Contextual Regulation of Inflammation: A Duet by Transforming Growth Factor-β and Interleukin-10

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

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

Interleukin-10 and the Interleukin-10 Receptor

Moore, K. W., de Waal Malefyt, R., Coffman, R. L., & O'Garra, A. (2001) · Annual Review of Immunology · doi:10.1146/annurev.immunol.19.1.683 · Cited by 6,737

Mechanisms of TGF-β Signaling from Cell Membrane to the Nucleus

Shi, Y., & Massagué, J. (2003) · Cell · doi:10.1016/s0092-8674(03)00432-x · Cited by 5,860

Smad-dependent and Smad-independent pathways in TGF-β family signalling

Derynck, R., & Zhang, Y. E. (2003) · Nature · doi:10.1038/nature02006 · Cited by 5,498

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

Conversion of Peripheral CD4+CD25− Naive T Cells to CD4+CD25+ Regulatory T Cells by TGF-β Induction of Transcription Factor Foxp3

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

Interleukin-10-deficient mice develop chronic enterocolitis

Kühn, R., Löhler, J., Rennick, D. M., Rajewsky, K., & Müller, W. (1993) · Cell · doi:10.1016/0092-8674(93)80068-p · Cited by 4,248

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

Applications of Antibody-Based Antigen Delivery Targeted to Dendritic Cells In Vivo

Bourque, J., & Hawiger, D. (2022) · Antibodies · doi:10.3390/antib11010008 · Cited by 14

The role of cytokines in the pathogenesis of SAPHO syndrome

Yang, Y., Chen, Q., & Zhong, W. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1427784 · Cited by 19

Regenerative Functions of Regulatory T Cells and Current Strategies Utilizing Mesenchymal Stem Cells in Immunomodulatory Tissue Regeneration

Ahn, J., Kim, B., Bello, A. B., Moon, J. J., Arai, Y., & Lee, S. (2025) · Tissue Engineering and Regenerative Medicine · doi:10.1007/s13770-024-00690-w · Cited by 15

A Snapshot of Cytokine Dynamics: A Fine Balance Between Health and Disease

Mallick, S., Duttaroy, A. K., & Bose, B. (2024) · Journal of Cellular Biochemistry · doi:10.1002/jcb.30680 · Cited by 15

Molecular profiling of tumor-specific TH1 cells activated in vivo

Lorvik, K. B., Haabeth, O. A. W., Clancy, T., Bogen, B., & Corthay, A. (2013) · OncoImmunology · doi:10.4161/onci.24383 · Cited by 14

Modulating T cell functions does not alleviate chronic inflammatory skin lesions in K5.TGFβ1 transgenic mice

Michaelis, K., Wallbrecht, K., Kerstan, A., Beyersdorf, N., Williams, C. A., Kerkau, T., Wang, X., Hünig, T., & Schön, M. P. (2010) · Experimental Dermatology · doi:10.1111/j.1600-0625.2009.01031.x · Cited by 13

Anti-allergic effect of a Korean traditional medicine, Biyeom-Tang on mast cells and allergic rhinitis

Jeong, K.-T., Kim, S.-G., Lee, J., Park, Y. N., Park, H.-H., Park, N.-Y., Kim, K., Lee, H.-D., Lee, Y. J., & Lee, E. (2014) · BMC Complementary and Alternative Medicine · doi:10.1186/1472-6882-14-54 · Cited by 14

The Inflammatory Response in Tissue Repair

Frangogiannis, N. G. (2017) · Wiley-VCH eBooks · doi:10.1002/9783527692156.ch60 · Cited by 15

Peripheral regulatory T cells and anti-inflammatory cytokines in children with juvenile idiopathic arthritis

Sznurkowska, K., Boćkowska, M., Zieliński, M., Plata‐Nazar, K., Trzonkowski, P., Liberek, A., Kamińska, B., & Szlagatys‐Sidorkiewicz, A. (2018) · Acta Biochimica Polonica · doi:10.18388/abp.2017_2308 · Cited by 14

Innovative engineering approaches to model host-microbiome interactions in vitro

Azamar, K. M. M., Sudi, S. D., Mohammadalizadeh, Z., Coffin, C., Parker, I., & Porras, A. M. (2025) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2025.115677 · Cited by 13

