CD69: from activation marker to metabolic gatekeeper

Control of Treg and TH17 cell differentiation by the aryl hydrocarbon receptor

Quintana, F. J., Basso, A. S., Iglesias, A. H., Korn, T., Farez, M. F., Bettelli, E., Caccamo, M., Oukka, M., & Weiner, H. L. (2008) · Nature · doi:10.1038/nature06880 · Cited by 1,865 · see citing works

Control of TH17/Treg Balance by Hypoxia-Inducible Factor 1

Dang, E. V., Barbi, J., Yang, H.-Y., Jinasena, D., Yu, H., Zheng, Y., Bordman, Z., Fu, J., Kim, Y., Yen, H.-R., et al. (2011) · Cell · doi:10.1016/j.cell.2011.07.033 · Cited by 1,595 · see citing works

The developmental pathway for CD103+CD8+ tissue-resident memory T cells of skin

Mackay, L. K., Rahimpour, A., Ma, J. Z., Collins, N., Stock, A. T., Hafon, M.-L., Vega-Ramos, J., Lauzurica, P., Mueller, S. N., Stefanovic, T., et al. (2013) · Nature Immunology · doi:10.1038/ni.2744 · Cited by 1,331 · see citing works

CD69 acts downstream of interferon-α/β to inhibit S1P1 and lymphocyte egress from lymphoid organs

Shiow, L. R., Rosen, D. B., Brdičková, N., Xu, Y., An, J., Lanier, L. L., Cyster, J. G., & Matloubian, M. (2006) · Nature · doi:10.1038/nature04606 · Cited by 1,189 · see citing works

The Glucose Transporter Glut1 Is Selectively Essential for CD4 T Cell Activation and Effector Function

Macintyre, A. N., Gerriets, V. A., Nichols, A., Michalek, R. D., Rudolph, M. C., Deoliveira, D., Anderson, S. M., Abel, E. D., Chen, B. J., Hale, L. P., et al. (2014) · Cell Metabolism · doi:10.1016/j.cmet.2014.05.004 · Cited by 1,129 · see citing works

Control of amino-acid transport by antigen receptors coordinates the metabolic reprogramming essential for T cell differentiation

Sinclair, L. V., Rolf, J., Emslie, E., Shi, Y.-B., Taylor, P. M., & Cantrell, D. A. (2013) · Nature Immunology · doi:10.1038/ni.2556 · Cited by 930 · see citing works

Inflammatory T Cell Responses Rely on Amino Acid Transporter ASCT2 Facilitation of Glutamine Uptake and mTORC1 Kinase Activation

Nakaya, M., Xiao, Y., Zhou, X., Chang, J., Chang, M., Cheng, X., Blonska, M., Lin, X., & Sun, S. (2014) · Immunity · doi:10.1016/j.immuni.2014.04.007 · Cited by 870 · see citing works

Glutamine Uptake and Metabolism Are Coordinately Regulated by ERK/MAPK during T Lymphocyte Activation

Carr, E. L., Kelman, A., Wu, G. S., Gopaul, R., Senkevitch, E., Aghvanyan, A., Turay, A. M., & Frauwirth, K. A. (2010) · The Journal of Immunology · doi:10.4049/jimmunol.0903586 · Cited by 830 · see citing works

Transcriptional downregulation of S1pr1 is required for the establishment of resident memory CD8+ T cells

Skon, C. N., Lee, J.-Y., Anderson, K. G., Masopust, D., Hogquist, K. A., & Jameson, S. C. (2013) · Nature Immunology · doi:10.1038/ni.2745 · Cited by 817 · see citing works

The outs and the ins of sphingosine-1-phosphate in immunity

Spiegel, S., & Milstien, S. (2011) · Nature Reviews Immunology · doi:10.1038/nri2974 · Cited by 810 · see citing works

mTORC1 couples immune signals and metabolic programming to establish Treg-cell function

Zeng, H., Yang, K., Cloer, C., Neale, G. A. M., Vogel, P., & Chi, H. (2013) · Nature · doi:10.1038/nature12297 · Cited by 789 · see citing works

