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T cell regeneration after immunological injury
Open accessAbstract
Following periods of haematopoietic cell stress, such as after chemotherapy, radiotherapy, infection and transplantation, patient outcomes are linked to the degree of immune reconstitution, specifically of T cells. Delayed or defective recovery of the T cell pool has significant clinical consequences, including prolonged immunosuppression, poor vaccine responses and increased risks of infections and malignancies. Thus, strategies that restore thymic function and enhance T cell reconstitution can provide considerable benefit to individuals whose immune system has been decimated in various settings. In this Review, we focus on the causes and consequences of impaired adaptive immunity and discuss therapeutic strategies that can recover immune function, with a particular emphasis on approaches that can promote a diverse repertoire of T cells through de novo T cell formation.
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“Since cytoreductive therapy significantly impairs the immune system [37], the potential to induce strong CD8+ T-cell responses is particularly relevant for an antigen-based immunotherapeutic for GBM, where chemotherapy and radiotherapy remain the standard of care, and induced T cells must cross the blood–brain barrier to invade the immunologically “cold” tumour.”
From Preclinical development of an mRNA-based multiepitope immunotherapeutic for glioblastoma (2025) · cites this paper as [37]
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Clinical features of patients infected with 2019 novel coronavirus in Wuhan, China
Huang, C., Wang, Y., Li, X., Ren, L., Zhao, J., Hu, Y., Zhang, L., Fan, G., Xu, J., Gu, X., et al. (2020) · The Lancet · doi:10.1016/s0140-6736(20)30183-5 · Cited by 48,884
PD-1 and PD-L1 Immune Checkpoint Blockade to Treat Breast Cancer
Hartkopf, A. D., Taran, F., Wallwiener, M., Walter, C. B., Krämer, B., Grischke, E., & Brucker, S. Y. (2016) · Breast Care · doi:10.1159/000453569 · Cited by 30,989
Mutational landscape determines sensitivity to PD-1 blockade in non–small cell lung cancer
Rizvi, N. A., Hellmann, M. D., Snyder, A., Kvistborg, P., Makarov, V., Havel, J. J., Lee, W., Yuan, J., Wong, P., Ho, T. S., et al. (2015) · Science · doi:10.1126/science.aaa1348 · Cited by 7,802
The trinity of COVID-19: immunity, inflammation and intervention
Tay, M. Z., Poh, C. M., Rénia, L., MacAry, P. A., & Ng, L. F. P. (2020) · Nature Reviews Immunology · doi:10.1038/s41577-020-0311-8 · Cited by 4,360
Genetic Basis for Clinical Response to CTLA-4 Blockade in Melanoma
Snyder, A., Makarov, V., Merghoub, T., Yuan, J., Zaretsky, J. M., Desrichard, A., Walsh, L. A., Postow, M. A., Wong, P., Ho, T. S., et al. (2014) · New England Journal of Medicine · doi:10.1056/nejmoa1406498 · Cited by 4,286
Mortality Associated With Influenza and Respiratory Syncytial Virus in the United States
Thompson, W. W., Shay, D. K., Weintraub, E., Brammer, L., Cox, N., Anderson, L. J., & Fukuda, K. (2003) · JAMA · doi:10.1001/jama.289.2.179 · Cited by 3,673
Clonal neoantigens elicit T cell immunoreactivity and sensitivity to immune checkpoint blockade
McGranahan, N., Furness, A. J. S., Rosenthal, R., Ramskov, S., Lyngaa, R., Saini, S. K., Jamal-Hanjani, M., Wilson, G. A., Birkbak, N. J., Hiley, C. T., et al. (2016) · Science · doi:10.1126/science.aaf1490 · Cited by 3,065
The evolving landscape of biomarkers for checkpoint inhibitor immunotherapy
Havel, J. J., Chowell, D., & Chan, T. A. (2019) · Nature Reviews Cancer · doi:10.1038/s41568-019-0116-x · Cited by 2,286
Changes in thymic function with age and during the treatment of HIV infection
Douek, D. C., McFarland, R. D., Keiser, P. H., Gage, E. A., Massey, J. M., Haynes, B. F., Polis, M. A., Haase, A. T., Feinberg, M. B., Sullivan#, J. L., et al. (1998) · Nature · doi:10.1038/25374 · Cited by 1,893
HIV Infection, Inflammation, Immunosenescence, and Aging
Deeks, S. G. (2011) · Annual Review of Medicine · doi:10.1146/annurev-med-042909-093756 · Cited by 1,349
Noguchi, M. (1993) · Cell · doi:10.1016/0092-8674(93)90167-o · Cited by 1,338
The twilight of immunity: emerging concepts in aging of the immune system
Nikolich-Žugich, J. (2018) · Nature Immunology · doi:10.1038/s41590-017-0006-x · Cited by 1,240
Cell intrinsic alterations underlie hematopoietic stem cell aging
Rossi, D. J., Bryder, D., Zahn, J. M., Ahlenius, H., Sonu, R., Wagers, A. J., & Weissman, I. L. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0503280102 · Cited by 1,152
Deficiencies in DNA damage repair limit the function of haematopoietic stem cells with age
Rossi, D. J., Bryder, D., Seita, J., Nussenzweig, A., Hoeijmakers, J., & Weissman, I. L. (2007) · Nature · doi:10.1038/nature05862 · Cited by 1,115
Haematopoietic stem cell activity and interactions with the niche
Pinho, S., & Frenette, P. S. (2019) · Nature Reviews Molecular Cell Biology · doi:10.1038/s41580-019-0103-9 · Cited by 1,064
Age, Thymopoiesis, and CD4+ T-Lymphocyte Regeneration after Intensive Chemotherapy
Mackall, C. L., Fleisher, T. A., Brown, M. R., Andrich, M. P., Chen, C. C., Feuerstein, I. M., Horowitz, M. E., Magrath, I. T., Shad, A. T., Steinberg, S. M., et al. (1995) · New England Journal of Medicine · doi:10.1056/nejm199501193320303 · Cited by 1,026
Fibroblastic reticular cells in lymph nodes regulate the homeostasis of naive T cells
Link, A., Vogt, T. K., Favre, S., Britschgi, M. R., Acha‐Orbea, H., Hinz, B., Cyster, J. G., & Luther, S. A. (2007) · Nature Immunology · doi:10.1038/ni1513 · Cited by 949
The bone marrow microenvironment at single-cell resolution
Tikhonova, A. N., Dolgalev, I., Hu, H., Sivaraj, K. K., Hoxha, E., Cuesta-Domínguez, Á., Pinho, S., Akhmetzyanova, I., Gao, J., Witkowski, M., et al. (2019) · Nature · doi:10.1038/s41586-019-1104-8 · Cited by 936
Advances in graft-versus-host disease biology and therapy
Blazar, B. R., Murphy, W. J., & Abedi, M. (2012) · Nature reviews. Immunology · doi:10.1038/nri3212 · Cited by 900
Viral and host factors related to the clinical outcome of COVID-19
Zhang, X., Tan, Y., Ling, Y., Lü, G., Liu, F., Yi, Z., Jia, X., Wu, M., Shi, B., Xu, S., et al. (2020) · Nature · doi:10.1038/s41586-020-2355-0 · Cited by 874
Defective IL7R expression in T(-)B(+)NK(+) severe combined immunodeficiency
Puel, A., Ziegler, S. F., Buckley, R. H., & Leonard., W. J. (1998) · Nature Genetics · doi:10.1038/3877 · Cited by 813
Journey through the thymus: stromal guides for T-cell development and selection
Takahama, Y. (2006) · Nature reviews. Immunology · doi:10.1038/nri1781 · Cited by 768
The many important facets of T-cell repertoire diversity
Nikolich‐Žugich, J., Slifka, M. K., & Messaoudi, I. (2004) · Nature reviews. Immunology · doi:10.1038/nri1292 · Cited by 681
Vonarbourg, C., Mortha, A., Bui, V. L., Hernández, P. P., Kiss, E. A., Hoyler, T., Flach, M., Bengsch, B., Thimme, R., Hölscher, C., et al. (2010) · Immunity · doi:10.1016/j.immuni.2010.10.017 · Cited by 669
Harnessing the biology of IL-7 for therapeutic application
Mackall, C. L., Fry, T. J., & Gress, R. E. (2011) · Nature reviews. Immunology · doi:10.1038/nri2970 · Cited by 602
Nikolich-Zugich, J., Knox, K. S., Rios, C. T., Natt, B., Bhattacharya, D., & Fain, M. J. (2020) · GeroScience · doi:10.1007/s11357-020-00186-0 · Cited by 577
Maintenance of peripheral naive T cells is sustained by thymus output in mice but not humans
den Braber, I., Mugwagwa, T., Vrisekoop, N., Westera, L., Mögling, R., Bregje de Boer, A., Willems, N., Schrijver, E. H. R., Spierenburg, G., Gaiser, K., et al. (2012) · Immunity · doi:10.1016/j.immuni.2012.02.006 · Cited by 572
Thymic involution and immune reconstitution.
