Beta cell-specific CD8+ T cells maintain stem cell memory-associated epigenetic programs during type 1 diabetes
Open accessAbstract
The pool of beta cell-specific CD8+ T cells in type 1 diabetes (T1D) sustains an autoreactive potential despite having access to a constant source of antigen. To investigate the long-lived nature of these cells, we established a DNA methylation-based T cell 'multipotency index' and found that beta cell-specific CD8+ T cells retained a stem-like epigenetic multipotency score. Single-cell assay for transposase-accessible chromatin using sequencing confirmed the coexistence of naive and effector-associated epigenetic programs in individual beta cell-specific CD8+ T cells. Assessment of beta cell-specific CD8+ T cell anatomical distribution and the establishment of stem-associated epigenetic programs revealed that self-reactive CD8+ T cells isolated from murine lymphoid tissue retained developmentally plastic phenotypic and epigenetic profiles relative to the same cells isolated from the pancreas. Collectively, these data provide new insight into the longevity of beta cell-specific CD8+ T cell responses and document the use of this methylation-based multipotency index for investigating human and mouse CD8+ T cell differentiation.
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
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?
A recent study found that circulating β-cell-specific CD8 T cells in T1D patients are epigenetically distinct from TCM, effector memory T (TEM) cells and exhausted CD8 T cells in chronic infection (for example, in HIV).
“In support of our findings, a recent study found that circulating β-cell–specific CD8 T cells in T1D patients are epigenetically distinct from TCM, effector memory T (TEM) cells and exhausted CD8 T cells in chronic infection26 (for example, in HIV).”
From An autoimmune stem-like CD8 T cell population drives type 1 diabetes (2022) · cites this paper as [26]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
Epigenetic modifications and human disease
Portela, A., & Esteller, M. (2010) · Nature Biotechnology · doi:10.1038/nbt.1685 · Cited by 2,843 · see citing works
The molecular hallmarks of epigenetic control
Allis, C. D., & Jenuwein, T. (2016) · Nature Reviews Genetics · doi:10.1038/nrg.2016.59 · Cited by 2,809 · see citing works
Machine Learning Identifies Stemness Features Associated with Oncogenic Dedifferentiation
Malta, T. M., Sokolov, A., Gentles, A. J., Burzykowski, T., Poisson, L., Weinstein, J. N., Kamińska, B., Huelsken, J., Omberg, L., Gevaert, O., et al. (2018) · Cell · doi:10.1016/j.cell.2018.03.034 · Cited by 2,180 · see citing works
A human memory T cell subset with stem cell–like properties
Gattinoni, L., Lugli, E., Ji, Y., Pos, Z., Paulos, C. M., Quigley, M. F., Almeida, J. R., Gostick, E., Yu, Z., Carpenito, C., et al. (2011) · Nature Medicine · doi:10.1038/nm.2446 · Cited by 1,974 · see citing works
Anti-CD3 monoclonal antibody in new-onset type 1 diabetes mellitus
Herold, K. C., Hagopian, W., Auger, J. A., Poumian-Ruiz, E., Taylor, L., Donaldson, D., Gitelman, S. E., Harlan, D. M., Xu, D., Zivin, R. A., et al. (2002) · New England Journal of Medicine · doi:10.1056/nejmoa012864 · Cited by 1,222 · see citing works
BSMAP: whole genome bisulfite sequence MAPping program
Xi, Y., & Li, W. (2009) · BMC Bioinformatics · doi:10.1186/1471-2105-10-232 · Cited by 1,216 · see citing works
An anti-CD3 antibody, teplizumab, in relatives at risk for type 1 diabetes
Herold, K. C., Bundy, B. N., Long, S. A., Bluestone, J. A., DiMeglio, L. A., Dufort, M. J., Gitelman, S. E., Gottlieb, P. A., Krischer, J. P., Linsley, P. S., et al. (2019) · New England Journal of Medicine · doi:10.1056/nejmoa1902226 · Cited by 1,189 · see citing works
TOX reinforces the phenotype and longevity of exhausted T cells in chronic viral infection
Alfei, F., Kanev, K., Hofmann, M., Wu, M., Ghoneim, H. E., Roelli, P., Utzschneider, D. T., von Hoesslin, M., Cullen, J. G., Fan, Y., et al. (2019) · Nature · doi:10.1038/s41586-019-1326-9 · Cited by 900 · see citing works
Self-citationDe Novo Epigenetic Programs Inhibit PD-1 Blockade-Mediated T Cell Rejuvenation
Ghoneim, H. E., Fan, Y., Moustaki, A., Abdelsamed, H. A., Dash, P., Dogra, P., Carter, R., Awad, W., Neale, G. A. M., Thomas, P. G., et al. (2017) · Cell · doi:10.1016/j.cell.2017.06.007 · Cited by 792 · see citing works
Self-citationAnalysis of islet inflammation in human type 1 diabetes
Willcox, A., Richardson, S. J., Bone, A. J., Foulis, A. K., & Morgan, N. G. (2009) · Clinical and Experimental Immunology · doi:10.1111/j.1365-2249.2008.03860.x · Cited by 712 · see citing works
Coppieters, K. T., Dotta, F., Amirian, N., Campbell, P. D., Kay, T. W. H., Atkinson, M. A., Roep, B. O., & von Herrath, M. G. (2012) · Journal of Experimental Medicine · doi:10.1084/jem.20111187 · Cited by 672 · see citing works
A Pathogenic Role for Myelin-Specific Cd8+ T Cells in a Model for Multiple Sclerosis