Differential glycosylation of TH1, TH2 and TH-17 effector cells selectively regulates susceptibility to cell death

Toscano, M. A., Bianco, G. A., Ilarregui, J. M., Croci, D. O., Correale, J., Hernandez, J. D., Zwirner, N. W., Poirier, F., Riley, E. M., Baum, L. G., et al. (2007) · Nature Immunology · doi:10.1038/ni1482 · Cited by 653 · see citing works

Opposing regulation of the locus encoding IL-17 through direct, reciprocal actions of STAT3 and STAT5

Yang, X.-P., Ghoreschi, K., Steward-Tharp, S. M., Rodriguez-Canales, J., Zhu, J., Grainger, J. R., Hirahara, K., Sun, H.-W., Wei, L., Vahedi, G., et al. (2011) · Nature Immunology · doi:10.1038/ni.1995 · Cited by 583 · see citing works

Cutting Edge: CD69 Interference with Sphingosine-1-Phosphate Receptor Function Regulates Peripheral T Cell Retention

Mackay, L. K., Braun, A., Macleod, B. L., Collins, N., Tebartz, C., Bedoui, S., Carbone, F. R., & Gebhardt, T. (2015) · The Journal of Immunology · doi:10.4049/jimmunol.1402256 · Cited by 503 · see citing works

Metabolic control of type 1 regulatory T cell differentiation by AHR and HIF1-α

Mascanfroni, I. D., Takenaka, M. C., Yeste, A., Patel, B., Wu, Y., Kenison, J. E., Siddiqui, S., Basso, A. S., Otterbein, L. E., Pardoll, D. M., et al. (2015) · Nature Medicine · doi:10.1038/nm.3868 · Cited by 441 · see citing works

Integrating canonical and metabolic signalling programmes in the regulation of T cell responses

Pollizzi, K. N., & Powell, J. D. (2014) · Nature reviews. Immunology · doi:10.1038/nri3701 · Cited by 379 · see citing works

The S1P1-mTOR axis directs the reciprocal differentiation of TH1 and Treg cells

Liu, G., Yang, K., Burns, S., Shrestha, S., & Chi, H. (2010) · Nature Immunology · doi:10.1038/ni.1939 · Cited by 322 · see citing works

CD69 Suppresses Sphingosine 1-Phosophate Receptor-1 (S1P1) Function through Interaction with Membrane Helix 4

Bankovich, A. J., Shiow, L. R., & Cyster, J. G. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m110.123299 · Cited by 310 · see citing works

Persistence of skin-resident memory T cells within an epidermal niche

Zaid, A., Mackay, L. K., Rahimpour, A., Braun, A., Veldhoen, M., Carbone, F. R., Manton, J. H., Heath, W. R., & Mueller, S. N. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1322292111 · Cited by 306 · see citing works

Molecular cloning, expression, and chromosomal localization of the human earliest lymphocyte activation antigen AIM/CD69, a new member of the C-type animal lectin superfamily of signal-transmitting receptors.

López‐Cabrera, M., Santis, A. G., Fernández‐Ruiz, E., Blacher, R. W., Esch, F. S., Sánchez‐Mateos, P., & Sánchez‐Madrid, F. (1993) · The Journal of Experimental Medicine · doi:10.1084/jem.178.2.537 · Cited by 279 · see citing works

Specific niches for lung-resident memory CD8+ T cells at the site of tissue regeneration enable CD69-independent maintenance

Takamura, S., Yagi, H., Hakata, Y., Motozono, C., McMaster, S. R., Masumoto, T., Fujisawa, M., Chikaishi, T., Komeda, J., Itoh, J., et al. (2016) · The Journal of Experimental Medicine · doi:10.1084/jem.20160938 · Cited by 240 · see citing works

Metabolic control of the Treg/Th17 axis

Barbi, J. J., Pardoll, D. M., & Pan, F. (2013) · Immunological Reviews · doi:10.1111/imr.12029 · Cited by 215 · see citing works

