The DOI matches its Crossref record, with a small difference in title or year; 71 of the 71 references it cites were found in a registry or an index.
NF‐κB: roles and regulation in different CD 4+ T‐cell subsets
Open accessAbstract
Summary: The nuclear factor‐κB (NF‐κB) family of transcription factors plays important roles in various biological processes including apoptosis, stress response, immunity, and inflammation. NF‐κB signaling is involved in both immune cell development and function, and it is critical in modulation of the immune response through the transcriptional regulation of cytokine and chemokine expression. An area of great interest in T‐cell‐mediated adaptive immunity is the ability of naive CD 4+ T cells generated in the thymus to differentiate into various subsets including T‐helper 1 (Th1), Th2, Th17, Th9, follicular helper T (Tfh), Th22, and regulatory T (Treg) cells, upon encountering different pathogens and microenvironments. In this review, we discuss the role of NF‐κB pathway in the development and functional divergence of the different helper T‐cell subsets as well as in regulatory T cells.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
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?
The check wasn’t confident either way, so it gives no verdict — never disputed.
In the citing paper
“Other studies have also shown that FOXK2 affects the activation of T lymphocytes77,78 and revealed the essential roles of NR4A1 in regulatory T cell differentiation79,80, suggesting that the identified TFs have important roles in naive CD4+ T cell response upon TCR stimulation.”
From Inferring gene regulatory networks from single-cell multiome data using atlas-scale external data (2025) · cites this paper as [78]
Experimental — accuracy not yet measured
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Park, J., Adoro, S., Guinter, T. I., Erman, B., Alag, A., Catálfamo, M., Kimura, M. Y., Cui, Y., Lucas, P. J., Gress, R. E., et al. (2010) · Nature Immunology · doi:10.1038/ni.1840 · Cited by 5,835
Sakaguchi, S., Sakaguchi, N., Asano, M., Itoh, M., & Toda, M. (1995) · The Journal of Immunology · doi:10.4049/jimmunol.155.3.1151 · Cited by 5,608 · cited 1×
“Since the original discovery of CD4CD25 Treg cells by Sakaguchi and colleagues (14), there has been much progress in understanding the role of Treg cells in immune homeostasis and function.”
BackgroundCTLA-4 Control over Foxp3 + Regulatory T Cell Function
Wing, K., Onishi, Y., Prieto-Martin, P., Yamaguchi, T., Miyara, M., Fehervari, Z., Nomura, T., & Sakaguchi, S. (2008) · Science · doi:10.1126/science.1160062 · Cited by 2,956
Follicular Helper CD4 T Cells (T FH )
Crotty, S. (2011) · Annual Review of Immunology · doi:10.1146/annurev-immunol-031210-101400 · Cited by 2,738 · cited 1×
“Also, Tfh cells express high level of ICOS, and the resulting costimulatory signal through the interaction between T-cell ICOS and B-cell ICOSL is critical for B-cell maturation (42).”
BackgroundDeaglio, S., Dwyer, K. M., Gao, W., Friedman, D. J., Usheva, A., Erat, A., Chen, J., Enjyoji, K., Linden, J. M., Oukka, M., et al. (2007) · The Journal of Experimental Medicine · doi:10.1084/jem.20062512 · Cited by 2,613
Zheng, W.-P., & Flavell, R. A. (1997) · Cell · doi:10.1016/s0092-8674(00)80240-8 · Cited by 2,384
Crosstalk in NF-κB Signaling Pathways
Oeckinghaus, A., Hayden, M. S., & Ghosh, S. (2011) · Nature Immunology · doi:10.1038/ni.2065 · Cited by 1,942
Self-citationTrans-endocytosis of CD80 and CD86: a molecular basis for the cell-extrinsic function of CTLA-4
Qureshi, O. S., Zheng, Y., Nakamura, K., Attridge, K., Manzotti, C., Schmidt, E. M., Baker, J., Jeffery, L. E., Kaur, S., Briggs, Z., et al. (2011) · Science · doi:10.1126/science.1202947 · Cited by 1,860
Modulation of tryptophan catabolism by regulatory T cells
Fallarino, F., Grohmann, U., Hwang, K. W., Orabona, C., Vacca, C., Bianchi, R., Belladonna, M. L., Fioretti, M. C., Alegre, M., & Puccetti, P. (2003) · Nature Immunology · doi:10.1038/ni1003 · Cited by 1,375
Autoimmune disease as a consequence of developmental abnormality of a T cell subpopulation.
