Cited by 1,842Psoriasis: Treatment and PathogenesisT-cell and B-cell ImmunologyIL-33, ST2, and ILC Pathways

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IL-17 Family Cytokines and the Expanding Diversity of Effector T Cell Lineages

Weaver, Casey T., Hatton, Robin D., Mangan, Paul R., Harrington, Laurie E.·2007·Annual Review of Immunology

DOI 10.1146/annurev.immunol.25.022106.141557

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Abstract

Since its conception two decades ago, the Th1-Th2 paradigm has provided a framework for understanding T cell biology and the interplay of innate and adaptive immunity. Naive T cells differentiate into effector T cells with enhanced functional potential for orchestrating pathogen clearance largely under the guidance of cytokines produced by cells of the innate immune system that have been activated by recognition of those pathogens. This secondary education of post-thymic T cells provides a mechanism for appropriately matching adaptive immunity to frontline cues of the innate immune system. Owing in part to the rapid identification of novel cytokines of the IL-17 and IL-12 families using database searches, the factors that specify differentiation of a new effector T cell lineage-Th17-have now been identified, providing a new arm of adaptive immunity and presenting a unifying model that can explain many heretofore confusing aspects of immune regulation, immune pathogenesis, and host defense.

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TH1 and TH2 Cells: Different Patterns of Lymphokine Secretion Lead to Different Functional Properties
Mosmann, T. R., & Coffman, R. L. (1989) · Annual Review of Immunology · doi:10.1146/annurev.iy.07.040189.001045 · Cited by 7,692
Two types of murine helper T cell clone. I. Definition according to profiles of lymphokine activities and secreted proteins.
Mosmann, T. R., Cherwinski, H. M., Bond, M. W., Giedlin, M. A., & Coffman, R. L. (1986) · The Journal of Immunology · doi:10.4049/jimmunol.136.7.2348 · Cited by 7,553
Reciprocal developmental pathways for the generation of pathogenic effector TH17 and regulatory T cells
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
The Orphan Nuclear Receptor RORγt Directs the Differentiation Program of Proinflammatory IL-17+ T Helper Cells
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
Interleukin 17-producing CD4+ effector T cells develop via a lineage distinct from the T helper type 1 and 2 lineages
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
Self-citation
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
IL-23 drives a pathogenic T cell population that induces autoimmune inflammation
Langrish, C. L., Chen, Y., Blumenschein, W. M., Mattson, J., Basham, B., Sedgwick, J. D., McClanahan, T., Kastelein, R. A., & Cua, D. J. (2005) · The Journal of Experimental Medicine · doi:10.1084/jem.20041257 · Cited by 4,099
TGFβ in the Context of an Inflammatory Cytokine Milieu Supports De Novo Differentiation of IL-17-Producing T Cells
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
A Novel Transcription Factor, T-bet, Directs Th1 Lineage Commitment
Szabo, S. J., Kim, S. T., Costa, G. L., Zhang, X., Fathman, C. G., & Glimcher, L. H. (2000) · Cell · doi:10.1016/s0092-8674(00)80702-3 · Cited by 3,589
Development of T H 1 CD4 + T Cells Through IL-12 Produced by Listeria -Induced Macrophages
Hsieh, C.-S., Macatonia, S. E., Tripp, C. S., Wolf, S. F., O'Garra, A., & Murphy, K. M. (1993) · Science · doi:10.1126/science.8097338 · Cited by 3,134

