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Intersection of mTOR and STAT signaling in immunity
Open accessAbstract
Optimal regulation of immune networks is essential for the generation of effective immune responses, and defects in such networks can lead to immunodeficiency while uncontrolled responses can result in autoimmune disorders. mTOR and STAT signaling cascades are key regulators of the differentiation and function of cells of the immune system. Both pathways act as sensors and transducers of environmental stimuli, and recent evidence has revealed points of crosstalk between these pathways, highlighting synergistic regulation of immune cell differentiation and function. We review here the current understanding of mTOR and STAT interactions in T cells and innate immune cells, and discuss potential mechanisms underlying these events. We further outline models for the intersection of these pathways in the regulation of immunity and highlight important areas for future research.
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“mTOR has also been shown to regulate STAT signaling175, and studies in older humans show that the elevation in baseline phosphorylation of STAT proteins in T cells distinguishes healthy ageing from unhealthy ageing subjects based on cardiovascular ageing phenotypes17.”
From SARS-CoV-2, COVID-19 and the aging immune system (2021) · cites this paper as [175]
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Cites
mTOR Signaling in Growth Control and Disease
Laplante, M., & Sabatini, D. M. (2012) · Cell · doi:10.1016/j.cell.2012.03.017 · Cited by 8,509
Mechanisms of type-I- and type-II-interferon-mediated signalling
Platanias, L. C. (2005) · Nature reviews. Immunology · doi:10.1038/nri1604 · Cited by 3,631
Self-citationRegulation of type I interferon responses
Ivashkiv, L. B., & Donlin, L. T. (2013) · Nature reviews. Immunology · doi:10.1038/nri3581 · Cited by 3,442
Development of Monocytes, Macrophages, and Dendritic Cells
Geissmann, F., Manz, M. G., Jung, S., Sieweke, M. H., Merad, M., & Ley, K. (2010) · Science · doi:10.1126/science.1178331 · Cited by 3,049
Molecular mechanisms of mTOR-mediated translational control
Ma, X. M., & Blenis, J. (2009) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2672 · Cited by 2,558
Sancak, Y., Bar-Peled, L., Zoncu, R., Markhard, A. L., Nada, S., & Sabatini, D. M. (2010) · Cell · doi:10.1016/j.cell.2010.02.024 · Cited by 2,464 · cited 1×
“In response to increased amino acid levels, activated Rag GTPases promote the translocation of mTORC1 into the lysosomal surface, where its activator, RHEB, is located [66,67].”
BackgroundThoreen, C. C., Kang, S. A., Chang, J. W., Liu, Q., Zhang, J., Gao, Y., Reichling, L. J., Sim, T., Sabatini, D. M., & Gray, N. S. (2009) · Journal of Biological Chemistry · doi:10.1074/jbc.m900301200 · Cited by 1,803
SOCS proteins, cytokine signalling and immune regulation
Yoshimura, A., Naka, T., & Kubo, M. (2007) · Nature Reviews Immunology · doi:10.1038/nri2093 · Cited by 1,580
The JAK-STAT Pathway at Twenty
Stark, G. R., & Darnell, J. E., Jr. (2012) · Immunity · doi:10.1016/j.immuni.2012.03.013 · Cited by 1,577
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
mTOR differentially regulates effector and regulatory T cell lineage commitment
