The DOI matches its Crossref record; 43 of the 43 references it cites were found in a registry or an index.
Interleukins 1β and 6 but not transforming growth factor-β are essential for the differentiation of interleukin 17–producing human T helper cells
Abstract
Interleukin 17 (IL-17)-producing CD4(+) helper T cells (T(H)-17 cells) have been linked to host defense and autoimmune diseases. In mice, the differentiation of T(H)-17 cells requires transforming growth factor-beta and IL-6 and the transcription factor RORgammat. We report here that for human naive CD4(+) T cells, RORgammat expression and T(H)-17 polarization were induced by IL-1beta and enhanced by IL-6 but were suppressed by transforming growth factor-beta and IL-12. Monocytes and conventional dendritic cells, but not monocyte-derived dendritic cells activated by microbial stimuli, efficiently induced T(H)-17 priming, and this function correlated with antigen-presenting cell production of IL-1beta and IL-6 but not IL-12. Our results identify cytokines, antigen-presenting cells and microbial products that promote the polarization of human T(H)-17 cells and emphasize an important difference in the requirements for the differentiation of T(H)-17 cells in humans and mice.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
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?
In the citing paper
“The produced IL-6 further induces Th17 cell differentiation through STAT3 in the presence of TGFβ, IL-1β and IL-23, all of which are rich in inflammatory lesions and tumor microenvironments (164, 166, 169–171, 174, 175).”
From IL-6 in inflammation, autoimmunity and cancer (2021) · cites this paper as [169]
In the citing paper
“Importantly, IL-6, transforming growth factor-b, and IL-1b are required for Th17 differentiation from naïve CD4þ T cells.56,57”
From Autoimmune diseases and immune-checkpoint inhibitors for cancer therapy: Review of the literature and personalized risk-based prevention strategy (2020) · cites this paper as [56]
Citations
Cites
Bettelli, E., Carrier, Y., Gao, W., Korn, T., Strom, T. B., Oukka, M., Weiner, H. L., & Kuchroo, V. K. (2006) · Nature · doi:10.1038/nature04753 · Cited by 6,992
Ivanov, I. I., McKenzie, B. S., Zhou, L., Tadokoro, C. E., Lepelley, A., Lafaille, J. J., Cua, D. J., & Littman, D. R. (2006) · Cell · doi:10.1016/j.cell.2006.07.035 · Cited by 5,145
Sallusto, F., & Lanzavecchia, A. (1994) · The Journal of Experimental Medicine · doi:10.1084/jem.179.4.1109 · Cited by 5,129
Harrington, L. E., Hatton, R. D., Mangan, P. R., Turner, H., Murphy, T. L., Murphy, K. M., & Weaver, C. T. (2005) · Nature Immunology · doi:10.1038/ni1254 · Cited by 4,742
A distinct lineage of CD4 T cells regulates tissue inflammation by producing interleukin 17
Park, H., Li, Z., Yang, X. O., Chang, S. H., Nurieva, R., Wang, Y.-H., Wang, Y., Hood, L., Zhu, Z., Tian, Q., et al. (2005) · Nature Immunology · doi:10.1038/ni1261 · Cited by 4,265
Veldhoen, M., Hocking, R. J., Atkins, C. J., Locksley, R. M., & Stockinger, B. (2006) · Immunity · doi:10.1016/j.immuni.2006.01.001 · Cited by 3,605
Transforming growth factor-β induces development of the TH17 lineage
Mangan, P. R., Harrington, L. E., O'Quinn, D. B., Helms, W. S., Bullard, D. C., Elson, C. O., Hatton, R. D., Wahl, S. M., Schoeb, T. R., & Weaver, C. T. (2006) · Nature · doi:10.1038/nature04754 · Cited by 3,087
Interleukin-22, a TH17 cytokine, mediates IL-23-induced dermal inflammation and acanthosis