Huseby, E. S., Liggitt, D., Brabb, T., Schnabel, B., Öhlén, C., & Goverman, J. M. (2001) · The Journal of Experimental Medicine · doi:10.1084/jem.194.5.669 · Cited by 660 · see citing works
QUMA: quantification tool for methylation analysis
Kumaki, Y., Oda, M., & Okano, M. (2008) · Nucleic Acids Research · doi:10.1093/nar/gkn294 · Cited by 606 · see citing works
Origin and differentiation of human memory CD8 T cells after vaccination
Akondy, R. S., Fitch, M., Edupuganti, S., Yang, S., Kissick, H. T., Li, K. W., Youngblood, B. A., Abdelsamed, H. A., McGuire, D. J., Cohen, K. W., et al. (2017) · Nature · doi:10.1038/nature24633 · Cited by 517 · see citing works
Self-citationEpigenetic control of CD8+ T cell differentiation
Henning, A. N., Roychoudhuri, R., & Restifo, N. P. (2018) · Nature reviews. Immunology · doi:10.1038/nri.2017.146 · Cited by 501 · see citing works
Effector CD8 T cells dedifferentiate into long-lived memory cells
Youngblood, B., Hale, J. S., Kissick, H. T., Ahn, E., Xu, X., Wieland, A., Araki, K., West, E. E., Ghoneim, H. E., Fan, Y., et al. (2017) · Nature · doi:10.1038/nature25144 · Cited by 481 · see citing works
Self-citationMyelin Antigen-Specific CD8+ T Cells Are Encephalitogenic and Produce Severe Disease in C57BL/6 Mice
Sun, D., Whitaker, J. N., Huang, Z., Liu, D., Coleclough, C., Wekerle, H., & Raine, C. S. (2001) · The Journal of Immunology · doi:10.4049/jimmunol.166.12.7579 · Cited by 444 · see citing works
Chen, T., Ueda, Y., Xie, S., & Li, E. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m205312200 · Cited by 371 · see citing works
Skowera, A., Ellis, R. J., Varela‐Calviño, R., Arif, S., Huang, G. C., Van-Krinks, C., Zaremba, A., Rackham, C. L., Allen, J. S., Tree, T. I. M., et al. (2008) · Journal of Clinical Investigation · doi:10.1172/jci35449 · Cited by 362 · see citing works
Wu, H., Xu, T., Feng, H., Chen, L., Li, B., Yao, B., Qin, Z. S., Jin, P., & Conneely, K. N. (2015) · Nucleic Acids Research · doi:10.1093/nar/gkv715 · Cited by 350 · see citing works
Burrack, A. L., Martinov, T., & Fife, B. T. (2017) · Frontiers in Endocrinology · doi:10.3389/fendo.2017.00343 · Cited by 337 · see citing works
The epigenetic control of stemness in CD8 + T cell fate commitment
Pace, L., Goudot, C., Zueva, E., Gueguen, P., Burgdorf, N., Waterfall, J. J., Quivy, J., Almouzni, G., & Amigorena, S. (2018) · Science · doi:10.1126/science.aah6499 · Cited by 232 · see citing works
Tadokoro, Y., Ema, H., Okano, M., Li, E., & Nakauchi, H. (2007) · The Journal of Experimental Medicine · doi:10.1084/jem.20060750 · Cited by 203 · see citing works
Lugli, E., Gattinoni, L., Roberto, A., Mavilio, D., Price, D. A., Restifo, N. P., & Roederer, M. (2012) · Nature Protocols · doi:10.1038/nprot.2012.143 · Cited by 202 · see citing works
Utzschneider, D. T., Alfei, F., Roelli, P., Barras, D., Chennupati, V., Darbre, S., Delorenzi, M., Pinschewer, D. D., & Zehn, D. (2016) · The Journal of Experimental Medicine · doi:10.1084/jem.20150598 · Cited by 176 · see citing works
Self-citationYoungblood, B., Noto, A., Porichis, F., Akondy, R. S., Ndhlovu, Z. M., Austin, J. W., Bordi, R., Procopio, F. A., Miura, T., Allen, T. M., et al. (2013) · The Journal of Immunology · doi:10.4049/jimmunol.1203161 · Cited by 169 · see citing works
Self-citationAutoreactive CD8+ T cell exhaustion distinguishes subjects with slow type 1 diabetes progression
Wiedeman, A. E., Muir, V. S., Rosasco, M. G., DeBerg, H. A., Presnell, S., Haas, B., Dufort, M. J., Speake, C., Greenbaum, C. J., Serti, E., et al. (2019) · Journal of Clinical Investigation · doi:10.1172/jci126595 · Cited by 168 · see citing works
Self-citationHuman memory CD8 T cell effector potential is epigenetically preserved during in vivo homeostasis
Abdelsamed, H. A., Moustaki, A., Fan, Y., Dogra, P., Ghoneim, H. E., Zebley, C. C., Triplett, B. M., Sékaly, R., & Youngblood, B. (2017) · The Journal of Experimental Medicine · doi:10.1084/jem.20161760 · Cited by 147 · see citing works
Self-citationYang, J., Chow, I., Sosinowski, T., Torres-Chinn, N., Greenbaum, C. J., James, E. A., Kappler, J. W., Davidson, H. W., & Kwok, W. W. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1416864111 · Cited by 124 · see citing works
Self-citationIsoform‐specific localization of DNMT3A regulates DNA methylation fidelity at bivalent CpG islands
Manzo, M., Wirz, J., Ambrosi, C. M., Villaseñor, R., Roschitzki, B., & Baubec, T. (2017) · The EMBO Journal · doi:10.15252/embj.201797038 · Cited by 120 · see citing works
Crompton, J. G., Narayanan, M., Cuddapah, S., Roychoudhuri, R., Ji, Y., Yang, W., Patel, S. J., Sukumar, M., Palmer, D. C., Peng, W., et al. (2015) · Cellular and Molecular Immunology · doi:10.1038/cmi.2015.32 · Cited by 118 · see citing works
β-Cell–Specific CD8 T Cell Phenotype in Type 1 Diabetes Reflects Chronic Autoantigen Exposure
Skowera, A., Ladell, K., McLaren, J. E., Dolton, G. M., Matthews, K. K., Emma Gostick, D., Kronenberg‐Versteeg, D., Eichmann, M., Knight, R. R., Heck, S., et al. (2014) · Diabetes · doi:10.2337/db14-0332 · Cited by 118 · see citing works