Show all 135 references

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Song, J., Wu, C., Korpos, É., Zhang, X., Agrawal, S. M., Wang, Y., Faber, C., Schäfers, M. A., Körner, H., Opdenakker, G., et al. (2015) · Cell Reports · doi:10.1016/j.celrep.2015.01.037 · Cited by 218
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Nalbandian, A., Crispín, J. C., & Tsokos, G. C. (2009) · Clinical & Experimental Immunology · doi:10.1111/j.1365-2249.2009.03944.x · Cited by 218
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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
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Gómez‐Rodríguez, J., Sahu, N., Handon, R., Davidson, T. S., Anderson, S. M., Kirby, M., August, A., & Schwartzberg, P. L. (2009) · Immunity · doi:10.1016/j.immuni.2009.07.009 · Cited by 217
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Behçet’s disease physiopathology: a contemporary review
Zeidan, M. J., Saadoun, D., Garrido, M., Klatzmann, D., Six, A., & Cacoub, P. (2016) · Autoimmunity Highlights · doi:10.1007/s13317-016-0074-1 · Cited by 215
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Gasse, P., Riteau, N., Vacher, R., Michel, M.-L., Fautrel, A., di Padova, F., Fick, L., Charron, S., Lagente, V., Eberl, G., et al. (2011) · PLoS ONE · doi:10.1371/journal.pone.0023185 · Cited by 208
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Kim, V., Rogers, T. J., & Criner, G. J. (2008) · Proceedings of the American Thoracic Society · doi:10.1513/pats.200802-014et · Cited by 213
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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
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Moisan, J., Grenningloh, R., Bettelli, E., Oukka, M., & Ho, I. (2007) · The Journal of Experimental Medicine · doi:10.1084/jem.20070994 · Cited by 205
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Lan, R. Y. Z., Salunga, T. L., Tsuneyama, K., Lian, Z.-X., Yang, G.-X., Hsu, W., Moritoki, Y., Ansari, A. A., Kemper, C., Price, J., et al. (2009) · Journal of Autoimmunity · doi:10.1016/j.jaut.2008.11.001 · Cited by 202
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Amsen, D., Antov, A., & Flavell, R. A. (2009) · Nature reviews. Immunology · doi:10.1038/nri2488 · Cited by 213
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Ait‐Oufella, H., Sage, A. P., Mallat, Z., & Tedgui, A. (2014) · Circulation Research · doi:10.1161/circresaha.114.302761 · Cited by 201
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
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Hot, A., & Miossec, P. (2011) · Annals of the Rheumatic Diseases · doi:10.1136/ard.2010.143768 · Cited by 204
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Shi, R., Tang, Y., & Miao, H. (2020) · MedComm · doi:10.1002/mco2.6 · Cited by 210
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Su, D., Lu, Z., Shen, M., Li, X., & Sun, L. (2012) · BioMed Research International · doi:10.1155/2012/347141 · Cited by 202
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Ely, L. K., Fischer, S., & Garcia, K. C. (2009) · Nature Immunology · doi:10.1038/ni.1813 · Cited by 195
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Taming cancer by inducing immunity via dendritic cells
Palucka, A. K., Ueno, H., Fay, J. W., & Banchereau, J. (2007) · Immunological Reviews · doi:10.1111/j.1600-065x.2007.00575.x · Cited by 192
The gelatinases, MMP-2 and MMP-9, as fine tuners of neuroinflammatory processes
Hannocks, M., Zhang, X., Gerwien, H., Chashchina, A. A., Burmeister, M., Korpos, É., Song, J., & Sorokin, L. M. (2017) · Matrix Biology · doi:10.1016/j.matbio.2017.11.007 · Cited by 190
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Amicarella, F., Muraro, M. G., Hirt, C., Cremonesi, E., Padovan, E., Mele, V, Governa, V, Han, J., Huber, X., Droeser, R. A., et al. (2017) · Gut · doi:10.1136/gutjnl-2015-310016 · Cited by 189
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Simonian, P. L., Roark, C. L., Wehrmann, F., Lanham, A. K., del Valle, F. D., Born, W. K., O’Brien, R. L., & Fontenot, A. P. (2009) · The Journal of Immunology · doi:10.4049/jimmunol.182.1.657 · Cited by 195
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Niess, J. H., Leithäuser, F., Adler, G., & Reimann, J. (2008) · The Journal of Immunology · doi:10.4049/jimmunol.180.1.559 · Cited by 198
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Spolski, R. J., Kim, H., Zhu, W., Levy, D. E., & Leonard, W. J. (2009) · The Journal of Immunology · doi:10.4049/jimmunol.0802978 · Cited by 182
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Park, S. W., Chen, S. W. C., Kim, M., Brown, K. M., Kolls, J. K., D’Agati, V. D., & Lee, H. T. (2010) · Laboratory Investigation · doi:10.1038/labinvest.2010.151 · Cited by 179
Interleukin-17: A novel inflammatory cytokine that bridges innate and adaptive immunity
Jeffrey, J. Y. (2007) · Frontiers in bioscience · doi:10.2741/2667 · Cited by 182
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Cope, A. P. (2008) · Arthritis Research & Therapy · doi:10.1186/ar2412 · Cited by 177
Expression of IL-17A in human atherosclerotic lesions is associated with increased inflammation and plaque vulnerability
Erbel, C., Dengler, T. J., Wangler, S., Lasitschka, F., Bea, F., Wambsganss, N., Hakimi, M., Böckler, D., Katus, H. A., & Gleissner, C. A. (2010) · Basic Research in Cardiology · doi:10.1007/s00395-010-0135-y · Cited by 180
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Mayer, L. (2009) · Journal of Gastroenterology · doi:10.1007/s00535-009-0138-3 · Cited by 178
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Andoh, A. (2016) · Digestion · doi:10.1159/000444066 · Cited by 170
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Cannas, D., Loi, E., Serra, M., Firinu, D., Valera, P., & Zavattari, P. (2020) · Nutrients · doi:10.3390/nu12072074 · Cited by 175
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Cha, H., Chang, S.-Y., Chang, J., Kim, J., Yang, J., Kim, C., & Kweon, M. (2010) · The Journal of Immunology · doi:10.4049/jimmunol.0902944 · Cited by 169
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Thompson, A., & Lees, C. W. (2010) · Inflammatory Bowel Diseases · doi:10.1002/ibd.21375 · Cited by 171
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Chang, J., Cha, H., Lee, D., Seo, K. Y., & Kweon, M. (2010) · PLoS ONE · doi:10.1371/journal.pone.0012925 · Cited by 170
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Laurence, A. D. J., & O’Shea, J. J. (2007) · Nature Immunology · doi:10.1038/ni0907-903 · Cited by 168
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Alexander, K. L., Targan, S. R., & Elson, C. O. (2014) · Immunological Reviews · doi:10.1111/imr.12180 · Cited by 169
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Pflugfelder, S. C., Corrales, R. M., & de Paiva, C. S. (2013) · Experimental Eye Research · doi:10.1016/j.exer.2013.08.013 · Cited by 166
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Habicht, A., Dada, S., Jurewicz, M. M., Fife, B. T., Yagita∥, H., Azuma, M., Sayegh, M. H., & Guleria, I. (2007) · The Journal of Immunology · doi:10.4049/jimmunol.179.8.5211 · Cited by 166
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Huang, W. J. M., Thomas, B., Flynn, R. A., Gavzy, S. J., Wu, L., Kim, S. V., Hall, J. A., Miraldi, E. R., Ng, C., Rigo, F., et al. (2015) · Nature · doi:10.1038/nature16193 · Cited by 170
Retracted
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Self-citation