Zheng, Y., Danilenko, D. M., Valdez, P. A., Kasman, I. M., Eastham‐Anderson, J., Wu, J., & Ouyang, W. (2006) · Nature · doi:10.1038/nature05505 · Cited by 1,888
Aggarwal, S., Ghilardi, N., Xie, M.-H., de Sauvage, F. J., & Gurney, A. L. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m207577200 · Cited by 1,848
IL-17 family cytokines and the expanding diversity of effector T cell lineages
Weaver, C. T., Hatton, R. D., Mangan, P. R., & Harrington, L. E. (2007) · Annual Review of Immunology · doi:10.1146/annurev.immunol.25.022106.141557 · Cited by 1,842
Cited by
Sorted by citations
Items 201–300 of 1,003
Eyerich, K., Foerster, S., Rombold, S., Seidl, H., Behrendt, H., Hofmann, H., Ring, J., & Traidl‐Hoffmann, C. (2008) · Journal of Investigative Dermatology · doi:10.1038/jid.2008.139 · Cited by 251
IL-17 and IL-22: siblings, not twins
Eyerich, S., Eyerich, K., Cavani, A., & Schmidt‐Weber, C. B. (2010) · Trends in Immunology · doi:10.1016/j.it.2010.06.004 · Cited by 242
Prostaglandin E2 synergistically with interleukin-23 favors human Th17 expansion
Chizzolini, C., Chicheportiche, R., Alvarez, M., de Rham, C., Roux‐Lombard, P., Ferrari‐Lacraz, S., & Dayer, J. (2008) · Blood · doi:10.1182/blood-2008-05-155408 · Cited by 241
Inflammasomes and autoimmunity
Shaw, P. J., McDermott, M., & Kanneganti, T. (2010) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2010.11.001 · Cited by 240
IL-17 and GM-CSF Expression Are Antagonistically Regulated by Human T Helper Cells
Noster, R., Riedel, R., Mashreghi, M., Radbruch, H., Harms, L., Haftmann, C., Chang, H., Radbruch, A., & Zielinski, C. E. (2014) · Science Translational Medicine · doi:10.1126/scitranslmed.3008706 · Cited by 244
Nogueira, E., Hamour, S., Sawant, D., Henderson, S. R., Mansfield, N., Chavele, K.-M., Pusey, C. D., & Salama, A. D. (2010) · Nephrology Dialysis Transplantation · doi:10.1093/ndt/gfp783 · Cited by 237
T Helper Cells: The Modulators of Inflammation in Multiple Sclerosis
Kunkl, M., Frascolla, S., Amormino, C., Volpe, E., & Tuosto, L. (2020) · Cells · doi:10.3390/cells9020482 · Cited by 248
MicroRNA-146a expresses in interleukin-17 producing T cells in rheumatoid arthritis patients
Niimoto, T., Nakasa, T., Ishikawa, M., Okuhara, A., Izumi, B., Deie, M., Suzuki, O., Adachi, N., & Ochi, M. (2010) · BMC Musculoskeletal Disorders · doi:10.1186/1471-2474-11-209 · Cited by 235
Peters, A., Lee, Y., & Kuchroo, V. K. (2011) · Current Opinion in Immunology · doi:10.1016/j.coi.2011.08.007 · Cited by 242
Cardiac myosin-Th17 responses promote heart failure in human myocarditis
Myers, J. M., Cooper, L. T., Kem, D. C., Stavrakis, S., Kosanke, S. D., Shevach, E. M., Fairweather, D., Stoner, J. A., Cox, C. J., & Cunningham, M. W. (2016) · JCI Insight · doi:10.1172/jci.insight.85851 · Cited by 230
IFN-β Inhibits Human Th17 Cell Differentiation
Ramgolam, V. S., Sha, Y., Jin, J., Zhang, X., & Markovic‐Plese, S. (2009) · The Journal of Immunology · doi:10.4049/jimmunol.0803227 · Cited by 229
The Interplay Between Monocytes/Macrophages and CD4+ T Cell Subsets in Rheumatoid Arthritis
Roberts, C. A., Dickinson, A. K., & Taams, L. S. (2015) · Frontiers in Immunology · doi:10.3389/fimmu.2015.00571 · Cited by 238
The Th17 family: flexibility follows function
Basu, R., Hatton, R. D., & Weaver, C. T. (2013) · Immunological Reviews · doi:10.1111/imr.12035 · Cited by 229
Samson, M., Audia, S., Fraszczak, J., Trad, M., Ornetti, P., Lakomy, D., Ciudad, M., Seguin, V. L., Berthier, S., Vinit, J., et al. (2012) · Arthritis & Rheumatism · doi:10.1002/art.34647 · Cited by 236