Kronenberg‐Versteeg, D., Knight, R. R., Estorninho, M., Ellis, R. J., Kester, M. G. D., de Ru, A., Eichmann, M., Huang, G. C., Powrie, J., Dayan, C. M., et al. (2012) · Diabetes · doi:10.2337/db11-1520 · Cited by 111 · see citing works
Pathway-Based Genomics Prediction using Generalized Elastic Net
Sokolov, A., Carlin, D. E., Paull, E., Baertsch, R., & Stuart, J. M. (2016) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1004790 · Cited by 108 · see citing works
Levisetti, M. G., Suri, A., Petzold, S. J., & Unanue, E. R. (2007) · The Journal of Immunology · doi:10.4049/jimmunol.178.10.6051 · Cited by 101 · see citing works
Anti-CD3 clinical trials in type 1 diabetes mellitus
Daifotis, A. G., Koenig, S., Chatenoud, L., & Herold, K. C. (2013) · Clinical Immunology · doi:10.1016/j.clim.2013.05.001 · Cited by 96 · see citing works
Re-examining the Nature and Function of Self-Reactive T cells
Richards, D. M., Kyewski, B., & Feuerer, M. (2016) · Trends in Immunology · doi:10.1016/j.it.2015.12.005 · Cited by 80 · see citing works
Pagé, N., Klimek, B., Roo, M. D., Steinbach, K., Soldati, H., Lemeille, S., Wagner, I., Kreutzfeldt, M., Liberto, G. D., Vincenti, I., et al. (2018) · Immunity · doi:10.1016/j.immuni.2018.04.005 · Cited by 80 · see citing works
Self-citationAutoreactive T effector memory differentiation mirrors β cell function in type 1 diabetes
Yeo, L., Woodwyk, A., Sood, S., Lorenc, A., Eichmann, M., Pujol‐Autonell, I., Melchiotti, R., Skowera, A., Fidanis, E., Dolton, G. M., et al. (2018) · Journal of Clinical Investigation · doi:10.1172/jci120555 · Cited by 65 · see citing works
Knight, R. R., Kronenberg‐Versteeg, D., Zhao, M., Huang, G. C., Eichmann, M., Bulek, A. M., Wooldridge, L., Cole, D. K., Sewell, A. K., Peakman, M., et al. (2012) · Diabetes · doi:10.2337/db12-0315 · Cited by 65 · see citing works
The transcription factor Batf3 inhibits the differentiation of regulatory T cells in the periphery
Lee, W., Kim, H. S., Hwang, S. S., & Lee, G. R. (2017) · Experimental & Molecular Medicine · doi:10.1038/emm.2017.157 · Cited by 57 · see citing works
Vizier, C., Bercovici, N., Cornet, A. M., Cambouris, C., & Libiau, R. S. (1999) · Immunological Reviews · doi:10.1111/j.1600-065x.1999.tb01308.x · Cited by 40 · see citing works
Batf Promotes Growth Arrest and Terminal Differentiation of Mouse Myeloid Leukemia Cells
Liao, J., Humphrey, S. E., Poston, S., & Taparowsky, E. J. (2011) · Molecular Cancer Research · doi:10.1158/1541-7786.mcr-10-0375 · Cited by 35 · see citing works
Characterization of Diabetogenic CD8+ T Cells
Garyu, J., Uduman, M., Stewart, A., Rui, J., Deng, S., Shenson, J. A., Staron, M. M., Kaech, S. M., Kleinstein, S. H., & Herold, K. C. (2016) · Journal of Biological Chemistry · doi:10.1074/jbc.m115.713362 · Cited by 32 · see citing works
Obstacles and opportunities for targeting the effector T cell response in type 1 diabetes
Buckner, J. H., & Nepom, G. T. (2016) · Journal of Autoimmunity · doi:10.1016/j.jaut.2016.02.009 · Cited by 23 · see citing works
Self-citationLow-Affinity Major Histocompatibility Complex–Binding Peptides in Type 1 Diabetes
James, E. A., & Kwok, W. W. (2008) · Diabetes · doi:10.2337/db08-0530 · Cited by 11 · see citing works
Self-citation
Flagged first, then by citations
Cited by
Sorted by citations
An anti-CD3 antibody, teplizumab, in relatives at risk for type 1 diabetes
Herold, K. C., Bundy, B. N., Long, S. A., Bluestone, J. A., DiMeglio, L. A., Dufort, M. J., Gitelman, S. E., Gottlieb, P. A., Krischer, J. P., Linsley, P. S., et al. (2019) · New England Journal of Medicine · doi:10.1056/nejmoa1902226 · Cited by 1,189 · see citing works
Deleting DNMT3A in CAR T cells prevents exhaustion and enhances antitumor activity
Prinzing, B., Zebley, C. C., Petersen, C. T., Fan, Y., Anido, A. A., Yi, Z., Nguyen, P., Houke, H., Bell, M., Haydar, D., et al. (2021) · Science Translational Medicine · doi:10.1126/scitranslmed.abh0272 · Cited by 349 · see citing works
Self-citationAn autoimmune stem-like CD8 T cell population drives type 1 diabetes
Gearty, S. V., Dündar, F., Zumbo, P., Espinosa-Carrasco, G., Shakiba, M., Sanchez-Rivera, F. J., Socci, N. D., Trivedi, P., Lowe, S. W., Lauer, P., et al. (2022) · Nature · doi:10.1038/s41586-021-04248-x · Cited by 257 · see citing works
Collier, J. L., Weiss, S. A., Pauken, K. E., Sen, D. R., & Sharpe, A. H. (2021) · Nature Immunology · doi:10.1038/s41590-021-00949-7 · Cited by 237 · see citing works
The immunology of type 1 diabetes
Herold, K. C., Delong, T., Perdigoto, A. L., Biru, N., Brusko, T. M., & Walker, L. S. K. (2024) · Nature reviews. Immunology · doi:10.1038/s41577-023-00985-4 · Cited by 222 · see citing works
MEK inhibition reprograms CD8+ T lymphocytes into memory stem cells with potent antitumor effects
Verma, V., Jafarzadeh, N., Boi, S. K., Kundu, S., Jiang, Z., Fan, Y., Lopez, J., Nandre, R. M., Zeng, P., Alolaqi, F., et al. (2020) · Nature Immunology · doi:10.1038/s41590-020-00818-9 · Cited by 183 · see citing works
