The DOI matches its Crossref record; 49 of the 49 references it cites were found in a registry or an index.
Quantitative analysis of T cell proteomes and environmental sensors during T cell differentiation
Open accessAbstract
Quantitative mass spectrometry reveals how CD4+ and CD8+ T cells restructure proteomes in response to antigen and mammalian target of rapamycin complex 1 (mTORC1). Analysis of copy numbers per cell of >9,000 proteins provides new understanding of T cell phenotypes, exposing the metabolic and protein synthesis machinery and environmental sensors that shape T cell fate. We reveal that lymphocyte environment sensing is controlled by immune activation, and that CD4+ and CD8+ T cells differ in their intrinsic nutrient transport and biosynthetic capacity. Our data also reveal shared and divergent outcomes of mTORC1 inhibition in naïve versus effector T cells: mTORC1 inhibition impaired cell cycle progression in activated naïve cells, but not effector cells, whereas metabolism was consistently impacted in both populations. This study provides a comprehensive map of naïve and effector T cell proteomes, and a resource for exploring and understanding T cell phenotypes and cell context effects of mTORC1.
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?
The check wasn’t confident either way, so it gives no verdict — never disputed.
In the citing paper
“Naïve T cells express non-detectable levels of CDK8, which are upregulated upon T cells activation and differentiation (Howden et al., 2019).”
From CDK8 fine-tunes IL-6 transcriptional activities by limiting STAT3 resident time at the gene loci (2020) · cites this paper as Howden et al., 2019
Experimental — accuracy not yet measured
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
Cox, J., & Mann, M. (2008) · Nature Biotechnology · doi:10.1038/nbt.1511 · Cited by 14,855
Andromeda: A Peptide Search Engine Integrated into the MaxQuant Environment
Cox, J., Neuhauser, N., Michalski, A., Scheltema, R. A., Olsen, J. V., & Mann, M. (2011) · Journal of Proteome Research · doi:10.1021/pr101065j · Cited by 5,503
The integrated stress response
Pakos‐Zebrucka, K., Koryga, I., Mnich, K., Ljujic, M., Samali, A., & Gorman, A. M. (2016) · The EMBO Reports · doi:10.15252/embr.201642195 · Cited by 2,659
L-Arginine Modulates T Cell Metabolism and Enhances Survival and Anti-tumor Activity
Geiger, R., Rieckmann, J. C., Wolf, T., Basso, C., Feng, Y., Fuhrer, T., Kogadeeva, M., Picotti, P., Meissner, F., Mann, M., et al. (2016) · Cell · doi:10.1016/j.cell.2016.09.031 · Cited by 1,775
Barnden, M., Allison, J., Heath, W. R., & Carbone, F. (1998) · Immunology and Cell Biology · doi:10.1046/j.1440-1711.1998.00709.x · Cited by 1,491
Sestrin2 is a leucine sensor for the mTORC1 pathway
Wolfson, R. L., Chantranupong, L., Saxton, R. A., Shen, K., Scaria, S. M., Cantor, J. R., & Sabatini, D. M. (2016) · Science · doi:10.1126/science.aab2674 · Cited by 1,306
Pause, A., Belsham, G. J., Gingras, A., Donzé, O., Lin, T.-A., Lawrence, J. C., & Sonenberg, N. (1994) · Nature · doi:10.1038/371762a0 · Cited by 1,242
Ultrasensitive proteome analysis using paramagnetic bead technology
Hughes, C. S., Föehr, S., Garfield, D. A., Furlong, E. E. M., Steinmetz, L. M., & Krijgsveld, J. (2014) · Molecular Systems Biology · doi:10.15252/msb.20145625 · Cited by 1,226
Bar-Peled, L., Chantranupong, L., Cherniack, A. D., Chen, W. W., Ottina, K. A., Grabiner, B. C., Spear, E. D., Carter, S. L., Meyerson, M., & Sabatini, D. M. (2013) · Science · doi:10.1126/science.1232044 · Cited by 1,080