Regulation and function of interleukin-36 cytokines in homeostasis and pathological conditions
Gabay, C., & Towne, J. E. (2015) · Journal of Leukocyte Biology · doi:10.1189/jlb.3ri1014-495r · Cited by 227
Regulation of interleukin‐12/interleukin‐23 production and the T‐helper 17 response in humans
Lyakh, L. A., Trinchieri, G., Provezza, L., Carra, G., & Gerosa, F. (2008) · Immunological Reviews · doi:10.1111/j.1600-065x.2008.00700.x · Cited by 237
Signal transduction pathways and transcriptional regulation in the control of Th17 differentiation
Chen, Z., Laurence, A., & O'Shea, J. J. (2007) · Seminars in Immunology · doi:10.1016/j.smim.2007.10.015 · Cited by 274
Pouring fuel on the fire: Th17 cells, the environment, and autoimmunity
Burkett, P. R., zu Hörste, G. M., & Kuchroo, V. K. (2015) · Journal of Clinical Investigation · doi:10.1172/jci78085 · Cited by 225
Lim, H. W., Lee, J., Hillsamer, P., & Kim, C. H. (2008) · The Journal of Immunology · doi:10.4049/jimmunol.180.1.122 · Cited by 226
Fujimoto, M., Serada, S., Mihara, M., Uchiyama, Y., Yoshida, H., Koike, N., Ohsugi, Y., Nishikawa, T., Ripley, B., Kimura, A., et al. (2008) · Arthritis & Rheumatism · doi:10.1002/art.24126 · Cited by 227
Haanen, J., Ernstoff, M. S., Wang, Y., Menzies, A. M., Puzanov, I., Grivas, P., Larkin, J., Peters, S., Thompson, J. A., & Obeid, M. (2020) · Annals of Oncology · doi:10.1016/j.annonc.2020.03.285 · Cited by 222
Signal transduction pathways and transcriptional regulation in Th17 cell differentiation
Hirahara, K., Ghoreschi, K., Laurence, A. D. J., Yang, X., Kanno, Y., & O’Shea, J. J. (2010) · Cytokine & Growth Factor Reviews · doi:10.1016/j.cytogfr.2010.10.006 · Cited by 231
Vigne, S., Palmer, G., Martin, P., Lamacchia, C., Strebel, D., Rodriguez, E., Olleros, M. L., Vesin, D., Garcia, I., Ronchi, F., et al. (2012) · Blood · doi:10.1182/blood-2012-06-439026 · Cited by 218
Th17 Cells and Autoimmune Encephalomyelitis (EAE/MS)
Aranami, T., & Yamamura, T. (2008) · Allergology International · doi:10.2332/allergolint.r-07-159 · Cited by 218
From interleukin-23 to T-helper 17 cells: human T-helper cell differentiation revisited
Boniface, K., Blom, B., Liu, Y., & De Waal Malefyt, R. (2008) · Immunological Reviews · doi:10.1111/j.1600-065x.2008.00714.x · Cited by 218
Zhang, M. A., Rego, D., Moshkova, M., Kébir, H., Chruscinski, A. J., Nguyen, H. T., Akkermann, R., Stanczyk, F. Z., Prat, A., Steinman, L., et al. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1118458109 · Cited by 216
Das, J., Ren, G., Zhang, L., Roberts, A. I., Zhao, X., Bothwell, A. L. M., Kaer, L. V., Shi, Y., & Das, G. (2009) · The Journal of Experimental Medicine · doi:10.1084/jem.20082286 · Cited by 222
Dhodapkar, K. M., Barbuto, S., Matthews, P., Kukreja, A., Mazumder, A., Vesole, D. H., Jagannath, S., & Dhodapkar, M. V. (2008) · Blood · doi:10.1182/blood-2008-03-143222 · Cited by 217
TH-17 cells in rheumatoid arthritis
Shahrara, S., Huang, Q.-Q., Mandelin, A. M., & Pope, R. M. (2008) · Arthritis Research & Therapy · doi:10.1186/ar2477 · Cited by 213
The Role of Chemokines in the Recruitment of Lymphocytes to the Liver
Oo, Y. H., Shetty, S., & Adams, D. (2010) · Digestive Diseases · doi:10.1159/000282062 · Cited by 221
The role of IL‐21 in regulating B‐cell function in health and disease
Ettinger, R., Kuchen, S., & Lipsky, P. E. (2008) · Immunological Reviews · doi:10.1111/j.1600-065x.2008.00631.x · Cited by 216
Type 17 T helper cells-origins, features and possible roles in rheumatic disease.