CD69 downregulates autoimmune reactivity through active transforming growth factor-β production in collagen-induced arthritis

Sancho, D., Gómez, M., Viedma, F., Esplugues, E., Gordón‐Alonso, M., García-López, M. Á., de la Fuente, H., Martínez‐A, C., Lauzurica, P., & Sánchez‐Madrid, F. (2003) · Journal of Clinical Investigation · doi:10.1172/jci19112 · Cited by 199 · see citing works

Transcriptional Regulation of Tissue-Resident Lymphocytes

Mackay, L. K., & Kallies, A. (2016) · Trends in Immunology · doi:10.1016/j.it.2016.11.004 · Cited by 196 · see citing works

Is CD69 an effective brake to control inflammatory diseases?

González‐Amaro, R., Cortés, J. R., Sánchez‐Madrid, F., & Martı́n, P. (2013) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2013.07.006 · Cited by 188 · see citing works

The Pronounced Th17 Profile in Systemic Sclerosis (SSc) Together with Intracellular Expression of TGFβ and IFNγ Distinguishes SSc Phenotypes

Radstake, T. R. D. J., van Bon, L., Broen, J. C. A., Hussiani, A., Hesselstrand, R., Wuttge, D. M., Deng, Y., Simms, R., Lubberts, E., & Lafyatis, R. (2009) · PLoS ONE · doi:10.1371/journal.pone.0005903 · Cited by 177 · see citing works

Enhanced Antitumor Immunity in Mice Deficient in CD69

Esplugues, E., Sancho, D., Vega‐Ramos, J., Martínez‐A, C., Syrbe, U., Hamann, A., Engel, P., Sánchez‐Madrid, F., & Lauzurica, P. (2003) · The Journal of Experimental Medicine · doi:10.1084/jem.20021337 · Cited by 171 · see citing works

Defective sphingosine 1-phosphate receptor 1 (S1P1) phosphorylation exacerbates TH17-mediated autoimmune neuroinflammation

Garris, C., Wu, L., Acharya, S., Arac, A., Blaho, V. A., Huang, Y., Moon, B.-S., Axtell, R. C., Ho, P. P.-K., Steinberg, G. K., et al. (2013) · Nature Immunology · doi:10.1038/ni.2730 · Cited by 161 · see citing works

T Cell Trafficking through Lymphatic Vessels

Hunter, M. C., Teijeira, Á., & Halin, C. (2016) · Frontiers in Immunology · doi:10.3389/fimmu.2016.00613 · Cited by 154 · see citing works

Molecular characterization of the early activation antigen CD69: A type II membrane glycoprotein related to a family of natural killer cell activation antigens

Ziegler, S. F., Ramsdell, F., Hjerrild, K. A., Armitage, R. J., Grabstein, K. H., Hennen, K. B., Farrah, T., Fanslow, W. C., Shevach, E. M., & Alderson, M. R. (1993) · European Journal of Immunology · doi:10.1002/eji.1830230737 · Cited by 148 · see citing works

A potential role for CD69 in thymocyte emigration

Feng, C., Woodside, K. J., Vance, B. A., El‐Khoury, D., Canelles, M., Lee, J., Gress, R., Fowlkes, B. J., Shores, E. W., & Love, P. E. (2002) · International Immunology · doi:10.1093/intimm/dxf020 · Cited by 145 · see citing works

Phenotype and function of natural killer cells in systemic lupus erythematosus: Excess interferon-γ production in patients with active disease

Hervier, B., Béziat, V., Haroche, J., Mathian, A., Lebon, P., Ghillani‐Dalbin, P., Musset, L., Debré, P., Amoura, Z., & Vieillard, V. (2011) · Arthritis & Rheumatism · doi:10.1002/art.30313 · Cited by 143 · see citing works

Type II membrane protein CD69 regulates the formation of resting T-helper memory

Shinoda, K., Tokoyoda, K., Hanazawa, A., Hayashizaki, K., Zehentmeier, S., Hosokawa, H., Iwamura, C., Koseki, H., Tumes, D. J., Radbruch, A., et al. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1118539109 · Cited by 143 · see citing works