Self-citationChromatin accessibility: biological functions, molecular mechanisms and therapeutic application
Chen, Y., Liang, R., Li, Y., Jiang, L., Ma, D., Luo, Q., & Song, G. (2024) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-024-02030-9 · Cited by 174 · see citing works
In vivo labeling reveals continuous trafficking of TCF-1+ T cells between tumor and lymphoid tissue
Li, Z., Tuong, Z. K., Dean, I., Willis, C., Gaspal, F., Fiancette, R., Idris, S., Kennedy, B. C., Ferdinand, J. R., Peñalver, A., et al. (2022) · The Journal of Experimental Medicine · doi:10.1084/jem.20210749 · Cited by 114 · see citing works
Autoreactive CD8+ T cells are restrained by an exhaustion-like program that is maintained by LAG3
Grebinoski, S., Zhang, Q., Cillo, A. R., Manne, S., Xiao, H., Brunazzi, E. A., Tabib, T., Cardello, C., Lian, C. G., Murphy, G. F., et al. (2022) · Nature Immunology · doi:10.1038/s41590-022-01210-5 · Cited by 107 · see citing works
Zebley, C. C., Brown, C., Tian, M., Fan, Y., Alli, S., Boi, S. K., Galletti, G., Lugli, E., Langfitt, D. M., Métais, J., et al. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.110079 · Cited by 108 · see citing works
Self-citationNew developments implicating IL-21 in autoimmune disease
Ren, H. M., Lukacher, A. E., Rahman, Z. S. M., & Olsen, N. J. (2021) · Journal of Autoimmunity · doi:10.1016/j.jaut.2021.102689 · Cited by 99 · see citing works
Epigenetic regulators of clonal hematopoiesis control CD8 T cell stemness during immunotherapy
Kang, T. G., Lan, X., Tian, M., Chen, H., Alli, S., Lim, S.-E., Bhatara, S., Vasandan, A. B., Ward, G., Bentivegna, S., et al. (2024) · Science · doi:10.1126/science.adl4492 · Cited by 98 · see citing works
Self-citationZheng, W., Wei, J., Zebley, C. C., Jones, L. L., Dhungana, Y., Wang, Y., Mavuluri, J., Long, L., Fan, Y., Youngblood, B., et al. (2021) · Blood · doi:10.1182/blood.2020009309 · Cited by 89 · see citing works
Self-citationTonic-signaling chimeric antigen receptors drive human regulatory T cell exhaustion
Lamarche, C., Ward‐Hartstonge, K. A., Tian, M., Lin, D. T. S., Huang, Q. B., Brown, A., Edwards, K., Novakovsky, G., Qi, C. N., Kobor, M. S., et al. (2023) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2219086120 · Cited by 86 · see citing works
Self-citationHumblin, É., Korpas, I., Lu, J., Filipescu, D., van der Heide, V., Goldstein, S., Vaidya, A. B., Schanoski, A. S., Casati, B., Selvan, M. E., et al. (2023) · Science Immunology · doi:10.1126/sciimmunol.adg0878 · Cited by 74 · see citing works
Rewriting History: Epigenetic Reprogramming of CD8+ T Cell Differentiation to Enhance Immunotherapy
Zebley, C. C., Gottschalk, S. M., & Youngblood, B. (2020) · Trends in Immunology · doi:10.1016/j.it.2020.06.008 · Cited by 69 · see citing works
Self-citationThe beta cell-immune cell interface in type 1 diabetes (T1D)
James, E. A., Joglekar, A. V., Linnemann, A. K., Russ, H. A., & Kent, S. C. (2023) · Molecular Metabolism · doi:10.1016/j.molmet.2023.101809 · Cited by 68 · see citing works
Self-citationMechanisms of T cell exhaustion guiding next-generation immunotherapy
Zebley, C. C., & Youngblood, B. (2022) · Trends in Cancer · doi:10.1016/j.trecan.2022.04.004 · Cited by 65 · see citing works
Self-citationHu, H., Zakharov, P. N., Peterson, O. J., & Unanue, E. R. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2019743117 · Cited by 62 · see citing works
Cencioni, M. T., Genchi, A., Brittain, G., de Silva, T. I., Sharrack, B., Snowden, J. A., Alexander, T., Greco, R., & Muraro, P. A. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2021.813957 · Cited by 60 · see citing works
Lledó-Delgado, A., Preston-Hurlburt, P., Currie, S., Clark, P., Linsley, P. S., Long, S. A., Liu, C., Koroleva, G., Martins, A. J., Tsang, J. S., et al. (2024) · Journal of Clinical Investigation · doi:10.1172/jci177492 · Cited by 58 · see citing works
A human mutation in STAT3 promotes type 1 diabetes through a defect in CD8+ T cell tolerance
Warshauer, J. T., Belk, J. A., Chan, A. Y. K., Wang, J., Gupta, A. R., Shi, Q., Skartsis, N., Peng, Y., Phipps, J. D., Acenas, D. D., II, et al. (2021) · The Journal of Experimental Medicine · doi:10.1084/jem.20210759 · Cited by 58 · see citing works
Passeri, L., Andolfi, G., Bassi, V., Russo, F., Giacomini, G., Laudisa, C., Marrocco, I., Cesana, L., Stefano, M. D., Fanti, L., et al. (2023) · Journal of Autoimmunity · doi:10.1016/j.jaut.2023.103051 · Cited by 56 · see citing works
Single-cell sorting based on secreted products for functionally defined cell therapies
Miwa, H., Dimatteo, R., de Rutte, J. M., Ghosh, R., & Carlo, D. D. (2022) · Microsystems & Nanoengineering · doi:10.1038/s41378-022-00422-x · Cited by 49 · see citing works
Saadey, A. A., Yousif, A., Osborne, N., Shahinfar, R., Chen, Y., Laster, B., Rajeev, M., Bauman, P., Webb, A., & Ghoneim, H. E. (2022) · Nature Immunology · doi:10.1038/s41590-022-01384-y · Cited by 45 · see citing works