Annunziato, F., Cosmi, L., Liotta, F., Maggi, E., & Romagnani, S. (2009) · Nature Reviews Rheumatology · doi:10.1038/nrrheum.2009.80 · Cited by 212
Interleukin-1 as Innate Mediator of T Cell Immunity
Eeckhout, B. V. D., Tavernier, J. H., & Gerlo, S. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2020.621931 · Cited by 227
Cholesterol Accumulation in Dendritic Cells Links the Inflammasome to Acquired Immunity
Westerterp, M., Gautier, E. L., Ganda, A., Molusky, M. M., Wang, W., Fotakis, P., Wang, N., Randolph, G. J., D'Agati, V. D., Yvan-Charvet, L., et al. (2017) · Cell Metabolism · doi:10.1016/j.cmet.2017.04.005 · Cited by 218
Activation of c-Kit in dendritic cells regulates T helper cell differentiation and allergic asthma
Krishnamoorthy, N., Oriss, T. B., Paglia, M., Fei, M., Yarlagadda, M., Vanhaesebroeck, B., Ray, A., & Ray, P. (2008) · Nature Medicine · doi:10.1038/nm1766 · Cited by 216
IL-17–producing T cells in lung immunity and inflammation
Nembrini, C., Marsland, B. J., & Köpf, M. (2009) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2009.03.033 · Cited by 216
Hedegaard, C. J., Krakauer, M., Bendtzen, K., Lund, H., Sellebjerg, F. T., & Nielsen, C. H. (2008) · Immunology · doi:10.1111/j.1365-2567.2008.02837.x · Cited by 215
T helper 17 cell heterogeneity and pathogenicity in autoimmune disease
Ghoreschi, K., Laurence, A. D. J., Yang, X., Hirahara, K., & O’Shea, J. J. (2011) · Trends in Immunology · doi:10.1016/j.it.2011.06.007 · Cited by 207
Evans, H. G., Gullick, N., Kelly, S., Pitzalis, C., Lord, G. M., Kirkham, B. W., & Taams, L. S. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0808144106 · Cited by 210
Annunziato, F., Cosmi, L., Liotta, F., Maggi, E., & Romagnani, S. (2008) · International Immunology · doi:10.1093/intimm/dxn106 · Cited by 209
Adverse functions of IL‐17A in experimental sepsis
Flierl, M. A., Rittirsch, D., Gao, H., Hoesel, L. M., Nadeau, B. A., Day, D. E., Zetoune, F. S., Sarma, J. V., Huber-Lang, M. S., Ferrara, J. L. M., et al. (2008) · The FASEB Journal · doi:10.1096/fj.07-105221 · Cited by 209
Iezzi, G., Sonderegger, I., Ampenberger, F., Schmitz, N., Marsland, B. J., & Köpf, M. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0810769106 · Cited by 204
IL-17 receptor and its functional significance in psoriatic arthritis
Raychaudhuri, S. P., Raychaudhuri, S. K., & Genovese, M. C. (2011) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-011-1036-6 · Cited by 203
Regulation and Function of Proinflammatory TH17 Cells
Martínez, G., Nurieva, R., Yang, X. O., & Dong, C. (2008) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1443.021 · Cited by 213
Zhang, X., Jin, J., Peng, X., Ramgolam, V. S., & Markovic‐Plese, S. (2008) · The Journal of Immunology · doi:10.4049/jimmunol.180.10.6988 · Cited by 203
Neveu, W. A., Allard, J. L., Raymond, D. M., Bourassa, L. M., Burns, S. M., Bunn, J. Y., Irvin, C. G., Kaminsky, D. A., & Rincón, M. (2010) · Respiratory Research · doi:10.1186/1465-9921-11-28 · Cited by 203
Roles of Pro- and Anti-Inflammatory Cytokines in the Pathogenesis of SLE
