1- School of Medicine, Bam University of Medical Sciences, Bam, Iran. 2- Department of Basic Medical Sciences, Neyshabur University of Medical Sciences, Neyshabur, Iran. 3- Department of Basic Medical Sciences, Neyshabur University of Medical Sciences, Neyshabur, Iran. , mohammadians@nums.ac.ir
Abstract: (22 Views)
Background: Multiple sclerosis (MS) is an autoimmune disease of the central nervous system, which is characterized by chronic inflammation. Evidence indicates that dysfunction of microglia, B cells, and T cells plays crucial roles in the pathogenesis of disease. Curcumin, the bioactive compound derived from turmeric (Curcuma longa), has gained attention due to its anti-inflammatory and immunomodulatory properties. This study aimed to explore the modulatory microglia, B cells, and T cells in MS.
Methods: This narrative review was conducted through a systematic search in PubMed, Scopus, and Web of Science databases up to 2026, with no time restriction and limited to English-language publications. Experimental, animal, and human studies investigating the modulatory effects of curcumin on T cells in MS were selected based on predefined inclusion criteria.
Results: The findings demonstrate that curcumin could suppress the inflammatory responses of microglia cells. On the one hand, curcumin decreases the function of inflammatory B cells and increases the activity of regulatory B cells. Also, curcumin inhibits the differentiation and function of TH1 and TH17 cells and subsequently reduces the production of inflammatory cytokines. In contrast, curcumin enhances the differentiation and function of Treg cells. These effects led to the correction of the TH17/Treg imbalance and subsequently reduced neuroinflammation.
Conclusion: Curcumin shows considerable potential as a supplementary therapeutic agent in MS by modulating both pro-inflammatory and regulatory immune pathways. However, further research in human studies IS required to confirm its clinical efficacy and long-term safety.
Keywords: B cells, Curcumin, Immune modulation, Microglia, Multiple sclerosis, T cellsAcknowledgments: None.
Data and Materials Availability: This is a narrative review article and does not constitute original research; therefore, no primary data are available for sharing. Responsibility for data availability rests with the corresponding author.
Conflict of Interest: The authors declare no conflict of interest.
Publication Consent: Not applicable.
Ethics Approval and Consent to Participate: This article was conducted as a narrative review and did not involve human participants or animal subjects. The study was conducted in accordance with the ethical principles outlined in the Declaration of Helsinki. Confidentiality of all information and data was maintained throughout the research process.
Funding Disclosure: No funding was received from any organization or institution for this article.
Author Contributions: All authors have read and approved the final version of the manuscript and accept responsibility for the accuracy and integrity of its content.
1. Dendrou CA, Fugger L, Friese MA. Immunopathology of multiple sclerosis. Nature reviews Immunology. 2015;15(9):545-58.
https://doi.org/10.1038/nri3871 [DOI:10.1038/nri3871.]
2. Voet S, Prinz M, van Loo G. Microglia in Central Nervous System Inflammation and Multiple Sclerosis Pathology. Trends in molecular medicine. 2019;25(2):112-23.
https://doi.org/10.1016/j.molmed.2018.11.005 [DOI:10.1016/j.molmed.2018.11.005.]
3. Zrzavy T, Hametner S, Wimmer I, Butovsky O, Weiner HL, Lassmann H. Loss of 'homeostatic' microglia and patterns of their activation in active multiple sclerosis. Brain : a journal of neurology. 2017;140(7):1900-13.
https://doi.org/10.1093/brain/awx113 [DOI:10.1093/brain/awx113.]
4. Chu F, Shi M, Lang Y, Shen D, Jin T, Zhu J, et al. Gut Microbiota in Multiple Sclerosis and Experimental Autoimmune Encephalomyelitis: Current Applications and Future Perspectives. Mediators of inflammation. 2018;2018:8168717.
https://doi.org/10.1155/2018/8168717 [DOI:10.1155/2018/8168717.]
5. Ponath G, Ramanan S, Mubarak M, Housley W, Lee S, Sahinkaya FR, et al. Myelin phagocytosis by astrocytes after myelin damage promotes lesion pathology. Brain : a journal of neurology. 2017;140(2):399-413.
https://doi.org/10.1093/brain/aww298 [DOI:10.1093/brain/aww298.]
6. Haider L. Inflammation, Iron, Energy Failure, and Oxidative Stress in the Pathogenesis of Multiple Sclerosis. Oxidative medicine and cellular longevity. 2015;2015:725370.
https://doi.org/10.1155/2015/725370 [DOI:10.1155/2015/725370.]