Asano, M., Toda, M., Sakaguchi, N., & Sakaguchi, S. (1996) · The Journal of Experimental Medicine · doi:10.1084/jem.184.2.387 · Cited by 1,328
Flagged first, then by citations
Cited by
Sorted by citations
Items 301–400 of 407
Gholizadeh, F., Hajiaghayi, M., Choi, J. S., Little, S. R., Rahbari, N., Kargar, M., Brotto, K., Han, E., Shih, S. C. C., & Darlington, P. J. (2025) · The Journal of Immunology · doi:10.1093/jimmun/vkaf086 · Cited by 4
Li, H., Zheng, T., Wan, X., Yuan, R., Bao, L., Long, T., Zhou, Y. N., & Jiang, H. (2025) · Molecular Immunology · doi:10.1016/j.molimm.2025.05.021 · Cited by 4
Pearson, R. A., Krish, K. N., Whatney, W. E., Jaoko, W. G., Mandaliya, K. N., Overbaugh, J. M., Graham, S. M., McClelland, R. S., Hicks, S. L., Maurer, J., et al. (2025) · The Journal of Infectious Diseases · doi:10.1093/infdis/jiaf354 · Cited by 4
Agil, M., Laswati, H., Kuncoro, H., & Ma’arif, B. (2021) · Research Journal of Pharmacy and Technology · doi:10.52711/0974-360x.2021.01102 · Cited by 4
NFAT1 and NFκB regulates expression of the common γ-chain cytokine receptor in activated T cells
Shim, J. A., Lee, S. M., Jeong, J. W., Kim, H., Son, W. J., Park, J. H., Song, P., Im, S., Bae, S., Park, J., et al. (2023) · Cell Communication and Signaling · doi:10.1186/s12964-023-01326-7 · Cited by 4
Accurate differential analysis of transcription factor activity from gene expression
Amin, V. R., Çobanoğlu, D. A., Barnes, S. D., & Çobanoğlu, M. C. (2019) · Bioinformatics · doi:10.1093/bioinformatics/btz398 · Cited by 4
Inhibiting PDGF-D alleviates the symptoms of HELLP by suppressing NF-κB activation
Wang, H., Li, N., Li, Z., & Changhui, L. (2021) · Journal of Molecular Endocrinology · doi:10.1530/jme-20-0308 · Cited by 4
“As a part of the canonical NF-κB signaling pathway, p65 has a central role in regulating T cell receptor (TCR) signaling and inflammatory responses (Oh & Ghosh 2013, Liu et al.”
BackgroundPan, Y., Hou, X., Meng, Q., Yang, X., Shang, L., Wei, X., & Hao, W. (2019) · Toxicology and Applied Pharmacology · doi:10.1016/j.taap.2019.114705 · Cited by 4
Transcriptional regulation of Notch1 by nuclear factor-κB during T cell activation
Hwang, J.-R., Kim, D., Kang, J., Park, S., & Park, S. (2023) · Scientific Reports · doi:10.1038/s41598-022-26674-1 · Cited by 3
Wang, Y., Xiang, Q., Wu, Y., Zhang, X., Huang, Z., Hou, Y., Wang, Y., Yang, J., Wan, W., Zou, H., et al. (2025) · Biomaterials Research · doi:10.34133/bmr.0255 · Cited by 3
Cao, Y., Peng, X., Luo, S., Du, Y., & Zhao, R. (2025) · Current Eye Research · doi:10.1080/02713683.2025.2553644 · Cited by 3
“53 Study has also shown that NF-κB inhibited Foxp3 expression.”
Zheng, S., Deng, S., Yin, Y., Li, G., He, G., Li, J., He, J., He, H., Zeng, Y., Hu, W., et al. (2025) · Kidney Diseases · doi:10.1159/000548294 · Cited by 3
Sun, L., Xu, Z., Shuai, M., Li, C., Yang, G., & Xu, S. (2025) · Science China Life Sciences · doi:10.1007/s11427-024-2838-x · Cited by 4
“We also observed shared mutations in the NFkB2 gene, important for immune cell development and function (Oh and Ghosh, 2013), among the long-lived species (MLS>35 years).”
