The DOI matches its Crossref record; 101 of the 101 references it cites were found in a registry or an index.
Plasticity of CD4+ T Cell Lineage Differentiation
Open accessAbstract
The differentiation of naive CD4(+) T cells into lineages with distinct effector functions has been considered to be an irreversible event. T helper type 1 (Th1) cells stably express IFN-gamma, whereas Th2 cells express IL-4. The discovery and investigation of two other CD4(+) T cell subsets, induced regulatory T (iTreg) cells and Th17 cells, has led to a rethinking of the notion that helper T cell subsets represent irreversibly differentiated endpoints. Accumulating evidence suggests that CD4(+) T cells, particularly iTreg and Th17 cells, are more plastic than previously appreciated. It appears that expression of Foxp3 by iTreg cells or IL-17 by Th17 cells may not be stable and that there is a great degree of flexibility in their differentiation options. Here, we will discuss recent findings that demonstrate the plasticity of CD4(+) T cell differentiation and the biological implications of this flexibility.
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 former group encompasses functionally distinct populations including T H 1 cells responsible for host defense against intracellular microbes and implicated in systemic autoimmunity, T H 2 cells that fight off extracellular parasites and are involved in anaphylactic reactions and T H 17 cells that mediate immunity against extracellular bacteria and fungi as well as organspecific autoimmunity (Z”
From Iron in infection and immunity (2020) · cites this paper as Zhou et al., 2009
In the citing paper
“However, the current view is that CD4 Th cell subsets are not separate lineages but have plasticity and form a continuum of mixed functional capacities [177, 178].”
From Guidelines for the use of flow cytometry and cell sorting in immunological studies (third edition) (2021) · cites this paper as [177]
Citations
Cites
Control of Regulatory T Cell Development by the Transcription Factor Foxp3
Hori, S., Nomura, T., & Sakaguchi, S. (2003) · Science · doi:10.1126/science.1079490 · Cited by 8,187
Foxp3 programs the development and function of CD4+CD25+ regulatory T cells
Fontenot, J. D., Gavin, M. A., & Rudensky, A. Y. (2003) · Nature Immunology · doi:10.1038/ni904 · Cited by 7,745
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
Self-citationHarrington, 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
Chen, W., Jin, W., Hardegen, N. J., Lei, K.-J., Li, L., Marinos, N. J., McGrady, G., & Wahl, S. M. (2003) · The Journal of Experimental Medicine · doi:10.1084/jem.20030152 · Cited by 4,678
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
Vignali, D. A. A., Collison, L. W., & Workman, C. J. (2008) · Nature Reviews Immunology · doi:10.1038/nri2343 · Cited by 3,463
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
Cited by
Sorted by citations
Items 601–700 of 1,000
Transcriptional characteristics of CD4+ T cells in young asthmatic children: RORC and FOXP3 axis
Hamzaoui, A., Hamzaoui, A., Berraïes, A., Maalmi, H., Ammar, J., & Abid, H. (2011) · Journal of Inflammation Research · doi:10.2147/jir.s25314 · Cited by 39
Li, Y., Zhao, L., Tong, L., Qian, S.-N., Ren, Y., Zhang, L., Ding, X., Chen, Y., Wang, Y., Zhang, W., et al. (2012) · Arthritis Research & Therapy · doi:10.1186/ar3853 · Cited by 39