Lynch, H. E., Goldberg, G. L., Chidgey, A., Van den Brink, M. R. M., Boyd, R., & Sempowski, G. D. (2009) · Trends in Immunology · doi:10.1016/j.it.2009.04.003 · Cited by 522
DNA repair is limiting for haematopoietic stem cells during ageing
Nijnik, A., Woodbine, L., Marchetti, C., Dawson, S., Lambe, T., Liu, C., Rodrigues, N. P., Crockford, T. L., Cabuy, E., Vindigni, A., et al. (2007) · Nature · doi:10.1038/nature05875 · Cited by 518
Akiyama, T., Shimo, Y., Yanai, H., Qin, J., Ohshima, D., Maruyama, Y., Asaumi, Y., Kitazawa, J., Takayanagi, H., Penninger, J. M., et al. (2008) · Immunity · doi:10.1016/j.immuni.2008.06.015 · Cited by 503
Activation of Thymic Regeneration in Mice and Humans following Androgen Blockade
Sutherland, J. S., Goldberg, G. L., Hammett, M. V., Uldrich, A. P., Berzins, S. P., Heng, T. S. P., Blazar, B. R., Millar, J. L., Malin, M., Chidgey, A. P., et al. (2005) · The Journal of Immunology · doi:10.4049/jimmunol.175.4.2741 · Cited by 493
Rossi, S. W., Kim, M., Leibbrandt, A., Parnell, S. M., Jenkinson, W. E., Glanville, S. H., McConnell, F. M., Scott, H. S., Penninger, J. M., Jenkinson, E. J., et al. (2007) · The Journal of Experimental Medicine · doi:10.1084/jem.20062497 · Cited by 491
Yager, E. J., Ahmed, M., Lanzer, K., Randall, T. D., Woodland, D. L., & Blackman, M. A. (2008) · The Journal of Experimental Medicine · doi:10.1084/jem.20071140 · Cited by 490
Small, T., Papadopoulos, E. B., Boulad, F., Black, P., Castro-Malaspina, H. R., Childs, B. H., Collins, N. H., Gillio, A. P., George, D., Jakubowski, A. A., et al. (1999) · Blood · doi:10.1182/blood.v93.2.467 · Cited by 489
Reversal of epigenetic aging and immunosenescent trends in humans.
Fahy, G. M., Brooke, R. T., Watson, J. P., Good, Z., Vasanawala, S. S., Maecker, H., Leipold, M. D., Lin, D. T. S., Kobor, M. S., & Horvath, S. (2019) · Aging Cell · doi:10.1111/acel.13028 · Cited by 477
Sportès, C., Hakim, F. T., Memon, S. A., Zhang, H., Chua, K., Brown, M. R., Fleisher, T. A., Krumlauf, M., Babb, R. R., Chow, C. K., et al. (2008) · The Journal of Experimental Medicine · doi:10.1084/jem.20071681 · Cited by 476
Britanova, O. V., Putintseva, E. V., Shugay, M., Merzlyak, E. M., Turchaninova, M. A., Staroverov, D. B., Bolotin, D. A., Lukyanov, S., Bogdanova, E. A., Mamedov, I. Z., et al. (2014) · The Journal of Immunology · doi:10.4049/jimmunol.1302064 · Cited by 465
Developmental kinetics, turnover, and stimulatory capacity of thymic epithelial cells
Gray, D. H. D., Seach, N., Ueno, T., Milton, M. K., Liston, A., Lew, A. M., Goodnow, C. C., & Boyd, R. L. (2006) · Blood · doi:10.1182/blood-2006-02-004531 · Cited by 458
Rosenberg, S. A., Sportès, C., Ahmadzadeh, M., Fry, T. J., Ngo, L. T., Schwarz, S. L., Stetler-Stevenson, M., Morton, K. E., Mavroukakis, S. A., Morre, M., et al. (2006) · Journal of Immunotherapy · doi:10.1097/01.cji.0000210386.55951.c2 · Cited by 443
Kimmig, S., Przybylski, G. K., Schmidt, C. A., Laurisch, K., Möwes, B., Radbruch, A., & Thiel, A. (2002) · The Journal of Experimental Medicine · doi:10.1084/jem.20011756 · Cited by 439
Hikosaka, Y., Nitta, T., Ohigashi, I., Yano, K., Ishimaru, N., Hayashi, Y., Matsumoto, M., Matsuo, K., Penninger, J. M., Takayanagi, H., et al. (2008) · Immunity · doi:10.1016/j.immuni.2008.06.018 · Cited by 433
Efficient Transplantation via Antibody-Based Clearance of Hematopoietic Stem Cell Niches
Czechowicz, A. D., Kraft, D. L., Weissman, I. L., & Bhattacharya, D. (2007) · Science · doi:10.1126/science.1149726 · Cited by 432
A potential role for interleukin-7 in T-cell homeostasis
Fry, T. J. (2001) · Blood · doi:10.1182/blood.v97.10.2983 · Cited by 415
Lymphocyte depletion during treatment with intensive chemotherapy for cancer
Mackall, C. L., Fleisher, T. A., Brown, M., Magrath, I. T., Shad, A., Horowitz, M., Wexler, L., Adde, M., McClure, L., & Gress, R. (1994) · Blood · doi:10.1182/blood.v84.7.2221.bloodjournal8472221 · Cited by 402
Mackall, C. L., Fleisher, T. A., Brown, M. R., Andrich, M. P., Chen, C. C., Feuerstein, I. M., Magrath, I. T., Wexler, L. H., Dimitrov, D. S., & Gress, R. E. (1997) · Blood · doi:10.1182/blood.v89.10.3700 · Cited by 400
Interleukin-22 Drives Endogenous Thymic Regeneration in Mice
Dudakov, J. A., Hanash, A. M., Jenq, R. R., Young, L. F., Ghosh, A., Singer, N. V., West, M. L., Smith, O. M., Holland, A. M., Tsai, J. J.-Y., et al. (2012) · Science · doi:10.1126/science.1218004 · Cited by 392
Self-citationBiology of Immune Responses to Vaccines in Elderly Persons
Weinberger, B., Herndler‐Brandstetter, D., Schwanninger, A., Weiskopf, D., & Grubeck‐Loebenstein, B. (2008) · Clinical Infectious Diseases · doi:10.1086/529197 · Cited by 392
Proliferative arrest and rapid turnover of thymic epithelial cells expressing Aire
Gray, D. H. D., Abramson, J., Benoist, C. O., & Mathis, D. J. (2007) · The Journal of Experimental Medicine · doi:10.1084/jem.20070795 · Cited by 378
Generation of Functional Thymocytes in the Human Adult
Jamieson, B. D., Douek, D. C., Killian, S., Hultin, L. E., Scripture-Adams, D. D., Giorgi, J. V., Marelli, D., Koup, R. A., & Zack, J. A. (1999) · Immunity · doi:10.1016/s1074-7613(00)80056-4 · Cited by 367
Thymic involution and rising disease incidence with age
Palmer, S., Albergante, L., Blackburn, C. C., & Newman, T. J. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1714478115 · Cited by 364
Age-dependent incidence, time course, and consequences of thymic renewal in adults
Hakim, F. T., Memon, S. A., Cepeda, R., Jones, E. C., Chow, C. K., Kasten-Sportès, C., Odom, J., Vance, B. A., Christensen, B. L., Mackall, C. L., et al. (2005) · Journal of Clinical Investigation · doi:10.1172/jci200522492 · Cited by 362
Inflammatory signals regulate hematopoietic stem cells
Baldridge, M. T., King, K. Y., & Goodell, M. A. (2011) · Trends in Immunology · doi:10.1016/j.it.2010.12.003 · Cited by 351
Total body irradiation selectively induces murine hematopoietic stem cell senescence.