Tolerance induction in double specific T-cell receptor transgenic mice varies with antigen
Pircher, H., Bürki, K., Lang, R., Hengartner, H., & Zinkernagel, R. M. (1989) · Nature · doi:10.1038/342559a0 · Cited by 1,019
Cited by
Sorted by citations
Amino Assets: How Amino Acids Support Immunity
Kelly, B. L., & Pearce, E. L. (2020) · Cell Metabolism · doi:10.1016/j.cmet.2020.06.010 · Cited by 666
Immunometabolic Interplay in the Tumor Microenvironment
Kaymak, I., Williams, K. S., Cantor, J. R., & Jones, R. G. (2020) · Cancer Cell · doi:10.1016/j.ccell.2020.09.004 · Cited by 333
Single-cell metabolic profiling of human cytotoxic T cells
Hartmann, F. J., Mrdjen, D., McCaffrey, E., Glass, D. R., Greenwald, N. F., Bharadwaj, A., Khair, Z., Verberk, S. G. S., Baranski, A., Baskar, R., et al. (2020) · Nature Biotechnology · doi:10.1038/s41587-020-0651-8 · Cited by 305
Metabolic adaptation of lymphocytes in immunity and disease
Chapman, N. M., & Chi, H. (2022) · Immunity · doi:10.1016/j.immuni.2021.12.012 · Cited by 316
Rethinking peripheral T cell tolerance: checkpoints across a T cell’s journey
ElTanbouly, M. A., & Noelle, R. J. (2020) · Nature reviews. Immunology · doi:10.1038/s41577-020-00454-2 · Cited by 282
Signaling networks in immunometabolism
Saravia, J., Raynor, J. L., Chapman, N. M., Lim, S. A., & Chi, H. (2020) · Cell Research · doi:10.1038/s41422-020-0301-1 · Cited by 258
Dynamics in protein translation sustaining T cell preparedness
Wolf, T., Jin, W., Zoppi, G., Vogel, I. A., Akhmedov, M., Bleck, C. K. E., Beltraminelli, T., Rieckmann, J. C., Ramirez, N. J., Benevento, M., et al. (2020) · Nature Immunology · doi:10.1038/s41590-020-0714-5 · Cited by 225
Marchingo, J. M., Sinclair, L. V., Howden, A. J. M., & Cantrell, D. A. (2020) · eLife · doi:10.7554/elife.53725 · Cited by 202
Self-citationmTOR signaling at the crossroads of environmental signals and T‐cell fate decisions
Huang, H., Long, L., Zhou, P., Chapman, N. M., & Chi, H. (2020) · Immunological Reviews · doi:10.1111/imr.12845 · Cited by 193
Nicolini, A., & Ferrari, P. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1353787 · Cited by 209
Protein synthesis, degradation, and energy metabolism in T cell immunity
Marchingo, J. M., & Cantrell, D. A. (2022) · Cellular & Molecular Immunology · doi:10.1038/s41423-021-00792-8 · Cited by 169
Self-citationIron Deficiency in Heart Failure: Mechanisms and Pathophysiology
Alnuwaysir, R. I. S., Hoes, M. F., van Veldhuisen, D. J., van der Meer, P., & Beverborg, N. G. (2021) · Journal of Clinical Medicine · doi:10.3390/jcm11010125 · Cited by 175
Sun, D.-Y., Hu, Y.-J., Li, X., Peng, J., Dai, Z., & Wang, S. (2024) · International Immunopharmacology · doi:10.1016/j.intimp.2024.113392 · Cited by 162
Hepcidin-Mediated Hypoferremia Disrupts Immune Responses to Vaccination and Infection
Frost, J. N., Tan, T. K., Abbas, M., Wideman, S. K., Bonadonna, M., Stoffel, N. U., Wray, K., Kronsteiner, B., Smits, G. P., Campagna, D. R., et al. (2020) · Med · doi:10.1016/j.medj.2020.10.004 · Cited by 127
Mitochondrial translation is required for sustained killing by cytotoxic T cells
Lisci, M., Barton, P. R., Randzavola, L. O., Ma, C. Y., Marchingo, J. M., Cantrell, D. A., Paupe, V., Prudent, J., Stinchcombe, J. C., & Griffiths, G. M. (2021) · Science · doi:10.1126/science.abe9977 · Cited by 122