Su, D., Lu, Z., Shen, M., Li, X., & Sun, L. (2012) · BioMed Research International · doi:10.1155/2012/347141 · Cited by 202
Cheung, P. F., Wong, C. K., & Lam, C. W. K. (2008) · The Journal of Immunology · doi:10.4049/jimmunol.180.8.5625 · Cited by 202
Regulation and function of interleukin‐36 cytokines
Bassoy, E. Y., Towne, J. E., & Gabay, C. (2017) · Immunological Reviews · doi:10.1111/imr.12610 · Cited by 198
Life in the inflamed intestine, Salmonella style
Santos, R. L., Raffatellu, M., Bevins, C. L., Adams, L. G., Tükel, Ç., Tsolis, R. M., & Bäumler, A. J. (2009) · Trends in Microbiology · doi:10.1016/j.tim.2009.08.008 · Cited by 197
Ness-Schwickerath, K. J., Jin, C., & Morita, C. T. (2010) · The Journal of Immunology · doi:10.4049/jimmunol.1000600 · Cited by 204
Ifergan, I., Kébir, H., Bernard, M., Wosik, K., Dodelet-Devillers, A., Cayrol, R., Arbour, N., & Prat, A. (2007) · Brain · doi:10.1093/brain/awm295 · Cited by 199
Protective Effects of Natural Polysaccharides on Intestinal Barrier Injury: A Review
Huo, J., Wu, Z., Sun, W., Wang, Z., Wu, J., Huang, M., Wang, B., & Sun, B. (2022) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.1c05966 · Cited by 197
Annexin‐A1: a pivotal regulator of the innate and adaptive immune systems
D’Acquisto, F., Perretti, M., & Flower, R. J. (2008) · British Journal of Pharmacology · doi:10.1038/bjp.2008.252 · Cited by 194
Heterogeneity of human effector CD4+ T cells
Annunziato, F., & Romagnani, S. (2009) · Arthritis Research & Therapy · doi:10.1186/ar2843 · Cited by 194
Elevated serum levels of interleukin-17A in children with autism
AL-Ayadhi, L. Y., & Mostafa, G. A. (2012) · Journal of Neuroinflammation · doi:10.1186/1742-2094-9-158 · Cited by 198
Cheng, S.-C., van de Veerdonk, F. L., Lenardon, M., Stoffels, M., Plantinga, T., Smeekens, S., Rizzetto, L., Mukaremera, L., Preechasuth, K., Cavalieri, D., et al. (2011) · Journal of Leukocyte Biology · doi:10.1189/jlb.1210702 · Cited by 191
Defining the human T helper 17 cell phenotype
Annunziato, F., Cosmi, L., Liotta, F., Maggi, E., & Romagnani, S. (2012) · Trends in Immunology · doi:10.1016/j.it.2012.05.004 · Cited by 202
Akdiş, M., Palomares, Ó., van de Veen, W., van Splunter, M. E., & Akdiş, C. A. (2012) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2012.05.003 · Cited by 201
Dendritic Cell Reprogramming by Endogenously Produced Lactic Acid
Nasi, A., Fekete, T., Krishnamurthy, A., Snowden, S. G., Rajnavölgyi, É., Catrina, A. I., Wheelock, C. E., Vivar, N., & Réthi, B. (2013) · The Journal of Immunology · doi:10.4049/jimmunol.1300772 · Cited by 190
Scriba, T. J., Tameris, M. D., Mansoor, N., Smit, E., van der Merwe, L., Isaacs, F., Keyser, A. T., Moyo, S., Brittain, N. J., Lawrie, A. M., et al. (2009) · European Journal of Immunology · doi:10.1002/eji.200939754 · Cited by 194
Ramirez, J., Brembilla, N. C., Sorg, O., Chicheportiche, R., Matthes, T., Dayer, J., Saurat, J. ‐., Roosnek, E. E., & Chizzolini, C. (2010) · European Journal of Immunology · doi:10.1002/eji.201040461 · Cited by 200