Wang, Y., Schulte, B. A., LaRue, A. C., Ogawa, M., & Zhou, D. (2006) · Blood · doi:10.1182/blood-2005-04-1418 · Cited by 351
Expansion of human NK-22 cells with IL-7, IL-2, and IL-1β reveals intrinsic functional plasticity
Cella, M., Otero, K., & Colonna, M. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1005641107 · Cited by 348
Snyder, A., Nathanson, T., Funt, S. A., Ahuja, A., Buros, J. L., Hellmann, M. D., Chang, E., Aksoy, B. A., Al‐Ahmadie, H. A., Yusko, E. C., et al. (2017) · PLoS Medicine · doi:10.1371/journal.pmed.1002309 · Cited by 348
Inflammation and the reciprocal production of granulocytes and lymphocytes in bone marrow
Ueda, Y., Kondo, M., & Kelsoe, G. H. (2005) · The Journal of Experimental Medicine · doi:10.1084/jem.20041419 · Cited by 343
Immunosenescence: what does it mean to health outcomes in older adults?
McElhaney, J. E., & Effros, R. B. (2009) · Current Opinion in Immunology · doi:10.1016/j.coi.2009.05.023 · Cited by 340
Purification and Biological Activity of Thymosin, a Hormone of the Thymus Gland
Goldstein, A. L., Guha, A., Zatz, M. M., Hardy, M. A., & White, A. (1972) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.69.7.1800 · Cited by 306
Sempowski, G. D., Hale, L. P., Sundy, J. S., Massey, J. M., Koup, R. A., Douek, D. C., Patel, D. D., & Haynes, B. F. (2000) · The Journal of Immunology · doi:10.4049/jimmunol.164.4.2180 · Cited by 304
Mackall, C. L., Fry, T. J., Bare, C., Morgan, P. B., Galbraith, A., & Gress, R. E. (2001) · Blood · doi:10.1182/blood.v97.5.1491 · Cited by 300
The Thymus Is a Common Target Organ in Infectious Diseases
Savino, W. (2006) · PLoS Pathogens · doi:10.1371/journal.ppat.0020062 · Cited by 298
Rantes/Ccl5 influences hematopoietic stem cell subtypes and causes myeloid skewing
Ergen, A. V., Boles, N. C., & Goodell, M. A. (2012) · Blood · doi:10.1182/blood-2011-11-391730 · Cited by 280
The full spectrum of human naive T cells
van den Broek, T., Borghans, J. A. M., & van Wijk, F. (2018) · Nature reviews. Immunology · doi:10.1038/s41577-018-0001-y · Cited by 273
HIV Infection Rapidly Induces and Maintains a Substantial Suppression of Thymocyte Proliferation
Dion, M.-L., Poulin, J., Bordi, R., Sylvestre, M., Corsini, R., Kettaf, N., Dalloul, A. H., Boulassel, M., Debré, P., Routy, J., et al. (2004) · Immunity · doi:10.1016/j.immuni.2004.10.013 · Cited by 270
Min, D., Taylor, P. A., Panoskaltsis‐Mortari, A., Chung, B., Danilenko, D. M., Farrell, C. L., Lacey, D. L., Blazar, B. R., & Weinberg, K. I. (2002) · Blood · doi:10.1182/blood.v99.12.4592 · Cited by 261
Identification of a human recent thymic emigrant phenotype
McFarland, R., Douek, D. C., Koup, R. A., & Picker, L. J. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.070061597 · Cited by 254
Yoshida, H., Naito, A., Inoue, J., Satoh, M., Santee, S. M., Ware, C. F., Togawa, A., Nishikawa, S., & Nishikawa, S. (2002) · Immunity · doi:10.1016/s1074-7613(02)00479-x · Cited by 250
Analysis of the human thymic perivascular space during aging
Flores, K. G., Li, J., Sempowski, G. D., Haynes, B. F., & Hale, L. P. (1999) · Journal of Clinical Investigation · doi:10.1172/jci7558 · Cited by 246
Lévy, Y., Sereti, I., Tambussi, G., Routy, J. P., Lelièvre, J. D., Delfraissy, J. F., Molina, J. M., Fischl, M., Goujard, C., Rodriguez, B., et al. (2012) · Clinical Infectious Diseases · doi:10.1093/cid/cis383 · Cited by 240
Finch, P. W., & Rubin, J. S. (2004) · Advances in cancer research · doi:10.1016/s0065-230x(04)91003-2 · Cited by 239
Fry, T. J. (2002) · Blood · doi:10.1182/blood-2002-07-2297 · Cited by 234
Hopkins, A. C., Yarchoan, M., Durham, J. N., Yusko, E. C., Rytlewski, J. A., Robins, H. S., Laheru, D. A., Le, D. T., Lutz, E. R., & Jaffee, E. M. (2018) · JCI Insight · doi:10.1172/jci.insight.122092 · Cited by 233
Postow, M. A., Manuel, M., Wong, P., Yuan, J., Dong, Z., Liu, C., Perez, S., Tanneau, I., Noel, M., Courtier, A., et al. (2015) · Journal for ImmunoTherapy of Cancer · doi:10.1186/s40425-015-0070-4 · Cited by 232
Palchaudhuri, R., Sáez, B., Hoggatt, J., Schajnovitz, A., Sykes, D. B., Tate, T. A., Czechowicz, A. D., Kfoury, Y. S., Ruchika, F., Rossi, D. J., et al. (2016) · Nature Biotechnology · doi:10.1038/nbt.3584 · Cited by 226
Severe combined immunodeficiencies and related disorders
Fischer, A., Notarangelo, L. D., Neven, B., Cavazzana, M., & Puck, J. M. (2015) · Nature Reviews Disease Primers · doi:10.1038/nrdp.2015.61 · Cited by 226
T‐Cell Immunodeficiency Following Cytotoxic Antineoplastic Therapy: A Review
Mackall, C. L. (2000) · Stem Cells · doi:10.1634/stemcells.18-1-10 · Cited by 224
Keratinocyte growth factor (KGF) is required for postnatal thymic regeneration.