Wen, W., Wan, Z., Ren, K., Zhou, D. F., Gao, Q., Wu, Y. R., Wang, L., Yuan, Z., & Zhou, J. (2016) · Experimental and Molecular Pathology · doi:10.1016/j.yexmp.2016.03.009 · Cited by 40
Myeloid Cells as Targets for Therapy in Solid Tumors
Cotechini, T., Medler, T. R., & Coussens, L. M. (2015) · The Cancer Journal · doi:10.1097/ppo.0000000000000132 · Cited by 40
Tonic LAT-HDAC7 Signals Sustain Nur77 and Irf4 Expression to Tune Naive CD4 T Cells
Myers, D. R., Lau, T. A., Markegard, E., Lim, H. W., Kasler, H. G., Zhu, M., Barczak, A. J., Huizar, J., Zikherman, J., Erle, D. J., et al. (2017) · Cell Reports · doi:10.1016/j.celrep.2017.04.076 · Cited by 39
Cellular architecture shapes the naïve T cell response
Hale, B. D., Severin, Y., Gräbnitz, F., Stark, D., Guignard, D., Mena, J., Festl, Y., Lee, S., Hanimann, J., Zangger, N. S., et al. (2024) · Science · doi:10.1126/science.adh8967 · Cited by 44
Differentiation, Regulation and Function of Th9 Cells
Jia, L., & Wu, C. Y. (2014) · Advances in experimental medicine and biology · doi:10.1007/978-94-017-9487-9_7 · Cited by 41
TH17, TH22 and TReg Cells Are Enriched in the Healthy Human Cecum
Wolff, M. J., Leung, J. M., Davenport, M., Poles, M. A., Cho, I., & Loke, P. (2012) · PLoS ONE · doi:10.1371/journal.pone.0041373 · Cited by 38
Dual function of polycomb group proteins in differentiated murine T helper (CD4+) cells
Jacob, E., Hod-Dvorai, R., Ben-Mordechai, O. L., Boyko, Y., & Avni, O. (2011) · Journal of Molecular Signaling · doi:10.1186/1750-2187-6-5 · Cited by 38
Riaz, T., Sollid, L. M., Olsen, I., & de Souza, G. A. (2016) · Molecular & Cellular Proteomics · doi:10.1074/mcp.m115.050138 · Cited by 38
Thymic and Postthymic Regulation of Naïve CD4+T-Cell Lineage Fates in Humans and Mice Models
Belizário, J. E., Brandão, W. N., Rossato, C., & Peron, J. P. S. (2016) · Mediators of Inflammation · doi:10.1155/2016/9523628 · Cited by 40
Th17 cells in pathogenic simian immunodeficiency virus infection of macaques
Cecchinato, V., & Franchini, G. (2010) · Current Opinion in HIV and AIDS · doi:10.1097/coh.0b013e32833653ec · Cited by 39
miRNAs Alter T Helper 17 Cell Fate in the Pathogenesis of Autoimmune Diseases
Huang, J., Xu, X., & Yang, J. Y. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.593473 · Cited by 38
Zhang, Q., Geng, M., Li, K., Gao, H., Jiao, X., Ai, K., Wei, X., & Yang, J. (2022) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2022.102843 · Cited by 43
Effects of Aluminum on Immune Functions of Cultured Splenic T and B Lymphocytes in Rats
She, Y., Wang, N., Chen, C., Zhu, Y., Xia, S., Hu, C., & Li, Y. (2012) · Biological Trace Element Research · doi:10.1007/s12011-011-9307-3 · Cited by 37
Lin, X., Sun, A., Ruan, P., Zhang, Z., & Yan, J. (2011) · BMC Microbiology · doi:10.1186/1471-2180-11-21 · Cited by 37
Sang, L.-X., Chang, B., Zhu, J., Yang, F., Li, Y., Jiang, X., Wang, D., Lu, C., & Sun, X. (2017) · World Journal of Gastroenterology · doi:10.3748/wjg.v23.i21.3850 · Cited by 38
Brincks, E. L., Adams, J., Wang, L., Turner, B. A., Marcinowicz, A., Ke, J., Essmann, M., Mautino, L. M., Allen, C. V., Kumar, S., et al. (2020) · Oncotarget · doi:10.18632/oncotarget.27646 · Cited by 37
García‐Serna, A. M., Hernández‐Caselles, T., Jiménez‐Guerrero, P., Martín‐Orozco, E., Pérez‐Fernández, V., Cantero‐Cano, E., Muñoz‐García, M., Meseguer, C. B., Cobos, I. P. D. L., García‐Marcos, L., et al. (2020) · Environmental Research · doi:10.1016/j.envres.2020.110468 · Cited by 38