Tissue-resident memory CD8+ T cells: master deciphers of the hepatic environment

Romero, D. B., Finney, G. E., Dudek, M., & Pallett, L. J. (2025) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/s41575-025-01118-z · Cited by 13

Potential Using of Fat-derived Stromal Cells in the Treatment of Active Disease, and also, in Both Pre- and Post-Periods in COVID-19

Çöpçü, H. E. (2020) · Aging and Disease · doi:10.14336/ad.2020.0621 · Cited by 13

Systematic toxicological analysis of the effect of salinity on the physiological stress induced by triphenyltin in Nile tilapia

Li, Z., Xing, S., Li, P., He, S., Cao, Z., Wang, X., Cao, X., Liu, B., & You, H. (2023) · Aquatic Toxicology · doi:10.1016/j.aquatox.2023.106441 · Cited by 13

Overcoming the hurdles in using mouse genetic models that block TGF-β signaling

Sanjabi, S., & Flavell, R. A. (2010) · Journal of Immunological Methods · doi:10.1016/j.jim.2009.12.008 · Cited by 14

IL-10 control of dendritic cells in the skin

Clausen, B. E., & Girard-Madoux, M. J. H. (2013) · OncoImmunology · doi:10.4161/onci.23186 · Cited by 13

T cell sensitivity to TGF- is required for the effector function but not the generation of splenic CD8+ regulatory T cells induced via the injection of antigen into the anterior chamber

Cone, R. E., Chattopadhyay, S., Sharafieh, R., Lemire, Y., O’Rourke, J., Flavell, R. A., & Clark, R. B. (2009) · International Immunology · doi:10.1093/intimm/dxp023 · Cited by 13

Intestinal regulatory T cell induction by β-elemene alleviates the formation of fat tissue-related inflammation

Zhou, Y., Takano, T., Wang, Y., Li, X., Wang, R., Wakatsuki, Y., Nakajima‐Adachi, H., Tanokura, M., Miyakawa, T., & Hachimura, S. (2020) · iScience · doi:10.1016/j.isci.2020.101883 · Cited by 12

All‐Trans‐Retinoic Acid Ameliorates the Inflammation by Inducing Transforming Growth Factor Beta 1 and Interleukin 10 in Mouse Epididymitis

Cao, W. J., Chen, W., Liang, X., Zhou, J., Wei, C., Cui, S., & Liu, J. (2014) · American Journal of Reproductive Immunology · doi:10.1111/aji.12197 · Cited by 12

Expressions of TGF‐β1 and MMP‐9 in a guinea pig model of tympanosclerosis: Possible role in the pathogenesis of this disorder

Guo, W., Bai, X., Han, Y., Xu, L., Liu, W., Zhang, G., Li, J., Fan, Z., & Wang, H. (2012) · The Laryngoscope · doi:10.1002/lary.23415 · Cited by 12

Regulatory CD8+ T Cells Associated with Erosion of Immune Surveillance in Persistent Virus Infection Suppress In Vitro and Have a Reversible Proliferative Defect

Hu, Z., Zhang, W., & Usherwood, E. J. (2013) · The Journal of Immunology · doi:10.4049/jimmunol.1201773 · Cited by 11

Relationship between the IL-10 (−1082 A/G) polymorphism and the risk of immune/idiopathic thrombocytopenic purpura: A meta-analysis

Ou, Y., Yan, Y., Xiang, X., & Wu, Y. (2019) · Cytokine · doi:10.1016/j.cyto.2019.154820 · Cited by 12

Emerging trends in chromatin remodeler plasticity in mesenchymal stromal cell function

Chakraborty, S., Sinha, S., & Sengupta, A. (2020) · The FASEB Journal · doi:10.1096/fj.202002232r · Cited by 11

Responses to LPS boost effector CD8 T-cell accumulation outside of signals 1 and 2

Liu, W., Ménoret, A., & Vella, A. T. (2015) · Cellular and Molecular Immunology · doi:10.1038/cmi.2015.69 · Cited by 11

Repeated inhalation of sevoflurane inhibits airway inflammation in an OVA ‐induced mouse model of allergic airway inflammation

Shen, Q., Fang, L., Wu, H., He, F., Ding, P., & Liu, R. (2014) · Respirology · doi:10.1111/resp.12439 · Cited by 11

Combining Use of Captopril and Losartan Attenuates the Progress of Streptococcus pneumoniae-Induced Tympanosclerosis through the Suppression of TGF-β1 Expression