7. Masuda T, Sankowski R, Staszewski O, Prinz M. Microglia Heterogeneity in the Single-Cell Era. Cell reports. 2020;30(5):1271-81.
https://doi.org/10.1016/j.celrep.2020.01.010 [DOI:10.1016/j.celrep.2020.01.010.]
8. Guo S, Wang H, Yin Y. Microglia Polarization From M1 to M2 in Neurodegenerative Diseases. Frontiers in aging neuroscience. 2022;14:815347.
https://doi.org/10.3389/fnagi.2022.815347 [DOI:10.3389/fnagi.2022.815347.]
9. Miron VE, Boyd A, Zhao JW, Yuen TJ, Ruckh JM, Shadrach JL, et al. M2 microglia and macrophages drive oligodendrocyte differentiation during CNS remyelination. Nature neuroscience. 2013;16(9):1211-8.
https://doi.org/10.1038/nn.3469 [DOI:10.1038/nn.3469.]
10. Liddelow SA, Guttenplan KA, Clarke LE, Bennett FC, Bohlen CJ, Schirmer L, et al. Neurotoxic reactive astrocytes are induced by activated microglia. Nature. 2017;541(7638):481-7.
https://doi.org/10.1038/nature21029 [DOI:10.1038/nature21029.]
11. Ponath G, Park C, Pitt D. The Role of Astrocytes in Multiple Sclerosis. Front Immunol. 2018;9:217.
https://doi.org/10.3389/fimmu.2018.00217 [DOI:10.3389/fimmu.2018.00217.]
12. Bourdette D, Yadav V. B-cell depletin with rituximab in relapsing-remittingmultiple sclerosis. Current neurology and neuroscience reports. 2008;8(5):417-8.
https://doi.org/10.1007/s11910-008-0064-4 [DOI:10.1007/s11910-008-0064-4.]
13. Li R, Rezk A, Miyazaki Y, Hilgenberg E Touil H, Shen P, et al. Proinflammatory GMCSF-producing B cells in multiple sclerosis and B cell depletion therapy. Science translational medicine. 2015;7(310):310ra166.
https://doi.org/10.1126/scitranslmed.aab4176 [DOI:10.1126/scitranslmed.aab4176.]
14. Lamb YN. Ocrelizumab: A Review in Multiple Sclerosis. Drugs. 2022;82(3):323-34.
https://doi.org/10.1007/s40265-022-01672-9 [DOI:10.1007/s40265-022-01672-9.]
15. Saez-Calveras N, Stuve O. The role of the complement system in Multiple Sclerosis: A review. Front Immunol. 2022;13:970486.
https://doi.org/10.3389/fimmu.2022.970486 [DOI:10.3389/fimmu.2022.970486.]
16. Michel L, Touil H, Pikor NB, Gommerman JL, Prat A, Bar-Or A. B Cells in the Multiple Sclerosis Central Nervous System: Trafficking and Contribution to CNS-Compartmentalized Inflammation. Front Immunol. 2015;6:636.
https://doi.org/10.3389/fimmu.2015.00636 [DOI:10.3389/fimmu.2015.00636.]
17. Li R, Patterson KR, Bar-Or A. Reassessing B cell contributions in multiple sclerosis. Nat Immunol. 2018;19(7):696-707.
https://doi.org/10.1038/s41590-018-0135-x [DOI:10.1038/s41590-018-0135-x.]
18. Mosmann TR, Cherwinski H, Bond MW, Giedlin MA, Coffman RL. Two types of murine helper T cell clone. I. Definition according to profiles of lymphokine activities and secreted proteins. Journal of immunology (Baltimore, Md : 1950). 1986;136(7):2348-57. [DOI:10.4049/jimmunol.136.7.2348]
20. Zhu J, Yamane H, Paul WE. Differentiation of effector CD4 T cell populations (*). Annual review of immunology. 2010;28:445-89.
https://doi.org/10.1146/annurev-immunol-030409-101212 [DOI:10.1146/annurev-immunol-030409-101212.]
21. van den Berg WB, Miossec P. IL-17 as a future therapeutic target for rheumatoid arthritis. Nature reviews Rheumatology. 2009;5(10):549-53.
https://doi.org/10.1038/nrrheum.2009.179 [DOI:10.1038/nrrheum.2009.179.]
22. Kolls JK, Lindén A. Interleukin-17 Family Members and Inflammation. Immunity. 2004;21(4):467-76.
https://doi.org/10.1016/j.immuni.2004.08.018 [DOI:https://doi.org/10.1016/j.immuni.2004.08.018.]
23. Sun J, Li Q. Curcumin suppresses IL-23/Th17 axis in autoimmune diseases. Cytokine. 2021;140:155431. [DOI:10.1016/j.cyto.2020.155431.]