Self-citationMetabolic Interdependency of Th2 Cell-Mediated Type 2 Immunity and the Tumor Microenvironment
Schreiber, S., Hammers, C. M., Kaasch, A. J., Schraven, B. L., Dudeck, A., & Kahlfuß, S. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.632581 · Cited by 113
Ryan, D. G., Knatko, E. V., Casey, A. M., Hukelmann, J. L., Naidu, S. D., Brenes, A. J., Ekkunagul, T., Baker, C. P., Higgins, M., Tronci, L., et al. (2021) · iScience · doi:10.1016/j.isci.2022.103827 · Cited by 112
Self-citationRegulation of CD8+ T memory and exhaustion by the mTOR signals
Chen, Y., Xu, Z., Sun, H., Ouyang, X., Han, Y., Yu, H., Wu, N., Xie, Y., & Su, B. (2023) · Cellular and Molecular Immunology · doi:10.1038/s41423-023-01064-3 · Cited by 101
Nutrients: Signal 4 in T cell immunity
Raynor, J. L., & Chi, H. (2024) · The Journal of Experimental Medicine · doi:10.1084/jem.20221839 · Cited by 99
Targeting immunometabolism against acute lung injury
Ning, L., Shishi, Z., Wang, B., & Huiqing, L. (2023) · Clinical Immunology · doi:10.1016/j.clim.2023.109289 · Cited by 92
LINE1 are spliced in non-canonical transcript variants to regulate T cell quiescence and exhaustion
Marasca, F., Sinha, S., Vadalà, R., Polimeni, B., Ranzani, V., Paraboschi, E. M., Burattin, F. V., Ghilotti, M., Crosti, M., Negri, M. L., et al. (2022) · Nature Genetics · doi:10.1038/s41588-021-00989-7 · Cited by 87
Fueling T-cell Antitumor Immunity: Amino Acid Metabolism Revisited
Han, C., Ge, M., Ho, P., & Zhang, L. (2021) · Cancer Immunology Research · doi:10.1158/2326-6066.cir-21-0459 · Cited by 86
Single Cell Glucose Uptake Assays: A Cautionary Tale
Sinclair, L. V., Barthelemy, C., & Cantrell, D. A. (2020) · Immunometabolism · doi:10.20900/immunometab20200029 · Cited by 72
Self-citationUpregulation of RNA cap methyltransferase RNMT drives ribosome biogenesis during T cell activation
Galloway, A., Kaskar, A., Ditsova, D., Atrih, A., Yoshikawa, H., Gómez-Moreira, C., Suska, O., Warmiński, M., Grzela, R., Lamond, A. I., et al. (2021) · Nucleic Acids Research · doi:10.1093/nar/gkab465 · Cited by 74
Self-citationCD47 masks pro-phagocytic ligands in cis on tumor cells to suppress antitumor immunity
Tang, Z.-H., Zhong, M., Qian, J., Galindo, C. C., Davidson, D., Li, J., Zhao, Y., Hui, E., & Veillette, A. (2023) · Nature Immunology · doi:10.1038/s41590-023-01671-2 · Cited by 66
Mori, D., Grégoire, C., Voisinne, G., Celis‐Gutierrez, J., Aussel, R., Girard, L., Camus, M., Marcellin, M., Argenty, J., Burlet‐Schiltz, O., et al. (2020) · The Journal of Experimental Medicine · doi:10.1084/jem.20201011 · Cited by 65
Tumor-induced metabolic immunosuppression: Mechanisms and therapeutic targets
Ricci, J. (2025) · Cell Reports · doi:10.1016/j.celrep.2024.115206 · Cited by 73
Systems-based approaches to study immunometabolism
Purohit, V., Wagner, A., Yosef, N., & Kuchroo, V. K. (2022) · Cellular and Molecular Immunology · doi:10.1038/s41423-021-00783-9 · Cited by 64
Glutarate regulates T cell metabolism and anti-tumour immunity
Minogue, E., Cunha, P. P., Wadsworth, B. J., Grice, G. L., Sah‐Teli, S. K., Hughes, R. J. F., Bargiela, D., Quaranta, A., Zurita, J., Antrobus, R., et al. (2023) · Nature Metabolism · doi:10.1038/s42255-023-00855-2 · Cited by 60
A disease-linked lncRNA mutation in RNase MRP inhibits ribosome synthesis
Robertson, N., Shchepachev, V., Wright, D., Turowski, T. W., Spanos, C., Helwak, A., Zamoyska, R., & Tollervey, D. W. (2022) · Nature Communications · doi:10.1038/s41467-022-28295-8 · Cited by 57