Involvement and Therapeutic Implication of JAK-STAT Pathway in Cancer
Rehman, A., Khan, N. A., Rashid, G., Tamanna, S., Jindal, R., Seth, N., Bashir, B., Mushtaq, G., Salman, M., & Parveen, S. (2025) · Springer eBooks · doi:10.1007/978-981-96-2763-9_8 · Cited by 5
Basak, F., Jainul, M. A., & Yusof, A. M. (2019) · Journal of Biological Sciences · doi:10.3923/jbs.2019.272.279 · Cited by 3
CQMUH ‐011 mitigates autoimmune hepatitis via inhibiting the function of T lymphocytes
Ling, Q., Hu, X., Jiang, R., Liu, H., Qiu, H., Jiang, X., Zubreri, A., Zhu, H., Wan, J., & Ying-ju, L. (2021) · Drug Development Research · doi:10.1002/ddr.21813 · Cited by 3
“It also plays a crucial role in immune response, and many studies have shown that blocking the expression of NF-κB can attenuate hepatitis in mice by regulating the T cells and the release of inflammatory cytokines (Oh & Ghosh, 2013; Shen et al., 2014).”
A multiplexed siRNA screen identifies key kinase signaling networks of brain glia
Kim, J., Han, J., Afridi, R., Kim, J., Rahman, M. H., Park, D. H., Lee, W. S., Song, G. J., & Suk, K. (2023) · Life Science Alliance · doi:10.26508/lsa.202201605 · Cited by 3
“…involves a series of complex events in which TCR engagement evokes a cytoplasmic cascade of protein − protein interactions and posttranslational modi fi cations, leading to the nuclear translocation of NF-κ B. NF-κ B then promotes the differentiation of T helper type 1 cells (Oh & Ghosh, 2013).”
Ansari, S. R., Charantimath, S., Jirge, V. L., & Keluskar, V. K. (2023) · Brazilian journal of oral sciences/Brazilian Journal of Oral Sciences · doi:10.20396/bjos.v22i00.8668902 · Cited by 3
Potassium ion channel Kir2.1 negatively regulates protective responses to Mycobacterium bovis BCG
Sinha, V., Singh, A., Singh, A., Saraswati, S. S. K., Rana, A. K., Kalra, K., & Natarajan, K. (2024) · Journal of Leukocyte Biology · doi:10.1093/jleuko/qiae068 · Cited by 3
Control of CD4+ T Cell Differentiation and Function by PI3K Isoforms
Cameron, B., Zaheer, S. A., & Dominguez‐Villar, M. (2022) · Current topics in microbiology and immunology · doi:10.1007/978-3-031-06566-8_8 · Cited by 3
Regulatory T Lymphocytes (Treg): Modulation and Clinical Application
Reichert, C. O., da Cunha, J., Levy, D., Maselli, L. M. F., Bydlowski, S. P., & Spada, C. (2017) · InTech eBooks · doi:10.5772/intechopen.69152 · Cited by 3
“This decrease in Treg compromises immunotolerance and equilibration of the immune system [23].”
BackgroundThe effects of phenanthrene exposure on Treg and Th17 cells related cytokines in female rats
Ma, H., Guo, H., Zhang, W., Hu, F., Huang, Y., Zeng, Y., Liu, Y., Li, C., & Wang, J. (2020) · Toxicology Research · doi:10.1093/toxres/tfaa030 · Cited by 3
Epigenetic control of commensal induced Th2 Responses and Intestinal immunopathologyPreprint
Sangani, K. A., Parker, M. E., Anderson, H. D., Chen, L., Pandey, S. P., Pierre, J. F., Meisel, M., Riesenfeld, S. J., Hinterleitner, R., & Jabrì, B. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.08.30.610485 · Cited by 3
NF-κB and STAT3 activation in CD4 T cells in pediatric MOG antibody-associated disease
Corbali, O., Saxena, S., Patel, R. P., Lokhande, H. A., & Chitnis, T. (2023) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2023.578197 · Cited by 2
Nano-immunotherapy: Merging immunotherapy precision with nanomaterial delivery
Hà, N. T. T., Menon, S., & Rivero‐Müller, A. (2025) · iScience · doi:10.1016/j.isci.2025.112319 · Cited by 3
Huang, X., Lin, Z., Lu, D., & Li, H. (2025) · Journal of Environmental Sciences · doi:10.1016/j.jes.2025.06.037 · Cited by 2
Tian, Z., Chen, R., Jia, Y., Jiang, J., Dai, R., An, Y., Tang, X., Zhao, X., & Zhou, L. (2025) · Journal of Clinical Immunology · doi:10.1007/s10875-025-01921-y · Cited by 2
“Tregs are profoundly impaired in Malt1 -/- mice, with markedly reduced Treg numbers observed in the peripheral blood of young animals [17, 18, 23, 27–31].”