24. Sakaguchi S, Yamaguchi T, Nomura T, Ono M. Regulatory T Cells and Immune Tolerance. Cell. 2008;133(5):775-87.
https://doi.org/10.1016/j.cell.2008.05.009 [DOI:https://doi.org/10.1016/j.cell.2008.05.009.]
25. Wing K, Sakaguchi S. Regulatory T cells exert checks and balances on self tolerance and autoimmunity. Nature Immunology. 2010;11(1):7-13.
https://doi.org/10.1038/ni.1818 [DOI:10.1038/ni.1818.]
26. Zhang H-L, Zheng X-Y, Zhu J. Th1/Th2/Th17/Treg cytokines in Guillain-Barré syndrome and experimental autoimmune neuritis. Cytokine & Growth Factor Reviews. 2013;24(5):443-53.
https://doi.org/10.1016/j.cytogfr.2013.05.005 [DOI:https://doi.org/10.1016/j.cytogfr.2013.05.005.]
27. von Boehmer H, Daniel C. Therapeutic opportunities for manipulating TReg cells in autoimmunity and cancer. Nature Reviews Drug Discovery. 2013;12(1):51-63.
https://doi.org/10.1038/nrd3683 [DOI:10.1038/nrd3683.]
28. Kondelkova K, Vokurkova D, Krejsek J, Borska L, Fiala Z, Ctirad A. Regulatory T cells (TREG) and their roles in immune system with respect to immunopathological disorders. Acta Medica (Hradec Kralove). 2010;53(2):73-7. [DOI:10.14712/18059694.2016.63]
29. Haftcheshmeh SM, Abedi M, Mashayekhi K, Mousavi MJ, Navashenaq JG, Mohammadi A, et al. Berberine as a natural modulator of inflammatory signaling pathways in the immune system: Focus on NF-κB, JAK/STAT, and MAPK signaling pathways. 2022;36(3):1216-30.
https://doi.org/10.1002/ptr.7407 [DOI:https://doi.org/10.1002/ptr.7407.]
30. Abdollahi E, Momtazi AA, Johnston TP, Sahebkar A. Therapeutic effects of curcumin in inflammatory and immune-mediated diseases: A nature-made jack-of-all-trades? Journal of cellular physiology. 2018;233(2):830-48.
https://doi.org/10.1002/jcp.25778 [DOI:10.1002/jcp.25778.]
31. Mohammadian Haftcheshmeh S, Khosrojerdi A, Aliabadi A, Lotfi S, Mohammadi A, Momtazi-Borojeni AA. Immunomodulatory Effects of Curcumin in Rheumatoid Arthritis: Evidence from Molecular Mechanisms to Clinical Outcomes. Reviews of physiology, biochemistry and pharmacology. 2021;179:1-29.
https://doi.org/10.1007/112_2020_54 [DOI:10.1007/112_2020_54.]
32. Momtazi-Borojeni AA, Haftcheshmeh SM, Esmaeili SA, Johnston TP, Abdollahi E, Sahebkar A. Curcumin: A natural modulator of immune cells in systemic lupus erythematosus. Autoimmunity reviews. 2018;17(2):125-35.
https://doi.org/10.1016/j.autrev.2017.11.016 [DOI:10.1016/j.autrev.2017.11.016.]
33. Bhardwaj RS, Bhardwaj KS, Ranjeet D, Ganesh N. Curcuma longa leaves exhibits a potential antioxidant, antibacterial and immunomodulating properties. Intl J Phytomed. 2011;3(2):270-8.
34. Mohammadi A, Mashayekhi K, Navashenaq JG, Haftcheshmeh SM. Curcumin as a Natural Modulator of B Lymphocytes: Evidence from In Vitro and In Vivo Studies. Mini reviews in medicinal chemistry. 2022.
https://doi.org/10.2174/1389557522666220304122916 [DOI:10.2174/1389557522666220304122916.]
35. Mohammadian Haftcheshmeh S, Karimzadeh MR, Azhdari S, Vahedi P, Abdollahi E, Momtazi-Borojeni AA. Modulatory effects of curcumin on the atherogenic activities of inflammatory monocytes: Evidence from in vitro and animal models of human atherosclerosis. BioFactors (Oxford, England). 2020;46(3):341-55.
https://doi.org/10.1002/biof.1603 [DOI:10.1002/biof.1603.]
