, M., Guan, Y., et al. (2022) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2022.115913 · Cited by 52
Lapel, M., Weston, P., Strassheim, D., Karoor, V., Burns, N., Lyubchenko, T. A., Pauček, P., Stenmark, K. R., & Gerasimovskaya, E. V. (2016) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00250.2016 · Cited by 53
Song, B., Wang, Z., Liu, Y., Xu, S., Huang, G., Xiong, Y., Zhang, S., Xu, L., Deng, X., & Guan, S. (2014) · PLoS ONE · doi:10.1371/journal.pone.0096502 · Cited by 51
Epigenetic coordination of acute systemic inflammation: potential therapeutic targets
Vachharajani, V., Liu, T., & McCall, C. E. (2014) · Expert Review of Clinical Immunology · doi:10.1586/1744666x.2014.943192 · Cited by 52
Remodelling of primary human CD4+T cell plasma membrane order byn-3 PUFA
Fan, Y.-Y., Fuentes, N. R., Hou, T. Y., Barhoumi, R., Li, X. C., Deutz, N. E. P., ENGELEN, M. P. K. J., McMurray, D. N., & Chapkin, R. S. (2017) · British Journal Of Nutrition · doi:10.1017/s0007114517003385 · Cited by 53
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
Mitochondrial functionality and metabolism in T cells from progressive multiple sclerosis patients
Biasi, S. D., Simone, A. M., Bianchini, E., Tartaro, D. L., Pecorini, S., Nasi, M., Patergnani, S., Carnevale, G., Gibellini, L., Ferraro, D., et al. (2019) · European Journal of Immunology · doi:10.1002/eji.201948223 · 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
Reactive oxygen species formation and its effect on CD4+ T cell-mediated inflammation
Shu, P., Liang, H., Zhang, J., Lin, Y., Chen, W., & Zhang, D. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1199233 · Cited by 58
Mousset, C. M., Hobo, W. A., Ji, Y., Fredrix, H., Giorgi, V. D., Allison, R. D., Kester, M. G. D., Falkenburg, J. H. F., Schaap, N. P., Jansen, J. H., et al. (2018) · OncoImmunology · doi:10.1080/2162402x.2018.1488565 · Cited by 51
Fernández-García, J., Franco, F., Parik, S., Altea‐Manzano, P., Pane, A. A., Broekaert, D., Elsen, J. V., Conza, G. D., Vermeire, I., Schalley, T., et al. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.111639 · Cited by 53
Metadata
- Authors
- Pearce, E. L.
- Affiliations
- Trudeau Institute (US)
- Corresponding author
- Pearce, Erika L
- ORCID
- Pearce, Erika L
- Venue
- Current Opinion in Immunology
- Publisher
- Elsevier BV
- Published
- 2010-06
- Volume
- 22
- Issue
- 3
- Pages
- 314-320
- ISSN
- 0952-7915 (ISSN-L)
- PMC
- PMC4486663
- OpenAlex
- W1970662865
- Cited by
- 314
- References
- 82
- Citations by year
- 2026: 27 · 2025: 25 · 2024: 20 · 2023: 18 · 2022: 17 · 2021: 17 · 2020: 23 · 2019: 20 · 2018: 12 · 2017: 24 · 2016: 15 · 2015: 19 · 2014: 21 · 2013: 24 · 2012: 22
- FWCI
- 1.43
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Current Opinion in Immunology (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- MPG.PuRe (Max Planck Society) (submittedVersion, other-oa)
- Funders
- Emerald Foundation
- National Cancer Institute (R01CA181125)
- National Institute of Allergy and Infectious Diseases (R01AI091965)
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Cancer, Hypoxia, and Metabolism
- Life Sciences › Immunology and Microbiology › Immunology › Immune cells in cancer
- Keywords
- T cell metabolism, T cell activation, T cell differentiation, bioenergetics, clonal expansion, costimulation, memory T cells
- MeSH terms
- Animals, Cell Differentiation, Glucose, Humans, Lymphocyte Activation, T-Lymphocytes, Lipid Metabolism, Mice
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review