Three’s company: The cooperative signals behind the differentiation of Th9 cells
Rodriguez, J. A., Habib, H., & Olson, M. R. (2025) · Seminars in Immunology · doi:10.1016/j.smim.2025.101999 · Cited by 2
Dayem, A. A., Song, M., Park, J., Jeong, K., Lim, K. M., Kim, S., Song, K., & Cho, S. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms262110297 · Cited by 2
Yun, Y., Xu, G., Jiang, X., Ren, X., Lu, M., Chen, J., & Zhang, S. (2025) · Comprehensive physiology · doi:10.1002/cph4.70078 · Cited by 2
“…lipopolysaccharides (LPS), initiate nuclear factor κB (NF-κB) and mitogen-activated protein kinase (MAPK) signaling (Manfredo Vieira et al. 2018; Oh and Ghosh 2013; Thalhamer et al. 2008), upregulating expression of TNF-α, IL-6, IL-1β, and cyclooxygen- ase-2 that exacerbate synovial…”
Basnyat, P., Sumelahti, M., Lehtimäki, T. J., Elovaara, I., & Hagman, S. (2019) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2019.577020 · Cited by 2
Exposure to Secreted Bacterial Factors Promotes HIV-1 Replication in CD4 + T Cells
Znaidia, M., de Souza-Angelo, Y., Létoffé, S., Staropoli, I., Grzelak, L., Ghigo, J., Schwartz, O., & Casartelli, N. (2023) · Microbiology Spectrum · doi:10.1128/spectrum.04313-22 · Cited by 2
Qian, J., Xu, Z., Yin, M., Qin, Z., & Pinhu, L. (2023) · Transplant Immunology · doi:10.1016/j.trim.2023.101926 · Cited by 2
Alnawajha, A., Endharti, A. T., Santoso, S., Santosaningsih, D., & Satriotomo, I. (2023) · Journal of Tropical Life Science · doi:10.11594/jtls.13.03.03 · Cited by 2
Senotherapeutic Peptide 14 Suppresses Th1 and M1 Human T Cell and Monocyte Subsets In Vitro
Alencar‐Silva, T., de Barcelos, S. M., Silva‐Carvalho, A. É., Sousa, M. G. D. C., Rezende, T. M. B., Pogue, R. E., Saldanha‐Araújo, F., Franco, O. L., Boroni, M., Zonari, A. A. C., et al. (2024) · Cells · doi:10.3390/cells13100813 · Cited by 2
“…regulator REL ( c-REL ) (Figure 2F), and those involved in canonical and non-canonical activation pathways ( RELA and RELB , respectively) (Figure 2G,H) RELA is necessary for Th1 differentiation, but its recruitment to the IFN-γ enhancer region is dependent on TBET expression in Th1 cells [16].”
