GFP-specific CD8 T cells enable targeted cell depletion and visualization of T-cell interactions
Open accessAbstract
There are numerous cell types with scarcely understood functions, whose interactions with the immune system are not well characterized. To facilitate their study, we generated a mouse bearing enhanced green fluorescent protein (EGFP)-specific CD8+ T cells. Transfer of the T cells into EGFP reporter animals can be used to kill EGFP-expressing cells, allowing selective depletion of desired cell types, or to interrogate T-cell interactions with specific populations. Using this system, we eliminate a rare EGFP-expressing cell type in the heart and demonstrate its role in cardiac function. We also show that naive T cells are recruited into the mouse brain by antigen-expressing microglia, providing evidence of an immune surveillance pathway in the central nervous system. The just EGFP death-inducing (Jedi) T cells enable visualization of a T-cell antigen. They also make it possible to utilize hundreds of existing EGFP-expressing mice, tumors, pathogens and other tools, to study T-cell interactions with many different cell types, to model disease states and to determine the functions of poorly characterized cell populations.
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Jedi T cells express a T cell receptor that recognizes the immunodominant epitope of GFP loaded in the H-2Kd allele of MHC-I.
“we took advantage of just eGFP death inducing (Jedi) T cells, which express a T cell receptor that recognizes the immunodominant epitope of GFP loaded in the H-2Kd allele of MHC-I (Agudo et al., 2015).”
From Protein Barcodes Enable High-Dimensional Single-Cell CRISPR Screens (2018) · cites this paper as Agudo et al., 2015
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Cites
Jung, S., Aliberti, J., Graemmel, P., Sunshine, M. J., Kreutzberg, G. W., Sher, A., & Littman, D. R. (2000) · Molecular and Cellular Biology · doi:10.1128/mcb.20.11.4106-4114.2000 · Cited by 2,632 · see citing works
Regulatory T Cell Lineage Specification by the Forkhead Transcription Factor Foxp3
Fontenot, J. D., Rasmussen, J. P., Williams, L. M., Dooley, J., Farr, A. G., & Rudensky, A. Y. (2005) · Immunity · doi:10.1016/j.immuni.2005.01.016 · Cited by 2,255 · see citing works
A gene expression atlas of the central nervous system based on bacterial artificial chromosomes
Gong, S., Zheng, C., Doughty, M. L., Losos, K., Didkovsky, N., Schambra, U. B., Nowak, N. J., Joyner, A., Leblanc, G., Hatten, M. E., et al. (2003) · Nature · doi:10.1038/nature02033 · Cited by 2,108 · see citing works
Jung, S., Unutmaz, D., Wong, P., Sano, G., Santos, K. D. L., Sparwasser, T., Wu, S., Vuthoori, S., Ko, K., Zavala, F., et al. (2002) · Immunity · doi:10.1016/s1074-7613(02)00365-5 · Cited by 1,953 · see citing works
Regulatory T cells prevent catastrophic autoimmunity throughout the lifespan of mice
Kim, J. M., Rasmussen, J. P., & Rudensky, A. Y. (2006) · Nature Immunology · doi:10.1038/ni1428 · Cited by 1,827 · see citing works
Tolerance in T-cell-receptor transgenic mice involves deletion of nonmature CD4+8+ thymocytes
Kisielow, P., Blüthmann, H., Staerz, U., Steinmetz, M., & von Boehmer, H. (1988) · Nature · doi:10.1038/333742a0 · Cited by 1,793 · see citing works
Infiltrating monocytes trigger EAE progression, but do not contribute to the resident microglia pool