The Immunological Proteome Resource
Brenes, A. J., Hukelmann, J. L., Spinelli, L., Howden, A. J. M., Marchingo, J. M., Sinclair, L. V., Rollings, C. M., James, O. J., Phair, I. R., Matthews, S. P., et al. (2023) · Nature Immunology · doi:10.1038/s41590-023-01483-4 · Cited by 53
Self-citationExtracellular signal-regulated kinase (ERK) pathway control of CD8+ T cell differentiation
Damasio, M. P. S., Marchingo, J. M., Spinelli, L., Hukelmann, J. L., Cantrell, D. A., & Howden, A. J. M. (2020) · Biochemical Journal · doi:10.1042/bcj20200661 · Cited by 56
Self-citationAnalysis of Iron and Iron-Interacting Protein Dynamics During T-Cell Activation
Teh, M. R., Frost, J. N., Armitage, A. E., & Drakesmith, H. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.714613 · Cited by 54
Chen, X., Liu, L., Kang, S., Gnanaprakasam, J. R., & Wang, R. (2023) · Science Advances · doi:10.1126/sciadv.add9554 · Cited by 54
The Role of Non-essential Amino Acids in T Cell Function and Anti-tumour Immunity
Hope, H. C., & Salmond, R. J. (2021) · Archivum Immunologiae et Therapiae Experimentalis · doi:10.1007/s00005-021-00633-6 · Cited by 55
Wincup, C., Sawford, N., & Rahman, A. (2021) · Expert Review of Clinical Immunology · doi:10.1080/1744666x.2021.1953981 · Cited by 48
The proteome and transcriptome of stress granules and P bodies during human T lymphocyte activation
Curdy, N., Lanvin, O., Cerapio, J., Pont, F., Tosolini, M., Sarot, É., Valle, C., Saint‐Laurent, N., Lhuillier, É., Laurent, C., et al. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.112211 · Cited by 51
Targeting metabolic dysfunction of CD8 T cells and natural killer cells in cancer
Viel, S., Vivier, É., Walzer, T., & Marçais, A. (2024) · Nature Reviews Drug Discovery · doi:10.1038/s41573-024-01098-w · Cited by 53
CDK8 Fine-Tunes IL-6 Transcriptional Activities by Limiting STAT3 Resident Time at the Gene Loci
Martínez‐Fábregas, J., Wang, L., Pöhler, E., Cozzani, A., Wilmes, S., Kazemian, M., Mitra, S., & Moraga, I. (2020) · Cell Reports · doi:10.1016/j.celrep.2020.108545 · Cited by 49
A type I IFN, prothrombotic hyperinflammatory neutrophil signature is distinct for COVID-19 ARDS
Reyes, L., Sánchez-García, M. A., Morrison, T., Howden, A., Watts, E., Arienti, S., Sadiku, P., Coelho, P., Mirchandani, A. S., Zhang, A., et al. (2021) · Wellcome Open Research · doi:10.12688/wellcomeopenres.16584.1 · Cited by 59
Self-citationImmunometabolism: crosstalk with tumor metabolism and implications for cancer immunotherapy
Zhang, H., Fan, J., Kong, D., Sun, Y., Zhang, Q., Xiang, R., Lu, S., Yang, W., Feng, L., & Zhang, H. (2025) · Molecular Cancer · doi:10.1186/s12943-025-02460-1 · Cited by 49
Modulation of TCR Signaling by Tyrosine Phosphatases: From Autoimmunity to Immunotherapy
Castro-Sanchez, P., Teagle, A. R., Prade, S., & Zamoyska, R. (2020) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2020.608747 · Cited by 44
T cells at work: How post‐transcriptional mechanisms control T cell homeostasis and activation
Jurgens, A. P., Popović, B., & Wolkers, M. C. (2021) · European Journal of Immunology · doi:10.1002/eji.202049055 · Cited by 42
More TOR: The expanding role of mTOR in regulating immune responses
Patel, C. H., & Powell, J. D. (2025) · Immunity · doi:10.1016/j.immuni.2025.06.010 · Cited by 48
Nutrient inputs and social metabolic control of T cell fate
Bacigalupa, Z. A., Landis, M. D., & Rathmell, J. C. (2023) · Cell Metabolism · doi:10.1016/j.cmet.2023.12.009 · Cited by 45