BackgroundBouwman, W., Verhaegh, W., van Doorn, A., Raymakers, R. A. P., van der Poll, T., & van de Stolpe, A. (2024) · Scientific Reports · doi:10.1038/s41598-024-75666-w · Cited by 2
Revisiting Mastitis- An Immunopathophysiological View
Rahal, A., Sohal, J., & Kumar, A. (2021) · Journal of Immunology and Immunopathology · doi:10.5958/0973-9149.2021.00011.3 · Cited by 2
T Cells and Their Subsets in Autoimmunity
Burkett, P. R., Pawlak, M., Peters, A., & Kuchroo, V. K. (2019) · Elsevier eBooks · doi:10.1016/b978-0-12-812102-3.00006-3 · Cited by 2
Adaptive Immunity and Autoimmunity
Albani, S., Wedderburn, L. R., & Prakken, B. J. (2015) · Elsevier eBooks · doi:10.1016/b978-0-323-24145-8.00004-1 · Cited by 2
Prostaglandin-related immune suppression in cattle
Sajiki, Y., Konnai, S., Ikenaka, Y., Okagawa, T., Maekawa, N., Logullo, C., Vaz, I. D. S., Murata, S., & Ohashi, K. (2021) · Veterinary Immunology and Immunopathology · doi:10.1016/j.vetimm.2021.110238 · Cited by 2
New Molecular Mechanisms of Placental Dysfunction
Ventskovskaya, I. B., & Купчик, В. И. (2022) · Репродуктивное здоровье Восточная Европа · doi:10.34883/pi.2021.11.6.006 · Cited by 2
Tanaka, T., Tawara, M., Suzuki, H., Kaneko, M. K., & Kato, Y. (2023) · Antibodies · doi:10.3390/antib12020032 · Cited by 2
“These pathways play essential roles in the differentiation, migration, and plasticity of CD4 + T lymphcytes [33–36].”
Müller, E. K., Białas, N., Epple, M., & Hilger, I. (2022) · Biomedicines · doi:10.3390/biomedicines10071571 · Cited by 2
NF-kappaB and the Immune System
Gilmore, T. D., & Siggers, T. (2022) · Elsevier eBooks · doi:10.1016/b978-0-12-821618-7.00009-2 · Cited by 2
Wang, S., Wang, Y., Li, Y., Lai, X., Hu, M., Chen, M., Li, C., Liu, X., Song, Y., & Deng, Y. (2025) · ACS Nano · doi:10.1021/acsnano.5c09136 · Cited by 1
Qin, K., Zhou, H., Chen, Q., WU, C. C., Liu, J., & Zhou, L. (2026) · Toxicology Mechanisms and Methods · doi:10.1080/15376516.2026.2650438 · Cited by 1
“Previous studies have indicated that the activation of NF-κB and MaPK signaling pathways may be associated with the elevated expression levels of cytokines such as il-2, il-8, il-10, and tNF-α, which were significantly upregulated in Figure 4 (oh and Ghosh 2013;”
The dual role of TOX in regulating TH1 and CD8+ T cell fate
Kye, Y.-C., & Kuchroo, V. K. (2026) · Nature Immunology · doi:10.1038/s41590-026-02494-7 · Cited by 1
Multimodal single‐cell analysis provides novel insights on ankylosing spondylitis in females
Chen, H., Wang, J., Sung, H., Chao, W., Liu, K., Lin, F., & Ko, T. (2022) · Clinical and Translational Medicine · doi:10.1002/ctm2.1066 · Cited by 1
Tang, H., Zhang, J., Zhu, L., Jiang, X., Pei, C., Li, L., & Kong, X. (2023) · Fish & Shellfish Immunology · doi:10.1016/j.fsi.2023.109318 · Cited by 1
Gao, A., Xie, K., Gupta, S., Ahmad, G., & Witting, P. K. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25147863 · Cited by 1
“Therefore, SAA elicits inflammation via NF-κ B signalling including T-cell activation, which is further linked to the production of interferon gamma (IFN-γ ) and concomitant increases in inducible nitric oxide synthase (iNOS) [17–19].”
BackgroundCandidiasis in breast cancer: Tumor progression or not?
Ashrafi, S., Amini, A. A., Karimi, P., Bagherian, M., Sereshgi, M. M. A., Asgarhalvaei, F., Ahmadi, K., Yazdi, M. H., Jahantigh, H. R., Mahdavi, M., et al. (2024) · PubMed Central · doi:10.22038/ijbms.2024.75408.16379 · Cited by 1
“The extracellular signal-regulated kinase (Erk) MAPK pathway prevents apoptosis of CD8+ T cells by modulating the expression of Bcl-2-interacting mediator of cell death (BIM), B-cell lymphoma 2 (BCL-2), and B-cell lymphoma-extra-large (Bcl-XL) proteins (101).”
BackgroundAnti-inflammatory effects of LCB 03-0110 on human corneal epithelial and murine T helper 17 cells
Truong, D. V., Yang, B., & Song, C. (2024) · Korean Journal of Physiology and Pharmacology · doi:10.4196/kjpp.24.166 · Cited by 1
“It has been reported that not only ERK/p38 [53,54], but also other cell signaling pathways, including STAT3 [50], NF-κ B [55], and SMAD2/3 [56] regulate the expression of IL-17A.”