Ganor, Y., & Levite, M. (2012) · Springer eBooks · doi:10.1007/978-3-7091-0888-8_4 · Cited by 38
Fighting Viral Infections and Virus-Driven Tumors with Cytotoxic CD4+ T Cells
Muraro, E., Merlo, A., Martorelli, D., Cangemi, M., Santa, S. D., Dolcetti, R., & Rosato, A. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.00197 · Cited by 38
Interleukin-17 Links Inflammatory Cross-Talks Between Comorbid Psoriasis and Atherosclerosis
Wang, Y., Zang, J., Liu, C., Yan, Z., & Shi, D. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.835671 · Cited by 36
Lim, J. U., Lee, E., Lee, S., Cho, H. J., Ahn, D. H., Hwang, Y., Choi, J. Y., Yeo, C. D., Park, C. K., & Kim, S. J. (2023) · Translational Lung Cancer Research · doi:10.21037/tlcr-22-633 · Cited by 36
Optimizing vaccine development
Hoft, D. F., Brusić, V., & Sakala, I. G. (2011) · Cellular Microbiology · doi:10.1111/j.1462-5822.2011.01609.x · Cited by 36
Ahlers, J. D., & Belyakov, I. M. (2010) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2010.07.007 · Cited by 37
Flamant, M., Rigaill, J., Paul, S., & Roblin, X. (2017) · Drugs · doi:10.1007/s40265-017-0755-8 · Cited by 37
TLR7 Signaling Regulates Th17 Cells and Autoimmunity: Novel Potential for Autoimmune Therapy
Ye, J., Wang, Y., Liu, X., Li, L., Opejin, A., Hsueh, E. C., Luo, H., Wang, T., Hawiger, D., & Peng, G. (2017) · The Journal of Immunology · doi:10.4049/jimmunol.1601890 · Cited by 36
Brunner, K., Samassa, F., Sansonetti, P. J., & Phalipon, A. (2019) · Human Vaccines & Immunotherapeutics · doi:10.1080/21645515.2019.1594132 · Cited by 35
Role and plasticity of Th1 and Th17 responses in immunity to Staphylococcus aureus
Ferraro, A., Buonocore, S. M., Auquier, P., Nicolas, I., Wallemacq, H., Boutriau, D., & der Most, R. G. V. (2019) · Human Vaccines & Immunotherapeutics · doi:10.1080/21645515.2019.1613126 · Cited by 36
T cell populations in children with autism spectrum disorder and co-morbid gastrointestinal symptoms
Rose, D. R., Yang, H. T., Careaga, M., Angkustsiri, K., de Water, J. V., & Ashwood, P. (2020) · Brain Behavior & Immunity - Health · doi:10.1016/j.bbih.2020.100042 · Cited by 39
A peptide encoded by pri‐miRNA‐31 represses autoimmunity by promoting Treg differentiation
Zhou, H., Lou, F., Bai, J., Sun, Y., Cai, W., Sun, L., Xu, Z., Liu, Z., Zhang, L., Yin, Q., et al. (2022) · EMBO Reports · doi:10.15252/embr.202153475 · Cited by 34
Impact of Lipid Metabolism on Antitumor Immune Response
Mabrouk, N., Lecoeur, B., Bettaı̈eb, A., Paul, C., & Végran, F. (2022) · Cancers · doi:10.3390/cancers14071850 · Cited by 36
Increased serum IL-2, IL-4, IL-5 and IL-12p70 levels in AChR subtype generalized myasthenia gravis
Huan, X., Zhao, R., Song, J., Zhong, H., Su, M., Yan, C., Wang, Y., Chen, S., Zhou, Z., Lu, J., et al. (2022) · BMC Immunology · doi:10.1186/s12865-022-00501-8 · Cited by 36
Regulatory T Cell as a Target for Cancer Therapy
de Rezende, L. C. D., Silva, I. V., Rangel, L. B. A., & Guimarães, M. C. C. (2010) · Archivum Immunologiae et Therapiae Experimentalis · doi:10.1007/s00005-010-0075-0 · Cited by 36
The autoimmunity in Graves's disease
Li, H. (2012) · Frontiers in bioscience · doi:10.2741/4141 · Cited by 36
Neves, P., Rudersdorf, R. A., Galler, R., Bonaldo, M. C., de Santana, M. G. V., Mudd, P. A., Martins, M. A., Rakasz, E. G., Wilson, N. A., & Watkins, D. I. (2010) · Vaccine · doi:10.1016/j.vaccine.2010.09.090 · Cited by 36