Self-citationJiang, W., Xia, T., Liu, C., Li, J., Zhang, W., & Sun, C. (2021) · Frontiers in Oncology · doi:10.3389/fonc.2021.705903 · Cited by 46 · see citing works
Srivastava, N., Hu, H., Peterson, O. J., Vomund, A. N., Stremska, M. E., Zaman, M., Giri, S., Li, T., Lichti, C. F., Zakharov, P. N., et al. (2024) · Immunity · doi:10.1016/j.immuni.2024.04.017 · Cited by 45 · see citing works
Schrödinger’s T Cells: Molecular Insights Into Stemness and Exhaustion
Gonzalez, N. M., Zou, D., Gu, A., & Chen, W. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.725618 · Cited by 45 · see citing works
IL-12 Signaling Promotes TET2-Mediated DNA Demethylation During CD8 T Cell Effector Differentiation
Zebley, C. C., Abdelsamed, H. A., Ghoneim, H. E., Alli, S., Brown, C., Haydar, D., Tian, M., Harris, T. L., McGargill, M. A., Krenciute, G., et al. (2020) · Cell Reports · doi:10.1016/j.celrep.2021.109796 · Cited by 45 · see citing works
Self-citationDNA Methylation and Immune Memory Response
Mittelstaedt, N. N., Becker, A. L., de Freitas, D. N., Zanin, R. F., Stein, R. T., & de Souza, A. P. D. (2021) · Cells · doi:10.3390/cells10112943 · Cited by 43 · see citing works
Mallone, R., Halliez, C., Rui, J., & Herold, K. C. (2022) · Diabetes · doi:10.2337/dbi21-0036 · Cited by 43 · see citing works
Early methionine availability attenuates T cell exhaustion
Sharma, P., Guo, A., Poudel, S., Boada-Romero, E., Verbist, K., Palacios, G., Immadisetty, K., Chen, J., Haydar, D., Mishra, A., et al. (2025) · Nature Immunology · doi:10.1038/s41590-025-02223-6 · Cited by 43 · see citing works
Epigenetic regulation of T cell adaptive immunity
Frias, A. B., Boi, S. K., Lan, X., & Youngblood, B. (2021) · Immunological Reviews · doi:10.1111/imr.12943 · Cited by 44 · see citing works
Self-citationEpigenetics and CD8+ T cell memory*
Montacchiesi, G., & Pace, L. (2021) · Immunological Reviews · doi:10.1111/imr.13057 · Cited by 42 · see citing works
Uncovering Pathways to Personalized Therapies in Type 1 Diabetes
Linsley, P. S., Greenbaum, C. J., & Nepom, G. T. (2021) · Diabetes · doi:10.2337/db20-1185 · Cited by 37 · see citing works
Self-citationThe Role of T Cell Receptor Signaling in the Development of Type 1 Diabetes
Clark, M., Kroger, C. J., Qi, K., & Tisch, R. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2020.615371 · Cited by 35 · see citing works
Persistence of self-reactive CD8+ T cells in the CNS requires TOX-dependent chromatin remodeling
Pagé, N., Lemeille, S., Vincenti, I., Klimek, B., Mariotte, A., Wagner, I., Liberto, G. D., Kaye, J. G., & Merkler, D. (2021) · Nature Communications · doi:10.1038/s41467-021-21109-3 · Cited by 34 · see citing works
Collier, J. L., Pauken, K. E., Lee, C. A. A., Patterson, D. G., Markson, S. C., Conway, T. S., Fung, M. E., France, J. A., Mucciarone, K., Lian, C. G., et al. (2023) · The Journal of Experimental Medicine · doi:10.1084/jem.20221920 · Cited by 33 · see citing works
An update on epigenetic regulation in autoimmune diseases
Mei, X., Zhang, B., Zhao, M., & Lu, Q. (2022) · Journal of Translational Autoimmunity · doi:10.1016/j.jtauto.2022.100176 · Cited by 33 · see citing works
Riegel, D., Romero-Fernández, E., Simon, M., Adenugba, A. R., Singer, K., Mayr, R., Weber, F., Kleemann, M., Imbusch, C. D., Kreutz, M. P., et al. (2023) · Molecular Cell · doi:10.1016/j.molcel.2022.12.029 · Cited by 33 · see citing works
Epigenetic regulation of T cell exhaustion in cancer
Kang, T. G., Johnson, J. T., Zebley, C. C., & Youngblood, B. (2025) · Nature reviews. Cancer · doi:10.1038/s41568-025-00883-y · Cited by 35 · see citing works
Self-citationStem cell-like memory T cells: A perspective from the dark side
Gao, S., Liang, X., Wang, H., Bao, B., Zhang, K., Zhu, Y., & Shao, Q. (2021) · Cellular Immunology · doi:10.1016/j.cellimm.2020.104273 · Cited by 31 · see citing works
Conserved epigenetic hallmarks of T cell aging during immunity and malignancy
Tian, M., Soerens, A. G., Alli, S., Kang, T. G., Vasandan, A. B., Wang, Z., Vezys, V., Kimura, S., Iacobucci, I., Baylin, S. B., et al. (2024) · Nature Aging · doi:10.1038/s43587-024-00649-5 · Cited by 30 · see citing works
Self-citationAljobaily, N. A., Allard, D., Perkins, B., Raugh, A., Galland, T., Jing, Y., Stephens, W. Z., Bettini, M. L., Hale, J. S., & Bettini, M. (2024) · Immunity · doi:10.1016/j.immuni.2024.09.016 · Cited by 30 · see citing works
Chen, Z., Zhu, Z., Hu, T., Yao, C., & Wu, T. (2025) · Cellular and Molecular Immunology · doi:10.1038/s41423-025-01378-4 · Cited by 36 · see citing works
Yang, K., Zhang, Y., Ding, J., Li, Z., Zhang, H., & Zou, F. (2024) · Frontiers in Endocrinology · doi:10.3389/fendo.2024.1377322 · Cited by 28 · see citing works
Ou, K., Hamo, D., Schulze, A. S., Roemhild, A., Kaiser, D., Gasparoni, G., Salhab, A., Zarrinrad, G., Amini, L., Schlickeiser, S., et al. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.751590 · Cited by 27 · see citing works
Personalized Immunotherapies for Type 1 Diabetes: Who, What, When, and How?