Schmechel, S., Konrad, A., Diegelmann, J., Glas, J., Wetzke, M., Paschos, E., Lohse, P., Göke, B., & Brand, S. (2007) · Inflammatory Bowel Diseases · doi:10.1002/ibd.20315 · Cited by 193
Boniface, K., Blumenschein, W. M., Brovont-Porth, K., McGeachy, M. J., Basham, B., Desai, B., Pierce, R. H., McClanahan, T. K., Sadekova, S., & Malefyt, R. D. W. (2010) · The Journal of Immunology · doi:10.4049/jimmunol.1000366 · Cited by 193
Th17 immune responses contribute to the pathophysiology of aplastic anemia
de Latour, R. P., Visconte, V., Takaku, T., Wu, C. O., Erie, A. J., Sarcon, A. K., Desierto, M. J., Scheinberg, P., Keyvanfar, K., Núñez, O., et al. (2010) · Blood · doi:10.1182/blood-2010-01-266098 · Cited by 189
Murugaiyan, G., Mittal, A., & Weiner, H. L. (2008) · The Journal of Immunology · doi:10.4049/jimmunol.181.11.7480 · Cited by 186
Alternative Pathways of IL-1 Activation, and Its Role in Health and Disease
Pyrillou, K., Burzynski, L. C., & Clarke, M. C. H. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.613170 · Cited by 202
Cytokines in Sjögren’s syndrome
Roescher, N., Tak, P. P., & Illei, G. G. (2009) · Oral Diseases · doi:10.1111/j.1601-0825.2009.01582.x · Cited by 188
Th17 and regulatory T cells: rebalancing pro- and anti-inflammatory forces in autoimmune arthritis
Nistala, K., & Wedderburn, L. R. (2009) · Rheumatology · doi:10.1093/rheumatology/kep028 · Cited by 185
IL ‐17: overview and role in oral immunity and microbiome
Abusleme, L., & Moutsopoulos, N. M. (2016) · Oral Diseases · doi:10.1111/odi.12598 · Cited by 189
The role of transforming growth factor β in T helper 17 differentiation
Zhang, S. (2018) · Immunology · doi:10.1111/imm.12938 · Cited by 194
CD4 T cell differentiation in type 1 diabetes
Walker, L. S. K., & von Herrath, M. (2015) · Clinical & Experimental Immunology · doi:10.1111/cei.12672 · Cited by 189
IL-22 is related to development of human colon cancer by activation of STAT3
Jiang, R., Wang, H., Deng, L., Hou, J., Shi, R., Yao, M., Gao, Y., Yao, A., Wang, X., Yu, L., et al. (2013) · BMC Cancer · doi:10.1186/1471-2407-13-59 · Cited by 190
Harada, K., Shimoda, S., Sato, Y., Isse, K., Ikeda, H., & Nakanuma, Y. (2009) · Clinical & Experimental Immunology · doi:10.1111/j.1365-2249.2009.03947.x · Cited by 179
Properties and origin of human Th17 cells
Romagnani, S., Maggi, E., Liotta, F., Cosmi, L., & Annunziato, F. (2009) · Molecular Immunology · doi:10.1016/j.molimm.2008.12.019 · Cited by 190
IL-1β and IL-2 convert human Treg into TH17 cells
Deknuydt, F., Bioley, G., Valmori, D., & Ayyoub, M. (2009) · Clinical Immunology · doi:10.1016/j.clim.2008.12.008 · Cited by 188
Seo, W., Eun, H. S., Kim, S. Y., Yi, H., Lee, Y., Park, S., Jang, M., Jo, E., Kim, S. C., Han, Y., et al. (2016) · Hepatology · doi:10.1002/hep.28644 · Cited by 175
Cytokines in Autoimmune Uveitis
Horai, R., & Caspi, R. R. (2011) · Journal of Interferon & Cytokine Research · doi:10.1089/jir.2011.0042 · Cited by 181
FOXP3 and the regulation of Treg/Th17 differentiation
Ziegler, S. F., & Buckner, J. H. (2009) · Microbes and Infection · doi:10.1016/j.micinf.2009.04.002 · Cited by 177