Yan, W., Li, J., Chai, R., Guo, W., Xu, L., Han, Y., Bai, X., & Wang, H. (2014) · PLoS ONE · doi:10.1371/journal.pone.0111620 · Cited by 11

Production of LPS-induced inflammatory mediators in murine peritoneal macrophages: neocuproine as a broad inhibitor and ATP7A as a selective regulator

Patel, O., Wilson, W. B., & Qin, Z. (2013) · BioMetals · doi:10.1007/s10534-013-9624-4 · Cited by 11

The attenuating effect of aqueous extract of licorice on bleomycin-induced pulmonary fibrosis in mice

Ghorashi, M., Rezaee, M. A., Rezaie, M. J., Mohammadi, M., Jalili, A., & Rahmani, M. R. (2016) · Food and Agricultural Immunology · doi:10.1080/09540105.2016.1203294 · Cited by 11

Micro RNA-155 participates in re-activation of encephalitogenic T cells

Jevtić, B., Timotijević, G. S., Stanisavljević, S., Momčilović, M. B., Stojković, M. M., & Miljković, D. M. (2015) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2015.08.011 · Cited by 11

Suppression of breast tumor growth by DNA vaccination against phosphatase of regenerating liver 3

Lv, J., Liu, C., Huang, H., Meng, L., Jiang, B., Cao, Y., Zhou, Z., She, T., Qu, L., Song, S., et al. (2013) · Gene Therapy · doi:10.1038/gt.2013.5 · Cited by 11

Le lymphocyte TH17 dernier-né de la famille des lymphocytes T CD4+

Essakalli, M., Brick, C., Bennani, N., Benseffaj, N., Ouadghiri, S., & Atouf, O. (2009) · Pathologie Biologie · doi:10.1016/j.patbio.2009.01.001 · Cited by 11

The Role of TGF-β, Activin and Follistatin in Inflammatory Bowel Disease

Esfahani, N. H., & Day, A. S. (2023) · Gastrointestinal Disorders · doi:10.3390/gidisord5020015 · Cited by 11

Bifidobacterium breve CCFM1310 enhances immunity in immunosuppressed mice via modulating immune response and gut microbiota

Fang, H., Li, H., Chen, Y., Liu, X., Zhao, J., Ross, R. P., Stanton, C., Chen, W., & Yang, B. K. (2024) · Food Bioscience · doi:10.1016/j.fbio.2024.104058 · Cited by 10

Pathophysiology of bone remodelling cycle: Role of immune system and lipids

Parolini, C. (2025) · Biochemical Pharmacology · doi:10.1016/j.bcp.2025.116844 · Cited by 10

Cellular immune responses to platelet factor 4 and heparin complexes in patients with heparin‐induced thrombocytopenia

Nazy, I., Clare, R., Staibano, P., Warkentin, T. E., Larché, M., Moore, J. C., Smith, J. W., Whitlock, R. P., Kelton, J. G., & Arnold, D. M. (2018) · Journal of Thrombosis and Haemostasis · doi:10.1111/jth.14132 · Cited by 10

Negative regulation of innate lymphoid cell responses in inflammation and cancer

Sciumè, G., Fionda, C., Stabile, H., Gismondi, A., & Santoni, A. (2019) · Immunology Letters · doi:10.1016/j.imlet.2019.01.011 · Cited by 10

Tumour Derived Extracellular Vesicles: Challenging Target to Blunt Tumour Immune Evasion

Lopatina, T., Sarcinella, A., & Brizzi, M. F. (2022) · Cancers · doi:10.3390/cancers14164020 · Cited by 10

In Vitro Expression Analysis of Cytokines and ROS-Related Genes in Human Corneal Fibroblasts and Keratocytes of Healthy and Keratoconus Corneas

Berger, T., Szentmáry, N., Chai, N., Flockerzi, E., Daas, L., Stachon, T., & Seitz, B. (2023) · Ocular Immunology and Inflammation · doi:10.1080/09273948.2023.2176325 · Cited by 10

Cells with dendritic cell morphology and immunophenotype, binuclear morphology, and immunosuppressive function in dendritic cell cultures

Dong, R., MOULDING, D. A., Himoudi, N., Adams, S. P., Bouma, G., Eddaoudi, A., Basu, B. P., Derniame, S., Chana, P. S., Duncan, A., et al. (2011) · Cellular Immunology · doi:10.1016/j.cellimm.2011.09.012 · Cited by 10