36. Rahimi K, Hassanzadeh K, Khanbabaei H, Haftcheshmeh SM, Ahmadi A, Izadpanah E, et al. Curcumin: A Dietary Phytochemical for Targeting the Phenotype and Function of Dendritic Cells. Current medicinal chemistry. 2021;28(8):1549-64.
https://doi.org/10.2174/0929867327666200515101228 [DOI:10.2174/0929867327666200515101228.]
37. Kahkhaie KR, Mirhosseini A, Aliabadi A, Mohammadi A, Mousavi MJ, Haftcheshmeh SM, et al. Curcumin: a modulator of inflammatory signaling pathways in the immune system. Inflammopharmacology. 2019;27(5):885-900.
https://doi.org/10.1007/s10787-019-00607-3 [DOI:10.1007/s10787-019-00607-3.]
38. Zhou Y, Cui C, Ma X, Luo W, Zheng SG, Qiu W. Nuclear Factor κB (NF-κB)-Mediated Inflammation in Multiple Sclerosis. Front Immunol. 2020;11:391.
https://doi.org/10.3389/fimmu.2020.00391 [DOI:10.3389/fimmu.2020.00391.]
39. Karlstetter M, Lippe E, Walczak Y, Moehle C, Aslanidis A, Mirza M, et al. Curcumin is a potent modulator of microglial gene expression and migration. Journal of neuroinflammation. 2011;8:125.
https://doi.org/10.1186/1742-2094-8-125 [DOI:10.1186/1742-2094-8-125.]
40. Yu Y, Shen Q, Lai Y, Park SY, Ou X, Lin D, et al. Anti-inflammatory Effects of Curcumin in Microglial Cells. Frontiers in pharmacology. 2018;9:386.
https://doi.org/10.3389/fphar.2018.00386 [DOI:10.3389/fphar.2018.00386.]
41. Fitzgerald KA, Kagan JC. Toll-like Receptors and the Control of Immunity. Cell. 2020;180(6):1044-66.
https://doi.org/10.1016/j.cell.2020.02.041 [DOI:10.1016/j.cell.2020.02.041.]
42. Zhang J, Zheng Y, Luo Y, Du Y, Zhang X, Fu J. Curcumin inhibits LPS-induced neuroinflammation by promoting microglial M2 polarization via TREM2/ TLR4/ NF-κB pathways in BV2 cells. Molecular immunology. 2019;116:29-37.
https://doi.org/10.1016/j.molimm.2019.09.020 [DOI:10.1016/j.molimm.2019.09.020.]
43. Gao Y, Zhuang Z, Lu Y, Tao T, Zhou Y, Liu G, et al. Curcumin Mitigates Neuro-Inflammation by Modulating Microglia Polarization Through Inhibiting TLR4 Axis Signaling Pathway Following Experimental Subarachnoid Hemorrhage. Frontiers in neuroscience. 2019;13:1223.
https://doi.org/10.3389/fnins.2019.01223 [DOI:10.3389/fnins.2019.01223.]
44. Ohl K, Tenbrock K, Kipp M. Oxidative stress in multiple sclerosis: Central and peripheral mode of action. Experimental neurology. 2016;277:58-67.
https://doi.org/10.1016/j.expneurol.2015.11.010 [DOI:10.1016/j.expneurol.2015.11.010.]
45. Chen Y, Peng DW, Jiang SR, Shao QC, Zhang YC, Chi ZL. Curcuma longa-derived extracellular vesicle-like particles ameliorate retinal neovascularization through HIF-1α and NRF2 signaling. Journal of nanobiotechnology. 2026;24(1).
https://doi.org/10.1186/s12951-026-04303-7 [DOI:10.1186/s12951-026-04303-7.]
46. Wu F, Lin Y, Xiao L, Chen Q, Lin F, Li R. Administration with curcumin alleviates spinal cord ischemia-reperfusion injury by regulating anti-oxidative stress and microglia activation-mediated neuroinflammation via Nrf2/NF-κB axis. In vitro cellular & developmental biology Animal. 2024;60(2):172-82.
https://doi.org/10.1007/s11626-023-00846-3 [DOI:10.1007/s11626-023-00846-3.]
47. Duan C, Wang H, Jiao D, Geng Y, Wu Q, Yan H, et al. Curcumin Restrains Oxidative Stress of After Intracerebral Hemorrhage in Rat by Activating the Nrf2/HO-1 Pathway. Frontiers in pharmacology. 2022;13:889226.
https://doi.org/10.3389/fphar.2022.889226 [DOI:10.3389/fphar.2022.889226.]