Alpdogan, O., Hubbard, V. M., Smith, O. M., Patel, N., Lu, S., Goldberg, G. L., Gray, D. H., Feinman, J., Kochman, A. A., Eng, J. M., et al. (2006) · Blood · doi:10.1182/blood-2005-07-2831 · Cited by 220
Immunosenescence: deficits in adaptive immunity in the elderly
Hakim, F. T., & Gress, R. E. (2007) · Tissue Antigens · doi:10.1111/j.1399-0039.2007.00891.x · Cited by 218
Effects of Castration on Thymocyte Development in Two Different Models of Thymic Involution
Heng, T. S. P., Goldberg, G. L., Gray, D. H. D., Sutherland, J. S., Chidgey, A. P., & Boyd, R. L. (2005) · The Journal of Immunology · doi:10.4049/jimmunol.175.5.2982 · Cited by 216
Reduction in the Developmental Potential of Intrathymic T Cell Progenitors with Age
Min, H., Montecino-Rodriguez, E., & Dorshkind, K. (2004) · The Journal of Immunology · doi:10.4049/jimmunol.173.1.245 · Cited by 216
Rossi, S. W., Jeker, L. T., Ueno, T., Kuse, S., Keller, M. P., Zuklys, S., Gudkov, A. V., Takahama, Y., Krenger, W., Blazar, B. R., et al. (2007) · Blood · doi:10.1182/blood-2006-10-049767 · Cited by 215
Min, D., Panoskaltsis-Mortari, A., Kuro-o, M., Holländer, G. A., Blazar, B. R., & Weinberg, K. I. (2007) · Blood · doi:10.1182/blood-2006-08-043794 · Cited by 214
Perales, M., Goldberg, J. D., Yuan, J. D., Koehne, G., Lechner, L., Papadopoulos, E. B., Young, J. W., Jakubowski, A. A., Zaidi, B., Gallardo, H. F., et al. (2012) · Blood · doi:10.1182/blood-2012-06-437236 · Cited by 213
Stem cells and the aging hematopoietic system
Beerman, I., Maloney, W. J., Weissman, I. L., & Rossi, D. J. (2010) · Current Opinion in Immunology · doi:10.1016/j.coi.2010.06.007 · Cited by 212
Alpdoğan, Ö., Schmaltz, C., Muriglan, S. J., Kappel, B. J., Perales, M., Rotolo, J. A., Halm, J. A., Rich, B. E., & van den Brink, M. R. M. (2001) · Blood · doi:10.1182/blood.v98.7.2256 · Cited by 209
Quantitative assessment of T cell repertoire recovery after hematopoietic stem cell transplantation
van Heijst, J. W. J., Ceberio, I., Lipuma, L., Samilo, D., Wasilewski, G., Gonzales, A. M., Nieves, J., van den Brink, M. R. M., Perales, M., & Pamer, E. G. (2013) · Nature Medicine · doi:10.1038/nm.3100 · Cited by 206
Ghrelin promotes thymopoiesis during aging
Dixit, V. D., Yang, H., Sun, Y., Weeraratna, A. T., Youm, Y., Smith, R. G., & Taub, D. D. (2007) · Journal of Clinical Investigation · doi:10.1172/jci30248 · Cited by 206
Hattori, N. (2009) · Growth Hormone & IGF Research · doi:10.1016/j.ghir.2008.12.001 · Cited by 205
Tumanov, A. V., Koroleva, E. P., Guo, X., Wang, Y., Kruglov, A., Nedospasov, S. A., & Fu, Y. (2011) · Cell Host & Microbe · doi:10.1016/j.chom.2011.06.002 · Cited by 199
Czechowicz, A. D., Palchaudhuri, R., Scheck, A., Hu, Y., Hoggatt, J., Sáez, B., Pang, W. W., Mansour, M. K., Tate, T. A., Chan, Y. Y., et al. (2019) · Nature Communications · doi:10.1038/s41467-018-08201-x · Cited by 198
Rossi, S. W., Blazar, B. R., Farrell, C. L., Danilenko, D. M., Lacey, D. L., Weinberg, K. I., Krenger, W., & Holländer, G. A. (2002) · Blood · doi:10.1182/blood.v100.2.682 · Cited by 193
Meng, A., Wang, Y., Zant, G. E. V., & Zhou, D. (2003) · PubMed · Cited by 193
Zakrzewski, J. L., Kochman, A. A., Lu, S. X., Terwey, T. H., Kim, T. D., Hubbard, V. M., Muriglan, S. J., Suh, D. Y., Smith, O. M., Grubin, J., et al. (2006) · Nature Medicine · doi:10.1038/nm1463 · Cited by 190
Haines, C. J., Giffon, T. D., Lu, L.-S., Lu, X., Tessier-Lavigne, M., Ross, D. T., & Lewis, D. B. (2009) · Journal of Experimental Medicine · doi:10.1084/jem.20080996 · Cited by 189
Roberts, N. A., White, A. J., Jenkinson, W. E., Turchinovich, G., Nakamura, K., Withers, D. R., McConnell, F. M., Desanti, G. E., Bénézech, C., Parnell, S. M., et al. (2012) · Immunity · doi:10.1016/j.immuni.2012.01.016 · Cited by 185
Shono, Y., Ueha, S., Wang, Y., Abe, J., Kurachi, M., Matsuno, Y., Sugiyama, T., Nagasawa, T., Imamura, M., & Matsushima, K. (2010) · Blood · doi:10.1182/blood-2009-11-253559 · Cited by 184
Alpdoğan, Ö., Muriglan, S. J., Eng, J. M., Willis, L. M., Greenberg, A. S., Kappel, B. J., & van den Brink, M. R. M. (2003) · Journal of Clinical Investigation · doi:10.1172/jci17865 · Cited by 182
Flow cytometric analysis of the V? repertoire in healthy controls
van den Beemd, R., Boor, P. P. C., van Lochem, E. G., Hop, W. C. J., Langerak, A. W., Wolvers-Tettero, I. L. M., Hooijkaas, H., & van Dongen, J. J. M. (2000) · Cytometry · doi:10.1002/1097-0320(20000801)40:4 · Cited by 178
IL-7–producing stromal cells are critical for lymph node remodeling
Onder, L., Narang, P., Scandella, E., Chai, Q., Iolyeva, M. E., Hoorweg, K., Halin, C., Richie, E. R., Kaye, P. M., Westermann, J., et al. (2012) · Blood · doi:10.1182/blood-2012-03-416859 · Cited by 178
Clave, E., Busson, M., Douay, C., de Latour, R. P., Berrou, J., Rabian, C., Carmagnat, M., Rocha, V., Charron, D. J., Socié, G., et al. (2009) · Blood · doi:10.1182/blood-2008-09-176594 · Cited by 173
Parent, A. V., Russ, H. A., Khan, I. S., LaFlam, T. N., Metzger, T. C., Anderson, M. S., & Hebrok, M. (2013) · Cell stem cell · doi:10.1016/j.stem.2013.04.004 · Cited by 173
An organized and functional thymus generated from FOXN1-reprogrammed fibroblasts
Bredenkamp, N., Ulyanchenko, S., O’Neill, K. E., Manley, N. R., Vaidya, H. J., & Blackburn, C. C. (2014) · Nature Cell Biology · doi:10.1038/ncb3023 · Cited by 172
BMP Signaling Is Required for Normal Thymus Development
Bleul, C. C., & Boehm, T. L. J. (2005) · The Journal of Immunology · doi:10.4049/jimmunol.175.8.5213 · Cited by 169
Specific bone cells produce DLL4 to generate thymus-seeding progenitors from bone marrow
Yu, V. W. C., Sáez, B., Cook, C., Lotinun, S., Pardo–Saganta, A., Wang, Y., Lymperi, S., Ferraro, F., Raaijmakers, M. H. G. P., Wu, J. Y., et al. (2015) · The Journal of Experimental Medicine · doi:10.1084/jem.20141843 · Cited by 163