Neves, P., dos Santos, J. R., Tubarão, L. N., Bonaldo, M. C., & Galler, R. (2013) · PLoS ONE · doi:10.1371/journal.pone.0081953 · Cited by 35
Park, M.-J., Park, K.-S., Park, H.-S., Cho, M., Hwang, S., Min, S., Park, M., Park, S., & Kim, H. (2012) · Cellular Immunology · doi:10.1016/j.cellimm.2012.06.009 · Cited by 37
Zhang, G. H., Xie, D., Ye, Y., Lin, C., Zhang, X., Zheng, Y., Huang, Z., Peng, L., & Gao, Z. (2013) · Liver International · doi:10.1111/liv.12268 · Cited by 36
Pham, D., Walline, C. C., Hollister, K., Dent, A. L., Blum, J. S., Firulli, A. B., & Kaplan, M. H. (2013) · Journal of Biological Chemistry · doi:10.1074/jbc.m113.497248 · Cited by 35
Park, M., Park, J., Park, E., Lim, M., Kim, S., Lee, D., Baek, S.-Y., Yang, E., Woo, J., Lee, J. J., et al. (2013) · Arthritis & Rheumatology · doi:10.1002/art.38313 · Cited by 35
Wang, Y., Gu, X., Zhang, G., Wang, L., Wang, T., Zhao, Y., Zhang, X., Zhou, Y., Kadin, M. E., & Tu, P. (2014) · Blood · doi:10.1182/blood-2013-10-534693 · Cited by 35
Park, S., Chen, W., Esmaeil, N., Lucas, B., Marsh, L. M., Reibman, J., & Grünig, G. (2014) · Pulmonary Circulation · doi:10.1086/678511 · Cited by 35
Measuring Cellular Immunity to Influenza: Methods of Detection, Applications and Challenges
Coughlan, L., & Lambe, T. (2015) · Vaccines · doi:10.3390/vaccines3020293 · Cited by 35
Current Knowledge of Th22 Cell and IL-22 Functions in Infectious Diseases
Zhang, K., Chen, L., Zhu, C., Zhang, M., & Liang, C. Y. (2023) · Pathogens · doi:10.3390/pathogens12020176 · Cited by 40
Zhu, Y. T., Yu, J., Zhu, X., Yuan, J., Dai, M., Bao, Y., & Jiang, Y. (2023) · Scientific Reports · doi:10.1038/s41598-023-32507-6 · Cited by 35
Multifaceted role of the ubiquitin ligase Itch in immune regulation
Venuprasad, K., Zeng, M., Baughan, S. L., & Massoumi, R. (2015) · Immunology and Cell Biology · doi:10.1038/icb.2014.118 · Cited by 35
Th17 Cells and Transplant Acceptance
Burrell, B. E., & Bishop, D. K. (2010) · Transplantation · doi:10.1097/tp.0b013e3181f5c3de · Cited by 35
TET Proteins and 5-Methylcytosine Oxidation in the Immune SystemPreprint
Tsagaratou, A., & Rao, A. (2013) · Cold Spring Harbor Symposia on Quantitative Biology · doi:10.1101/sqb.2013.78.020248 · Cited by 36
Zhou, Y., Wang, S., Liang, X., Heger, Z., Xu, M., Lü, Q., Yu, M., Adam, V., & Li, N. (2022) · ACS Nano · doi:10.1021/acsnano.2c01778 · Cited by 34
The therapeutic potential of immune cross-talk in leishmaniasis
Hartley, M., Kohl, K., Ronet, C., & Fasel, N. J. (2012) · Clinical Microbiology and Infection · doi:10.1111/1469-0691.12095 · Cited by 34
Zhang, G., Ducatelle, R., Pasmans, F., D'Herde, K. G. M. A., Huang, L., Smet, A., Haesebrouck, F., & Flahou, B. (2013) · PLoS ONE · doi:10.1371/journal.pone.0077966 · Cited by 36
Immunogenicity Assessment of Tumor Necrosis Factor Antagonists in the Clinical Laboratory
Lázár‐Molnár, E., & Delgado, J. C. (2016) · Clinical Chemistry · doi:10.1373/clinchem.2015.242875 · Cited by 34
Nedoszytko, B., Lange, M., Sokołowska‐Wojdyło, M., Renke, J., Trzonkowski, P., Sobjanek, M., Szczerkowska‐Dobosz, A., Niedoszytko, M., Górska, A., Romantowski, J., et al. (2017) · Advances in Dermatology and Allergology · doi:10.5114/ada.2017.69305 · Cited by 36