Post-Transcriptional and Translational Mechanisms of Regulation of Gene Expression in T Cell Subsets
Istomine, R., & Piccirillo, C. A. (2018) · InTech eBooks · doi:10.5772/intechopen.73319 · Cited by 1
“While NFAT and NF-κB are necessary during the initial stages of T cell activation, they are also necessary for the differentiation o CD4+ T cells into distinct Th cell subset each endowed with its cytokine signature and specific effector functions [12, 13].”
BackgroundRizk, J., Agerholm, R., Jönsson, A., Doğan, A. A., Dufva, M., & Bekiaris, V. (2021) · European Journal of Immunology · doi:10.1002/eji.202048983 · Cited by 1
Handono, K., Pratama, M. Z., Yuniati, M. G., Sermoati, I. A., Norahmawati, E., Endharti, A. T., Irwanto, Y., Hidayat, S., Solikhin, M. B., Indahwati, L., et al. (2023) · AIP conference proceedings · doi:10.1063/5.0117337 · Cited by 1
Bouwman, W., Verhaegh, W., van Doorn, A., & van de Stolpe, A. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.10.06.463309 · Cited by 1
“…(ER) and androgen (AR) receptor pathways, to regulate functions such as immune cell maturation and activation (Han et al., 2012),(Platanias, 2005),(Oh and Ghosh, 2013),(Li et al., 2007),(Goodman et al., 2011),(Perchet et al., 2018),(Deftos and Bevan, 2000),(Liu et al., 2007),(Lai et al.,…”
BackgroundElizaldi, S. R., Hawes, C. E., Verma, A., Dinasarapu, A. R., Lakshmanappa, Y. S., Schlegel, B. T., Rajasundaram, D., Li, J., Durbin-Johnson, B. P., Ma, Z.-M., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.08.28.555037 · Cited by 1
“Furthermore, the notable increase in the inflammatory mediator NFκB1 is of significance due to 584 its role in promoting Th1 cell differentiation and inducing cytokine production in innate immune 585 cells, such as IL-12, which drives Th1 fate (101, 102).”
BackgroundA Subset Apart? Th9 cell regulation and current limitations to study
Zheng, Z., & Kang, J. (2015) · Journal of nature and science
Knudsen, E., Carlsen, H., Bøyum, A., Benestad, H. B., & Iversen, P. O. (2014) · International Journal of Hematology · doi:10.1007/s12185-014-1598-7
Thymidine Glycol: The Effect on DNA Structure and DNA Binding by Site-Specific Proteins
Kubareva, E. A., Yang, F., Ryazanova, A. Y., Dolinnaya, N. G., Golovin, A. V., Molochkov, N. V., Romanova, E. A., Karpova, E. A., Zatsepin, T. S., & Oretskaya, T. S. (2015) · Natural Science · doi:10.4236/ns.2015.711051
The possible role of heat shock protein-70 induction in collagen-induced arthritis in rats
EL-SAKA, M. D. S. A. E.-S. M. H., Madi, N., & Shahba, A. (2019) · Physiology International · doi:10.1556/2060.106.2019.17
“The later is one of the major factors stimulating the proliferation of Th-17 cells, hence increasing IL-17 expression (2, 41).”