The Road to Memory: An Early Rest for the Long Journey

Ho, L. P., Yit, P. S., Ng, L. H., Linn, Y. C., Zhao, Y., Sun, L. J., Ling, K. L., Koh, M., Shih, M.-C. M., Li, S., et al. (2013) · The Journal of Immunology · doi:10.4049/jimmunol.1301175 · Cited by 10

Impaired immune regulation after radioiodine therapy for Graves’ disease and the protective effect of Methimazole

Côté‐Bigras, S., Tran, V., Turcotte, S., Rola‐Pleszczynski, M., Verreault, J., & Rottembourg, D. (2015) · Endocrine · doi:10.1007/s12020-015-0832-2 · Cited by 14

Impact of Inflammation on White Matter Integrity and Functional Connectivity in Chronic Major Depressive Disorder

Cha, J., Raj, D., Choi, K. S., Rajendra, J. K., Nemeroff, C. B., Felger, J. C., Craighead, W. E., Mayberg, H. S., & Dunlop, B. W. (2025) · Biological Psychiatry · doi:10.1016/j.biopsych.2025.06.026 · Cited by 12

Single cell multi-omic analysis identifies key genes differentially expressed in innate lymphoid cells from COVID-19 patients

Kaushik, A., Chang, I., Han, X., He, Z., Komlósi, Z. I., Ji, X., Cao, S., Akdiş, C. A., Boyd, S. D., Pulendran, B., et al. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1374828 · Cited by 9

Natural Tr1-like cells do not confer long-term tolerogenic memory

Yadava, K., Medina, C. O., Ishak, H. D., Gurevich, I., Kuipers, H. F., Shamskhou, E. A., Koliesnik, I. O., Moon, J. J., Weaver, C. T., Nadeau, K. C., et al. (2019) · eLife · doi:10.7554/elife.44821 · Cited by 9

miR-129-5p Regulates the Immunomodulatory Functions of Adipose-Derived Stem Cells via Targeting Stat1 Signaling

Zhang, H., Wang, Y., Wang, Y., Qu, Y., Huang, X., Yang, H., Zhao, C.-M., He, Y., Li, S., Zhou, J., et al. (2019) · Stem Cells International · doi:10.1155/2019/2631024 · Cited by 9

Validation of Gene Profiles for Analysis of Regional Lymphatic Metastases in Head and Neck Squamous Cell Carcinoma

Hu, Z., Yang, R., Li, L., Mao, L., Liu, S., Qiao, S., Ren, G., & Hu, J. (2020) · Frontiers in Molecular Biosciences · doi:10.3389/fmolb.2020.00003 · Cited by 9

A non-inflammatory form of immune competence prevails in acute pre-pubescent malnutrition: new evidence based on critical mRNA transcripts in the mouse

Monk, J. M., Richard, C. L., & Woodward, B. D. (2011) · British Journal Of Nutrition · doi:10.1017/s0007114511004399 · Cited by 9

Mysm1 epigenetically regulates the immunomodulatory function of adipose‐derived stem cells in part by targeting miR‐150

Wang, Y., Huang, X., Yang, Y., He, Y., Dong, X., Yang, H., Zhang, L., Wang, Y., Zhou, J., Wang, C., et al. (2019) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.14281 · Cited by 9

MAGE-A4 induces non–small cell lung cancer and tumor-promoting plasma cell accumulation

Armstrong, D., Chang, C.-Y., Hong, M. J., Green, L., Shen, Y., Hudson, W., Mauk, K. E., Song, L., Jammi, S., Casal, B., et al. (2025) · Science Advances · doi:10.1126/sciadv.ads4227 · Cited by 9

Oxidant-Based Cytotoxic Agents During Aging: From Disturbed Energy Metabolism to Chronic Inflammation and Disease Progression

Arnhold, J. (2025) · Biomolecules · doi:10.3390/biom15040547 · Cited by 8

Single nucleotide polymorphisms, gene expression and evaluation of immunological, antioxidant, and pathological parameters associated with bacterial pneumonia in Barki sheep

El-Sayed, A., Hafez, A., Ateya, A. I., Darwish, A. A., & Tahoun, A. A. E. (2025) · Irish Veterinary Journal · doi:10.1186/s13620-025-00296-1 · Cited by 8