48. Lan Z, Tan F, He J, Liu J, Lu M, Hu Z, et al. Curcumin-primed olfactory mucosa-derived mesenchymal stem cells mitigate cerebral ischemia/reperfusion injury-induced neuronal PANoptosis by modulating microglial polarization. Phytomedicine : international journal of phytotherapy and phytopharmacology. 2024;129:155635.
https://doi.org/10.1016/j.phymed.2024.155635 [DOI:10.1016/j.phymed.2024.155635.]
49. Zhang J, Gu Y, Sun W, Yu L, Li T. Tetrahydrocurcumin Protects Against GSK3β/PTEN/PI3K/Akt-Mediated Neuroinflammatory Responses and Microglial Polarization Following Traumatic Brain Injury. Molecular neurobiology. 2024;61(9):7026-36.
https://doi.org/10.1007/s12035-024-04034-6 [DOI:10.1007/s12035-024-04034-6.]
50. I EL-D, Manai M, Neili NE, Marzouki S, Sahraoui G, Ben Achour W, et al. Dual Mechanism of Action of Curcumin in Experimental Models of Multiple Sclerosis. International journal of molecular sciences. 2022;23(15).
https://doi.org/10.3390/ijms23158658 [DOI:10.3390/ijms23158658.]
51. Azimzadeh M, Shapoori S, Jafarinia M. Synergistic effects of melatonin and curcumin in ameliorating experimental autoimmune encephalomyelitis: insights into anti-inflammatory, antioxidant, and neuroprotective mechanisms. Inflammopharmacology. 2025;33(12):7373-86.
https://doi.org/10.1007/s10787-025-02035-y [DOI:10.1007/s10787-025-02035-y.]
52. McKenzie BA, Mamik MK, Saito LB, Boghozian R, Monaco MC, Major EO, et al. Caspase-1 inhibition prevents glial inflammasome activation and pyroptosis in models of multiple sclerosis. Proceedings of the National Academy of Sciences of the United States of America. 2018;115(26):E6065-e74.
https://doi.org/10.1073/pnas.1722041115 [DOI:10.1073/pnas.1722041115.]
53. Gong Z, Zhou J, Li H, Gao Y, Xu C, Zhao S, et al. Curcumin suppresses NLRP3 inflammasome activation and protects against LPS-induced septic shock. Molecular nutrition & food research. 2015;59(11):2132-42.
https://doi.org/10.1002/mnfr.201500316 [DOI:10.1002/mnfr.201500316.]
54. Zhou T, Chen Z, Li S, Wang F, Tian W. Curcumin suppresses NLRP3 inflammasome activation by inducing autophagy to alleviate neuropathic pain in rats. Molecular biology reports. 2025;52(1):859.
https://doi.org/10.1007/s11033-025-10984-4 [DOI:10.1007/s11033-025-10984-4.]
55. Nedzvetsky VS, Agca CA, Kyrychenko SV. Neuroprotective Effect of Curcumin on LPS-activated Astrocytes Is Related to the Prevention of GFAP and NF-κB Upregulation. Neurophysiology. 2017;49(4):305-7.
https://doi.org/10.1007/s11062-017-9687-x [DOI:10.1007/s11062-017-9687-x.]
56. Zhang W, Sun M, Liu N, Li X, Sun J, Wang M. Curcumin ameliorates astrocyte inflammation through AXL in cuprizone-induced mice. Toxicology and applied pharmacology. 2025;494:117170.
https://doi.org/10.1016/j.taap.2024.117170 [DOI:10.1016/j.taap.2024.117170.]
57. Miron VE. Microglia-driven regulation of oligodendrocyte lineage cells, myelination, and remyelination. Journal of leukocyte biology. 2017;101(5):1103-8.
https://doi.org/10.1189/jlb.3RI1116-494R [DOI:10.1189/jlb.3RI1116-494R.]
58. Keren-Shaul H, Spinrad A, Weiner A, Matcovitch-Natan O, Dvir-Szternfeld R, Ulland TK, et al. A Unique Microglia Type Associated with Restricting Development of Alzheimer's Disease. Cell. 2017;169(7):1276-90.e17.
https://doi.org/10.1016/j.cell.2017.05.018 [DOI:10.1016/j.cell.2017.05.018.]
59. Su QY, Jiang ZQ, Song XY, Zhang SX. Regulatory B cells in autoimmune diseases: Insights and therapeutic potential. Journal of autoimmunity. 2024;149:103326.
https://doi.org/10.1016/j.jaut.2024.103326 [DOI:10.1016/j.jaut.2024.103326.]
60. Huang J, Wu T, Zhong Y, Huang J, Kang Z, Zhou B, et al. Effect of curcumin on regulatory B cells in chronic colitis mice involving TLR/MyD88 signaling pathway. Phytotherapy research : PTR. 2023;37(2):731-42.
https://doi.org/10.1002/ptr.7656 [DOI:10.1002/ptr.7656.]