Downs‐Canner, S., Berkey, S. E., Delgoffe, G. M., Edwards, R. P., Curiel, T. J., Odunsi, K. O., Bartlett, D. L., & Obermajer, N. (2017) · Nature Communications · doi:10.1038/ncomms14649 · Cited by 184
The inflammatory function of human IgA
Hansen, I. S., Baeten, D. L. P., & den Dunnen, J. (2019) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-018-2976-8 · Cited by 170
Chen, L., Wang, C., Nan, L., & Zhu, P. (2011) · Journal of Clinical Immunology · doi:10.1007/s10875-011-9542-6 · Cited by 176
Vogelpoel, L. T. C., Hansen, I. S., Rispens, T., Muller, F. J. M., van Capel, T. M. M., Turina, M. C., Vos, J. B., Baeten, D., Kapsenberg, M. L., de Jong, E. C., et al. (2014) · Nature Communications · doi:10.1038/ncomms6444 · Cited by 176
Steinman, L. (2008) · The Journal of Experimental Medicine · doi:10.1084/jem.20072066 · Cited by 177
Yi, H., Guo, C., Yu, X., Zuo, D., & Wang, X. (2012) · The Journal of Immunology · doi:10.4049/jimmunol.1200086 · Cited by 177
IL-17A is increased in the serum and in spinal cord CD8 and mast cells of ALS patients
Fiala, M., Chattopadhay, M., Cava, A. L., Tse, E., Liu, G., Lourenço, E. V., Eskin, A., Liu, P. T., Magpantay, L. I., Tse, S., et al. (2010) · Journal of Neuroinflammation · doi:10.1186/1742-2094-7-76 · Cited by 180
Interleukin-17 in human inflammatory diseases
Shabgah, A. G., Fattahi, E., & Shahneh, F. Z. (2014) · Advances in Dermatology and Allergology · doi:10.5114/pdia.2014.40954 · Cited by 181
Safety and Immunogenicity of a New Tuberculosis Vaccine, MVA85A, in Healthy Adults in South Africa
Hawkridge, T., Scriba, T. J., Gelderbloem, S., Smit, E., Tameris, M. D., Moyo, S., Lang, T. A., Veldsman, A., Hatherill, M., van der Merwe, L., et al. (2008) · The Journal of Infectious Diseases · doi:10.1086/590185 · Cited by 172
IL-17 Induces Monocyte Migration in Rheumatoid Arthritis
Shahrara, S., Pickens, S. R., Dorfleutner, A., & Pope, R. M. (2009) · The Journal of Immunology · doi:10.4049/jimmunol.0802246 · Cited by 175
The Potential Role of Interleukin-17 in Severe Asthma
Wang, Y., & Wills-Karp, M. A. (2011) · Current Allergy and Asthma Reports · doi:10.1007/s11882-011-0210-y · Cited by 177
The Role of the IL23/IL17 Axis in Bronchiolitis Obliterans Syndrome After Lung Transplantation
Vanaudenaerde, B. M., Vleeschauwer, S. I. D., Vos, R., Meyts, I., Bullens, D. M. A., Reynders, V., Wuyts, W. A., Raemdonck, D. E. V., Dupont, L., & Verleden, G. M. (2008) · American Journal of Transplantation · doi:10.1111/j.1600-6143.2008.02321.x · Cited by 172
Mouse and human intestinal immunity: same ballpark, different players; different rules, same score
Gibbons, D. L., & Spencer, J. (2011) · Mucosal Immunology · doi:10.1038/mi.2010.85 · Cited by 174
Cutting Edge: Phenotypic Characterization and Differentiation of Human CD8+ T Cells Producing IL-17
Kondo, T., Takata, H., Matsuki, F., & Takiguchi, M. (2009) · The Journal of Immunology · doi:10.4049/jimmunol.0801347 · Cited by 172
Khayrullina, T., Yen, J.-H. J., Jing, H., & Ganea, D. (2008) · The Journal of Immunology · doi:10.4049/jimmunol.181.1.721 · Cited by 172
Inflammasomes as mediators of immunity against influenza virus