Wu, T., Young, J. S., Johnston, H. F., Ni, X., Deng, R., Racine, J. J., Wang, M., Wang, A., Todorov, I., Wang, J., et al. (2013) · The Journal of Immunology · doi:10.4049/jimmunol.1300657 · Cited by 160
Aging alters the epigenetic asymmetry of HSC division
Florian, M. C., Klose, M., Saçma, M., Jablanovic, J., Knudson, L. A., Nattamai, K., Marka, G., Vollmer, A., Soller, K., Sakk, V., et al. (2018) · PLoS Biology · doi:10.1371/journal.pbio.2003389 · Cited by 160
Kalayjian, R. C., LANDAY, A. L., Pollard, R. B., Taub, D. D., Gross, B. H., Francis, I. R., Sevin, A. D., Pu, M., Spritzler, J., Chernoff, M., et al. (2003) · The Journal of Infectious Diseases · doi:10.1086/375372 · Cited by 158
Marie‐Cardine, A., Divay, F., Dutot, I., Green, A. S., Perdrix, A., Boyer, O., Contentin, N., Tilly, H., Tron, F., Vannier, J., et al. (2008) · Clinical Immunology · doi:10.1016/j.clim.2007.11.013 · Cited by 156
Alpdoğan, Ö., Muriglan, S. J., Eng, J. M., et al. (2003) · Journal of Clinical Investigation · doi:10.1172/jci200317865 · Cited by 156
Regulation of thymic epithelium by keratinocyte growth factor
Erickson, M., Morkowski, S., Lehar, S. M., Gillard, G. O., Beers, C., Dooley, J., Rubin, J. S., Rudensky, A. Y., & Farr, A. G. (2002) · Blood · doi:10.1182/blood-2002-04-1036 · Cited by 154
Nixon, A. B., Schalper, K. A., Jacobs, I. A., Potluri, S., Wang, I., & Fleener, C. (2019) · Journal for ImmunoTherapy of Cancer · doi:10.1186/s40425-019-0799-2 · Cited by 154
Liu, Y., Pan, Y., Hu, Z., Wu, M., Wang, C., Feng, Z., Mao, C., Tan, Y., Liu, Y., Chen, L., et al. (2020) · Clinical Infectious Diseases · doi:10.1093/cid/ciaa630 · Cited by 154
Napolitano, L. A., Lo, J. C.-M., Gotway, M. B., Mulligan, K. M., Barbour, J. D., Schmidt, D. K., Grant, R. M., Halvorsen, R. A., Schambelan, M., & McCune, J. M. (2002) · AIDS · doi:10.1097/00002030-200205240-00003 · Cited by 153
Maury, S., Mary, J., Rabian, C., Schwarzinger, M., Toubert, A., Scieux, C., Carmagnat, M., Espérou, H., Ribaud, P., Devergié, A., et al. (2001) · British Journal of Haematology · doi:10.1046/j.1365-2141.2001.03135.x · Cited by 153
Čičin‐Šain, L., Smyk-Pearson, S., Currier, N., Byrd, L., Koudelka, C. W., Robinson, T., Swarbrick, G. M., Tackitt, S., Legasse, A. W., Fischer, M. B., et al. (2010) · The Journal of Immunology · doi:10.4049/jimmunol.0904193 · Cited by 151
Enterocyte Expression of Interleukin 7 Induces Development of γδ T Cells and Peyer's Patches
Laky, K., Lefrançois, L., Lingenheld, E. G., Ishikawa, H., Lewis, J. M., Olson, S., Suzuki, K., Tigelaar, R. E., & Puddington, L. (2000) · The Journal of Experimental Medicine · doi:10.1084/jem.191.9.1569 · Cited by 142
Small, T., KEEVER, C. A., Weiner-Fedus, S., Heller, G., O’Reilly, R., & Flomenberg, N. (1990) · Blood · doi:10.1182/blood.v76.8.1647.1647 · Cited by 141
Zoller, A. L., & Kersh, G. J. (2006) · The Journal of Immunology · doi:10.4049/jimmunol.176.12.7371 · Cited by 140
Interleukin-15 enhances immune reconstitution after allogeneic bone marrow transplantation
Alpdoğan, Ö., Eng, J. M., Muriglan, S. J., Willis, L. M., Hubbard, V. M., Tjoe, K. H., Terwey, T. H., Kochman, A. A., & van den Brink, M. R. M. (2004) · Blood · doi:10.1182/blood-2003-09-3344 · Cited by 139
Kim, D. H., Sohn, S. K., Won, D. I., Lee, N. Y., Suh, J. S., & Lee, K. B. (2006) · Bone Marrow Transplantation · doi:10.1038/sj.bmt.1705381 · Cited by 139
Toubert, A., Glauzy, S., Douay, C., & Clave, E. (2012) · Tissue Antigens · doi:10.1111/j.1399-0039.2011.01820.x · Cited by 136
Thymic atrophy and regrowth in response to chemotherapy: CT evaluation
Choyke, P. L., Zeman, R. K., Gootenberg, J. E., Greenberg, J. S., Hoffer, F. A., & Frank, J. (1987) · American Journal of Roentgenology · doi:10.2214/ajr.149.2.269 · Cited by 134
Tn, S., Avigan, D., Dupont, B., Smith, K. M., Black, P., Heller, G., Polyak, T., & O’Reilly, R. (1997) · PubMed · Cited by 133
Murray, J. M., Kaufmann, G. R., Hodgkin, P. D., Lewin, S. R., Kelleher, A. D., Davenport, M. P., & Zaunders, J. (2003) · Immunology and Cell Biology · doi:10.1046/j.1440-1711.2003.01191.x · Cited by 132
Sutherland, J. S., Spyroglou, L., Muirhead, J., Heng, T. S. P., Hinojosa, A. I. P., Prince, H. M., Chidgey, A. P., Schwarer, A. P., & Boyd, R. L. (2008) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-07-1784 · Cited by 132
Production of BMP4 by endothelial cells is crucial for endogenous thymic regeneration
Wertheimer, T., Velardi, E., Tsai, J. J.-Y., Cooper, K., Xiao, S., Kloss, C. C., Jarick, K. J., Mokhtari, Z., Brede, C., DeRoos, P. C., et al. (2018) · Science Immunology · doi:10.1126/sciimmunol.aal2736 · Cited by 132
Self-citationThe aged lymphoid tissue environment fails to support naïve T cell homeostasis
Becklund, B. R., Purton, J. F., Ramsey, C., Favre, S., Vogt, T. K., Martin, C. E., Spasova, D. S., Sarkisyan, G., LeRoy, E., Tan, J. T., et al. (2016) · Scientific Reports · doi:10.1038/srep30842 · Cited by 129
Impaired hematopoietic stem cell functioning after serial transplantation and during normal aging
Kamminga, L. M., van Os, R., Ausema, A., Noach, E. J. K., Weersing, E., Dontje, B., Vellenga, E., & de Haan, G. (2005) · STEM CELLS · doi:10.1634/stemcells.2004-0066 · Cited by 128
BMP4 acts upstream of FGF in modulating thymic stroma and regulating thymopoiesis
Tsai, P. T., Lee, R. A., & Wu, H. (2003) · Blood · doi:10.1182/blood-2003-05-1657 · Cited by 126
Yew, P., Alachkar, H., Yamaguchi, R., Kiyotani, K., Fang, H., Yap, K. L., Liu, H. T., Wickrema, A., Artz, A. S., van Besien, K., et al. (2015) · Bone Marrow Transplantation · doi:10.1038/bmt.2015.133 · Cited by 125
Powles, R., Singhal, S., Treleaven, J. G., Kulkarni, S., Horton, C., & Mehta, J. (1998) · Blood · doi:10.1182/blood.v91.9.3481 · Cited by 123
Sex steroid blockade enhances thymopoiesis by modulating Notch signaling