61. Dolati S, Ahmadi M, Aghebti-Maleki L, Nikmaram A, Marofi F, Rikhtegar R, et al. Nanocurcumin is a potential novel therapy for multiple sclerosis by influencing inflammatory mediators. Pharmacological reports : PR. 2018;70(6):1158-67.
https://doi.org/10.1016/j.pharep.2018.05.008 [DOI:10.1016/j.pharep.2018.05.008.]
62. Natarajan C, Bright JJ. Curcumin inhibits experimental allergic encephalomyelitis by blocking IL-12 signaling through Janus kinase-STAT pathway in T lymphocytes. Journal of immunology (Baltimore, Md : 1950). 2002;168(12):6506-13. [DOI:10.4049/jimmunol.168.12.6506]
63. Ranjan D, Chen C, Johnston TD, Jeon H, Nagabhushan M. Curcumin inhibits mitogen stimulated lymphocyte proliferation, NFkappaB activation, and IL-2 signaling. The Journal of surgical research. 2004;121(2):171-7.
https://doi.org/10.1016/j.jss.2004.04.004 [DOI:10.1016/j.jss.2004.04.004.]
64. Zhang M, Deng CS, Zheng JJ, Xia J. Curcumin regulated shift from Th1 to Th2 in trinitrobenzene sulphonic acid-induced chronic colitis. Acta pharmacologica Sinica. 2006;27(8):1071-7.
https://doi.org/10.1111/j.1745-7254.2006.00322.x [DOI:10.1111/j.1745-7254.2006.00322.x.]
65. Larmonier CB, Uno JK, Lee KM, Karrasch T, Laubitz D, Thurston R, et al. Limited effects of dietary curcumin on Th-1 driven colitis in IL-10 deficient mice suggest an IL-10-dependent mechanism of protection. American journal of physiology Gastrointestinal and liver physiology. 2008;295(5):G1079-91.
https://doi.org/10.1152/ajpgi.90365.2008 [DOI:10.1152/ajpgi.90365.2008.]
66. Shin HS, See H-J, Jung SY, Choi DW, Kwon D-A, Bae M-J, et al. Turmeric (Curcuma longa) attenuates food allergy symptoms by regulating type 1/type 2 helper T cells (Th1/Th2) balance in a mouse model of food allergy. Journal of Ethnopharmacology. 2015;175:21-9.
https://doi.org/10.1016/j.jep.2015.08.038 [DOI:https://doi.org/10.1016/j.jep.2015.08.038.]
67. Shin HS, See HJ, Jung SY, Choi DW, Kwon DA, Bae MJ, et al. Turmeric (Curcuma longa) attenuates food allergy symptoms by regulating type 1/type 2 helper T cells (Th1/Th2) balance in a mouse model of food allergy. J Ethnopharmacol. 2015;175:21-9.
https://doi.org/10.1016/j.jep.2015.08.038 [DOI:10.1016/j.jep.2015.08.038.]
68. Kim GY, Kim KH, Lee SH, Yoon MS, Lee HJ, Moon DO, et al. Curcumin inhibits immunostimulatory function of dendritic cells: MAPKs and translocation of NF-kappa B as potential targets. Journal of immunology (Baltimore, Md : 1950). 2005;174(12):8116-24. [DOI:10.4049/jimmunol.174.12.8116]
69. Shirley SA, Montpetit AJ, Lockey RF, Mohapatra SS. Curcumin prevents human dendritic cell response to immune stimulants. Biochemical and biophysical research communications. 2008;374(3):431-6.
https://doi.org/10.1016/j.bbrc.2008.07.051 [DOI:10.1016/j.bbrc.2008.07.051.]
70. Zhao HM, Xu R, Huang XY, Cheng SM, Huang MF, Yue HY, et al. Curcumin Suppressed Activation of Dendritic Cells via JAK/STAT/SOCS Signal in Mice with Experimental Colitis. Frontiers in pharmacology. 2016;7:455.
https://doi.org/10.3389/fphar.2016.00455 [DOI:10.3389/fphar.2016.00455.]
71. Kanakasabai S, Casalini E, Walline CC, Mo C, Chearwae W, Bright JJ. Differential regulation of CD4(+) T helper cell responses by curcumin in experimental autoimmune encephalomyelitis. J Nutr Biochem. 2012;23(11):1498-507.
https://doi.org/10.1016/j.jnutbio.2011.10.002 [DOI:10.1016/j.jnutbio.2011.10.002.]