Ajami, B., Bennett, J. L., Krieger, C., McNagny, K. M., & Rossi, F. M. V. (2011) · Nature Neuroscience · doi:10.1038/nn.2887 · Cited by 1,061 · see citing works
MECHANISMS OF MHC CLASS I–RESTRICTED ANTIGEN PROCESSING
Pamer, E. G., & Cresswell, P. (1998) · Annual Review of Immunology · doi:10.1146/annurev.immunol.16.1.323 · Cited by 1,007 · see citing works
Differential roles of microglia and monocytes in the inflamed central nervous system
Yamasaki, R., Lu, H., Butovsky, O., Ohno, N., Rietsch, A. M., Cialic, R., Wu, P. M., Doykan, C. E., Lin, J., Cotleur, A. C., et al. (2014) · Journal of Experimental Medicine · doi:10.1084/jem.20132477 · Cited by 855 · see citing works
The myeloid cells of the central nervous system parenchyma
Ransohoff, R. M., & Cardona, A. E. (2010) · Nature · doi:10.1038/nature09615 · Cited by 804 · see citing works
Capture, crawl, cross: the T cell code to breach the blood–brain barriers
Engelhardt, B., & Ransohoff, R. M. (2012) · Trends in Immunology · doi:10.1016/j.it.2012.07.004 · Cited by 686 · see citing works
Brown, B. D., Gentner, B., Cantore, A., Colleoni, S., Amendola, M., Zingale, A., Baccarini, A., Lazzari, G., Galli, C., & Naldini, L. (2007) · Nature Biotechnology · doi:10.1038/nbt1372 · Cited by 559 · see citing works
Self-citationStromal cell contributions to the homeostasis and functionality of the immune system
Mueller, S. N., & Germain, R. N. (2009) · Nature reviews. Immunology · doi:10.1038/nri2588 · Cited by 524 · see citing works
Diphtheria toxin receptor–mediated conditional and targeted cell ablation in transgenic mice
Saito, M., Iwawaki, T., Taya, C., Yonekawa, H., Noda, M., Inui, Y., Mekada, E., Kimata, Y., Tsuru, A., & Kohno, K. (2001) · Nature Biotechnology · doi:10.1038/90795 · Cited by 512 · see citing works
Berg, L. J., Pullen, A. M., Groth, B. F. D. S., Mathis, D. J., Benoist, C. O., & Davis, M. M. (1989) · Cell · doi:10.1016/0092-8674(89)90502-3 · Cited by 374 · see citing works
Visualizing priming of virus-specific CD8+ T cells by infected dendritic cells in vivo
Norbury, C. C., Malide, D. A., Gibbs, J. S., Bennink, J. R., & Yewdell, J. W. (2002) · Nature Immunology · doi:10.1038/ni762 · Cited by 339 · see citing works
Clarke, S. R. M., Barnden, M., Kurts, C., Carbone, F., Miller, J. F. A. P., & Heath, W. R. (2000) · Immunology and Cell Biology · doi:10.1046/j.1440-1711.2000.00889.x · Cited by 296 · see citing works
Transgenic mice with green fluorescent protein-labeled pancreatic β-cells
Hara, M., Wang, X., Kawamura, T., Bindokas, V. P., Dizon, R. F., Alcoser, S. Y., Magnuson, M. A., & Bell, G. I. (2003) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00321.2002 · Cited by 293 · see citing works
Gambotto, A. A., Dworacki, G., Cicinnati, V. R., Kenniston, T. W., Steitz, J., Tüting, T., Robbins, P., & Deleo, A. (2000) · Gene Therapy · doi:10.1038/sj.gt.3301335 · Cited by 183 · see citing works
Thuan, N. V., Bui, H., Kim, J., Hikichi, T., Wakayama, S., Kishigami, S., Mizutani, E., & Wakayama, T. (2009) · Reproduction · doi:10.1530/rep-08-0299 · Cited by 151 · see citing works
The miR-126-VEGFR2 axis controls the innate response to pathogen-associated nucleic acids
Agudo, J., Ruzo, A., Tung, N., Salmon, H., Leboeuf, M., Hashimoto, D., Becker, C., Garrett-Sinha, L.-A., Baccarini, A., Merad, M., et al. (2014) · Nature Immunology · doi:10.1038/ni.2767 · Cited by 122 · see citing works
Self-citationLymph node stroma broaden the peripheral tolerance paradigm