BackgroundRizk, J., Mörbe, U. M., Agerholm, R., Ulmert, I., Tardos, E. C., Kadekar, D., Baglioni, M. V., Viñals, M. T., & Bekiaris, V. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.05.14.094334
Sampurna, I. S. R., Rifa’i, M., & Rahayu, S. (2020) · The Journal of Experimental Life Sciences · doi:10.21776/ub.jels.2019.010.01.11
Resistance to human immunodeficiency virus infection: a rare but neglected state
Tamalet, C., Devaux, C. A., Dubourg, G., & Colson, P. (2020) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.14452
Marei, E. S., & Khattab, N. (2021) · Egyptian Journal of Radiation Sciences and Applications · doi:10.21608/ejrsa.2021.61555.1115
Kelsey, K. T., Eliot, M., Butler, R. A., Koestler, D. C., Salas, L. A., Bell-Glenn, S., Warrier, G., Molinaro, A. M., Christensen, B. C., & Wiencke, J. K. (2021) · SSRN Electronic Journal · doi:10.2139/ssrn.3921282
Analysis of Sterols in Human T Helper Cells
Yutuc, E. (2017) · Cronfa (Swansea University) · doi:10.23889/suthesis.60641
Immunodeficiency, Leukemia, and Lymphoma
Srinivasan, A., Sinha, A. A., & Frazer, J. K. (2022) · Interdisciplinary cancer research · doi:10.1007/16833_2022_82
Novel Targets and Therapies in T Cell Lymphoma
Kesavan, M., & Collins, G. P. (2018) · EMJ Oncology · doi:10.33590/emjoncol/10310205
Chu, G.-G., Wang, J., Ding, Z., Yin, J., Song, L.-J., Wang, Q., Huang, J.-J., Xiao, B., & Ma, C. (2023) · International Immunopharmacology · doi:10.1016/j.intimp.2023.110791
Peripheral Blood Transcriptome Profiles of Adults with Type I HypersensitivityPreprint
Adamovský, O., Vespalcová, H., Rudzanová, B., Thon, V., Martyniuk, C. J., Piler, P., Zvonař, M., Klánová, J., & Bláha, L. (2023) · doi:10.22541/au.169379466.66510286/v1
Galli, T. T. (2023) · doi:10.11606/t.5.2023.tde-01122023-160533
Multiple layers of innate immune response antagonism of SARS-CoV-2Preprint
Zhou, F., Periasamy, S., Jackson, N. D., Cheng, W. S., Soto-Acosta, R., Ilinykh, P. A., Ye, C., Chauhan, S., Nudelman, G., Zaslavsky, E., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.01.29.577695
ABCD of IA: A multi-scale agent-based model of T cell activation in inflammatory arthritis
McBride, D. A., Wang, J. S., Johnson, W. T., Bottini, N., & Shah, N. J. (2024) · Biomaterials Science · doi:10.1039/d3bm01674a
Li, C., Wang, B., Tu, J., Liu, C., Wang, Y., Chen, J., Huang, Y., Liu, B., & Yuan, X. (2024) · Research Square · doi:10.21203/rs.3.rs-4116540/v1
Jin, W., Xia, Y. X., Thela, S. R., Liu, Y., & Chen, L. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.06.25.600715
“MPRA experiment is performed to screen noncoding SNVs in 25 significant GWAS loci associated with AD and nine loci associated with PSP in the HEK293T cell line [41] loci associated with melanoma [43].”
MethodLevonorgestrel enhanced Toxoplasma gondii infection risk via progesterone receptor upregulation
Wang, S., Sun, T., Huang, Y., Mi, R., Zhang, Y., Gong, H., & Chen, Z. (2024) · Veterinary Parasitology · doi:10.1016/j.vetpar.2024.110330
Future prospective of microbiome-gut brain axis for treatment of CNS disorders
Mane, R., Kashid, S., Mazahir, F., & Yadav, A. K. (2025) · Elsevier eBooks · doi:10.1016/b978-0-443-21680-0.00019-5
Role of NF-KB signaling in recurrent pregnancy loss
Ramzan, K., Fazili, K. M., Ramzan, A., dar, B. M. U. D., & Khan, A. S. (2025) · Elsevier eBooks · doi:10.1016/b978-0-443-13617-7.00035-9
БИОЛОГИЧЕСКАЯ ЗНАЧИМОСТЬ МЕХАНИЗМА NF-κB ПРИ СТАРЕНИИ
В., А. О. (2025) · Успехи геронтологии · doi:10.34922/ae.2025.38.3.016
CD94/NKG2A-Qa-1b axis as a key modulator of vaccine responsiveness in aging populations
Chen, L., Bai, Z., Wan, D., Ren, W., Que, H., Wang, J., Lu, Y., He, X., Hong, W., Alu, A., et al. (2025) · Cell Reports · doi:10.1016/j.celrep.2025.116514