Metabolic rewiring and communication in cancer immunity
Chapman, N. M., & Chi, H. (2024) · Cell chemical biology · doi:10.1016/j.chembiol.2024.02.001 · Cited by 44
The low-density lipoprotein receptor–mTORC1 axis coordinates CD8+ T cell activation
Bonacina, F., Moregola, A., Svecla, M., Coe, D., Uboldi, P., Fraire, S., Beretta, S., Beretta, G., Pellegatta, F., Catapano, A. L., et al. (2022) · The Journal of Cell Biology · doi:10.1083/jcb.202202011 · Cited by 41
Frost, J. N., & Drakesmith, H. (2025) · Nature reviews. Immunology · doi:10.1038/s41577-025-01193-y · Cited by 42
Johansen, K. H., Golec, D. P., Huang, B., Park, C., Thomsen, J. H., Preite, S., Cannons, J. L., Garçon, F., Schrom, E. C., Courrèges, C. J. F., et al. (2022) · Science Signaling · doi:10.1126/scisignal.abl9169 · Cited by 37
Lloyd, A. F., Martínez‐Muriana, A., Davis, E., Daniels, M. J. D., Hou, P., Mancuso, R., Brenes, A. J., Sinclair, L. V., Geric, I., Snellinx, A., et al. (2024) · Cell Reports · doi:10.1016/j.celrep.2024.114908 · Cited by 47
Self-citationPelgrom, L. R., Davis, G. M., O’Shaughnessy, S., Wezenberg, E. J. M., van Kasteren, S. I., Finlay, D. K., & Sinclair, L. V. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.112828 · Cited by 34
Self-citationIL-15 and PIM kinases direct the metabolic programming of intestinal intraepithelial lymphocytes
James, O. J., Vandereyken, M., Marchingo, J. M., Singh, F., Bray, S. E., Wilson, J., Love, A. G., & Swamy, M. (2021) · Nature Communications · doi:10.1038/s41467-021-24473-2 · Cited by 34
Cell Cycle Entry Control in Naïve and Memory CD8+ T Cells
Lewis, D. A., & Ly, T. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.727441 · Cited by 32
Sinclair, L. V., Youdale, T., Spinelli, L., Gakovic, M., Langlands, A. J., Pathak, S., Howden, A. J. M., Ganley, I. G., & Cantrell, D. A. (2025) · Nature Immunology · doi:10.1038/s41590-025-02090-1 · Cited by 33
Self-citationArming a killer: mitochondrial regulation of CD8+ T cell cytotoxicity
Lisci, M., & Griffiths, G. M. (2022) · Trends in Cell Biology · doi:10.1016/j.tcb.2022.05.007 · Cited by 29
TYK2 in Tumor Immunosurveillance
Karjalainen, A., Shoebridge, S., Krunic, M., Simonović, N., Tebb, G., Macho‐Maschler, S., Strobl, B., & Müller, M. M. (2020) · Cancers · doi:10.3390/cancers12010150 · Cited by 31
Absolute and functional iron deficiency: Biomarkers, impact on immune system, and therapy
Iriarte‐Gahete, M., Tarancón‐Díez, L., Garrido‐Rodríguez, V., Leal, M., & Pacheco, Y. M. (2024) · Blood Reviews · doi:10.1016/j.blre.2024.101227 · Cited by 39
Kedia-Mehta, N., Pisarska, M. M., Rollings, C. M., O’Neill, C. A., Barra, C. D., Foley, C., Wood, N., Wrigley-Kelly, N., Veerapen, N., Besra, G. S., et al. (2023) · Science Signaling · doi:10.1126/scisignal.abo2709 · Cited by 32
Self-citationSalerno, F., Howden, A. J. M., Matheson, L. S., Gizlenci, Ö., Screen, M., Lingel, H., Brunner-Weinzierl, M. C., & Turner, M. (2023) · Nature Communications · doi:10.1038/s41467-023-40621-2 · Cited by 29
Self-citationLoss of Phosphatidylinositol 3-Kinase Activity in Regulatory T Cells Leads to Neuronal Inflammation
Stark, A., Davenport, E. C. M., Patton, D. T., Scudamore, C. L., Vanhaesebroeck, B., Veldhoen, M., Garden, O. A., & Okkenhaug, K. (2020) · The Journal of Immunology · doi:10.4049/jimmunol.2000043 · Cited by 29
Tissue environment, not ontogeny, defines murine intestinal intraepithelial T lymphocytes