Fletcher, A. L., Malhotra, D., & Turley, S. J. (2011) · Trends in Immunology · doi:10.1016/j.it.2010.11.002 · Cited by 120 · see citing works
Low Dose Cranial Irradiation-Induced Cerebrovascular Damage Is Reversible in Mice
Sándor, N., Walter, F. R., Bocsik, A., Sántha, P., Schilling-Tóth, B. M., Lener, V., Varga, Z., Kahán, Z., Deli, M. A., Sáfrány, G., et al. (2014) · PLoS ONE · doi:10.1371/journal.pone.0112397 · Cited by 71 · see citing works
BAC Transgenic Mice and the GENSAT Database of Engineered Mouse StrainsPreprint
Schmidt, E. F., Kus, L., Gong, S., & Heintz, N. (2013) · Cold Spring Harbor Protocols · doi:10.1101/pdb.top073692 · Cited by 65 · see citing works
Funny Current and Cardiac Rhythm: Insights from HCN Knockout and Transgenic Mouse Models
Bucchi, A., Barbuti, A., DiFrancesco, D., & Baruscotti, M. (2012) · Frontiers in Physiology · doi:10.3389/fphys.2012.00240 · Cited by 63 · see citing works
Kirak, O., Frickel, E., Grotenbreg, G. M., Suh, H., Jaenisch, R., & Ploegh, H. L. (2010) · Science · doi:10.1126/science.1178590 · Cited by 53 · see citing works
HCN channels in the heart: lessons from mouse mutants
Herrmann, S., Hofmann, F. B., Stieber, J., & Ludwig, A. (2011) · British Journal of Pharmacology · doi:10.1111/j.1476-5381.2011.01798.x · Cited by 52 · see citing works
Tissue destruction caused by cytotoxic T lymphocytes induces deletional tolerance
Parish, I. A., Waithman, J. C., Davey, G. M., Belz, G. T., Mintern, J. D., Kurts, C., Sutherland, R. M., Carbone, F., & Heath, W. R. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0810427106 · Cited by 23 · see citing works
T-cell receptor transgenic mice in the study of autoimmune diseases
Lafaille, J. J. (2004) · Journal of Autoimmunity · doi:10.1016/j.jaut.2003.10.007 · Cited by 20 · see citing works
Wu, M., Peng, S., & Zhao, Y. B. (2013) · genesis · doi:10.1002/dvg.22730 · Cited by 18 · see citing works
Self-citationNuclear Transfer into Mouse Oocytes
Egli, D. M., & Eggan, K. C. (2006) · Journal of Visualized Experiments · doi:10.3791/116 · Cited by 7 · see citing works
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Maier, B. B., Leader, A. M., Chen, S. T., Tung, N., Chang, C., Bérichel, J. L., Chudnovskiy, A., Maskey, S., Walker, L. A., Finnigan, J. P., et al. (2020) · Nature · doi:10.1038/s41586-020-2134-y · Cited by 950 · see citing works
Self-citationQuiescent cancer cells resist T cell attack by forming an immunosuppressive niche
Baldominos, P., Barbera-Mourelle, A., Barreiro, O., Huang, Y., Wight, A. E., Cho, J.-W., Zhao, X., Estivill, G., Adam, I., Sanchez, X., et al. (2022) · Cell · doi:10.1016/j.cell.2022.03.033 · Cited by 315 · see citing works
Self-citationQuiescent tissue stem cells evade immune surveillance
Agudo, J., Park, E. S., Rose, S. A., Alibo, E., Sweeney, R., Dhainaut, M., Kobayashi, K. S., Sachidanandam, R., Baccarini, A., Merad, M., et al. (2018) · Immunity · doi:10.1016/j.immuni.2018.02.001 · Cited by 244 · see citing works
Self-citationCancers make their own luck: theories of cancer origins
Jassim, A., Rahrmann, E. P., Simons, B. D., & Gilbertson, R. J. (2023) · Nature reviews. Cancer · doi:10.1038/s41568-023-00602-5 · Cited by 226 · see citing works
Integrin αvβ6–TGFβ–SOX4 Pathway Drives Immune Evasion in Triple-Negative Breast Cancer
Bagati, A., Kumar, S., Jiang, P., Pyrdol, J. W., Zou, A. E., Godicelj, A., Mathewson, N. D., Cartwright, A. N. R., Cejas, P., Brown, M. A., et al. (2020) · Cancer Cell · doi:10.1016/j.ccell.2020.12.001 · Cited by 216 · see citing works