Velardi, E., Tsai, J. J.-Y., Holland, A. M., Wertheimer, T., Yu, V. W. C., Zakrzewski, J. L., Tuckett, A. Z., Singer, N. V., West, M. L., Smith, O. M., et al. (2014) · The Journal of Experimental Medicine · doi:10.1084/jem.20131289 · Cited by 121
Self-citationGriffith, A. V., Fallahi, M., Venables, T., & Petrie, H. T. (2011) · Aging Cell · doi:10.1111/j.1474-9726.2011.00773.x · Cited by 120
Rejuvenation of the aging thymus: growth hormone-mediated and ghrelin-mediated signaling pathways
Taub, D. D., Murphy, W. J., & Longo, D. L. (2010) · Current Opinion in Pharmacology · doi:10.1016/j.coph.2010.04.015 · Cited by 119
Fan, Y., Tajima, A., Goh, S. K., Geng, X., Gualtierotti, G., Grupillo, M., Coppola, A., Bertera, S., Rudert, W. A., Banerjee, I., et al. (2015) · Molecular Therapy · doi:10.1038/mt.2015.77 · Cited by 119
Tumor immunotherapy across MHC barriers using allogeneic T-cell precursors
Zakrzewski, J. L., Suh, D. Y., Markley, J. C., Smith, O. M., King, C. G., Goldberg, G. L., Jenq, R. R., Holland, A. M., Grubin, J., Cabrera-Pérez, J., et al. (2008) · Nature Biotechnology · doi:10.1038/nbt1395 · Cited by 119
Evidence for an early role for BMP4 signaling in thymus and parathyroid morphogenesis
Gordon, J., Patel, S. R., Mishina, Y. M., & Manley, N. R. (2010) · Developmental Biology · doi:10.1016/j.ydbio.2009.12.026 · Cited by 116
Ki, S., Park, D., Selden, H. J., Seita, J., Chung, H., Kim, J., Iyer, V. R., & Ehrlich, L. I. R. (2014) · Cell Reports · doi:10.1016/j.celrep.2014.08.070 · Cited by 116
Genetic and epigenetic regulation of aging
Fraga, M. F. (2009) · Current Opinion in Immunology · doi:10.1016/j.coi.2009.04.003 · Cited by 114
Sano, S., Takahama, Y., Sugawara, T., Kosaka, H., Itami, S., Yoshikawa, K., Miyazaki, J., van Ewijk, W., & Takeda, J. (2001) · Immunity · doi:10.1016/s1074-7613(01)00180-7 · Cited by 110
Chu, Y.-W., Schmitz, S., Choudhury, B., Telford, W., Kapoor, V., Garfield, S., Howe, D., & Gress, R. E. (2008) · Blood · doi:10.1182/blood-2008-04-149435 · Cited by 107
Kelly, R. M., Highfill, S. L., Panoskaltsis‐Mortari, A., Taylor, P. A., Boyd, R. L., Holländer, G. A., & Blazar, B. R. (2008) · Blood · doi:10.1182/blood-2008-01-136531 · Cited by 107
Verfuerth, S., Peggs, K. S., Vyas, P., Barnett, L., O’Reilly, R. J., & Mackinnon, S. (2000) · Blood · doi:10.1182/blood.v95.12.3990 · Cited by 104
Lymphohematopoietic progenitors do not have a synchronized defect with age‐related thymic involution
Zhu, X., Gui, J., Dohkan, J., Cheng, L., Barnes, P. F., & Su, D. (2007) · Aging Cell · doi:10.1111/j.1474-9726.2007.00325.x · Cited by 104
Chu, Y., Memon, S. A., Sharrow, S. O., Hakim, F. T., Eckhaus, M., Lucas, P. J., & Gress, R. E. (2004) · Blood · doi:10.1182/blood-2003-10-3635 · Cited by 102
Seggewiss, R., Loré, K., Guenaga, J., Pittaluga, S., Mattapallil, J. J., Chow, C. K., Koup, R. A., Camphausen, K. A., Nason, M., Meier‐Schellersheim, M., et al. (2007) · Blood · doi:10.1182/blood-2006-12-065623 · Cited by 101
Age-related changes in localization of thymosin in the human thymus.
Hirokawa, K., McClure, J. E., & Al, G. (1982) · PubMed · Cited by 101
Shah, N. J., Mao, A. S., Shih, T., Kerr, M. D., Sharda, A., Raimondo, T. M., Weaver, J. C., Vrbanac, V. D., Déruaz, M., Tager, A. M., et al. (2019) · Nature Biotechnology · doi:10.1038/s41587-019-0017-2 · Cited by 100
Blanc, K. L., Barrett, A. J., Schaffer, M., Hägglund, H., Ljungman, P. T., Ringdén, O. T. H., & Remberger, M. (2009) · Transplantation and Cellular Therapy · doi:10.1016/j.bbmt.2009.05.015 · Cited by 99
Hauri-Hohl, M. M., Keller, M. P., Gill, J. W., Hafen, K., Pachlatko, E., Boulay, T., Peter, A., Holländer, G. A., & Krenger, W. (2007) · Blood · doi:10.1182/blood-2006-07-034157 · Cited by 98
Fletcher, A. L., Lowen, T. E., Sakkal, S., Reiseger, J. J., Hammett, M. V., Seach, N., Scott, H. S., Boyd, R. L., & Chidgey, A. P. (2009) · The Journal of Immunology · doi:10.4049/jimmunol.0900225 · Cited by 97
Flt3 ligand enhances thymic-dependent and thymic-independent immune reconstitution
Fry, T. J., Sinha, M. L., Milliron, M., Chu, Y., Kapoor, V., Gress, R. E., Thomas, E., & Mackall, C. L. (2004) · Blood · doi:10.1182/blood-2003-11-3789 · Cited by 95
Goldberg, G. L., Alpdoğan, Ö., Muriglan, S. J., Hammett, M. V., Milton, M. K., Eng, J. M., Hubbard, V. M., Kochman, A. A., Willis, L. M., Greenberg, A. S., et al. (2007) · The Journal of Immunology · doi:10.4049/jimmunol.178.11.7473 · Cited by 94
Studies on the thymus in chagas' disease
Savino, W., Leite‐de‐Moraes, M., Hontebeyrie-Joskowicz, M., & Dardenne, M. (1989) · European Journal of Immunology · doi:10.1002/eji.1830190930 · Cited by 90
B Cells in Chronic Graft-versus-Host Disease
Sarantopoulos, S., Blazar, B. R., Cutler, C. S., & Ritz, J. (2014) · Transplantation and Cellular Therapy · doi:10.1016/j.bbmt.2014.10.029 · Cited by 87
Azevedo, R. I., Soares, M. V. D., Barata, J. T., Rego, R. T., Serra‐Caetano, A., Victorino, R. M. M., & Sousa, A. E. (2008) · Blood · doi:10.1182/blood-2008-07-166223 · Cited by 87
Thymic Atrophy: Experimental Studies and Therapeutic Interventions
Majumdar, S., & Nandi, D. (2017) · Scandinavian Journal of Immunology · doi:10.1111/sji.12618 · Cited by 84
Goldberg, G. L., King, C. G., Nejat, R. A., Suh, D. Y., Smith, O. M., Bretz, J. C., Samstein, R. M., Dudakov, J. A., Chidgey, A. P., Chen‐Kiang, S., et al. (2009) · The Journal of Immunology · doi:10.4049/jimmunol.0801458 · Cited by 82
Abdul-Hai, A., Or, R., Slavin, S., Friedman, G., Weiss, L., Matsa, D., & Ben-Yehuda, A. (1996) · PubMed · Cited by 82
CCL25 increases thymopoiesis after androgen withdrawal
Williams, K. M., Lucas, P. J., Bare, C. V., Wang, J., Chu, Y., Tayler, E. B., Kapoor, V., & Gress, R. E. (2008) · Blood · doi:10.1182/blood-2008-04-153627 · Cited by 81
Administration of interleukin-7 increases CD4 T cells in idiopathic CD4 lymphocytopenia
Sheikh, V., Porter, B. O., DerSimonian, R., Kovacs, S. B., Thompson, W. L., Pérez‐Díez, A., Freeman, A. F., Roby, G. A., Mican, J. M., Pau, A. K., et al. (2015) · Blood · doi:10.1182/blood-2015-05-645077 · Cited by 81