Delgoffe, G. M., Kole, T., Zheng, Y., Zarek, P. E., Matthews, K., Xiao, B., Worley, P., Kozma, S., & Powell, J. (2009) · Immunity · doi:10.1016/j.immuni.2009.04.014 · Cited by 1,293
JAK and STAT Signaling Molecules in Immunoregulation and Immune-Mediated Disease
O’Shea, J. J., & Plenge, R. M. (2012) · Immunity · doi:10.1016/j.immuni.2012.03.014 · Cited by 1,186
Delgoffe, G. M., Pollizzi, K. N., Waickman, A. T., Heikamp, E., Meyers, D. J., Horton, M. R., Xiao, B., Worley, P. F., & Powell, J. D. (2011) · Nature Immunology · doi:10.1038/ni.2005 · Cited by 1,141
Active-Site Inhibitors of mTOR Target Rapamycin-Resistant Outputs of mTORC1 and mTORC2
Feldman, M. E., Apsel, B., Uotila, A., Loewith, R., Knight, Z. A., Ruggero, D., & Shokat, K. M. (2009) · PLoS Biology · doi:10.1371/journal.pbio.1000038 · Cited by 1,111
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 · cited 1×
“Recently, it was reported that GAP activity toward Rags (GATOR) complex controls Rag A and B [68], whereas folliculin and folliculin interacting protein Saleiro and Platanias Page 2”
BackgroundRegulation and function of mTOR signalling in T cell fate decisions
Chi, H. (2012) · Nature Reviews Immunology · doi:10.1038/nri3198 · Cited by 1,035
Rapamycin passes the torch: a new generation of mTOR inhibitors
Benjamin, D., Colombi, M., Moroni, C., & Hall, M. N. (2011) · Nature Reviews Drug Discovery · doi:10.1038/nrd3531 · Cited by 1,013
JAKs and STATs in immunity, immunodeficiency, and cancer
O'Shea, J. J., Holland, S. M., & Staudt, L. M. (2013) · New England Journal of Medicine · doi:10.1056/nejmra1202117 · Cited by 927
Ragulator Is a GEF for the Rag GTPases that Signal Amino Acid Levels to mTORC1
Bar-Peled, L., Schweitzer, L. D., Zoncu, R., & Sabatini, D. M. (2012) · Cell · doi:10.1016/j.cell.2012.07.032 · Cited by 918 · cited 1×
“In response to increased amino acid levels, activated Rag GTPases promote the translocation of mTORC1 into the lysosomal surface, where its activator, RHEB, is located [66,67].”
BackgroundRegulation 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
The TSC-mTOR Signaling Pathway Regulates the Innate Inflammatory Response
Weichhart, T., Costantino, G., Poglitsch, M., Rosner, M., Zeyda, M., Stuhlmeier, K. M., Kolbe, T., Stulnig, T. M., Hörl, W. H., Hengstschläger, M., et al. (2008) · Immunity · doi:10.1016/j.immuni.2008.08.012 · Cited by 801
Regulation of mTORC1 and its impact on gene expression at a glance
Laplante, M., & Sabatini, D. M. (2013) · Journal of Cell Science · doi:10.1242/jcs.125773 · Cited by 697
Rao, R. R., Li, Q., Odunsi, K., & Shrikant, P. A. (2010) · Immunity · doi:10.1016/j.immuni.2009.10.010 · Cited by 656 · cited 7×
“STAT-dependent gene products are required for cytokine-induced activation of mTOR [19, 20, 36].”
BackgroundInfluentialActivation of mTORC2 by Association with the Ribosome
Zinzalla, V., Stracka, D., Oppliger, W., & Hall, M. N. (2011) · Cell · doi:10.1016/j.cell.2011.02.014 · Cited by 648
TBC1D7 Is a Third Subunit of the TSC1-TSC2 Complex Upstream of mTORC1
Dibble, C. C., Elis, W., Menon, S., Qin, W., Klekota, J., Asara, J. M., Finan, P. M., Kwiatkowski, D. J., Murphy, L. O., & Manning, B. D. (2012) · Molecular Cell · doi:10.1016/j.molcel.2012.06.009 · Cited by 612
Tsun, Z.-Y., Bar-Peled, L., Chantranupong, L., Zoncu, R., Wang, T., Kim, C., Spooner, E., & Sabatini, D. M. (2013) · Molecular Cell · doi:10.1016/j.molcel.2013.09.016 · Cited by 565