Feeding Buttermilk-Derived Choline Forms During Gestation and Lactation Modulates Ex Vivo T-Cell Response in Rat Dams

Azarcoya‐Barrera, J., Goruk, S., Lewis, E. D., Pouliot, Y., Curtis, J. M., Steele, R., Wadge, E., Field, C. J., Jacobs, R. L., & Richard, C. (2020) · Journal of Nutrition · doi:10.1093/jn/nxaa089 · Cited by 8

New Insights into the Mechanism of Immune-Mediated Tissue Injury in Yellow Fever: The Role of Immunopathological and Endothelial Alterations in the Human Lung Parenchyma

Vasconcelos, D. B., Falcão, L. F. M., da Ponte, L. C. T., Silva, C. C., Martins, L. C., Nunes, B. T. D., Filho, A. J. M., Franco, E. C. S., Duarte, M. I. S., de Sousa, J. R., et al. (2022) · Viruses · doi:10.3390/v14112379 · Cited by 7

Co‐initiators of polymerization can modulate the inflammatory cytokine release without major cytotoxic effects in human dental pulp cells

Agostinelli, B. G., Andia, D. C., & Lima, A. F. (2023) · Journal of Biomedical Materials Research Part B Applied Biomaterials · doi:10.1002/jbm.b.35218 · Cited by 8

Integrative Single-Cell RNA-Seq and ATAC-Seq Analysis of Mesenchymal Stem/Stromal Cells Derived from Human Placenta

Li, J., Wang, Q., An, Y., Chen, X., Xing, Y., Deng, Q., Li, Z., Wang, S., Dai, X., Liang, N., et al. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.836887 · Cited by 8

Immunosuppressive and metabolic agents that influence allo‐ and xenograft survival by in vivo expansion of T regulatory cells

Zhao, Y., Hu, W., Chen, P., Cao, M., Zhang, Y., Zeng, C., Hara, H., Cooper, D. K. C., Mou, L., Luan, S., et al. (2020) · Xenotransplantation · doi:10.1111/xen.12640 · Cited by 8

nSARS-Cov-2, pulmonary edema and thrombosis: possible molecular insights using miRNA-gene circuits in regulatory networks

Khurana, P., Gupta, A., Sugadev, R., Sharma, Y. K., Varshney, R. K., Ganju, L., & Kumar, B. (2020) · ExRNA · doi:10.1186/s41544-020-00057-y · Cited by 8

Analysis of Changes in Viral Load and Inflammatory Cytokines, as Well as the Occurrence of Secondary Infections, in SFTS Patients Treated with Specific Treatments: A Prospective Multicenter Cohort Study

Seo, J.-W., Lee, Y. M., Tamanna, S., Bang, M.-S., Kim, C., Kim, D. Y., Yun, N. R., Kim, J., Jung, S., Kim, U. J., et al. (2024) · Viruses · doi:10.3390/v16121906 · Cited by 7

Mast cells in autoimmune disease: Unveiling their multifaceted roles and therapeutic potential

Javan, M. R., Akhlaghi, M., Hormozi, A., Hosseini, M., & Khosrojerdi, A. (2025) · Human Immunology · doi:10.1016/j.humimm.2025.111334 · Cited by 8

Tumor Suppressor Adenomatous Polyposis Coli Sustains Dendritic Cell Tolerance through IL-10 in a β-Catenin–Dependent Manner

Cao, W., Liu, J., Jiang, Z., Tao, Y., Wang, H., Li, J., Ni, J., & Wu, X. (2023) · The Journal of Immunology · doi:10.4049/jimmunol.2300046 · Cited by 7

Dietary Pediastrum boryanum microalgal extract improves growth, enhances immunity, and regulates immune-related genes in Nile tilapia

Al-Wakeel, A. H., Elbahnaswy, S., Risha, E., & Zahran, E. (2024) · BMC Veterinary Research · doi:10.1186/s12917-024-04155-z · Cited by 7

Nucleotide sequence variants, gene expression and serum profile of immune and antioxidant markers associated with bacterial diarrhea susceptibility in Barki lambs

Darwish, A. A., Ebissy, E., Hafez, A., Ateya, A. I., & El-Sayed, A. (2024) · BMC Veterinary Research · doi:10.1186/s12917-024-04288-1 · Cited by 7

SCUBE3 Is Likely a Susceptibility Gene for Systemic Lupus Erythematosus for Chinese Populations