Liu, R.-T., Zhang, P., Yang, C.-L., Pang, Y., Zhang, M., Zhang, N., Yue, L.-T., Li, X.-L., Li, H., & Duan, R. (2017) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2017.08.005 · Cited by 33
T cells and their function in the immune response to viruses
Beňová, K., Hancková, M., Koči, K., Kúdelová, M., & Betáková, T. (2020) · Acta Virologica · doi:10.4149/av_2020_203 · Cited by 36
Candida Pathogenicity and Interplay with the Immune System
Valand, N., & Girija, U. V. (2021) · Advances in experimental medicine and biology · doi:10.1007/978-3-030-67452-6_11 · Cited by 38
Shi, G., Zhou, Y., Liu, W., Chen, C., Wei, Y., Yan, X., Wu, L., Wang, W., Sun, L., & Zhang, T. (2023) · Acta Pharmaceutica Sinica B · doi:10.1016/j.apsb.2023.04.003 · Cited by 36
Drug targets in the cytokine universe for autoimmune disease
Liu, X., Fang, L., Guo, T. B., Mei, H., & Zhang, J. Z. (2012) · Trends in Immunology · doi:10.1016/j.it.2012.10.003 · Cited by 34
CD4+ T Cell Plasticity—Th2 Cells Join the Crowd
Zhu, J., & Paul, W. E. (2010) · Immunity · doi:10.1016/j.immuni.2010.01.001 · Cited by 34
They Must Hold Tight: Junction Proteins, Microbiota And Immunity In Intestinal Mucosa
Castoldi, Â., de Aguiar, C. F., Moraes‐Vieira, P. M., & Câmara, N. O. S. (2015) · Current Protein and Peptide Science · doi:10.2174/1389203716666150630133141 · Cited by 33
Zeng, W., Liu, Z., Zhang, S., Ren, J., Ma, X., Qin, C., Tian, F., Zhang, Y., & Lin, Y. (2016) · Scientific Reports · doi:10.1038/srep36560 · Cited by 35
Won, H. Y., Jang, E. J., Lee, K., Oh, S., Kim, H. K., Woo, H. A., Kang, S. W., Yu, D., Rhee, S.-G., & Hwang, E. S. (2013) · The Journal of Immunology · doi:10.4049/jimmunol.1203247 · Cited by 32
Robertson, S. A., Petroff, M. G., & Hunt, J. S. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-397175-3.00041-7 · Cited by 35
miR-340 Alleviates Psoriasis in Mice through Direct Targeting of IL-17A
Bian, J., Liu, R., Fan, T., Liao, L., Wang, S., Geng, W., Wang, T., Shi, W., & Ruan, Q. (2018) · The Journal of Immunology · doi:10.4049/jimmunol.1800189 · Cited by 33
Wang, C., Shen, Z., Li, L., Li, Y., Zhao, H., & Jiang, X. (2020) · Food & Function · doi:10.1039/c9fo02444a · Cited by 33
Lim, Y., Kim, H. Y., An, S., & Choi, B. (2022) · Journal of Oral Microbiology · doi:10.1080/20002297.2022.2123550 · Cited by 35
T cells: an emerging cast of roles in bipolar disorder
Chen, Z., Huang, Y., Wang, B., Peng, H., Wang, X., Wu, H., Chen, W., & Wang, M. (2023) · Translational Psychiatry · doi:10.1038/s41398-023-02445-y · Cited by 35
Human Th9 cells: inflammatory cytokines modulate IL‐9 production through the induction of IL‐21
Ma, C. S., Tangye, S. G., & Deenick, E. K. (2010) · Immunology and Cell Biology · doi:10.1038/icb.2010.73 · Cited by 33
Regulation of Toll-like Receptor 5 Gene Expression and Function on Mucosal Dendritic Cells
Feng, T., Cong, Y., Alexander, K. L., & Elson, C. O. (2012) · PLoS ONE · doi:10.1371/journal.pone.0035918 · Cited by 33
Parekh, D., Dancer, R. C. A., Lax, S., Cooper, M. S., Martineau, A. R., Fraser, W. D., Tucker, O., Alderson, D., Perkins, G. D., Smith, F. G., et al. (2013) · Trials · doi:10.1186/1745-6215-14-100 · Cited by 33
Xu, W., Ren, M., Ghosh, S., Qian, K., Luo, Z., Zhang, A., Zhang, C., & Cui, J. (2020) · Mediators of Inflammation · doi:10.1155/2020/3645157 · Cited by 32
Teng, T., Yang, H., Xu, T., Sun, G., Song, X., Bai, G., & Shi, B. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms231810697 · Cited by 33