Direct Effects of Type I Interferons on Cells of the Immune System
Hervás‐Stubbs, S., Perez‐Gracia, J. L., Rouzaut, A., Sanmamed, M. F., Bon, A. L., & Melero, I. (2011) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-10-1114 · Cited by 535
JAK/STAT signaling in hematological malignancies
Vainchenker, W., & Constantinescu, S. N. (2013) · Oncogene · doi:10.1038/onc.2012.347 · Cited by 528
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
Regulation of mTORC1 by the Rag GTPases is necessary for neonatal autophagy and survival
Efeyan, A., Zoncu, R., Chang, S. H., Gumper, I., Snitkin, H., Wolfson, R. L., Kirak, O., Sabatini, D. M., & Sabatini, D. M. (2012) · Nature · doi:10.1038/nature11745 · Cited by 473
Lee, K., Gudapati, P., Dragovic, S. M., Spencer, C. T., Joyce, S., Killeen, N. P., Magnuson, M. A., & Boothby, M. R. (2010) · Immunity · doi:10.1016/j.immuni.2010.06.002 · Cited by 471
Biology and significance of the JAK/STAT signalling pathways
Kiu, H., & Nicholson, S. E. (2012) · Growth Factors · doi:10.3109/08977194.2012.660936 · Cited by 470
Wofford, J. A., Wieman, H. L., Jacobs, S. R., Zhao, Y., & Rathmell, J. C. (2007) · Blood · doi:10.1182/blood-2007-06-096297 · Cited by 424
Cui, W., Liu, Y., Weinstein, J. S., Craft, J., & Kaech, S. M. (2011) · Immunity · doi:10.1016/j.immuni.2011.09.017 · Cited by 410
Naive T cell homeostasis: from awareness of space to a sense of place
Takada, K., & Jameson, S. C. (2009) · Nature reviews. Immunology · doi:10.1038/nri2657 · Cited by 393
STATs Shape the Active Enhancer Landscape of T Cell Populations
Vahedi, G., Takahashi, H., Nakayamada, S., Sun, H., Sartorelli, V., Kanno, Y., & O’Shea, J. J. (2012) · Cell · doi:10.1016/j.cell.2012.09.044 · Cited by 380
Regulation of mTORC1 and mTORC2 Complex Assembly by Phosphatidic Acid: Competition with Rapamycin
Toschi, A., Lee, E., Xu, L., Garcia, A., Gadir, N., & Foster, D. A. (2008) · Molecular and Cellular Biology · doi:10.1128/mcb.00782-08 · Cited by 341
Effective and selective targeting of leukemia cells using a TORC1/2 kinase inhibitor
Janes, M. R., Limon, J. J., So, L., Chen, J., Lim, R. J., Chavez, M. A., Vu, C., Lilly, M. B., Mallya, S., Ong, S. T., et al. (2010) · Nature Medicine · doi:10.1038/nm.2091 · Cited by 341
PD‐L1 expression on tolerogenic APCs is controlled by STAT‐3
Wölfle, S. J., Strebovsky, J., Bartz, H., Sähr, A., Arnold, C., Kaiser, C., Dalpke, A. H., & Heeg, K. M. (2010) · European Journal of Immunology · doi:10.1002/eji.201040979 · Cited by 325
Genomic views of STAT function in CD4+ T helper cell differentiation
O'Shea, J. J., Lahesmaa, R., Vahedi, G., Laurence, A., & Kanno, Y. (2011) · Nature Reviews Immunology · doi:10.1038/nri2958 · Cited by 295
Cohney, S., Sanden, D., Cacalano, N., Yoshimura, A., Mui, A., Migone, T., & Johnston, J. (1999) · Molecular and Cellular Biology · doi:10.1128/mcb.19.7.4980 · Cited by 293
Siegel, A., Heimall, J. R., Freeman, A. F., Hsu, A. P., Brittain, E., Brenchley, J. M., Douek, D. C., Fahle, G. H., Cohen, J. I., Holland, S. M., et al. (2011) · Immunity · doi:10.1016/j.immuni.2011.09.016 · Cited by 284
Rac1 Regulates the Activity of mTORC1 and mTORC2 and Controls Cellular Size
Saci, A., Cantley, L. C., & Carpenter, C. L. (2011) · Molecular Cell · doi:10.1016/j.molcel.2011.03.017 · Cited by 275