Self-citationA Critical Role for Fas-Mediated Off-Target Tumor Killing in T-cell Immunotherapy
Upadhyay, R., Boiarsky, J., Pantsulaia, G., Svensson‐Arvelund, J., Lin, M. J., Wroblewska, A., Bhalla, S., Scholler, N., Bot, A. I., Rossi, J. M., et al. (2021) · Cancer Discovery · doi:10.1158/2159-8290.cd-20-0756 · Cited by 210 · see citing works
Self-citationRitzel, R. M., Crapser, J. D., Patel, A. R., Verma, R., Grenier, J. M., Chauhan, A., Jellison, E. R., & McCullough, L. D. (2016) · The Journal of Immunology · doi:10.4049/jimmunol.1502021 · Cited by 182 · see citing works
Protein Barcodes Enable High-Dimensional Single-Cell CRISPR Screens
Wroblewska, A., Dhainaut, M., Ben-Zvi, B., Rose, S. A., Park, E. S., Amir, E.-A. D., Bektesevic, A., Baccarini, A., Merad, M., Rahman, A. H., et al. (2018) · Cell · doi:10.1016/j.cell.2018.09.022 · Cited by 168 · see citing works
Self-citationTsao, L.-C., Wang, J. S., Ma, X., Sodhi, S. S., Ragusa, J. V., Liu, B., McBane, J., Wang, T., Wei, J.-P., Liu, C.-X., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-58266-8 · Cited by 177 · see citing works
Sampaziotis, F., de Brito, M. C., Geti, I., Bertero, A., Hannan, N. R. F., & Vallier, L. (2017) · Nature Protocols · doi:10.1038/nprot.2017.011 · Cited by 115 · see citing works
Grzelak, C. A., Goddard, E. T., Lederer, E. E., Rajaram, K., Dai, J., Shor, R. E., Lim, A. R., Kim, J., Beronja, S., Funnell, A. P. W., et al. (2021) · Cancer Cell · doi:10.1016/j.ccell.2021.11.004 · Cited by 93 · see citing works
Bowman’s capsule provides a protective niche for podocytes from cytotoxic CD8+ T cells
Chen, A., Lee, K., D’Agati, V. D., Wei, C., Fu, J., Guan, T., He, C., Schlöndorff, D., & Agudo, J. (2018) · Journal of Clinical Investigation · doi:10.1172/jci97879 · Cited by 92 · see citing works
Self-citationGoddard, E. T., Linde, M. H., Srivastava, S., Klug, G., Shabaneh, T. B., Iannone, S., Grzelak, C. A., Marsh, S. A., Riggio, A. I., Shor, R. E., et al. (2024) · Cancer Cell · doi:10.1016/j.ccell.2023.12.011 · Cited by 93 · see citing works
Svensson‐Arvelund, J., Cuadrado‐Castano, S., Pantsulaia, G., Kim, K., Aleynick, M., Hammerich, L., Upadhyay, R., Yellin, M. J., Marsh, H. C., Oreper, D., et al. (2022) · Nature Communications · doi:10.1038/s41467-022-34791-8 · Cited by 79 · see citing works
Self-citationIRE1α silences dsRNA to prevent taxane-induced pyroptosis in triple-negative breast cancer
Xu, L., Peng, F., Luo, Q., Ding, Y., Yuan, F., Zheng, L., He, W., Zhang, S. S., Fu, X., Liu, J., et al. (2024) · Cell · doi:10.1016/j.cell.2024.09.032 · Cited by 81 · see citing works
Adamopoulos, C., Ahmed, T. A., Tucker, M. R., Ung, P. M. U., Xiao, M., Karoulia, Z., Amabile, A., Wu, X., Aaronson, S. A., Ang, C., et al. (2021) · Cancer Discovery · doi:10.1158/2159-8290.cd-20-1351 · Cited by 69 · see citing works
Self-citationStemness in solid malignancies: coping with immune attack
Agudo, J., & Miao, Y. (2024) · Nature reviews. Cancer · doi:10.1038/s41568-024-00760-0 · Cited by 54 · see citing works
Self-citationInducible de novo expression of neoantigens in tumor cells and mice
Damo, M., Fitzgerald, B., Lu, Y., Nader, M., William, I., Cheung, J. F., Connolly, K. A., Foster, G. G., Akama‐Garren, E. H., Lee, D.-Y., et al. (2020) · Nature Biotechnology · doi:10.1038/s41587-020-0613-1 · Cited by 54 · see citing works
