The DOI matches its Crossref record; 107 of the 107 references it cites were found in a registry or an index.
T-bet: a bridge between innate and adaptive immunity
Open accessAbstract
Originally described over a decade ago as a T cell transcription factor regulating T helper 1 cell lineage commitment, T-bet is now recognized as having an important role in many cells of the adaptive and innate immune system. T-bet has a fundamental role in coordinating type 1 immune responses by controlling a network of genetic programmes that regulate the development of certain immune cells and the effector functions of others. Many of these transcriptional networks are conserved across innate and adaptive immune cells and these shared mechanisms highlight the biological functions that are regulated by T-bet.
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Citations
Cites
Master Transcription Factors and Mediator Establish Super-Enhancers at Key Cell Identity Genes
Whyte, W. A., Orlando, D. A., Hnisz, D., Abraham, B. J., Lin, C. Y., Kagey, M. H., Rahl, P. B., Lee, T. I., & Young, R. A. (2013) · Cell · doi:10.1016/j.cell.2013.03.035 · Cited by 4,143
A Novel Transcription Factor, T-bet, Directs Th1 Lineage Commitment
Szabo, S. J., Kim, S. T., Costa, G. L., Zhang, X., Fathman, C. G., & Glimcher, L. H. (2000) · Cell · doi:10.1016/s0092-8674(00)80702-3 · Cited by 3,589
Self-citationZheng, W.-P., & Flavell, R. A. (1997) · Cell · doi:10.1016/s0092-8674(00)80240-8 · Cited by 2,384
Innate lymphoid cells — a proposal for uniform nomenclature
Spits, H., Artis, D., Colonna, M., Diefenbach, A., Disanto, J. D., Eberl, G., Koyasu, S., Locksley, R., McKenzie, A., Mebius, R., et al. (2013) · Nature reviews. Immunology · doi:10.1038/nri3365 · Cited by 2,380
Blackburn, S. D., Shin, H., Haining, W. N., Zou, T., Workman, C. J., Polley, A., Betts, M. R., Freeman, G. J., Vignali, D. A. A., & Wherry, E. J. (2009) · Nature Immunology · doi:10.1038/ni.1679 · Cited by 2,062
Joshi, N. S., Cui, W., Chandele, A., Lee, H. K., Urso, D. R., Hagman, J., Gapin, L., & Kaech, S. M. (2007) · Immunity · doi:10.1016/j.immuni.2007.07.010 · Cited by 1,861
Generation of pathogenic TH17 cells in the absence of TGF-β signalling
Ghoreschi, K., Laurence, A., Yang, X.-P., Tato, C. M., McGeachy, M. J., Konkel, J. E., Ramos, H. L., Wei, L., Davidson, T. S., Bouladoux, N., et al. (2010) · Nature · doi:10.1038/nature09447 · Cited by 1,388
Effector and memory CD8+ T cell fate coupled by T-bet and eomesodermin
Intlekofer, A. M., Takemoto, N., Wherry, E. J., Longworth, S. A., Northrup, J. T., Palanivel, V., Mullen, A. C., Gasink, C. R., Kaech, S. M., Miller, J. D., et al. (2005) · Nature Immunology · doi:10.1038/ni1268 · Cited by 1,293
Koch, M. A., Tucker-Heard, G., Perdue, N. R., Killebrew, J. R., Urdahl, K. B., & Campbell, D. J. (2009) · Nature Immunology · doi:10.1038/ni.1731 · Cited by 1,258
Fate mapping of IL-17-producing T cells in inflammatory responses
Hirota, K., Duarte, J. H., Veldhoen, M., Hornsby, E., Li, Y., Cua, D. J., Ahlfors, H., Wilhelm, C., Tolaini, M., Menzel, U., et al. (2011) · Nature Immunology · doi:10.1038/ni.1993 · Cited by 1,176
Cited by
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McKenna, N. J., Ochsner, S. A., Waich, A., Cala-García, J., Echartrea, M. E. R., Grimm, S. L., Poli, F., Castillo, R. C., Zuluaga, J. D., Poli, S., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.06.16.659944 · Cited by 3
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Ivarsson, M. A. (2014) · Figshare
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Urban, S. L. (2015) · The Journal of the American Medical Association (JAMA) Network (American Medical Association) · doi:10.13028/m2wk5z
“Conversely, IL-12 has been shown to inhibit Eomes induction thus inhibiting effector memory formation (159).”
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Awe, O. (2015) · IUScholarWorks (Indiana University) · doi:10.7912/c2/1724
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Reiner, S. L. (2015) · The Journal of Immunology · doi:10.4049/jimmunol.1500289
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BackgroundInfluentialChavkin, A. (2015) · doi:10.7282/t38w3g82
“The transcription factor T-bet has also been found to play a role in the development of NKT cells [45, 47, 51].”