Ohtani, M., Nagai, S., Kondo, S., Mizuno, S., Nakamura, K., Tanabe, M., Takeuchi, T., Matsuda, S., & Koyasu, S. (2008) · Blood · doi:10.1182/blood-2008-02-137430 · Cited by 269
Henson, S. M., Franzese, O., Macaulay, R., Libri, V., Azevedo, R. I., Kiani-Alikhan, S., Plunkett, F. J., Masters, J. E., Jackson, S., Griffiths, S. J., et al. (2009) · Blood · doi:10.1182/blood-2009-01-199588 · Cited by 262
Tasian, S. K., Doral, M. Y., Borowitz, M. J., Wood, B. L., Chen, I., Harvey, R. C., Gastier, J. M., Willman, C. L., Hunger, S. P., Mullighan, C. G., et al. (2012) · Blood · doi:10.1182/blood-2011-12-389932 · Cited by 240
Differential effects of STAT5 and PI3K/AKT signaling on effector and memory CD8 T-cell survival
Hand, T. W., Cui, W., Jung, Y. W., Sefik, E., Joshi, N. S., Chandele, A., Liu, Y., & Kaech, S. M. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1003457107 · Cited by 232
Haidinger, M., Poglitsch, M., Geyeregger, R., Kasturi, S. P., Zeyda, M., Zlabinger, G. J., Pulendran, B., Hörl, W. H., Säemann, M. D., & Weichhart, T. (2010) · The Journal of Immunology · doi:10.4049/jimmunol.1000296 · Cited by 226
Evidence for Direct Activation of mTORC2 Kinase Activity by Phosphatidylinositol 3,4,5-Trisphosphate
Gan, X., Wang, J., Su, B., & Wu, D. (2011) · Journal of Biological Chemistry · doi:10.1074/jbc.m110.195016 · Cited by 217
Role of the Akt pathway in mRNA translation of interferon-stimulated genes
Kaur, S., Sassano, A., Dolniak, B., Joshi, S., Majchrzak-Kita, B., Baker, D., Hay, N., Fish, E., & Platanias, L. (2008) · Proceedings of the National Academy of Sciences of the United States of America · doi:10.1073/pnas.0710907105 · Cited by 215
Self-citationRiou, C., Yassine‐Diab, B., van Grevenynghe, J., Somogyi, R., Greller, L. D., Gagnon, D., Gimmig, S., Wilkinson, P. A., Shi, Y., Cameron, M. J., et al. (2006) · The Journal of Experimental Medicine · doi:10.1084/jem.20061681 · Cited by 209
Suppression of cytokine signaling: The SOCS perspective
Linossi, E. M., Babon, J. J., Hilton, D. J., & Nicholson, S. E. (2013) · Cytokine & Growth Factor Reviews · doi:10.1016/j.cytogfr.2013.03.005 · Cited by 197
Carayol, N., Vakana, E., Sassano, A., Kaur, S., Goussetis, D. J., Glaser, H., Druker, B. J., Donato, N. J., Altman, J. K., Barr, S. M., et al. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1005114107 · Cited by 179
Self-citationLi, Q., Rao, R. R., Araki, K., Pollizzi, K. N., Odunsi, K. O., Powell, J. D., & Shrikant, P. A. (2011) · Immunity · doi:10.1016/j.immuni.2011.04.006 · Cited by 166
The evolution of the TOR pathway and its role in cancer
Beauchamp, E. M., & Platanias, L. C. (2012) · Oncogene · doi:10.1038/onc.2012.567 · Cited by 158
Self-citationER Stress Inhibits mTORC2 and Akt Signaling Through GSK-3β–Mediated Phosphorylation of Rictor
Chen, C.-H., Shaiken, T. E., Peterson, T. R., Aimbetov, R., Bissenbaev, A. K., Lee, S.-W., Wu, J., Lin, H., & Sarbassov, D. D. (2011) · Science Signaling · doi:10.1126/scisignal.2001731 · Cited by 147
TSC1 regulates the balance between effector and regulatory T cells
Park, Y., Jin, H., Lopez, J. M., Elly, C., Kim, G., Murai, M., Kronenberg, M., & Liu, Y. (2013) · Journal of Clinical Investigation · doi:10.1172/jci69751 · Cited by 140
Sun, Y., Chin, Y. E., Weisiger, E., Malter, C., Tawara, I., Toubai, T., Gatza, E., Mascagni, P., Dinarello, C. A., & Reddy, P. R. (2009) · The Journal of Immunology · doi:10.4049/jimmunol.0804388 · Cited by 127