Qi, Y., Zhao, Y., Zhai, Y., Zhang, X., Wang, X., Liu, X., Cui, Y., Ning, X., & Zhao, Z. (2020) · Journal of Immunology Research · doi:10.1155/2020/8897936 · Cited by 7

Effect of IL-10 Deficiency on TGFβ Expression during Fatal Alphavirus Encephalomyelitis in C57Bl/6 Mice

Martin, N., & Griffin, D. E. (2022) · Viruses · doi:10.3390/v14081791 · Cited by 7

Special Focus on the Cellular Anti-Inflammatory Effects of Several Micro-Immunotherapy Formulations: Considerations Regarding Intestinal-, Immune-Axis-Related- and Neuronal-Inflammation Contexts

Jacques, C., & Floris, I. (2022) · Journal of Inflammation Research · doi:10.2147/jir.s389614 · Cited by 7

Differential Pattern of Cytokine Production by Depressed Medical Students; Evidence for Involvement of Cytokine Network in Pathology of Depression

Momeni, M., Ghorban, K., Dadmanesh, M., Hajebrahimi, B., Khodadadi, H., & Hassanshahi, G. (2014) · Clinical Laboratory · doi:10.7754/clin.lab.2013.130238 · Cited by 8

Cowpox virus induces interleukin-10 both in vitro and in vivo

Spesock, A. H., Barefoot, B. E., Ray, C. A., Kenan, D. J., Gunn, M. D., Ramsburg, E. A., & Pickup, D. J. (2011) · Virology · doi:10.1016/j.virol.2011.05.010 · Cited by 7

Whole-Proteome Analysis of Human Craniosynostotic Tissue Suggests a Link between Inflammatory Signaling and Osteoclast Activation in Human Cranial Suture Patency

Lyon, S. M., Mayampurath, A. M., Song, D., Ye, J., Januszyk, M., Rogers, M., Ralston, A., Frim, D. M., He, T., & Reid, R. R. (2018) · Plastic & Reconstructive Surgery · doi:10.1097/prs.0000000000004025 · Cited by 7

Rapid Identification of Genome-Edited Mesenchymal Stem Cell Colonies via Cas9

Jiang, W., Lian, W., Chen, J., Li, W., Huang, J., Lai, B., Li, L., Huang, Z. W., & Xu, J. (2019) · BioTechniques · doi:10.2144/btn-2018-0183 · Cited by 7

Inflammation-Associated Cytotoxic Agents in Tumorigenesis

Arnhold, J. (2023) · Cancers · doi:10.3390/cancers16010081 · Cited by 7

Novel plant-derived compounds modulate gut microbiome dysbiosis in colitis mice: A potential therapeutic avenue for inflammatory bowel disease

Rahaman, M. M., Yeshi, K., Bappi, M. H., Islam, Z., Wangchuk, P., & Sarker, S. (2025) · Microbiological Research · doi:10.1016/j.micres.2025.128343 · Cited by 6

Early Oral Ovalbumin Exposure during Maternal Milk Feeding Prevents Spontaneous Allergic Sensitization in Allergy-Prone Rat Pups

El-Merhibi, A., Lymn, K. A., Kanter, I., & Penttila, I. (2011) · Clinical and Developmental Immunology · doi:10.1155/2012/396232 · Cited by 6

Microglia in Gliomas: Friend or Foe?

Kaminska, B. (2014) · Springer eBooks · doi:10.1007/978-3-7091-1431-5_9 · Cited by 6

The positive impacts of tea polyphenols on the growth performance, immune responses, and hepatic health of largemouth bass (Micropterus salmoides) under high fat diets

Du, Q., Chen, J., Li, J., Liu, Z., Huang, W., Liu, H., Song, H., Cai, W., Tan, B., & Dong, X. (2025) · Aquaculture Reports · doi:10.1016/j.aqrep.2025.102850 · Cited by 6

Role of Cytokines in Tumor Immunity and Immune Tolerance to Cancer

Murugaiyan, G. (2014) · Springer eBooks · doi:10.1007/978-3-662-44006-3_7 · Cited by 6

Fallen Angels or Risen Apes? A Tale of the Intricate Complexities of Imbalanced Immune Responses in the Pathogenesis and Progression of Immune-Mediated and Viral Cancers

Ondondo, B. (2014) · Frontiers in Immunology · doi:10.3389/fimmu.2014.00090 · Cited by 6