Glucocorticoid (GC) sensitivity and GC receptor expression differ in thymocyte subpopulations
Berki, T., Pàlinkàs, L., Boldizsár, F., & Németh, P. (2002) · International Immunology · doi:10.1093/intimm/14.5.463 · Cited by 80
van der Maas, N. G., Berghuis, D., van der Burg, M., & Lankester, A. C. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.00782 · Cited by 80
Multiple prethymic defects underlie age-related loss of T progenitor competence
Zediak, V. P., Maillard, I., & Bhandoola, A. (2007) · Blood · doi:10.1182/blood-2007-01-071605 · Cited by 79
Awong, G., Singh, J., Mohtashami, M., Malm, M., Motte-Mohs, R. N. L., Benveniste, P. M., Serra, P., Herer, E., van den Brink, M. R. M., & Zúñiga‐Pflücker, J. C. (2013) · Blood · doi:10.1182/blood-2012-12-472803 · Cited by 79
Montecino‐Rodriguez, E., Kong, Y., Casero, D., Rouault, A., Dorshkind, K. A., & Pioli, P. D. (2019) · Stem Cell Reports · doi:10.1016/j.stemcr.2019.01.016 · Cited by 79
The immunopathology of thymic GVHD
Krenger, W., & Holländer, G. A. (2008) · Seminars in Immunopathology · doi:10.1007/s00281-008-0131-6 · Cited by 78
Dudakov, J. A., Mertelsmann, A. M., O'Connor, M. H., Jenq, R. R., Velardi, E., Young, L. F., Smith, O. M., Boyd, R. L., van den Brink, M. R. M., & Hanash, A. M. (2017) · Blood · doi:10.1182/blood-2017-01-762658 · Cited by 78
Self-citationDertschnig, S., Hauri-Hohl, M. M., Vollmer, M., Holländer, G. A., & Krenger, W. (2015) · Blood · doi:10.1182/blood-2014-08-597245 · Cited by 75
Mensen, A., Jöhrens, K., Anagnostopoulos, I., Demski, S., Oey, M., Stroux, A., Hemmati, P., Westermann, J., Blau, O., Wittenbecher, F., et al. (2014) · Blood · doi:10.1182/blood-2013-11-539031 · Cited by 75
Hemopoietic reconstitution after bone marrow transplantation.
Arnold, R., SCHMEISER, T., Heit, W. F. W., Frickhofen, N., Pabst, G., Heimpel, H., & Kubanek, B. (1986) · PubMed · Cited by 75
Lymph nodes as barriers to T‐cell rejuvenation in aging mice and nonhuman primates
Thompson, H. L., Smithey, M. J., Uhrlaub, J. L., Jeftic, I. D., Jergović, M., White, S. E., Currier, N., Lang, A. M., Okoye, A. A., Park, B. S., et al. (2018) · Aging Cell · doi:10.1111/acel.12865 · Cited by 75
Young, Proliferative Thymic Epithelial Cells Engraft and Function in Aging Thymuses
Kim, M., Miller, C. M., Shadrach, J. L., Wagers, A. J., & Serwold, T. F. (2015) · The Journal of Immunology · doi:10.4049/jimmunol.1403158 · Cited by 74
Neonatal and adult recent thymic emigrants produce IL-8 and express complement receptors CR1 and CR2
Pękalski, M. Ł., García, A. R., Ferreira, R. C., Rainbow, D. B., Smyth, D. J., Mashar, M., Brady, J., Yarkoni, N. S., Dopico, X. C., Mahmood, S., et al. (2017) · JCI Insight · doi:10.1172/jci.insight.93739 · Cited by 74
Arakawa, A., Vollmer, S., Tietze, J., Galinski, A., Heppt, M. V., Bürdek, M., Berking, C., & Prinz, J. C. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.01336 · Cited by 74
Meyer, E. H., Hsu, A. R., Liliental, J., Löhr, A., Florek, M., Zehnder, J. L., Strober, S., Lavori, P. W., Miklos, D. B., Johnson, D. S., et al. (2013) · Blood · doi:10.1182/blood-2013-03-489757 · Cited by 71
Cell generation dynamics underlying naive T-cell homeostasis in adult humans
Mold, J. E., Réu, P., Olin, A., Bernard, S., Michaëlsson, J., Rane, S., Yates, A. J., Khosravi, A., Salehpour, M., Possnert, G., et al. (2019) · PLoS Biology · doi:10.1371/journal.pbio.3000383 · Cited by 70
Pao, M., Papadopoulos, E. B., Chou, J. F., Heller, G., Castro-Malaspina, H. R., Jakubowski, A. A., Kernan, N. A., Perales, M., Prokop, S., Scaradavou, A., et al. (2008) · Transplantation and Cellular Therapy · doi:10.1016/j.bbmt.2008.06.012 · Cited by 69
Chen, B. J., Cui, X., Sempowski, G. D., & Chao, N. J. A. (2003) · Experimental Hematology · doi:10.1016/s0301-472x(03)00196-6 · Cited by 69
Wils, E., van der Holt, B., Broers, A. E. C., Sluijs, S. J. P.-V., Gratama, J. W., Braakman, E., & Cornelissen, J. J. (2011) · Haematologica · doi:10.3324/haematol.2011.047696 · Cited by 69
Knutsen, A. P., Freeman, J. J., Mueller, K. R., Roodman, S. T., & Bouhasin, J. D. (1999) · International Journal of Immunopharmacology · doi:10.1016/s0192-0561(98)00060-5 · Cited by 68
Fagnoni, F. F., Lozza, L., Zibera, C., Zambelli, A., Ponchio, L., Gibelli, N., Oliviero, B., Pavesi, L., Gennari, R., Vescovini, R., et al. (2002) · Immunology · doi:10.1046/j.1365-2567.2002.01400.x · Cited by 67
Age‐related thymic activity in adults following chemotherapy‐induced lymphopenia
Sfikakis, P. P., Gourgoulis, G.-M., Moulopoulos, L. A., Kouvatseas, G., Theofilopoulos, A. N., & Dimopoulos, M. A. (2005) · European Journal of Clinical Investigation · doi:10.1111/j.1365-2362.2005.01499.x · Cited by 67
Trédan, O., Ménétrier‐Caux, C., Ray-Coquard, I., Garin, G., Cropet, C., Verronèse, E., Bachelot, T., Rebattu, P., Heudel, P., Cassier, P. A., et al. (2015) · Annals of Oncology · doi:10.1093/annonc/mdv173 · Cited by 67
IL-12 Inhibits Thymic Involution by Enhancing IL-7- and IL-2-Induced Thymocyte Proliferation
Li, L., Hsu, H., Stockard, C. R., Yang, P., Zhou, J., Wu, Q., Grizzle, W. E., & Mountz, J. D. (2004) · The Journal of Immunology · doi:10.4049/jimmunol.172.5.2909 · Cited by 66
Clise-Dwyer, K., Huston, G. E., Buck, A. L., Duso, D. K., & Swain, S. L. (2007) · The Journal of Immunology · doi:10.4049/jimmunol.178.3.1321 · Cited by 65
Abdel‐Azim, H., Elshoury, A., Mahadeo, K. M., Parkman, R., & Kapoor, N. (2017) · Transplantation and Cellular Therapy · doi:10.1016/j.bbmt.2017.05.005 · Cited by 65
Lakshmikanth, T., Olin, A., Chen, Y., Mikeš, J., Fredlund, E., Remberger, M., Omazic, B., & Brodin, P. (2017) · Cell Reports · doi:10.1016/j.celrep.2017.08.021 · Cited by 64