Galectin-1 Triggers an Immunoregulatory Signature in Th Cells Functionally Defined by IL-10 Expression

Cedeno‐Laurent, F., Opperman, M. J., Barthel, S. R., Kuchroo, V. K., & Dimitroff, C. J. (2012) · The Journal of Immunology · doi:10.4049/jimmunol.1103433 · Cited by 131 · see citing works

Transcriptional Regulation of the Gene Encoding the Human C-type Lectin Leukocyte Receptor AIM/CD69 and Functional Characterization of Its Tumor Necrosis Factor-α-responsive Elements

López‐Cabrera, M., Muñóz, E., Blazquez, M. V., Ursa, M. A., Santis, A. G., & Sánchez‐Madrid, F. (1995) · Journal of Biological Chemistry · doi:10.1074/jbc.270.37.21545 · Cited by 127 · see citing works

CD69 Association with Jak3/Stat5 Proteins Regulates Th17 Cell Differentiation

Martı́n, P., Gómez, M., Lamana, A., Cruz‐Adalia, A., Ramírez‐Huesca, M., Ursa, M. A., Yáñez‐Mó, M., & Sánchez‐Madrid, F. (2010) · Molecular and Cellular Biology · doi:10.1128/mcb.00456-10 · Cited by 127 · see citing works

CD69 controls the uptake of L-tryptophan through LAT1-CD98 and AhR-dependent secretion of IL-22 in psoriasis

Cibrián, D., Sáiz, M. L., de la Fuente, H., Sánchez‐Díaz, R., Moreno-Gonzalo, O., Jorge, I., Ferrarini, A., Vázquez, J., Punzón, C., Fresno, M., et al. (2016) · Nature Immunology · doi:10.1038/ni.3504 · Cited by 125 · see citing works

Evidence for New Light-Independent Pathways for Generation of the Endogenous Aryl Hydrocarbon Receptor Agonist FICZ

Smirnova, A. V., Wincent, E., Bergander, L. V., Alsberg, T. E., Bergman, J., Rannug, A., & Rannug, U. (2015) · Chemical Research in Toxicology · doi:10.1021/acs.chemrestox.5b00416 · Cited by 122 · see citing works

The Generation of Mature, Single-Positive Thymocytes In Vivo Is Dysregulated by CD69 Blockade or Overexpression

Nakayama, T., Kasprowicz, D. J., Yamashita, M., Schubert, L. A., Gillard, G., Kimura, M. Y., Didierlaurent, A. M., Koseki, H., & Ziegler, S. F. (2002) · The Journal of Immunology · doi:10.4049/jimmunol.168.1.87 · Cited by 105 · see citing works

Phenotypic and functional characteristics of hematopoietic cell lineages in CD69-deficient mice

Lauzurica, P., Sancho, D., Torres, M., Albella, B., Marazuela, M., Merino, T., Bueren, J. A., Martínez‐A, C., & Sánchez‐Madrid, F. (2000) · Blood · doi:10.1182/blood.v95.7.2312 · Cited by 101 · see citing works

The Leukocyte Activation Receptor CD69 Controls T Cell Differentiation through Its Interaction with Galectin-1

de la Fuente, H., Cruz‐Adalia, A., del Hoyo, G. M., Cibrián, D., Bonay, P., Pérez-Hernández, D., Vázquez, J., Navarro, P., Gallego, R. G., Ramírez‐Huesca, M., et al. (2014) · Molecular and Cellular Biology · doi:10.1128/mcb.00348-14 · Cited by 100 · see citing works

Expression of the leukocyte early activation antigen CD69 is regulated by the transcription factor AP-1

Castellanos, M. C., Muñoz, C., Montoya, M. C., Lara‐Pezzi, E., López‐Cabrera, M., & Landázuri, M. O. (1997) · The Journal of Immunology · doi:10.4049/jimmunol.159.11.5463 · Cited by 100 · see citing works