Effects of peptides derived from traditional Greek yoghurt on expression of pro- and anti-inflammatory genes by ovine monocytes and neutrophils

Θεοδώρου, Γ., & Politis, I. (2016) · Food and Agricultural Immunology · doi:10.1080/09540105.2015.1129598 · Cited by 6

Autorestriction and resolution of allergic process

Gushchin, I. S. (2020) · Immunologiya · doi:10.33029/0206-4952-2020-41-6-557-580 · Cited by 8

Maturation of human cardiac organoids enables complex disease modelling and drug discoveryPreprint

Pocock, M., Reid, J. D., Robinson, H., Charitakis, N., Krycer, J. R., Foster, S. R., Fitzsimmons, R. L., Lor, M., Tuano, N., Howden, S. E., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.09.05.611336 · Cited by 6

Alkaline Treatment Enhances the Anti-Inflammatory and Reparative Potential of Dentin Matrix Proteins in Inflamed Pulp

Jia, P., Li, J., Wu, J., Li, X., Mao, S., Wang, S., & Dong, Y. (2025) · Journal of Endodontics · doi:10.1016/j.joen.2025.06.002 · Cited by 5

Assessment of 10-MDP and GPDM monomers on viability and inflammatory response in human dental pulp stem cells

Cavallaro, F. D., Esposo, G. D. M. N., Kury, M., Fronza, B. M., Saraceni, C. H. C., Andia, D. C., & Lima, A. F. (2024) · Dental Materials · doi:10.1016/j.dental.2024.10.008 · Cited by 5

Subcutaneous delivery of mesenchymal stromal cells induces immunoregulatory effects in the lymph node prior to their apoptosis

Zheng, D., Bhuvan, T., Payne, N. L., Pang, S. H. M., Mendonca, S., Hutchinson, M. R., Mckinnirey, F., Morgan, C., Vesey, G., Meagher, L., et al. (2024) · Stem Cell Research & Therapy · doi:10.1186/s13287-024-04060-0 · Cited by 5

The potential targets in immunotherapy of atherosclerosis

Aghamajidi, A., Gorgani, M., Shahba, F., Shafaghat, Z., & Mojtabavi, N. (2021) · International Reviews of Immunology · doi:10.1080/08830185.2021.1988591 · Cited by 6

Treg cell abnormality and its potential treatments in patients with primary immune thrombocytopenia

Ji, L., & Cheng, Y. (2022) · Clinical and Translational Discovery · doi:10.1002/ctd2.77 · Cited by 5

Acupuncture and moxibustion stimulate fibroblast proliferation and neoangiogenesis during tissue repair of experimental excisional injuries in adult female Wistar rats

Alonso, H. R., Kuroda, F. C., Passarini, J. R., Quispe-Cabanillas, J. G., Mendonça, F. A. S., dos Santos, G. M. T., de Aro, A. A., do Amaral, M. E. C., & Esquisatto, M. A. M. (2020) · Acupuncture in Medicine · doi:10.1136/acupmed-2016-011314 · Cited by 5

Immune Response and Tissue Damage

Arnhold, J. (2019) · Elsevier eBooks · doi:10.1016/b978-0-12-816388-7.00006-1 · Cited by 5

TMEM16F phospholipid scramblase regulates tumorigenesis by modulating the tumor immune microenvironment

Wu, M., Shi, P., Huang, J., Ni, X., Lai, R., Cao, K., Cai, M., Yu, H., Zhao, W., & Zhang, Y. (2025) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2513910122 · Cited by 4

Interferon-Gamma Increases the Immune Modulation of Umbilical Cord-Derived Mesenchymal Stem Cells but Decreases Their Chondrogenic Potential

Truong, N. C., Phan, T. N. M., Huynh, N. T., Pham, K. D., & Pham, P. V. (2023) · Advances in experimental medicine and biology · doi:10.1007/5584_2023_776 · Cited by 4

Analysis of Inflammatory and Regulatory Cytokines in the Milk of Dairy Cows with Mastitis: A Comparative Study with Healthy Animals

Lohova, E., Pilmane, M., Šerstņova, K., Melderis, I., Gontar, Ł., Kochański, M., Drutowska, A., Maróti, G., & Prieto‐Simón, B. (2024) · Immunological Investigations · doi:10.1080/08820139.2024.2404623 · Cited by 5