STAT5 Is Critical To Maintain Effector CD8+ T Cell Responses
Tripathi, P., Kurtuluş, S., Wojciechowski, S., Sholl, A., Hoebe, K. H. N., Morris, S. C., Finkelman, F. D., Grimes, H. L., & Hildeman, D. A. (2010) · The Journal of Immunology · doi:10.4049/jimmunol.1000842 · Cited by 123
Kaur, S., Lal, L., Sassano, A., Majchrzak-Kita, B., Srikanth, M., Baker, D. P., Petroulakis, E., Hay, N., Sonenberg, N., Fish, E. N., et al. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m607365200 · Cited by 110
Self-citationWang, H., Brown, J. R., Gu, Z., Garcia, C. A., Liang, R., Alard, P., Beurel, E., Jope, R. S., Greenway, T., & Martin, M. (2011) · The Journal of Immunology · doi:10.4049/jimmunol.1002513 · Cited by 104
Bogani, C., Bartalucci, N., Martinelli, S., Tozzi, L., Guglielmelli, P., Bosi, A., Vannucchi, A. M., & Mieloproliferative, A. I. P. L. R. S. C. A. G. I. M. (2013) · PLoS ONE · doi:10.1371/journal.pone.0054826 · Cited by 103
mTOR, linking metabolism and immunity
Xu, X., Ye, L., Araki, K., & Ahmed, R. (2012) · Seminars in Immunology · doi:10.1016/j.smim.2012.12.005 · Cited by 99
Altman, J. K., Sassano, A., Kaur, S., Glaser, H., Kroczyńska, B., Redig, A. J., Russo, S. M., Barr, S. M., & Platanias, L. C. (2011) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-10-2285 · Cited by 98
Self-citationFielhaber, J. A., Carroll, S. F., Dydensborg, A. B., Shourian, M., Triantafillopoulos, A., Harel, S., Hussain, S. N. A., Bouchard, M., Qureshi, S. T., & Kristof, A. S. (2012) · The Journal of Immunology · doi:10.4049/jimmunol.1003655 · Cited by 95
Kim, J.-H., Yoon, M.-S., & Chen, J. (2009) · Journal of Biological Chemistry · doi:10.1074/jbc.m109.051516 · Cited by 92
Fish, E. N., & Platanias, L. C. (2014) · Molecular Cancer Research · doi:10.1158/1541-7786.mcr-14-0450 · Cited by 92
Self-citationTuberous sclerosis 1 (Tsc1)-dependent metabolic checkpoint controls development of dendritic cells
Wang, Y., Huang, G., Zeng, H., Yang, K., Lamb, R. F., & Chi, H. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1308905110 · Cited by 87
TOR kinase complexes and cell migration
Liu, L., & Parent, C. A. (2011) · Journal of Cell Biology · doi:10.1083/jcb.201102090 · Cited by 87
Busch, S., Renaud, S. J., Schleußner, E., Graham, C. H., & Markert, U. R. (2009) · Experimental Cell Research · doi:10.1016/j.yexcr.2009.01.026 · Cited by 81
A Role for Stat5 in CD8+ T Cell Homeostasis
Kelly, J., Spolski, R. J., Imada, K., Bollenbacher, J., Lee, S., & Leonard, W. J. (2003) · The Journal of Immunology · doi:10.4049/jimmunol.170.1.210 · Cited by 80
Differentiating the roles of STAT5B and STAT5A in human CD4+ T cells
Jenks, J. A., Seki, S. M., Kanai, T., Huang, J. J., Morgan, A. A., Scalco, R. C., Nath, R., Bucayu, R., Wit, J. M., Al–Herz, W., et al. (2013) · Clinical Immunology · doi:10.1016/j.clim.2013.04.014 · Cited by 60
Yamada, O., Ozaki, K., Akiyama, M., & Kawauchi, K. (2012) · Molecular Cancer Therapeutics · doi:10.1158/1535-7163.mct-11-0850 · Cited by 58
Kaur, S., Sassano, A., Majchrzak-Kita, B., Baker, D., Su, B., Fish, E., & Platanias, L. (2012) · Proceedings of the National Academy of Sciences of the United States of America · doi:10.1073/pnas.1118122109 · Cited by 52
Self-citationRosborough, B. R., Regué, D. R., Matta, B. M., Lee, K., Gan, B., DePinho, R. A., Hackstein, H., Boothby, M. R., Turnquist, H. R., & Thomson, A. W. (2013) · Blood · doi:10.1182/blood-2012-08-448290 · Cited by 50