Brenes, A. J., Vandereyken, M., James, O. J., Watt, H. J., Hukelmann, J. L., Spinelli, L., Dikovskaya, D., Lamond, A. I., & Swamy, M. (2021) · eLife · doi:10.7554/elife.70055 · Cited by 28
Self-citationXu, Y., Li, P., Li, K., Li, N., Liu, H., Zhang, X., Liu, W., & Liu, Y. (2022) · Journal of Autoimmunity · doi:10.1016/j.jaut.2022.102890 · Cited by 30
Subbannayya, Y., Haug, M., Pinto, S. M., Mohanty, V., Meås, H. Z., Flo, T. H., Prasad, T. S. K., & Kandasamy, R. K. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms22010275 · Cited by 29
Modulating the polyamine/hypusine axis controls generation of CD8+ tissue-resident memory T cells
Elmarsafawi, A. G., Hesterberg, R. S., Fernandez, M. R., Yang, C., Darville, L. N. F., Liu, M., Koomen, J. M., Phanstiel, O., Atkins, R. M., Mullinax, J. E., et al. (2023) · JCI Insight · doi:10.1172/jci.insight.169308 · Cited by 27
A glutamine ‘tug-of-war’: targets to manipulate glutamine metabolism for cancer immunotherapy
Pallett, L. J., Dimeloe, S., Sinclair, L. V., Byrne, A. J., & Schurich, A. (2021) · Immunotherapy Advances · doi:10.1093/immadv/ltab010 · Cited by 28
Self-citationReuschl, A., Mesner, D., Shivkumar, M., Whelan, M. V. X., Pallett, L. J., Guerra‐Assunção, J. A., Madansein, R., Dullabh, K. J., Sigal, A., Thornhill, J. P., et al. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.110650 · Cited by 31
Salt inducible kinases 2 and 3 are required for thymic T cell development
Nefla, M., Darling, N. J., van Gijsel‐Bonnello, M., Cohen, P., & Arthur, J. S. C. (2021) · Scientific Reports · doi:10.1038/s41598-021-00986-0 · Cited by 25
Response Surface Methodology to Efficiently Optimize Intracellular Delivery by Photoporation
Goemaere, I., Punj, D., Harizaj, A., Woolston, J., Thys, S., Sterck, K., Smedt, S. C. D., Vos, W. H. D., & Braeckmans, K. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24043147 · Cited by 27
The E3 ubiquitin ligase Cul4b promotes CD4+ T cell expansion by aiding the repair of damaged DNA
Dar, A. A., Sawada, K., Dybas, J. M., Moser, E. K., Lewis, E. L., Park, E., Fazelinia, H., Spruce, L. A., Ding, H., Seeholzer, S. H., et al. (2021) · PLoS Biology · doi:10.1371/journal.pbio.3001041 · Cited by 28
The ubiquitin ligase Cul5 regulates CD4+ T cell fate choice and allergic inflammation
Kumar, B., Field, N. S., Kim, D. D., Dar, A. A., Chen, Y., Suresh, A., Pastore, C., Hung, L., Porter, N., Sawada, K., et al. (2022) · Nature Communications · doi:10.1038/s41467-022-30437-x · Cited by 25
Liu, X., Hao, J., Wei, P., Zhao, X., Lan, Q., Ni, L., Chen, Y., Bai, X., Ni, L., & Dong, C. (2022) · Science Advances · doi:10.1126/sciadv.abo4577 · Cited by 26
Darling, N. J., Arthur, J. S. C., & Cohen, P. (2021) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2021.100428 · Cited by 25
RNA-Binding Protein Expression Alters Upon Differentiation of Human B Cells and T Cells
Zandhuis, N. D., Nicolet, B. P., & Wolkers, M. C. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.717324 · Cited by 23
Weerakoon, H. T. W., Mohamed, A., Wong, Y., Chen, J., Senadheera, B., Haigh, O. L., Watkins, T. S., Kazakoff, S. H., Mukhopadhyay, P., Mulvenna, J. P., et al. (2024) · npj Systems Biology and Applications · doi:10.1038/s41540-024-00346-4 · Cited by 24
Zhang, J., Han, X., Lin, L., Chen, J., Wang, F., Ding, Q., Li, H., Wang, L., Wei, J., Wang, Y., et al. (2022) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2022/3583985 · Cited by 21