Role of Cytokines in Tumor Immunity and Immune Tolerance to Cancer

Garo, L. P., & Murugaiyan, G. (2020) · Springer eBooks · doi:10.1007/978-3-030-30845-2_13 · Cited by 5

C5a drives the inflammatory response with bacterial dose effect by binding to C5aR1 in zebrafish infected with Aeromonas hydrophila

Liu, X., Wang, W., Tan, S., Liu, H., Li, Z., Wang, N. N., Ma, J., Han, S., Wu, Z., Shi, K., et al. (2023) · Fish & Shellfish Immunology · doi:10.1016/j.fsi.2023.108873 · Cited by 4

Milk and Lacticaseibacillus paracasei BL23 effects on intestinal responses in a murine model of colitis

Bui, G., Torres‐Fuentes, C., Pusceddu, M. M., Gareau, M. G., & Marco, M. L. (2024) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00259.2023 · Cited by 4

Checks and Balances: IL-23 in the Intestine

Huber, S., & Flavell, R. A. (2010) · Immunity · doi:10.1016/j.immuni.2010.08.005 · Cited by 4

Transforming Growth Factor-β Partially Reversed the Immunosuppressive Effect of Mesenchymal Stem Cells in Mice

Zhao, J., Qi, Y., Wang, X., Jiao, Y., Gong, H., Zhang, J.-X., & Jiang, D. (2018) · Transplantation Proceedings · doi:10.1016/j.transproceed.2018.08.054 · Cited by 4

Serum levels of transforming growth factor β1 and C-reactive protein as possible markers of intra uterine insemination outcome

Sahin, A., Üstün, Y. E., Tokmak, A., Sahin, H., Erkaya, S., & Ozgu-Erdinc, A. S. (2018) · European Cytokine Network · doi:10.1684/ecn.2018.0418 · Cited by 4

Cranial Mandibular Fibrosis Syndrome in Adult Farmed Rainbow Trout Oncorhynchus mykiss

Cano, I., Worswick, J., Mulhearn, B., Green, M., Feist, S. W., & Clinton, M. (2021) · Pathogens · doi:10.3390/pathogens10050542 · Cited by 4

The Immune System and Inflammation in Type 2 Diabetes

García-Macedo, R., & Fortis, M. D. L. Á. (2023) · Springer eBooks · doi:10.1007/978-3-031-25519-9_12 · Cited by 6

Cerebrospinal Fluid Biomarkers of Simian Immunodeficiency Virus Encephalitis

Bissel, S. J., Kofler, J., Nyaundi, J., Murphey‐Corb, M., Wisniewski, S. R., & Wiley, C. A. (2016) · Journal of Neuroimmune Pharmacology · doi:10.1007/s11481-016-9666-9 · Cited by 4

New normal: two aspects of adipose tissue in COVID-19—treat and threat?

Çöpçü, H. E. (2020) · Expert Opinion on Biological Therapy · doi:10.1080/14712598.2020.1822812 · Cited by 4

The blood level of transforming growth factor-β rises in the early stages of acute protein and energy deficit in the weanling mouse

Monk, J. M., & Woodward, B. D. (2009) · British Journal Of Nutrition · doi:10.1017/s0007114509992443 · Cited by 4

TGF-b Directly Targets Effector T Cells

(2015)

The Interrelated Roles of TGF-β and IL-10 in the Regulation of Experimental Colitis

Fuss, I. J., Boirivant, M., Lacy, B. E., & Strober, W. (2002) · The Journal of Immunology · doi:10.4049/jimmunol.168.2.900 · Cited by 259

Regulation of TGF-β Response During T Cell Activation Is Modulated by IL-10

Cottrez, F., & Groux, H. (2001) · The Journal of Immunology · doi:10.4049/jimmunol.167.2.773 · Cited by 178

TRANSFORMING GROWTH FACTOR-β REGULATION OF IMMUNE RESPONSES

Li, M. O., Wan, Y. Y., Sanjabi, S., Robertson, A.-K. L., & Flavell, R. A. (2005) · Annual Review of Immunology · doi:10.1146/annurev.immunol.24.021605.090737 · Cited by 2,264

Cellular and molecular basis for the regulation of inflammation by TGF-

Yoshimura, A., Wakabayashi, Y., & Mori, T. (2010) · The Journal of Biochemistry · doi:10.1093/jb/mvq043 · Cited by 405