van de Laar, L., Buitenhuis, M., Wensveen, F. M., Janssen, H. L. A., Coffer, P. J., & Woltman, A. M. (2010) · The Journal of Immunology · doi:10.4049/jimmunol.0903089 · Cited by 49
Intrinsic and extrinsic control of effector T cell survival and memory T cell development
Hand, T. W., & Kaech, S. M. (2008) · Immunologic Research · doi:10.1007/s12026-008-8027-z · Cited by 49
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
Chen, H., Zhang, L., Zhang, H., Xiao, Y., Shao, L., Li, H., Yin, H., Wang, R., Liu, G., Corley, D. A., et al. (2013) · The FASEB Journal · doi:10.1096/fj.13-235408 · Cited by 40
An overview of the mTOR pathway as a target in cancer therapy
Gentzler, R. D., Altman, J. K., & Platanias, L. C. (2012) · Expert Opinion on Therapeutic Targets · doi:10.1517/14728222.2012.677439 · Cited by 36
Self-citationKim, H., Hwang, K., & Kang, I. (2007) · The Journal of Immunology · doi:10.4049/jimmunol.179.10.6734 · Cited by 31
Kaur, S., Kroczyńska, B., Sharma, B., Sassano, A., Arslan, A. D., Majchrzak-Kita, B., Stein, B. L., McMahon, B., Altman, J. K., Su, B., et al. (2014) · Journal of Biological Chemistry · doi:10.1074/jbc.m113.537852 · Cited by 22
Self-citationNext generation of mammalian target of rapamycin inhibitors for the treatment of cancer
Nelson, V. M., Altman, J. K., & Platanias, L. C. (2013) · Expert Opinion on Investigational Drugs · doi:10.1517/13543784.2013.787066 · Cited by 20
Self-citationTuning mTOR activity for immune balance
Yang, K., & Chi, H. (2013) · Journal of Clinical Investigation · doi:10.1172/jci73202 · Cited by 11
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Metadata
- Authors
- Saleiro, D., & Platanias, L. C.
- Affiliations
- Northwestern University (US)
- Corresponding author
- Platanias, Leonidas C.
- Venue
- Trends in Immunology
- Publisher
- Elsevier BV
- Published
- 2015-01
- Volume
- 36
- Issue
- 1
- Pages
- 21-29
- ISSN
- 1471-4906 (ISSN-L)
- PMC
- PMC4297313
- OpenAlex
- W2028684481
- Cited by
- 142
- References
- 84
- Citations by year
- 2026: 9 · 2025: 10 · 2024: 10 · 2023: 9 · 2022: 12 · 2021: 17 · 2020: 14 · 2019: 13 · 2018: 12 · 2017: 12 · 2016: 16 · 2015: 7
- FWCI
- 1.32
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Trends in Immunology (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institutes of Health
- National Cancer Institute (R01CA161796, CA-77816, CA121192, R01CA121192, R01CA155566, CA161196, R01CA077816, CA155566, P30CA060553)
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › Cytokine Signaling Pathways and Interactions
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › PI3K/AKT/mTOR signaling in cancer
- Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
- Keywords
- mTOR signaling, STAT signaling, pathway crosstalk, immune cell differentiation, T cells, innate immune cells, immune regulation, immunodeficiency, autoimmunity, signal transduction
- MeSH terms
- Mechanistic Target of Rapamycin Complex 2, Animals, Dendritic Cells, Humans, Immune System, Immunity, Macrophages, Protein Binding, T-Lymphocytes, Signal Transduction, Multiprotein Complexes, STAT Transcription Factors, Receptor, Interferon alpha-beta, 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 ›
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