Delivery of macromolecules in unstimulated T cells by photoporation with polydopamine nanoparticles
Berdecka, D., Harizaj, A., Goemaere, I., Punj, D., Goetgeluk, G., Munter, S. D., Keersmaecker, H. D., Boterberg, V., Dubruel, P., Vandekerckhove, B., et al. (2023) · Journal of Controlled Release · doi:10.1016/j.jconrel.2023.01.047 · Cited by 22
Ma, C. Y., Marioni, J. C., Griffiths, G. M., & Richard, A. C. (2020) · eLife · doi:10.7554/elife.53948 · Cited by 22
Cattley, R. T., Lee, M., Boggess, B., & Hawse, W. F. (2020) · Journal of Biological Chemistry · doi:10.1074/jbc.ra120.012572 · Cited by 21
Villegas-Méndez, A., Khandelwal, G., McGowan, L. M., Dookie, R. S., Haley, M., George, C. L., Sims, D., Lord, G. M., Sinclair, L. V., Jenner, R. G., et al. (2020) · The Journal of Immunology · doi:10.4049/jimmunol.2000450 · Cited by 22
Self-citationAba, Ü., Maslak, İ. C., İpşir, C., Pehlivan, D., Warnock, N. I., Tumes, D. J., Cildir, G., & Erman, B. (2024) · Journal of Clinical Immunology · doi:10.1007/s10875-024-01658-0 · Cited by 20
Wang, X., Li, Y., Li, Y., Wang, X., Song, H., Wang, Y., Huang, C., Mao, C., Wang, L., Zhong, C., et al. (2025) · Science Advances · doi:10.1126/sciadv.adn8402 · Cited by 21
Lu, W., Helou, Y. A., Shrinivas, K., Liou, J., Au‐Yeung, B. B., & Weiss, A. (2022) · Nature Immunology · doi:10.1038/s41590-022-01372-2 · Cited by 22
NADPH Oxidase 2–Derived Reactive Oxygen Species Promote CD8+ T Cell Effector Function
Chen, J., Liu, C., Chernatynskaya, A., Newby, B. N., Brusko, T. M., Xu, Y., Barra, J. M., Morgan, N. N., Santarlas, C., Reeves, W. H., et al. (2023) · The Journal of Immunology · doi:10.4049/jimmunol.2200691 · Cited by 21
d'Aria, S., Maquet, C., Li, S., Dhup, S., Lepez, A., Köhler, A., Hée, V. F. V., Dadhich, R. K., Frenière, M., Andris, F., et al. (2024) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2306763121 · Cited by 20
Iron deficiency causes aspartate-sensitive dysfunction in CD8+ T cells
Teh, M. R., Gudgeon, N. H., Frost, J. N., Sinclair, L. V., Smith, A., Millington, C. L., Kronsteiner, B., Roberts, J., Marzullo, B. P., Murray, H., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-60204-7 · Cited by 20
Self-citationStress Granules in the Post-transcriptional Regulation of Immune Cells
Curdy, N., Lanvin, O., Cadot, S., Laurent, C., Fournié, J., & Franchini, D. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2020.611185 · Cited by 21
Zhang, L., Jin, G., Chen, Z., Yu, C., Li, Y., Li, Y., Chen, J., & Yu, L. (2021) · Hematology · doi:10.1080/16078454.2021.1981534 · Cited by 19
Protein Synthesis and Metabolism in T Cells
Sinclair, L. V., & Cantrell, D. A. (2025) · Annual Review of Immunology · doi:10.1146/annurev-immunol-082323-035253 · Cited by 19
Self-citationStaggered starts in the race to T cell activation
Richard, A. C., Frazer, G. L., Ma, C. Y., & Griffiths, G. M. (2021) · Trends in Immunology · doi:10.1016/j.it.2021.09.004 · Cited by 15
The Coordination of mTOR Signaling and Non-Coding RNA in Regulating Epileptic Neuroinflammation
Zeng, C., Hu, J. J., Chen, F., Huang, T., & Zhang, L. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.924642 · Cited by 20
Mitochondrial calcium uniporter complex controls T-cell-mediated immune responses
Shumanska, M., Lodygin, D., Gibhardt, C. S., Ickes, C., Stejerean‐Todoran, I., Krause, L. C. M., Pahl, K., Jacobs, L. H. C., Paluschkiwitz, A., Liu, S., et al. (2024) · EMBO Reports · doi:10.1038/s44319-024-00313-4 · Cited by 17