Shim, J. A., Lee, S. M., Jeong, J. W., Kim, H., Son, W. J., Park, J. H., Song, P., Im, S.-H., Bae, S., Park, J.-H., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26634105
Zhang, Z., Butler, R. A., Koestler, D. C., Bell-Glenn, S., Warrier, G., Molinaro, A. M., Christensen, B. C., Wiencke, J. K., Kelsey, K. T., & Salas, L. A. (2023) · Figshare · doi:10.6084/m9.figshare.22600465
Shim, J. A., Lee, S. M., Jeong, J. W., Kim, H., Son, W. J., Park, J. H., Song, P., Im, S.-H., Bae, S., Park, J.-H., et al. (2023) · Figshare · doi:10.6084/m9.figshare.24465078
Shim, J. A., Lee, S. M., Jeong, J. W., Kim, H., Son, W. J., Park, J. H., Song, P., Im, S.-H., Bae, S., Park, J.-H., et al. (2023) · Figshare · doi:10.6084/m9.figshare.24465335
Shim, J. A., Lee, S. M., Jeong, J. W., Kim, H., Son, W. J., Park, J. H., Song, P., Im, S.-H., Bae, S., Park, J.-H., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26634108
Meshaal, S., Hawary, R. E., Elaziz, D. S. A., Eldash, A., Darwish, R. K., Erfan, A., Lotfy, S., Saad, M., Chohayeb, E. A., Alkady, R., et al. (2024) · Figshare · doi:10.6084/m9.figshare.25200585
Brunialti, E., Panzeri, A., Rizzi, N., Villa, A. M., Meda, C., Sfogliarini, C., Persano, S., Arlati, F., Lopez, M. L. G., Martelli, C., et al. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.01.29.702227
“In draining lymph nodes, sustained yet tightly regulated NF-κ B activity over 6–24 hours further fine-91 tunes T-cell activation, thereby ensuring an effective adaptive immune response 11,12 .”
Prospects for leveraging knowledge on ISG and NF-kB effector functions into anti-HBV therapies
Zhao, K., & Xia, Y. (2026) · Antiviral Research · doi:10.1016/j.antiviral.2026.106397
Mao, Y., Gao, Y., Zhou, J., Yimin, R., & Zhao, Y. (2026) · Human Immunology · doi:10.1016/j.humimm.2026.111729
Etude du rôle de NF-kB dans les lymphocytes T régulateurs chez la souris
Ronin, É. (2017) · theses.fr (ABES) · doi:10.70675/ea12e750z64e5z437fza120z3bbe647a2642
Metadata
- Authors
- Oh, H., & Ghosh, S.
- Affiliations
- Department of Microbiology and Immunology Columbia University New York NY
- Columbia University (US)
- Corresponding author
- Ghosh, Sankar
- ORCID
- Ghosh, Sankar
- Venue
- Immunological Reviews
- Publisher
- Wiley
- Published
- 2013-02-13
- Volume
- 252
- Issue
- 1
- Pages
- 41-51
- ISSN
- 0105-2896 (ISSN-L)
- 1600-065X
- PMC
- PMC3576882
- OpenAlex
- W2070085523
- Cited by
- 408
- References
- 71
- Citations by year
- 2026: 16 · 2025: 36 · 2024: 43 · 2023: 46 · 2022: 43 · 2021: 39 · 2020: 28 · 2019: 25 · 2018: 27 · 2017: 26 · 2016: 26 · 2015: 24 · 2014: 21 · 2013: 7
- FWCI
- 2.15
- Type
- journal article
- Language
- en
- Open access
- green
- europepmc.org
- Locations
- Immunological Reviews (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- U.S. Public Health Service (R37-33443, R01-68977)
- National Institute of Allergy and Infectious Diseases (R01AI068977, R37AI033443)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › NF-κB Signaling Pathways
- Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
- Life Sciences › Immunology and Microbiology › Immunology › Psoriasis: Treatment and Pathogenesis
- Keywords
- NF-κB signaling, CD4+ T cells, T helper cell differentiation, Th1 cells, Th2 cells, Th17 cells, Th9 cells, Th22 cells, T follicular helper cells, regulatory T cells, transcriptional regulation, cytokine and chemokine expression, adaptive immunity, inflammation
- MeSH terms
- Animals, Cell Differentiation, Gene Expression Regulation, Humans, Lymphocyte Activation, Transcription Factors, Transcription, Genetic, Signal Transduction, CD4-Positive T-Lymphocytes, T-Lymphocyte Subsets, Cytokines, NF-kappa B, Mice, Adaptive Immunity
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