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Calefi, A. S. (2016) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.10.2016.tde-07102016-124200
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Chen, J. K. (2017) · doi:10.7916/d84m9gxs
“T-bet ablated memory CD4+ T cells produced significant increased levels of IL-17 following stimulation, concomitant with significant elevation of RORγt expression.”
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“In addition, T-bet also contributes to gene regulatory programs in multiple immune cell types, including CD8 T cells, innate lymphoid cells, natural killer (NK) cells, and even subsets of Tregs and Th17 cells [12].”
BackgroundMicroRNA and T Helper Cell-Mediated Immune Responses
Garo, L. P., Beynon, V., & Murugaiyan, G. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-809912-4.00004-0
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Whiting, J. R. (2018) · Nottingham ePrints (University of Nottingham)
T ‐Box Genes: Developmental Functions in Mammals
Papaioannou, V. E. (2017) · Encyclopedia of Life Sciences · doi:10.1002/9780470015902.a0026975
Huber, K. (2018) · Eötvös Loránd Tudományegyetem · doi:10.15476/elte.2017.171
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Discovery of Novel Epigenetic Regulators of CD8+ T Cell Effector Function
Tay, R. E. (2019) · Digital Access to Scholarship at Harvard (DASH) (Harvard University)
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“Differentiation of naïve T cells into TH1 effectors requires the T-box transcription factor T-bet, encoded by Tbx21, which is upregulated via IL12-dependent activation of STAT4 (2, 3).”
BackgroundInfluentialSelf-citationMULTI-FUNCTIONAL EFFECTOR RESPONSES ELICITED FROM IgM MEMORY STEM CELLS
Kenderes, K. J. (2017) · SUNY Digital Repository Support (State University of New York System)
Bofarull, S. (2003) · La Aventura de la historia
Grant, N. L., Maiello, P. A., Klein, E. C., Lin, P. L., Borish, H. J., Tomko, J. A., Frye, L. J., White, A. G., Kirschner, D. E., Mattila, J. T., et al. (2022) · SSRN Electronic Journal · doi:10.2139/ssrn.4000884
Grant, N. L., Maiello, P. A., Klein, E. C., Lin, P. L., Borish, H. J., Tomko, J. A., Frye, L. J., White, A. G., Kirschner, D. E., Mattila, J. T., et al. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.01.25.477732
“…diseases, including TB, revealing its critical function in controlling infection through production of pro-inflammatory mediators, T cell trafficking, and inhibition of other T cell fates (Pritchard et al., 2019, Szabo et al., 2000, Sullivan et al., 2005, Lazarevic et al., 2013, Lord et al., 2005).”
Molofsky, A. B. (2017) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.728639681.793538742
Zareie, P. (2017) · Open Access Victoria University of Wellington | Te Herenga Waka (Figshare) · doi:10.26686/wgtn.17065139 · Cited by 1
Wittmann, M., & Stacey, M. A. (2015) · Encyclopedia of Inflammatory Diseases · doi:10.1007/978-3-0348-0620-6_128-1
Roy, S. (2019) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.725800935.793557322
Frasch, M. (2017) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/s0070-2153(16)30226-5
Wittmann, M., & Stacey, M. A. (2016) · Compendium of Inflammatory Diseases · doi:10.1007/978-3-7643-8550-7_128
Абатуров, А. Е., & Tovarnytska, A. O. (2022) · Modern pediatrics Ukraine · doi:10.15574/sp.2022.128.6
Wittmann, M., & Stacey, M. A. (2016) · Encyclopedia of Inflammatory Diseases · doi:10.1007/978-3-0348-0620-6_128-2
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Badeaux, M. D., Rolig, A. S., Agnello, G., Enzler, D., Kasiewicz, M. J., Priddy, L., Wiggins, J. F., Muir, A., Sullivan, M. R., Cleef, J. V., et al. (2023) · doi:10.1158/2326-6066.c.6550171.v1
Mine, K., Nagafuchi, S., Akazawa, S., Abiru, N., Mori, H., Kurisaki, H., Yoshikai, Y., Takahashi, H., & Anzai, K. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.07.14.548984
“It was 330 reported that a target gene of T-bet is Cxcr3 (Lazarevic et al., 2013), a receptor for Cxcl9 331”
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Milotay, G., Little, M., Watson, R. A., Muldoon, D., Tong, O., Taylor, C. A., MacKay, S., Nassiri, I., Sun, B., Webb, L. M., et al. (2024) · medRxiv · doi:10.1101/2024.10.09.24315144
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ResultИгоревна, К. А., Nikiforov, V. S., Андреевна, Б. Е., & Akleyev, А. V. (2025) · Doklady Biochemistry and Biophysics · doi:10.1134/s1607672925700024
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“Specific transcription factors like T-box transcription factor 21 (T-bet), GATA binding protein-3 (GATA-3), RAR-related orphan receptor gamma t (RORγt), and Forkhead box P3 (Foxp3) are crucial for the development of Th1, Th2, Th17, and Treg cells, respectively [12, 13].”