Pang, I. K., & Iwasaki, A. (2010) · Trends in Immunology · doi:10.1016/j.it.2010.11.004 · Cited by 176
Resveratrol modulates murine collagen-induced arthritis by inhibiting Th17 and B-cell function
Xuzhu, G., Komai‐Koma, M., Leung, B. P. L., Howe, H. S., McSharry, C. P., McInnes, I. B., & Xu, D. (2011) · Annals of the Rheumatic Diseases · doi:10.1136/ard.2011.149831 · Cited by 173
Teng, X., Hu, Z., Wei, X., Wang, Z., Guan, T., Liu, N., Liu, X., Ye, N., Deng, G., Luo, C., et al. (2014) · The Journal of Immunology · doi:10.4049/jimmunol.1300047 · Cited by 170
Raida, M. K., & Buchmann, K. (2008) · Fish & Shellfish Immunology · doi:10.1016/j.fsi.2008.07.008 · Cited by 169
Th17 Cells and Activated Dendritic Cells Are Increased in Vitiligo Lesions
Wang, C. Q. F., Cruz‐Inigo, A. E., Fuentes‐Duculan, J., Moussai, D., Gulati, N., Sullivan-Whalen, M. M., Gilleaudeau, P., Cohen, J. A., & Krueger, J. G. (2011) · PLoS ONE · doi:10.1371/journal.pone.0018907 · Cited by 169
IL-23 and Autoimmunity: New Insights into the Pathogenesis of Inflammatory Bowel Disease
Abraham, C., & Cho, J. H. (2008) · Annual Review of Medicine · doi:10.1146/annurev.med.60.051407.123757 · Cited by 169
Metadata
- Authors
- Acosta-Rodriguez, E. V., Napolitani, G., Lanzavecchia, A., & Sallusto, F.
- Affiliations
- Institute for Research in Biomedicine (CH)
- Corresponding author
- Sallusto, Federica
- Venue
- Nature Immunology
- Published
- 2007-08-05
- Volume
- 8
- Issue
- 9
- Pages
- 942-949
- ISSN
- 1529-2908 (ISSN-L)
- 1529-2916
- OpenAlex
- W2012680181
- Cited by
- 1,857
- References
- 43
- Citations by year
- 2026: 43 · 2025: 35 · 2024: 39 · 2023: 47 · 2022: 46 · 2021: 65 · 2020: 63 · 2019: 59 · 2018: 57 · 2017: 93 · 2016: 97 · 2015: 115 · 2014: 119 · 2013: 126 · 2012: 145
- FWCI
- 67.88
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature Immunology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institute for Health and Care Research
- Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung
- Bundesamt für Gesundheit
- National Institutes of Health
- National Institute of Allergy and Infectious Diseases (U19AI057266)
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › Psoriasis: Treatment and Pathogenesis
- Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
- Life Sciences › Immunology and Microbiology › Immunology › IL-33, ST2, and ILC Pathways
- Keywords
- Th17 cells, IL-17, IL-1β, interleukin-6, TGF-beta, RORγ, CD4+ T cell differentiation, IL-12, antigen-presenting cells, dendritic cells, monocytes, T cell polarization
- MeSH terms
- Antigen-Presenting Cells, Cell Differentiation, Cells, Cultured, Enzyme-Linked Immunosorbent Assay, Flow Cytometry, T-Lymphocytes, Helper-Inducer, Humans, Receptors, Thyroid Hormone, Interleukin-6, T-Lymphocyte Subsets, Cytokines, Transforming Growth Factor beta, Receptors, Retinoic Acid, Interleukin-12, Cell Lineage, Reverse Transcriptase Polymerase Chain Reaction, Interleukin-17, Interleukin-1beta, Nuclear Receptor Subfamily 1, Group F, Member 3
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