Deligne, C., You, S., & Mallone, R. (2022) · Journal of Personalized Medicine · doi:10.3390/jpm12040542 · Cited by 25 · see citing works
Immune perturbations in human pancreas lymphatic tissues prior to and after type 1 diabetes onset
Golden, G. J., Wu, V. H., Hamilton, J. T., Amses, K. R., Shapiro, M. R., Japp, A. S., Liu, C., Pampena, M. B., Kuri-Cervantes, L., Knox, J. J., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-59626-0 · Cited by 25 · see citing works
Mu-Mosley, H., Ostermann, L. B., Müftüoğlu, M., Vaidya, A. B., Bonifant, C. L., Velasquez, M. P., Gottschalk, S. M., & Andreeff, M. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.880108 · Cited by 20 · see citing works
Modeling cell-mediated immunity in human type 1 diabetes by engineering autoreactive CD8+ T cells
Peters, L. D., Yeh, W.-I., Arnoletti, J. M., Brown, M. E., Posgai, A. L., Mathews, C. E., & Brusko, T. M. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1142648 · Cited by 17 · see citing works
Kong, Y., Jing, Y., Allard, D., Scavuzzo, M. A., Sprouse, M. L., Borowiak, M., Bettini, M. L., & Bettini, M. (2022) · European Journal of Immunology · doi:10.1002/eji.202149690 · Cited by 16 · see citing works
Epitope-based precision immunotherapy of Type 1 diabetes
Firdessa-Fite, R., Genzano, C. B., Mallone, R., & Creusot, R. J. (2023) · Human Vaccines & Immunotherapeutics · doi:10.1080/21645515.2022.2154098 · Cited by 16 · see citing works
The many faces of islet antigen‐specific CD8 T cells: clues to clinical outcome in type 1 diabetes
WIEDEMAN, A. E., Speake, C., & Long, S. A. (2021) · Immunology and Cell Biology · doi:10.1111/imcb.12437 · Cited by 16 · see citing works
Self-citationHarnessing CD8+ T‐cell exhaustion to treat type 1 diabetes
Kwong, C.-T. J., Selck, C., Tahija, K., McAnaney, L. J., Le, D. V., Kay, T. W. H., Thomas, H. E., & Krishnamurthy, B. (2021) · Immunology and Cell Biology · doi:10.1111/imcb.12444 · Cited by 15 · see citing works
Autoreactive CD8 T cells in NOD mice exhibit phenotypic heterogeneity but restricted TCR gene usage
Kasmani, M. Y., Ciecko, A. E., Brown, A. K., Петрова, Г. В., Gorski, J., Chen, Y., & Cui, W. (2022) · Life Science Alliance · doi:10.26508/lsa.202201503 · Cited by 15 · see citing works
Self-antigens, benign autoimmunity and type 1 diabetes: a beta-cell and T-cell perspective
Samassa, F., & Mallone, R. (2022) · Current Opinion in Endocrinology Diabetes and Obesity · doi:10.1097/med.0000000000000735 · Cited by 15 · see citing works
Sun, F., Yang, C., Wang, F., Rong, S.-J., Luo, J., Lu, W.-Y., Yue, T., Wang, C., & Liu, S. (2023) · Cell & Bioscience · doi:10.1186/s13578-023-01110-7 · Cited by 14 · see citing works
Viruses as a potential environmental trigger of type 1 diabetes mellitus (Review)
Abrantes, J., de Azevedo, J. C. V., Fernandes, F., Almeida, V., de Oliveira, L. C., Oliveira, M. F. D., de Araújo, J. M. G., Lanza, D. C. F., Bezerra, F., Andrade, V. S., et al. (2024) · Biomedical Reports · doi:10.3892/br.2024.1770 · Cited by 14 · see citing works
Zhou, H., Zheng, Z., Fan, C., & Zhou, Z. (2025) · Seminars in Cancer Biology · doi:10.1016/j.semcancer.2025.01.001 · Cited by 15 · see citing works
Can fecal microbiota transplantations modulate autoimmune responses in type 1 diabetes?
Snethlage, C. M. F., de Wit, D. F., Wortelboer, K., Rampanelli, E., Hanssen, N., & Nieuwdorp, M. (2024) · Immunological Reviews · doi:10.1111/imr.13345 · Cited by 12 · see citing works
Grebinoski, S., Pieklo, G. P., Zhang, Q., Visperas, A., Cui, J., Goulet, J., Xiao, H., Brunazzi, E. A., Cardello, C., Herrada, A. A., et al. (2024) · The Journal of Immunology · doi:10.4049/jimmunol.2300216 · Cited by 13 · see citing works
Räuber, S. J., Schulte‐Mecklenbeck, A., Willison, A., Hagler, R., Jonas, M., Pul, D., Masanneck, L., Schroeter, C. B., Golombeck, K. S., Lichtenberg, S., et al. (2024) · Journal of Neuroinflammation · doi:10.1186/s12974-024-03269-3 · Cited by 13 · see citing works
Oligodendrocyte-derived IL-33 regulates self-reactive CD8+ T cells in CNS autoimmunity
Fonta, N., Pagé, N., Klimek, B., Piccinno, M., Liberto, G. D., Lemeille, S., Kreutzfeldt, M., Kastner, A. L., Ertuna, Y. I., Vincenti, I., et al. (2025) · The Journal of Experimental Medicine · doi:10.1084/jem.20241188 · Cited by 12 · see citing works
Stem-like T cells and niches: Implications in human health and disease
Yi, L., & Li, Y. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.907172 · Cited by 12 · see citing works
Activated-memory T cells influence naïve T cell fate: a noncytotoxic function of human CD8 T cells
Sasaki, K., Moussawy, M. A., Abou‐Daya, K. I., Macedo, C., Hosni-Ahmed, A., Liu, S., Juya, M., Zahorchak, A. F., Metes, D., Thomson, A. W., et al. (2022) · Communications Biology · doi:10.1038/s42003-022-03596-2 · Cited by 11 · see citing works
Self-citationMass cytometry and type 1 diabetes research in the age of single-cell data science
Rahman, A. H., & Homann, D. (2020) · Current Opinion in Endocrinology Diabetes and Obesity · doi:10.1097/med.0000000000000549 · Cited by 11 · see citing works
Defining the Molecular Hallmarks of T-Cell MemoryPreprint