72. Bakir B, Yetkin Ay Z, Buyukbayram HI, Kumbul Doguc D, Bayram D, Candan IA, et al. Effect of Curcumin on Systemic T Helper 17 Cell Response; Gingival Expressions of Interleukin-17 and Retinoic Acid Receptor-Related Orphan Receptor gammat; and Alveolar Bone Loss in Experimental Periodontitis. Journal of periodontology. 2016;87(11):e183-e91.
https://doi.org/10.1902/jop.2016.150722 [DOI:10.1902/jop.2016.150722.]
73. Okamoto Y, Tanaka M, Fukui T, Masuzawa T. Inhibition of interleukin 17 production by curcumin in mice with collagen-induced arthritis. Biomed Res (India). 2011;22(3):299-304.
74. Xie L, Li XK, Funeshima-Fuji N, Kimura H, Matsumoto Y, Isaka Y, et al. Amelioration of experimental autoimmune encephalomyelitis by curcumin treatment through inhibition of IL-17 production. Int Immunopharmacol. 2009;9(5):575-81.
https://doi.org/10.1016/j.intimp.2009.01.025 [DOI:https://doi.org/10.1016/j.intimp.2009.01.025.]
75. Chen D, Nie M. Curcumin suppresses STAT3 signaling and Th17 differentiation in rheumatoid arthritis. Clinical Immunology. 2015;161(2):146-53.
https://doi.org/10.1016/j.clim.2015.08.007 [DOI:10.1016/j.clim.2015.08.007.]
76. Cong Y, Wang L, Konrad A, Schoeb T, Elson CO. Curcumin induces the tolerogenic dendritic cell that promotes differentiation of intestine-protective regulatory T cells. European Journal of Immunology. 2009;39(11):3134-46.
https://doi.org/10.1002/eji.200939052 [DOI:10.1002/eji.200939052.]
77. Rogers NM, Kireta S, Coates PTH. Curcumin induces maturation-arrested dendritic cells that expand regulatory T cells in vitro and in vivo. Clinical & Experimental Immunology. 2010;162(3):460-73.
https://doi.org/10.1111/j.1365-2249.2010.04232.x [DOI:10.1111/j.1365-2249.2010.04232.x.]
78. Zhao G, Liu Y, Yi X, Wang Y, Qiao S, Li Z, et al. Curcumin inhibiting Th17 cell differentiation by regulating the metabotropic glutamate receptor-4 expression on dendritic cells. Int Immunopharmacol. 2017;46:80-6.
https://doi.org/10.1016/j.intimp.2017.02.017 [DOI:https://doi.org/10.1016/j.intimp.2017.02.017.]
79. Bruck J, Holstein J, Glocova I, Seidel U, Geisel J, Kanno T, et al. Nutritional control of IL-23/Th17-mediated autoimmune disease through HO-1/STAT3 activation. Scientific reports. 2017;7:44482.
https://doi.org/10.1038/srep44482 [DOI:10.1038/srep44482.]
80. Wang Q, Ye C, Sun S, Li R, Shi X, Wang S, et al. Curcumin attenuates collagen-induced rat arthritis via anti-inflammatory and apoptotic effects. Int Immunopharmacol. 2019;72:292-300.
https://doi.org/10.1016/j.intimp.2019.04.027 [DOI:10.1016/j.intimp.2019.04.027.]
81. Momtazi AA, Sahebkar A. Difluorinated Curcumin: A Promising Curcumin Analogue with Improved Anti-Tumor Activity and Pharmacokinetic Profile. Current pharmaceutical design. 2016;22(28):4386-97. [DOI:10.2174/1381612822666160527113501]
82. Yang M, Jiang J. Nano-curcumin suppresses Th17 differentiation in experimental autoimmune encephalomyelitis. Journal of Neuroimmunology. 2018;323:9-17.
https://doi.org/10.1016/j.jneuroim.2018.07.003 [DOI:10.1016/j.jneuroim.2018.07.003.]
83. Ma C, Ma Z, Fu Q, Ma S. Curcumin attenuates allergic airway inflammation by regulation of CD4+CD25+ regulatory T cells (Tregs)/Th17 balance in ovalbumin-sensitized mice. Fitoterapia. 2013;87:57-64.
https://doi.org/10.1016/j.fitote.2013.02.014 [DOI:10.1016/j.fitote.2013.02.014.]
84. Han F, Luo B, Shi R, Han C, Zhang Z, Xiong J, et al. Curcumin ameliorates rat experimental autoimmune neuritis. Journal of neuroscience research. 2014;92(6):743-50.
https://doi.org/10.1002/jnr.23357 [DOI:10.1002/jnr.23357.]