Rivero-Hinojosa, S., Grant, M., Panigrahi, A. K., Zhang, H., Caisová, V., Bollard, C. M., & Rood, B. R. (2021) · Nature Communications · doi:10.1038/s41467-021-26936-y · Cited by 52 · see citing works
Trinh, V. Q.-H., Lee, T.-F., Lemoinne, S., Ray, K. C., Ybanez, M. D., Tsuchida, T., Carter, J. K., Agudo, J., Brown, B. D., Akat, K. M., et al. (2023) · Science Signaling · doi:10.1126/scisignal.adf6696 · Cited by 45 · see citing works
Self-citationPD-1 blockade and CDK4/6 inhibition augment nonoverlapping features of T cell activation in cancer
Ali, L. R., Garrido-Castro, A., Lenehan, P., Bollenrucher, N., Stump, C. T., Dougan, M., Goel, S., Shapiro, G., Tolaney, S., & Dougan, S. (2023) · Journal of Experimental Medicine · doi:10.1084/jem.20220729 · Cited by 40 · see citing works
Role of CD8+ T cells in crescentic glomerulonephritis
Chen, A., Lee, K., Guan, T., He, C., & Schlöndorff, D. (2019) · Nephrology Dialysis Transplantation · doi:10.1093/ndt/gfz043 · Cited by 35 · see citing works
Tumors hijack macrophages for iron supply to promote bone metastasis and anemia
Han, Y., Sarkar, H., Xu, Z., Lopez-Darwin, S. L., Wei, Y., Hang, X., Liu, F., Tran, K., Wang, W., Miller, J. M., et al. (2025) · Cell · doi:10.1016/j.cell.2025.08.013 · Cited by 40 · see citing works
Long-term surviving influenza infected cells evade CD8+ T cell mediated clearance
Fiege, J. K., Stone, I. A., Dumm, R. E., Waring, B. M., Fife, B. T., Agudo, J., Brown, B. D., Heaton, N. S., & Langlois, R. A. (2019) · PLoS Pathogens · doi:10.1371/journal.ppat.1008077 · Cited by 29 · see citing works
Self-citationChimeric antigen receptor (CAR) T-cell therapy: Engineering immune cells to treat liver diseases
Jaeckel, E., Friedman, S. L., Hudecek, M., & Protzer, U. (2025) · Journal of Hepatology · doi:10.1016/j.jhep.2025.06.007 · Cited by 28 · see citing works
Intestinal tuft cell immune privilege enables norovirus persistence
Strine, M. S., Fagerberg, E., Darcy, P. W., Barrón, G. M., Filler, R. B., Alfajaro, M. M., D'Angelo-Gavrish, N. M., Wang, F., Graziano, V. R., Menasché, B. L., et al. (2024) · Science Immunology · doi:10.1126/sciimmunol.adi7038 · Cited by 25 · see citing works
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Ara, T., & Hashimoto, D. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.713631 · Cited by 26 · see citing works
Mapping the Chromosomal Insertion Site of the GFP Transgene of UBC-GFP Mice to the MHC Locus
Liu, S., Lockhart, J. R., Fontenard, S. D., Berlett, M., & Ryan, T. M. (2020) · The Journal of Immunology · doi:10.4049/jimmunol.1901338 · Cited by 23 · see citing works
Männ, L., Kochupurakkal, N. M., Martin, C., Verjans, E., Grüneboom, A., Sody, S., Kraus, A., Dalimot, J. J., Bergmüller, E., Jung, S., et al. (2016) · European Journal of Immunology · doi:10.1002/eji.201546245 · Cited by 22 · see citing works
You, Y., Dunst, J., Ye, K., Sandoz, P. A., Reinhardt, A., Sandrock, I., Comet, N. R., Sarkar, R. D., Yang, E., Duprez, E., et al. (2024) · Nature Immunology · doi:10.1038/s41590-024-01899-6 · Cited by 19 · see citing works
Self-citationMarshall, N., Hutchinson, K., Marron, T. U., Aleynick, M., Hammerich, L., Upadhyay, R., Svensson‐Arvelund, J., Brown, B. D., Mérad, M., & Brody, J. (2019) · Cancer Discovery · doi:10.1158/2159-8290.cd-19-0391 · Cited by 19 · see citing works
Self-citationImmune privilege of skin stem cells: What do we know and what can we learn?