Zebley, C. C., Akondy, R. S., Youngblood, B., & Kissick, H. T. (2021) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a037804 · Cited by 11 · see citing works
Self-citationYue, M., He, X., Min, X., Yang, H., Xu, H., Wu, W., Zhong, J., Mei, A., & Chen, J. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1462384 · Cited by 9 · see citing works
Selck, C., Jhala, G., George, D. J. D., Kwong, C.-T. J., Christensen, M. K., Pappas, E. G., Liu, X., Ge, T., Trivedi, P., Kallies, A., et al. (2024) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2315419121 · Cited by 10 · see citing works
Clinical and experimental treatment of type 1 diabetes
Long, S. A., & Buckner, J. H. (2022) · Clinical & Experimental Immunology · doi:10.1093/cei/uxac077 · Cited by 9 · see citing works
Obesity and Autoimmunity Epidemic: The Role of Immunometabolism
Colamatteo, A., Fusco, C., Matarese, A., & Matarese, G. (2025) · Annual Review of Nutrition · doi:10.1146/annurev-nutr-111324-122456 · Cited by 10 · see citing works
Niederlová, V., Neuwirth, A., Neuman, V., Michalik, J., Charvatova, B., Modrák, M., Šumnı́k, Z., & Štěpánek, O. (2025) · Nature Communications · doi:10.1038/s41467-025-66459-4 · Cited by 8 · see citing works
Ettinger, R. A., Buitinga, M., Vandamme, C., Afonso, G., Gómez, R., Arribas-Layton, D., Bissenova, S., Speake, C., Reijonen, H., Kinnunen, T. T., et al. (2023) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/clinem/dgad434 · Cited by 8 · see citing works
Self-citationApplications of single‐cell omics for chimeric antigen receptor T cell therapy
Ghaffari, S., Saleh, M., Akbari, B., Ramezani, F. M., & Mirzaei, H. R. (2023) · Immunology · doi:10.1111/imm.13720 · Cited by 8 · see citing works
Latent EBV enhances the efficacy of anti-CD3 mAb in Type 1 diabetes
Lledó-Delgado, A., Preston-Hurlburt, P., Higdon, L., Hu, A., James, E., Lim, N., Long, S. A., McNamara, J., Nguyen, H., Serti, E., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-60276-5 · Cited by 7 · see citing works
Self-citationEstablishment of CD8+ T Cell Thymic Central Tolerance to Tissue-Restricted Antigen Requires PD-1
May, J. F., Kelly, R. G., Suen, A. Y. W., Kim, J. I., Kim, J., Anderson, C. C., Rayat, G. R., & Baldwin, T. A. (2023) · The Journal of Immunology · doi:10.4049/jimmunol.2200775 · Cited by 7 · see citing works
Assessing effector T cells in type 1 diabetes
Arif, S., Pujol‐Autonell, I., & Eichmann, M. (2020) · Current Opinion in Endocrinology Diabetes and Obesity · doi:10.1097/med.0000000000000553 · Cited by 7 · see citing works
Zhao, R., Su, Z., Gu, J., Zhao, H., Bian, L., Yin, J., Cai, Y., Yang, T., Gu, Y., & Xu, X. (2025) · BMC Medicine · doi:10.1186/s12916-025-04001-5 · Cited by 6 · see citing works
CAR T cells need a pitstop to win the race
Zebley, C. C., & Youngblood, B. (2021) · Cancer Cell · doi:10.1016/j.ccell.2021.05.011 · Cited by 5 · see citing works
Self-citationThe role of memory T cells in type 1 diabetes: Phenotypes, mechanisms, and therapeutic implications
Fazeli, P., Abolhasani, S., Karamali, N., Hajivalili, M., Daryabor, G., Panji, M., Karimian, M., & Hosseini, M. (2025) · Autoimmunity Reviews · doi:10.1016/j.autrev.2025.103759 · Cited by 4 · see citing works
Innate-like memory T cells rapidly emerge in humans after gene therapy for SCID-X1
Vasandan, A. B., Abdelsamed, H. A., Boi, S. K., Ward, G., Alli, S., Mi, T., Lan, X., Zhang, X., Cowan, M. J., Puck, J. M., et al. (2025) · Immunity · doi:10.1016/j.immuni.2025.07.002 · Cited by 4 · see citing works
Self-citationAnti-CD3 mAb treatment reshapes infiltrating T and β cells in the islets in autoimmune diabetes
Wu, Y., Spurrell, M., Lledó-Delgado, A., Deng, S.-Y., Wang, D.-J., Liu, Y., Barkestani, M., Perdigoto, A., & Herold, K. (2026) · JCI Insight · doi:10.1172/jci.insight.192755 · Cited by 5 · see citing works
Zhang, Y., Lu, Y., Gao, Y., Liang, X., Zhang, R., Wang, X., Zou, X., & Yang, W. (2023) · International Immunopharmacology · doi:10.1016/j.intimp.2023.109890 · Cited by 4 · see citing works
Abdullatypov, A. V., Glushkova, O. V., Petriaikina, E. S., Bogdanov, V. P., Tabakov, D., Akimov, V. E., Yudin, V. S., Keskinov, A. A., Yudin, S. M., Volchkov, P., et al. (2025) · Frontiers in Endocrinology · doi:10.3389/fendo.2025.1663728 · Cited by 3 · see citing works
Developing a comprehensive database and search tool for single-cell ATAC-seq data
Gibson-Khademi, A., Wang, J., Christensen, E., & Shooshtari, P. (2026) · Scientific Reports · doi:10.1038/s41598-025-09962-4 · Cited by 3 · see citing works
Barman, S., Räuber, S. J., Eisenhut, K., Esser, D., VanDuijn, M. M., Scharf, M., Herrera-Rivero, M., Disse, P., Preuth, L.-M., Gulyaeva, V., et al. (2026) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2514753123 · Cited by 3 · see citing works
Yasumizu, Y., Hagiwara, M., Umezu, Y., Fuji, H., Iwaisako, K., Asagiri, M., Üemoto, S., Nakamura, Y., Thul, S., Ueyama, A., et al. (2024) · NAR Cancer · doi:10.1093/narcan/zcae022 · Cited by 3 · see citing works
Steenbuck, N., Damond, N., Engler, S., Kusmartseva, I., Posgai, A. L., Drotar, D. M., Williams, M. D., de Souza, N., Brusko, T. M., Brusko, M., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.03.05.641526 · Cited by 3 · see citing works
How do autoimmune CD4+ T cells handle exhaustion?