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“For instance, Foxp3 can be expressed in other regulatory cells [49–52 ] and macrophages [ 53 ], and Rorc is shared with innate lymphoid cells [ 51 ].”
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“T-bet is widely recognized as a master regulator of Th1 cell differentiation and essential for the production of IFN-γ , a key cytokine in cellular immunity(Lazarevic et al., 2013).”
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Akhter, W., Nakhle, J., Vaillant, L., Garcin, G., Saout, C. L., Simon, M., Crozet, C., Djouad, F., Jørgensen, C., Vignais, M., et al. (2023) · Figshare · doi:10.6084/m9.figshare.22598849
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Li, J., Luo, C., Lou, F., Zhang, X., Duan, J., Wei, Z., Hu, X., Tu, P., Du, X., Zhong, R., et al. (2026) · Animal Microbiome · doi:10.1186/s42523-026-00525-0
“It supports the development of naive T lymphocytes by controlling the expression of interferon-gamma ( IFN-γ ), and it controls the differentiation of Th1 cells through IFN-γ-STAT1 and IL-12-STAT4 pathways [37].”
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“Nous voudrions ici étudier comment la distribution inégale du contenu moléculaire lors des divisions cellulaires peut contribuer à l’émergence de deux sous-populations de lymphocytes T-CD8 effecteurs, la première étant composée de cellules capables de développer des propriétés de lymphocytes mémoires (ces cellules son…”
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Santamaria, K. (2020) · theses.fr (ABES) · doi:10.70675/0550da9bz6935z43d6z9117z2f2fdffb714c
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“…p38, JAK, JNK, and PKA signaling pathways) [39], HES1 (Notch pathway) [40], NFAT5 (IKK/NF-κ B signaling pathway) [41], SOX4 (NF-κ B signaling pathway) [42], and TBX21 (IFN-γ -STAT1 and IL-12-STAT4 signaling pathways) [43] were have also been reported to participate in inflammatory responses.”
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Marsal, C., Kashif, M., Borate, S., Hallstrand, C., Haazen, L., Gilljam, M., Dölalan, Y., Burduli, N., Meinke, S., Norman, A., et al. (2026) · Frontiers in Pharmacology · doi:10.3389/fphar.2026.1952429
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IMMUNOTHERAPEUTIC ACTION OF T-BET GENE MODIFIED DENDRITIC CELLS
Chen, L. (2013) · D-Scholarship@Pitt (University of Pittsburgh)
Metadata
- Authors
- Lazarevic, V., Glimcher, L. H., & Lord, G. M.
- Affiliations
- National Institutes of Health (US)
- Weill Cornell Medicine (US)
- King's College London (GB)
- Corresponding author
- Glimcher, Laurie H.
- Venue
- Nature Reviews Immunology
- Published
- 2013-10-11
- Volume
- 13
- Issue
- 11
- Pages
- 777-789
- ISSN
- 1474-1733 (ISSN-L)
- 1474-1741
- PMC
- PMC6290922
- OpenAlex
- W2055897422
- Cited by
- 486
- References
- 107
- Citations by year
- 2026: 19 · 2025: 38 · 2024: 26 · 2023: 34 · 2022: 40 · 2021: 41 · 2020: 42 · 2019: 36 · 2018: 50 · 2017: 47 · 2016: 48 · 2015: 32 · 2014: 30 · 2013: 2
- FWCI
- 3.16
- Type
- journal article
- Language
- en
- Open access
- green
- europepmc.org
- Locations
- Nature reviews. Immunology (publishedVersion)
- PubMed (publishedVersion)
- Research Explorer (The University of Manchester) (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Research Portal (King's College London) (submittedVersion)
- Funders
- Wellcome Trust (WT088747MA)
- British Heart Foundation (PG/12/36/29444)
- National Institutes of Health
- U.S. Public Health Service (P01NSO38037)
- Medical Research Council (MR/J006742/1)
- National Cancer Institute (R01CA112663, CA112663, ZIABC011431)
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
- Life Sciences › Immunology and Microbiology › Immunology › Psoriasis: Treatment and Pathogenesis
- Life Sciences › Immunology and Microbiology › Immunology › Immunotherapy and Immune Responses
- Keywords
- T-bet, transcription factors, innate immunity, adaptive immunity, memory CD8+ T cells, B cells, innate lymphoid cells, dendritic cells, natural killer cells, type 1 immune response, transcriptional regulatory networks, immune cell development
- MeSH terms
- T-bet Transcription Factor, Animals, B-Lymphocytes, Humans, Immunity, Innate, Immunologic Memory, T-Lymphocyte Subsets, T-Box Domain Proteins, Adaptive Immunity
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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