Luff, D. H., Wojdyła, K., Oxley, D., Chessa, T. A. M., Hudson, K., Hawkins, P. T., Stephens, L., Barry, S. T., & Okkenhaug, K. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.631271 · Cited by 17
Spinelli, L., Marchingo, J. M., Nomura, A., Damasio, M. P. S., & Cantrell, D. A. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.691997 · Cited by 18
Self-citationRoss, S. H., Rollings, C. M., & Cantrell, D. A. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.712402 · Cited by 17
Self-citationUncovering a novel role of PLCβ4 in selectively mediating TCR signaling in CD8+ but not CD4+ T cells
Sasai, M., Su, J., Okamoto, M., Nishino, K., Nagaoka, H., Takashima, E., Pradipta, A., Lee, Y., Kosako, H., Suh, P., et al. (2021) · The Journal of Experimental Medicine · doi:10.1084/jem.20201763 · Cited by 15
Mélique, S., Yang, C., & Lesourne, R. (2022) · Biomedical Journal · doi:10.1016/j.bj.2022.03.008 · Cited by 16
Zhou, D., Borsa, M., Puleston, D. J., Zellner, S., Capera, J., Sanderson, S., Schifferer, M., Hester, S. S., Ge, X., Fischer, R., et al. (2022) · Nature Communications · doi:10.1038/s41467-022-32718-x · Cited by 15
Li, M., Sun, X., Yao, H., Chen, W., Zhang, F., Gao, S., Zou, X., Chen, J., Qiu, S., Wei, H., et al. (2021) · Toxicology and Applied Pharmacology · doi:10.1016/j.taap.2021.115657 · Cited by 13
Lin, Y., Ruze, R., Zhang, R., Tuergan, T., Wang, M., Tulahong, A., Zhu, D., Yuan, Z., Jiang, T., Aji, T., et al. (2024) · Liver Cancer · doi:10.1159/000542578 · Cited by 17
Correa, L. O., Jankowski, S. E., Hong, H. S., Armas, N. D., Vijendra, A. I., Reynolds, M. B., Fogo, G. M., Awad, D., Dils, A. T., Inoki, K. A., et al. (2024) · Cell Reports · doi:10.1016/j.celrep.2024.114156 · Cited by 14
Metadata
- Authors
- Howden, A. J. M., Hukelmann, J. L., Brenes, A., Spinelli, L., Sinclair, L. V., Lamond, A. I., & Cantrell, D. A.
- Affiliations
- University of Dundee (GB)
- Corresponding author
- Lamond, Angus I.
- Cantrell, Doreen A.
- ORCID
- Venue
- Nature Immunology
- Published
- 2019-10-07
- Volume
- 20
- Issue
- 11
- Pages
- 1542-1554
- ISSN
- 1529-2908 (ISSN-L)
- 1529-2916
- PMC
- PMC6859072
- OpenAlex
- W2977451996
- Cited by
- 231
- References
- 49
- Citations by year
- 2026: 19 · 2025: 34 · 2024: 42 · 2023: 34 · 2022: 34 · 2021: 37 · 2020: 29 · 2019: 2
- FWCI
- 10.19
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Nature Immunology (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Discovery Research Portal (University of Dundee) (submittedVersion, other-oa)
- Funders
- Wellcome Trust (205023/Z/16/Z, 105024/Z/14/Z, 202950/Z/16/Z)
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
- Physical Sciences › Chemistry › Spectroscopy › Advanced Proteomics Techniques and Applications
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › PI3K/AKT/mTOR signaling in cancer
- Keywords
- T cell proteome, CD4+ T cells, CD8+ T cells, mTORC1, T cell differentiation, naive T cells, effector T cells, protein copy number, nutrient sensing, T cell metabolism, cell cycle progression, immune activation, quantitative mass spectrometry
- MeSH terms
- Mechanistic Target of Rapamycin Complex 1, Animals, Cell Differentiation, Cells, Cultured, Female, Gene Expression Regulation, Male, Mice, Transgenic, Mass Spectrometry, CD4-Positive T-Lymphocytes, CD8-Positive T-Lymphocytes, Gene Dosage, Sirolimus, Proteome, Gene Expression Profiling, Proteomics, Mice, Cell Cycle Checkpoints
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