CD69 Limits the Severity of Cardiomyopathy After Autoimmune Myocarditis

Cruz‐Adalia, A., Jiménez‐Borreguero, L. J., Ramírez‐Huesca, M., Chico‐Calero, I., Barreiro, O., López-Conesa, E., Fresno, M., Sánchez‐Madrid, F., & Martı́n, P. (2010) · Circulation · doi:10.1161/circulationaha.110.952820 · Cited by 100 · see citing works

Maintenance of immune tolerance by Foxp3+ regulatory T cells requires CD69 expression

Cortés, J. R., Sánchez‐Díaz, R., Bovolenta, E. R., Barreiro, O., Lasarte, S., Matesanz-Marín, A., Toribio, M. L., Sánchez‐Madrid, F., & Martı́n, P. (2014) · Journal of Autoimmunity · doi:10.1016/j.jaut.2014.05.007 · Cited by 94 · see citing works

CD69 Regulates Type I IFN-Induced Tolerogenic Signals to Mucosal CD4 T Cells That Attenuate Their Colitogenic Potential

Radulovic, K., Manta, C., Rossini, V., Holzmann, K., Kestler, H. A., Wegenka, U. M., Nakayama, T., & Niess, J. H. (2012) · The Journal of Immunology · doi:10.4049/jimmunol.1100765 · Cited by 77 · see citing works

Glycosylation‐dependent interaction between CD69 and S100A8/S100A9 complex is required for regulatory T‐cell differentiation

Lin, C., Wei, T. W., Tsai, H., Wu, Y., Wu, P., & Chen, S. (2015) · The FASEB Journal · doi:10.1096/fj.15-273987 · Cited by 75 · see citing works

The leukocyte activation antigen CD69 limits allergic asthma and skin contact hypersensitivity

Martı́n, P., Gómez, M., Lamana, A., Matesanz-Marín, A., Cortés, J. R., Ramírez‐Huesca, M., Barreiro, O., López‐Romero, P., Gutiérrez‐Vázquez, C., de la Fuente, H., et al. (2010) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2010.05.010 · Cited by 72 · see citing works

The Early Activation Marker CD69 Regulates the Expression of Chemokines and CD4 T Cell Accumulation in Intestine

Radulovic, K., Rossini, V., Manta, C., Holzmann, K., Kestler, H. A., & Niess, J. H. (2013) · PLoS ONE · doi:10.1371/journal.pone.0065413 · Cited by 64 · see citing works

Environmental and Metabolic Sensors That Control T Cell Biology

Ramsay, G., & Cantrell, D. A. (2015) · Frontiers in Immunology · doi:10.3389/fimmu.2015.00099 · Cited by 59 · see citing works

CD69 Modulates Sphingosine-1-Phosphate-Induced Migration of Skin Dendritic Cells

Lamana, A., Martı́n, P., de la Fuente, H., Martínez‐Muñoz, L., Cruz‐Adalia, A., Ramírez‐Huesca, M., Escribano, C., Gollmer, K., Mellado, M., Stein, J. V., et al. (2011) · Journal of Investigative Dermatology · doi:10.1038/jid.2011.54 · Cited by 57 · see citing works

Nutrient Sensing via mTOR in T Cells Maintains a Tolerogenic Microenvironment

Howie, D., Waldmann, H., & Cobbold, S. P. (2014) · Frontiers in Immunology · doi:10.3389/fimmu.2014.00409 · Cited by 57 · see citing works

Expression of CD69 antigen on synovial fluid T cells in patients with rheumatoid arthritis and other chronic synovitis.