Beyond FOXP3: a 20-year journey unravelling human regulatory T-cell heterogeneity
Nirmala, S. S., Kayani, K., Gliwiński, M., Hu, Y., Iwaszkiewicz‐Grześ, D., Piotrowska, M., Sakowska, J., Tomaszewicz, M., Morales, J. M. M., Lakshmi, K., et al. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1321228 · Cited by 37
The Role of Regulatory T Cells in Respiratory Infections and Allergy and Asthma
McGuirk, P., Higgins, S. C., & Mills, K. H. G. (2010) · Current Allergy and Asthma Reports · doi:10.1007/s11882-009-0078-2 · Cited by 33
Spectrum of T‐lymphocyte activities regulating allergic lung inflammation
Gelfand, E. W., Joetham, A., Wang, M., Takeda, K., & Schedel, M. (2017) · Immunological Reviews · doi:10.1111/imr.12561 · Cited by 32
Jacob, E. M., Borah, A., Pillai, S. C., & Kumar, D. S. (2020) · Nanomaterials · doi:10.3390/nano10122460 · Cited by 32
Zhan, X., Jiang, X. X., Dai, X., & Li, B. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.916411 · Cited by 34
Apple polyphenols suppress antigen presentation of ovalbumin by THP-1-derived dendritic cells
Katayama, S., Kukita, T., Ishikawa, E., Nakashima, S., Masuda, S., Kanda, T., Akiyama, H., Teshima, R., & Nakamura, S. (2012) · Food Chemistry · doi:10.1016/j.foodchem.2012.10.076 · Cited by 32
Rohlman, D., Pham, D., Yu, Z., Steppan, L. B., & Kerkvliet, N. I. (2012) · Frontiers in Immunology · doi:10.3389/fimmu.2012.00223 · Cited by 32
Regulatory T Cells and IL-17-Producing Cells in Graft-Versus-Host Disease
Teshima, T., Maeda, Y., & Ozaki, K. (2011) · Immunotherapy · doi:10.2217/imt.11.51 · Cited by 32
Lu, Y., Liu, F., Li, C., Chen, Y., Weng, D., & Chen, J. (2017) · Mediators of Inflammation · doi:10.1155/2017/8415094 · Cited by 32
Warner, K., Weit, N., Crispatzu, G., Admirand, J. H., Jones, D. M., & Herling, M. (2013) · Current Hematologic Malignancy Reports · doi:10.1007/s11899-013-0165-2 · Cited by 34
Interactions Between HDL and CD4+ T Cells: A Novel Understanding of HDL Anti-Inflammatory Properties
Atehortúa, L., Davidson, W. S., & Chougnet, C. A. (2024) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.124.320851 · Cited by 35
Malmhäll, C., Bossios, A., Rådinger, M., Sjöstrand, M., Lu, Y., Lundbäck, B., & Lötvall, J. O. (2012) · PLoS ONE · doi:10.1371/journal.pone.0040012 · Cited by 32
Matsuoka, K. (2017) · International Journal of Hematology · doi:10.1007/s12185-017-2386-y · Cited by 31
Recent advances in the development of vaccines for chronic inflammatory autoimmune diseases
Zhang, N., & Nandakumar, K. S. (2018) · Vaccine · doi:10.1016/j.vaccine.2018.04.062 · Cited by 31
Shakya, A. K., Lee, C. H., Uddin, M. J., & Gill, H. S. (2018) · Molecular Pharmaceutics · doi:10.1021/acs.molpharmaceut.8b00768 · Cited by 31
Guise, S. D., & Levin, M. (2021) · Toxicology Letters · doi:10.1016/j.toxlet.2021.09.002 · Cited by 31
Tian, H., Xing, J., Tang, X., Sheng, X., Chi, H., & Zhan, W. (2022) · Developmental & Comparative Immunology · doi:10.1016/j.dci.2022.104627 · Cited by 31
Caracciolo, D., Mancuso, A., Polerà, N., Froio, C., D’Aquino, G., Riillo, C., Tagliaferri, P., & Tassone, P. (2023) · Experimental Hematology and Oncology · doi:10.1186/s40164-022-00368-w · Cited by 36
Polyelectrolyte LbL microcapsules versus PLGA microparticles for immunization with a protein antigen