Agudo, J. (2020) · Experimental Dermatology · doi:10.1111/exd.14221 · Cited by 18 · see citing works
Self-citationHauptmann, M., Burkhardt, N. Y., Munderloh, U. G., Kuehl, S., Richardt, U., Krasemann, S., Hartmann, K., Krech, T., Fleischer, B., Keller, C. A., et al. (2017) · Infection and Immunity · doi:10.1128/iai.00156-17 · Cited by 17 · see citing works
Trotter, T. N., Dagotto, C. E., Serra, D. M., Wang, T., Yang, X. Y., Acharya, C. R., Wei, J.-P., Lei, G., Lyerly, H. K., & Hartman, Z. C. (2023) · JCI Insight · doi:10.1172/jci.insight.174458 · Cited by 13 · see citing works
Harper, M. M., Gramlich, O. W., Elwood, B. W., Boehme, N., Dutca, L. M., & Kuehn, M. H. (2022) · Experimental Eye Research · doi:10.1016/j.exer.2022.109272 · Cited by 12 · see citing works
Borroni, E., Borsotti, C., Cirsmaru, R. A., Kalandadze, V., Famà, R., Merlin, S., Brown, B. D., & Follenzi, A. (2024) · Molecular Therapy — Nucleic Acids · doi:10.1016/j.omtn.2024.102116 · Cited by 10 · see citing works
Self-citationA glucocorticoid–FAS axis controls immune evasion during metastatic seeding
Cassandras, M., Sanchez, X., Hsu, L., huang, Y., Getzler, A. J., Ganguly, D., Baldominos, P., Codinachs, I., Chuong, J., Martin, E. E., et al. (2026) · Nature · doi:10.1038/s41586-026-10222-2 · Cited by 9 · see citing works
Self-citationPattern recognition receptor agonists in pathogen vaccines mediate antitumor T-cell cross-priming
Aleynick, M., Svensson‐Arvelund, J., Pantsulaia, G., Kim, K., Rose, S. A., Upadhyay, R., Yellin, M. J., Marsh, H. C., Oreper, D., Jhunjhunwala, S., et al. (2023) · Journal for ImmunoTherapy of Cancer · doi:10.1136/jitc-2023-007198 · Cited by 5 · see citing works
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Agudo, J., & Baldominos, P. (2022) · Regular and Young Investigator Award Abstracts · doi:10.1136/jitc-2022-sitc2022.0947 · Cited by 5 · see citing works
Self-citationHan, Y., Sarkar, H., Xu, Z., Lopez-Darwin, S. L., Wei, Y. X., Hang, X., Liu, F., Tran, K., Wang, W., Miller, J. M., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.04.23.650120 · Cited by 5 · see citing works
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Self-citationNawy, T. (2015) · Nature Methods · doi:10.1038/nmeth.3723 · Cited by 2 · see citing works
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Sun, Q., & Schwabe, R. F. (2023) · Methods in molecular biology · doi:10.1007/978-1-0716-3207-9_12 · Cited by 1 · see citing works
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Alibo, E., Mollaoglu, G., Dhainaut, M., Zhao, R., Rose, S. A., Baccarini, A., Parsons, R. E., & Brown, B. D. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.05.24.445214 · Cited by 1 · see citing works
Self-citationAdamopoulos, C., Ahmed, T. A., Tucker, M. R., Ung, P. M. U., Xiao, M., Karoulia, Z., Amabile, A., Wu, X., Aaronson, S. A., Ang, C., et al. (2023) · doi:10.1158/2159-8290.c.6549364 · Cited by 1 · see citing works
Self-citationHoggatt, J. (2016) · The Hematologist · doi:10.1182/hem.v13.4.5655