Authors: Weaver, C. T., Hatton, R. D., Mangan, P. R., & Harrington, L. E.
Affiliations: University of Alabama at Birmingham (US)
ORCID: Weaver, Casey T.
Hatton, Robin D.
Harrington, Laurie E.
Venue: Annual Review of Immunology
Publisher: Annual Reviews
Published: 2007-04-01
Volume: 25
Issue: 1
Pages: 821-852
ISSN: 0732-0582 (ISSN-L)
1545-3278
DOI: 10.1146/annurev.immunol.25.022106.141557
OpenAlex: W2156451877
Cited by: 1,842
References: 135
Citations by year: 2026: 18 · 2025: 16 · 2024: 35 · 2023: 33 · 2022: 35 · 2021: 60 · 2020: 47 · 2019: 54 · 2018: 60 · 2017: 79 · 2016: 71 · 2015: 99 · 2014: 124 · 2013: 137 · 2012: 120
FWCI: 18.11
Type: journal article
Language: en
Open access: closed
Locations: Annual Review of Immunology (publishedVersion)
PubMed (publishedVersion)
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: IL-17 family cytokines, IL-12 family cytokines, Th17 cells, effector T cell differentiation, Th1/Th2 paradigm, naive T cell activation, innate-adaptive immune interaction, T cell lineage specification, immune regulation, immune pathogenesis, host defense
MeSH terms: Animals, Cell Differentiation, Humans, Immunity, Innate, Structure-Activity Relationship, Protein Structure, Tertiary, Th1 Cells, Th2 Cells, Interleukin-12, Interleukin-17

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IL-17 Family Cytokines and the Expanding Diversity of Effector T Cell Lineages

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