Alpdogan, N., Muriglan, S. J., Kappel, B. J., Doubrovina, E. S., Schmaltz, C., Schirò, R., Eng, J. M., Greenberg, A. S., Willis, L. M., Rotolo, J. A., et al. (2003) · Transplantation · doi:10.1097/01.tp.0000070167.81584.a2 · Cited by 63
Chen, T., Burke, K. A., Zhan, Y., Wang, X., Shibata, D. K., & Zhao, Y. (2007) · Experimental Hematology · doi:10.1016/j.exphem.2006.10.002 · Cited by 63
Goldberg, J. D., Zheng, J., Ratan, R., Small, T. N., Lai, K.-C., Boulad, F., Castro-Malaspina, H. R., Giralt, S. A., Jakubowski, A. A., Kernan, N. A., et al. (2017) · Leukemia & lymphoma/Leukemia and lymphoma · doi:10.1080/10428194.2016.1265113 · Cited by 61
Administration of RANKL boosts thymic regeneration upon bone marrow transplantation
Lopes, N., Vachon, H., Marie, J. C., & Irla, M. (2017) · EMBO Molecular Medicine · doi:10.15252/emmm.201607176 · Cited by 61
Dudakov, J. A., Goldberg, G. L., Reiseger, J. J., Vlahos, K., Chidgey, A. P., & Boyd, R. L. (2009) · The Journal of Immunology · doi:10.4049/jimmunol.0900196 · Cited by 60
Goldberg, G. L., Dudakov, J. A., Reiseger, J. J., Seach, N., Ueno, T., Vlahos, K., Hammett, M. V., Young, L. F., Heng, T. S. P., Boyd, R. L., et al. (2010) · The Journal of Immunology · doi:10.4049/jimmunol.0802445 · Cited by 59
Chen, W., KuoLee, R., Austin, J. W., Shen, H., Che, Y., & Conlan, J. W. (2005) · Microbial Pathogenesis · doi:10.1016/j.micpath.2005.08.005 · Cited by 59
Engineering the Human Thymic Microenvironment to Support Thymopoiesis In Vivo
Chung, B., Montel‐Hagen, A., Ge, S., Blumberg, G., Kim, K., Klein, S., Zhu, Y., Parekh, C., Balamurugan, A., Yang, O. O., et al. (2014) · Stem Cells · doi:10.1002/stem.1731 · Cited by 58
Immune memory and aging: an infinite or finite resource?
Nikolich-Žugich, J., & Rudd, B. D. (2010) · Current Opinion in Immunology · doi:10.1016/j.coi.2010.06.011 · Cited by 58
Activated T Cells Acquire Endothelial Cell Surface Determinants During Transendothelial Migration
Brezinschek, R. I., Oppenheimer‐Marks, N., & Lipsky, P. E. (1999) · The Journal of Immunology · doi:10.4049/jimmunol.162.3.1677 · Cited by 57
Dallas, M. H., Varnum‐Finney, B., Martin, P. J., & Bernstein, I. D. (2007) · Blood · doi:10.1182/blood-2006-08-039842 · Cited by 57
APOPTOSIS OF THYMOCYTES DURING ACUTE GRAFT-VERSUS-HOST DISEASE IS INDEPENDENT OF GLUCOCORTICOIDS1
Krenger, W., Rossi, S. W., & Holländer, G. A. (2000) · Transplantation · doi:10.1097/00007890-200005270-00040 · Cited by 51
Research works printed but not linked: 1
- Calzolari, A. Recherches experimentales sur un rapport probable entre la function du thymus et celle des testicules. Arch. Ital. Biol. 30, 71–77 (1898). This article presents one of the very first observations suggesting a relationship between sex steroids and thymic function.
Cited by
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Mittelbrunn, M., & Kroemer, G. (2021) · Nature Immunology · doi:10.1038/s41590-021-00927-z · Cited by 702
Immunosenescence: signaling pathways, diseases and therapeutic targets
Fu, Y., Wang, B., Alu, A., Hong, W., Hong, L., He, X., Shi, H., Cheng, P., & Yang, X. (2025) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-025-02371-z · Cited by 168
Dysregulation of Systemic Immunity in Aging and Dementia
Lutshumba, J., Nikolajczyk, B. S., & Bachstetter, A. D. (2021) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2021.652111 · Cited by 104
Age-related epithelial defects limit thymic function and regeneration
Kousa, A. I., Jahn, L., Zhao, K., Flores, A. E., Acenas, D. D., II, Lederer, E. E., Argyropoulos, K. V., Lemarquis, A. L., Granadier, D., Cooper, K., et al. (2024) · Nature Immunology · doi:10.1038/s41590-024-01915-9 · Cited by 116
Self-citationTissue-specific immunity for a changing world
Weisberg, S. P., Ural, B. B., & Färber, D. L. (2021) · Cell · doi:10.1016/j.cell.2021.01.042 · Cited by 104
Metadata
- Authors
- Velardi, E., Tsai, J. J., & van den Brink, M. R. M.
- Affiliations
- Bambino Gesù Children's Hospital (IT)
- State University of New York (US)
- Corresponding author
- Velardi, Enrico
- Venue
- Nature Reviews Immunology
- Published
- 2020-10-23
- Volume
- 21
- Issue
- 5
- Pages
- 277-291
- ISSN
- 1474-1733 (ISSN-L)
- 1474-1741
- PMC
- PMC7583557
- OpenAlex
- W3094124272
- Cited by
- 222
- References
- 282
- Citations by year
- 2026: 41 · 2025: 46 · 2024: 44 · 2023: 38 · 2022: 29 · 2021: 24
- FWCI
- 2.22
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Nature reviews. Immunology (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Memorial Sloan-Kettering Cancer Center (P01-CA023766, CA008748, P30 CA008748)
- Society of Memorial Sloan Kettering (P30-CA008748)
- Parker Institute for Cancer Immunotherapy
- Seres Therapeutics
- Ministero della Salute
- Associazione Italiana per la Ricerca sul Cancro
- National Institutes of Health (1r01hl147584-01a1, 7r01ca228308-07)
- National Institute on Aging (P01AG052359)
- National Heart, Lung, and Blood Institute (HL123340, R01‐HL147584, R01HL123340, CA008748, R01HL125571)
- National Cancer Institute (P01CA023766, R01‐CA228308, CA008748, R01CA228358, P30CA008748)
- National Institute of Allergy and Infectious Diseases (AI124275, U01AI124275)
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
- Health Sciences › Medicine › Hematology › Hematopoietic Stem Cell Transplantation
- Life Sciences › Immunology and Microbiology › Immunology › Immunotherapy and Immune Responses
- Keywords
- T cell reconstitution, immune reconstitution, thymic function, T cell depletion, chemotherapy, radiotherapy, transplantation, infection, adaptive immunity, T cell diversity, immunosuppression, vaccine response
- MeSH terms
- Immunosenescence, Animals, B-Lymphocytes, Graft vs Host Disease, Humans, Immunotherapy, Lymphopenia, Regeneration, Stress, Physiological, T-Lymphocytes, Hematopoietic Stem Cell Transplantation, Models, Immunological, Adaptive Immunity, Cellular Microenvironment
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