Afeltra, A., Galeazzi, M., Ferri, G. M., Amoroso, A., Pità, O. D., Porzio, F., & Bonomo, L. (1993) · Annals of the Rheumatic Diseases · doi:10.1136/ard.52.6.457 · Cited by 57 · see citing works

Participation of the CD69 Antigen in the T‐Cell Activation Process of Patients with Systemic Lupus Erythematosus

Crispín, J. C., Martı́nez, M. L., de Pablo, P., Velasquillo, & Alcocer‐Varela (1998) · Scandinavian Journal of Immunology · doi:10.1046/j.1365-3083.1998.00366.x · Cited by 56 · see citing works

CD69 limits early inflammatory diseases associated with immune response to Listeria monocytogenes infection

Vega‐Ramos, J., Alari‐Pahissa, E., del Valle-Mendoza, J., Carrasco-Marı́n, E., Esplugues, E., Borràs, M., Martínez‐A, C., & Lauzurica, P. (2010) · Immunology and Cell Biology · doi:10.1038/icb.2010.62 · Cited by 45 · see citing works

Thymus-Derived Regulatory T Cell Development Is Regulated by C-Type Lectin-Mediated BIC/MicroRNA 155 Expression

Sánchez‐Díaz, R., Blanco-Domínguez, R., Lasarte, S., Tsilingiri, K., Martín‐Gayo, E., Linillos-Pradillo, B., de la Fuente, H., Sánchez‐Madrid, F., Nakagawa, R., Toribio, M. L., et al. (2017) · Molecular and Cellular Biology · doi:10.1128/mcb.00341-16 · Cited by 42 · see citing works

CD69 surface expression on human lung eosinophils after segmental allergen provocation

Julius, P., Luttmann, W., Knöchel, B., Kroegel, C., Matthys, H., & Virchow, J. C. (1999) · European Respiratory Journal · doi:10.1183/09031936.99.13612609 · Cited by 36 · see citing works

CD69 is a direct HIF-1α target gene in hypoxia as a mechanism enhancing expression on tumor-infiltrating T lymphocytes

Labiano, S., Meléndez-Rodríguez, F., Palazón, A., Teijeira, Á., Garasa, S., Etxeberria, I., Aznar, M. Á., Sánchez-Paulete, A. R., Azpilikueta, A., Bolaños, E., et al. (2017) · OncoImmunology · doi:10.1080/2162402x.2017.1283468 · Cited by 35 · see citing works

Expansion of activated eosinophils in infants with severe atopic dermatitis

Toma, T., Mizuno, K., Okamoto, H. H., Kanegane, C., Ohta, K., Ikawa, Y., Miura, M., Kuroda, M., Niida, Y., Koizumi, S., et al. (2005) · Pediatrics International · doi:10.1111/j.1442-200x.2004.02004.x · Cited by 32 · see citing works

Hypertrophy of infected Peyer's patches arises from global, interferon-receptor, and CD69-independent shutdown of lymphocyte egress

Schulz, O., Ugur, M., Friedrichsen, M., Radulovic, K., Niess, J. H., Jalkanen, S., Krueger, A., & Pabst, O. (2013) · Mucosal Immunology · doi:10.1038/mi.2013.105 · Cited by 26 · see citing works

CD69 Does Not Affect the Extent of T Cell Priming

Alari‐Pahissa, E., Notario, L., Lorente, E., Vega‐Ramos, J., Justel, A., López, D., Villadangos, J. A., & Lauzurica, P. (2012) · PLoS ONE · doi:10.1371/journal.pone.0048593 · Cited by 25 · see citing works

Distinct recirculation potential of CD69+CD103− and CD103+ thymic memory CD8+ T cells

Park, S. L., Mackay, L. K., & Gebhardt, T. (2016) · Immunology and Cell Biology · doi:10.1038/icb.2016.60 · Cited by 20 · see citing works

Crucial Role for CD69 in the Pathogenesis of Dextran Sulphate Sodium-Induced Colitis

Hasegawa, A., Iwamura, C., Kitajima, M., Hashimoto, K., Otsuyama, K., Ogino, H., Nakayama, T., & Shirai, M. (2013) · PLoS ONE · doi:10.1371/journal.pone.0065494 · Cited by 20 · see citing works

Anti-CD69 antibodies enhance phorbol-dependent glucose metabolism and Ca2+ levels in human thymocytes. Antagonist effect of cyclosporin A