Fabri, A., & Walker, L. S. K. (2024) · Trends in Immunology · doi:10.1016/j.it.2024.11.004 · Cited by 2 · see citing works
Codazzi, V., Salvatore, V., Ragogna, F., Marzinotto, I., Anselmo, A., Baldoni, N., Pastore, M. R., Martinenghi, S., Stabilini, A., Bosi, E., et al. (2024) · Journal of Endocrinological Investigation · doi:10.1007/s40618-024-02497-x · Cited by 2 · see citing works
The Role of Epigenetics in Autoimmune Disorders
Klein, K. (2022) · Elsevier eBooks · doi:10.1016/b978-0-323-91909-8.00004-9 · Cited by 2 · see citing works
Mueller, A. L., Lamcaj, S., Garforth, S., Hiner, C. R., Woodley, D., Paraiso, K. D., Tian, M., Low, S., Youngblood, B., Almo, S. C., et al. (2025) · Journal of Virology · doi:10.1128/jvi.00188-25 · Cited by 1 · see citing works
Self-citationZhao, Y., Samir, J., Keoshkerian, E., Li, H., An, H., Bull, R. A., Luciani, F., & Lloyd, A. R. (2025) · The Journal of Immunology · doi:10.1093/jimmun/vkaf299 · Cited by 1 · see citing works
Epigenetic Modifications and Their Role in Type 1 Diabetes Development: A Review
de Azevedo, J. C. V., Fernandes, F. L., Rodrigues, T. D., de Medeiros, I. A. C. M., Andrade, V. S., de Araújo, J. M. G., Bezerra, F. L., Bezerra, C. M., Fernandes, T. A. A. D. M., & Fernandes, J. V. (2026) · Current Diabetes Reviews · doi:10.2174/0115733998399336251122042738 · Cited by 1 · see citing works
CD8+ T cells in atherosclerosis and coronary artery disease
Tandon, I., yosri, M., Soliman, H., Khalifa, A. M., Ley, K. F., & Abdelsamed, H. A. (2026) · Nature Reviews Cardiology · doi:10.1038/s41569-026-01295-7 · Cited by 1 · see citing works
Self-citationLEF1 and niche factors determine T cell stemness across chronic diseases
Miakicheva, S., Hawley, K. M., Zumbo, P., Gearty, S. V., Grassmann, S. A., Naizir, B., Chiu, E., Carson, S., Kissner, M., Owyong, M., et al. (2026) · Cell · doi:10.1016/j.cell.2026.06.022 · Cited by 1 · see citing works
Immune dysregulation and stem-like CD8+ T cell enrichment in type 1 diabetes pancreatic lymph nodes
Peters, L. D., Seay, H. R., Smith, J. A., Posgai, A. L., Berkowitz, R. L., Wasserfall, C. H., Atkinson, P. M. A., Bacher, R. L., Brusko, M., & Brusko, T. M. (2026) · Journal of Clinical Investigation · doi:10.1172/jci196445 · Cited by 1 · see citing works
UTX coordinates TCF1 and STAT3 to control progenitor CD8+ T cell fate in autoimmune diabetes
Chen, H.-C., Bang, M. F., Wang, H., Shpargel, K. B., Kohn, L. A., Sailer, D., Zhang, S. C., McCarthy, E. C., Seyedsadr, M., Stevens, S., et al. (2025) · Journal of Clinical Investigation · doi:10.1172/jci196325 · Cited by 1 · see citing works
IL-12 Signaling Promotes TET2-Mediated DNA Demethylation During CD8 T Cell Effector DifferentiationPreprint
Zebley, C. C., Abdelsamed, H. A., Ghoneim, H. E., Alli, S., Haydar, D., Harris, T. L., McGargill, M. A., Krenciute, G., & Youngblood, B. (2020) · SSRN Electronic Journal · doi:10.2139/ssrn.3720007 · Cited by 1 · see citing works
Self-citation
- Authors
- Abdelsamed, H. A., Zebley, C. C., Nguyen, H., Rutishauser, R. L., Fan, Y., Ghoneim, H. E., Crawford, J. C., Alfei, F., Alli, S., Ribeiro, S. P., Castellaw, A. H., McGargill, M. A., Jin, H., Boi, S. K., Speake, C., Serti, E., Turka, L. A., Busch, M. E., Stone, M., Deeks, S. G., Sekaly, R.-P., Zehn, D., James, E. A., Nepom, G. T., & Youngblood, B.
- Affiliations
- St. Jude Children's Research Hospital (US)
- Benaroya Research Institute (US)
- University of California, San Francisco (US)
- Technical University of Munich (DE)
- Case Western Reserve University (US)
- Immune Tolerance Network (US)
- Harvard University (US)
- Vitalant Research Institute (US)
- Corresponding author
- Youngblood, Ben
- ORCID
- Abdelsamed, Hossam A.
- Zebley, Caitlin C.
- Nguyen, Hai
- Rutishauser, Rachel L.
- Fan, Yiping
- Ghoneim, Hazem E.
- Crawford, Jeremy Chase
- Alli, Shanta
- Ribeiro, Susan Pereira
- Castellaw, Ashley H.
- McGargill, Maureen A.
- Jin, Hongjian
- Boi, Shannon K.
- Speake, Cate
- Serti, Elisavet
- Turka, Laurence A.
- Stone, Mars
- Deeks, Steven G.
- Zehn, Dietmar
- James, Eddie A.
- Nepom, Gerald T.
- Youngblood, Ben
- Venue
- Nature Immunology
- Published
- 2020-03-30
- Volume
- 21
- Issue
- 5
- Pages
- 578-587
- ISSN
- 1529-2908 (ISSN-L)
- 1529-2916
- PMC
- PMC7183435
- OpenAlex
- W3013298623
- Cited by
- 121
- References
- 46
- Citations by year
- 2026: 14 · 2025: 23 · 2024: 20 · 2023: 14 · 2022: 20 · 2021: 23 · 2020: 6 · 2019: 1
- FWCI
- 9.24
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Nature Immunology (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- eScholarship (California Digital Library) (submittedVersion)
- Funders
- U.S. Department of Health & Human Services | National Institutes of Health (1R01AI114442, UM1AI109565)
- American Lebanese Syrian Associated Charities
- Assisi Foundation of Memphis
- U.S. Department of Health & Human Services | NIH | Division of Loan Repayment
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Diabetes and associated disorders
- Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
- Life Sciences › Immunology and Microbiology › Immunology › Psoriasis: Treatment and Pathogenesis
- Keywords
- type 1 diabetes, autoreactive T cells, DNA methylation, T cell differentiation, chromatin accessibility, T cell plasticity, T cell longevity, pancreatic beta cells
- MeSH terms
- Cell Plasticity, Adolescent, Adult, Animals, Autoantigens, Cells, Cultured, Diabetes Mellitus, Type 1, Female, Flow Cytometry, Humans, Immunologic Memory, Male, CD8-Positive T-Lymphocytes, DNA Methylation, Pluripotent Stem Cells, Epigenesis, Genetic, Insulin-Secreting Cells, Mice, Young Adult, Single-Cell Analysis
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