Rivero-Hinojosa, S., Grant, M., Panigrahi, A. K., Zhang, H., Caisová, V., Bollard, C. M., & Rood, B. R. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.08.13.456263 · Cited by 1 · see citing works
Judith Agudo: Beware of your inner self-immune attack
Morgado-Palacin, L. (2023) · The Journal of Cell Biology · doi:10.1083/jcb.202302027
LSpECifying transgene expression
Annoni, A., & Cantore, A. (2024) · Molecular Therapy — Nucleic Acids · doi:10.1016/j.omtn.2024.102144
Atomistic TCR-ligand interactions instruct memory T-cell differentiation 2330211
Akitsu, A., Tan, K., Mallis, R. J., Booker, M. A., Duke‐Cohan, J. S., Brazin, K. N., Kirkpatrick, E. H., Parkins, A., Seabury, A., Aryal, S., et al. (2026) · The Journal of Immunology · doi:10.1093/jimmun/vkag141.1794
Schmitt, T., Furiya, K., Black, C., Vazquez, A., Sharma, J., Hailemariam, M., Paushter, D., Trieu, L., Lam, J., Lee, B. M., et al. (2026) · Journal for ImmunoTherapy of Cancer · doi:10.1136/jitc-2025-013520
Atomistic TCR-pMHC interactions bias CD8 memory fate within a single antigen-specific repertoire
Akitsu, A., Tan, K., Mallis, R. J., Booker, M. A., Duke‐Cohan, J. S., Brazin, K. N., Kirkpatrick, E. H., Parkins, A., Seabury, A. G., Aryal, S., et al. (2026) · Cell Reports · doi:10.1016/j.celrep.2026.117908
Elevated Intraocular Pressure Facilitates T-Cell–Mediated Retinal Ganglion Cell Loss
Mayberry, J. E., Xian, S., Roy, S., & Kuehn, M. H. (2026) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.67.12.68
- Authors
- Agudo, J., Ruzo, A., Park, E. S., Sweeney, R., Kana, V., Wu, M., Zhao, Y., Egli, D., Merad, M., & Brown, B. D.
- Affiliations
- Icahn School of Medicine at Mount Sinai (US)
- New York Stem Cell Foundation (US)
- Tisch Cancer Institute (US)
- Corresponding author
- Brown, Brian D
- Venue
- Nature Biotechnology
- Published
- 2015-11-02
- Volume
- 33
- Issue
- 12
- Pages
- 1287-1292
- ISSN
- 0733-222X (ISSN-L)
- 1087-0156
- 1546-1696
- PMC
- PMC4675673
- OpenAlex
- W1963130477
- Cited by
- 64
- References
- 31
- Citations by year
- 2026: 7 · 2025: 5 · 2024: 9 · 2023: 11 · 2022: 5 · 2021: 8 · 2020: 6 · 2019: 3 · 2018: 4 · 2017: 2 · 2016: 3 · 2015: 1
- FWCI
- 1.64
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature Biotechnology (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Heart, Lung, and Blood Institute (K02HL103597, R01HL107376)
- National Cancer Institute (R01CA173861, R01CA190400, P30CA196521)
- National Institute of Allergy and Infectious Diseases (R01AI104848, R01AI113221)
- National Institute of Diabetes and Digestive and Kidney Diseases (P30DK026687)
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Animal Genetics and Reproduction
- Life Sciences › Immunology and Microbiology › Immunology › Immunotherapy and Immune Responses
- Keywords
- T cell interactions, naive T cells, microglia, central nervous system, cardiac function, T cell transfer
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