85. Xie L, Li X-K, Funeshima-Fuji N, Kimura H, Matsumoto Y, Isaka Y, et al. Amelioration of experimental autoimmune encephalomyelitis by curcumin treatment through inhibition of IL-17 production. Int Immunopharmacol. 2009;9(5):575-81.
https://doi.org/10.1016/j.intimp.2009.01.025 [DOI:https://doi.org/10.1016/j.intimp.2009.01.025.]
86. Dolati S, Ahmadi M, Rikhtegar R, Babaloo Z, Ayromlou H, Aghebati-Maleki L, et al. Changes in Th17 cells function after nanocurcumin use to treat multiple sclerosis. Int Immunopharmacol. 2018;61:74-81.
https://doi.org/10.1016/j.intimp.2018.05.018 [DOI:https://doi.org/10.1016/j.intimp.2018.05.018.]
87. Chen J. Curcumin enhances Treg responses in viral infection. Antiviral Res. 2015;123:1-8.
https://doi.org/10.1016/j.antiviral.2015.08.001 [DOI:10.1016/j.antiviral.2015.08.001.]
88. Kim G, Jang MS, Son YM, Seo MJ, Ji SY, Han SH, et al. Curcumin Inhibits CD4+ T Cell Activation, but Augments CD69 Expression and TGF-β1-Mediated Generation of Regulatory T Cells at Late Phase. PLOS ONE. 2013;8(4):e62300.
https://doi.org/10.1371/journal.pone.0062300 [DOI:10.1371/journal.pone.0062300.]
89. Ohno M, Nishida A, Sugitani Y, Nishino K, Inatomi O, Sugimoto M, et al. Nanoparticle curcumin ameliorates experimental colitis via modulation of gut microbiota and induction of regulatory T cells. PLoS One. 2017;12(10):e0185999.
https://doi.org/10.1371/journal.pone.0185999 [DOI:10.1371/journal.pone.0185999.]
90. Gao W. Curcumin induces Foxp3+ regulatory T cells. Int Immunopharmacol. 2012;12(3):431-7.
https://doi.org/10.1016/j.intimp.2011.12.016 [DOI:10.1016/j.intimp.2011.12.016.]
91. Kim HR. Curcumin promotes regulatory T cell development in autoimmune arthritis. J Clin Immunol. 2010;30(3):363-73. [DOI:10.1007/s10875-010-9382-2.]
92. Liu Z. Curcumin promotes Treg-mediated immune tolerance in psoriasis model. J Dermatol Sci. 2017;87(2):131-9.
https://doi.org/10.1016/j.jdermsci.2017.05.004 [DOI:10.1016/j.jdermsci.2017.05.004.]
93. Sun J. Curcumin ameliorates autoimmune myocarditis via Treg expansion. J Cardiovasc Pharmacol. 2013;61(2):149-58. [DOI:10.1097/FJC.0b013e31827a2f40.]
94. Sun Y. Curcumin promotes Foxp3 stability in regulatory T cells. Front Immunol. 2020;11:589-.
https://doi.org/10.3389/fimmu.2020.00589 [DOI:10.3389/fimmu.2020.00589.]
95. Wang J. Curcumin increases Foxp3 expression through STAT5 pathway. Biochemical and biophysical research communications. 2011;407(3):421-6.
https://doi.org/10.1016/j.bbrc.2011.03.058 [DOI:10.1016/j.bbrc.2011.03.058.]
96. Dolati S, Babaloo Z, Ayromlou H, Ahmadi M, Rikhtegar R, Rostamzadeh D, et al. Nanocurcumin improves regulatory T-cell frequency and function in patients with multiple sclerosis. Journal of Neuroimmunology. 2019;327:15-21.
https://doi.org/10.1016/j.jneuroim.2019.01.007 [DOI:https://doi.org/10.1016/j.jneuroim.2019.01.007.]
97. Lassmann H, Brück W, Lucchinetti CF. The immunopathology of multiple sclerosis: an overview. Brain pathology (Zurich, Switzerland). 2007;17(2):210-8.
https://doi.org/10.1111/j.1750-3639.2007.00064.x [DOI:10.1111/j.1750-3639.2007.00064.x.]
Gholizadeh J, Gowhari Shabgah A, Majidiani H, Mohammadian Haftcheshmeh S. Modulatory Effects of Curcumin on Microglia, B and T Lymphocytes in Multiple Sclerosis: A Comprehensive Review of Findings from In vitro, In vivo and Human Studies. Iran J Health Res Dev 2026; 4 (4) :56-77 URL: http://jhrd.trjums.ac.ir/article-1-195-en.html
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