Temmerman, M. D., Rejman, J., Vandenbroucke, R. E., Koker, S. D., Libert, C., Grooten, J., Demeester, J., Gander, B. A., & Smedt, S. C. D. (2011) · Journal of Controlled Release · doi:10.1016/j.jconrel.2011.10.029 · Cited by 31
Ting, H.-A., Nagata, D. D. A., Rasky, A. J., Malinczak, C., Maillard, I. P., Schaller, M. A., & Lukacs, N. W. (2018) · Mucosal Immunology · doi:10.1038/s41385-018-0052-1 · Cited by 31
Semaphorin Signals Tweaking the Tumor Microenvironment
Muratori, C., & Tamagnone, L. (2012) · Advances in cancer research · doi:10.1016/b978-0-12-386503-8.00003-x · Cited by 30
Immunological perspectives on atherosclerotic plaque formation and progression
Pi, H., Wang, G., Wang, Y., Zhang, M., He, Q., Zheng, X., Yin, K., Zhao, G., & Jiang, T. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1437821 · Cited by 35
Li, L., Kim, H. T., Nellore, A., Patsoukis, N., Petkova, V., McDonough, S. M., Politikos, I., Nikiforow, S., Soiffer, R. J., Antin, J. H., et al. (2014) · Blood Cancer Journal · doi:10.1038/bcj.2013.75 · Cited by 30
Trans-presentation of IL-15 modulates STAT5 activation and Bcl-6 expression in TH1 cells
Cooley, I. D., Read, K. A., & Oestreich, K. J. (2015) · Scientific Reports · doi:10.1038/srep15722 · Cited by 29
Th1high in tumor microenvironment is an indicator of poor prognosis for patients with NSCLC
Huang, J. A., Fangrong, S., Hai-tao, H., Chunhua, L., & Guangbo, Z. (2017) · Oncotarget · doi:10.18632/oncotarget.14471 · Cited by 30
Choi, D. W., Jung, S. Y., Shon, D., & Shin, H. S. (2020) · Molecules · doi:10.3390/molecules25092186 · Cited by 30
Inflammation Determines the Capacity of Allogenic Endothelial Cells to Regulate Human Treg Expansion
Cross, A. R., Lion, J., Poussin, K., Glotz, D., & Mooney, N. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.666531 · Cited by 30
Metadata
- Authors
- Zhou, L., Chong, M. M. W., & Littman, D. R.
- Affiliations
- Howard Hughes Medical Institute (US)
- New York University (US)
- Corresponding author
- Littman, Dan R.
- Venue
- Immunity
- Publisher
- Elsevier BV
- Published
- 2009-05
- Volume
- 30
- Issue
- 5
- Pages
- 646-655
- ISSN
- 1074-7613 (ISSN-L)
- OpenAlex
- W2016827757
- Cited by
- 1,551
- References
- 101
- Citations by year
- 2026: 33 · 2025: 48 · 2024: 51 · 2023: 61 · 2022: 73 · 2021: 96 · 2020: 73 · 2019: 61 · 2018: 68 · 2017: 77 · 2016: 90 · 2015: 99 · 2014: 110 · 2013: 145 · 2012: 134
- FWCI
- 11.46
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- www.elsevier.com/tdm/userlicense/1.0/ (tdm)
- www.elsevier.com/legal/tdmrep-license (tdm)
- www.elsevier.com/open-access/userlicense/1.0/ (vor, 1574 d)
- doi.org/10.15223/policy-017 (stm-asf)
- doi.org/10.15223/policy-037 (stm-asf)
- doi.org/10.15223/policy-012 (stm-asf)
- doi.org/10.15223/policy-029 (stm-asf)
- doi.org/10.15223/policy-004 (stm-asf)
- Locations
- Immunity (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
- Life Sciences › Immunology and Microbiology › Immunology › Psoriasis: Treatment and Pathogenesis
- Life Sciences › Immunology and Microbiology › Immunology › IL-33, ST2, and ILC Pathways
- Keywords
- CD4+ T cell differentiation, T cell plasticity, Th1 cells, Th2 cells, induced regulatory T cells, Th17 cells, Foxp3, IL-17, T helper cell subsets
- MeSH terms
- Animals, Cell Differentiation, T-Lymphocytes, Helper-Inducer, Humans, T-Lymphocyte Subsets, Cytokines, Cell Lineage, T-Lymphocytes, Regulatory, Forkhead Transcription Factors
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