Conde, M., Montaño, R., Moreno-aurioles, V. R., Ramı́rez, R., Sánchez‐Mateos, P., Sánchez‐Madrid, F., & Sobrino, F. (1996) · Journal of Leukocyte Biology · doi:10.1002/jlb.60.2.278 · Cited by 14 · see citing works

Severe COVID-19 Is Marked by a Dysregulated Myeloid Cell Compartment

Schulte-Schrepping, J., Reusch, N., Paclik, D., Baßler, K., Schlickeiser, S., Zhang, B., Krämer, B., Krammer, T., Brumhard, S., Bonaguro, L., et al. (2020) · Cell · doi:10.1016/j.cell.2020.08.001 · Cited by 1,461 · see citing works

Human T cell development, localization, and function throughout life

Kumar, B. V., Connors, T. J., & Farber, D. L. (2018) · Immunity · doi:10.1016/j.immuni.2018.01.007 · Cited by 1,257 · see citing works

C-type lectins in immunity and homeostasis

Brown, G. D., Willment, J. A., & Whitehead, L. (2018) · Nature reviews. Immunology · doi:10.1038/s41577-018-0004-8 · Cited by 747 · see citing works

Trial watch: Immunogenic cell death induction by anticancer chemotherapeutics

Garg, A. D., More, S., Rufo, N., Meçe, O., Sassano, M. L., Agostinis, P., Zitvogel, L., Kroemer, G., & Galluzzi, L. (2017) · OncoImmunology · doi:10.1080/2162402x.2017.1386829 · Cited by 277 · see citing works

Host-Directed Antiviral Therapy

Kumar, N., Sharma, S., Kumar, R., Tripathi, B. N., Barua, S., Ly, H., & Rouse, B. T. (2020) · Clinical Microbiology Reviews · doi:10.1128/cmr.00168-19 · Cited by 281 · see citing works

Commensal bacteria and fungi differentially regulate tumor responses to radiation therapy

Shiao, S. L., Kershaw, K. M., Limon, J. J., You, S., Yoon, J., Ko, E. Y., Guarnerio, J., Potdar, A. A., McGovern, D. P. B., Bose, S., et al. (2021) · Cancer Cell · doi:10.1016/j.ccell.2021.07.002 · Cited by 279 · see citing works

Trial watch: chemotherapy-induced immunogenic cell death in immuno-oncology

Vanmeerbeek, I., Sprooten, J., Ruysscher, D. D., Tejpar, S., Vandenberghe, P., Fucikova, J. P., Špíšek, R., Zitvogel, L., Kroemer, G., Galluzzi, L., et al. (2020) · OncoImmunology · doi:10.1080/2162402x.2019.1703449 · Cited by 228 · see citing works

Neural stem cell delivery of an oncolytic adenovirus in newly diagnosed malignant glioma: a first-in-human, phase 1, dose-escalation trial

Fares, J., Ahmed, A. U., Ulasov, I. V., Sonabend, A. M., Miska, J. M., Lee-Chang, C., Balyasnikova, I. V., Chandler, J. P., Portnow, J., Tate, M. C., et al. (2021) · The Lancet Oncology · doi:10.1016/s1470-2045(21)00245-x · Cited by 223 · see citing works

Metabolic Pathways That Control Skin Homeostasis and Inflammation

Cibrián, D., de la Fuente, H., & Sánchez‐Madrid, F. (2020) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2020.04.004 · Cited by 210 · see citing works

Tissue‐resident memory T cells in tissue homeostasis, persistent infection, and cancer surveillance

Gebhardt, T., Palendira, U., Tscharke, D. C., & Bedoui, S. (2018) · Immunological Reviews · doi:10.1111/imr.12650 · Cited by 199 · see citing works

Tissue-Resident Memory T Cells in Cancer Immunosurveillance

Park, S. L., Gebhardt, T., & Mackay, L. K. (2019) · Trends in Immunology · doi:10.1016/j.it.2019.06.002 · Cited by 190 · see citing works

Distinct molecular profiles of skull bone marrow in health and neurological disorders

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The Functional Requirement for CD69 in Establishment of Resident Memory CD8+ T Cells Varies with Tissue Location

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