Journals / Turkish Journal of Medical Sciences / 2019 / Cilt: 49 - Sayı: 6

IFN-γ stimulated dental follicle mesenchymal stem cells regulate activated lymphocyte response in rheumatoid arthritis patients in vitro

Pages
1779–1788
Publication Date
2022-11-05
DOI
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After culture period, lymphocyte proliferation and viability, the frequency of CD4+CD25+FoxP3+ T regulatory cells, IL-10 and TNF-α levels in the culture supernatants were measured via flow cytometry.Results: Our results demonstrated that DFSCs suppressed proliferation of T lymphocytes by increasing the number of FoxP3 expressingCD4+CD25+ T regulatory cells and suppressed lymphocyte apoptosis in RA patients.

📌 3 Key Takeaways

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Objective & Hypothesis:Background/aim: Multipotent mesenchymal stem cells (MSCs) have been investigated in autoimmune diseases such as rheumatoidarthritis (RA) due to their immunomodulatory and regenerative properties.
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Key Findings & Data:Lymphocytes were isolated from peripheral venous blood of RA patients (n = 5) andhealthy individuals (n = 5).
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Conclusion & Impact:After culture period, lymphocyte proliferation and viability, the frequency of CD4+CD25+FoxP3+ T regulatory cells, IL-10 and TNF-α levels in the culture supernatants were measured via flow cytometry.Results: Our results demonstrated that DFSCs suppressed proliferation of T lymphocytes by increasing the number of FoxP3 expressingCD4+CD25+ T regulatory cells and suppressed lymphocyte apoptosis in RA patients.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Background/aim: Multipotent mesenchymal stem cells (MSCs) have been investigated in autoimmune diseases such as rheumatoidarthritis (RA) due to their immunomodulatory and regenerative properties. In this study, their immunosuppressive effects on peripheralblood mononuclear cells (PBMC) of RA patients were studied.Materials and methods: Dental follicle stem cells (DFSCs) were isolated from follicle tissue in the orofacial region. Characterizationand multipotency analyses were performed. Lymphocytes were isolated from peripheral venous blood of RA patients (n = 5) andhealthy individuals (n = 5). DFSCs were preincubated with IFN-γ for 48 h. PBMCs of RA patients and healthy individuals wereseparately cultured with or without DFSCs for 72 h. After culture period, lymphocyte proliferation and viability, the frequency of CD4+CD25+FoxP3+ T regulatory cells, IL-10 and TNF-α levels in the culture supernatants were measured via flow cytometry.Results: Our results demonstrated that DFSCs suppressed proliferation of T lymphocytes by increasing the number of FoxP3 expressingCD4+CD25+ T regulatory cells and suppressed lymphocyte apoptosis in RA patients. Also, DFSCs reduced TNF-α cytokine secretionand upregulated IL-10 secreting cells.Conclusions: Such cells could potentially be a source for future immunomodulatory treatments of RA patients.

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Cite This Article

AKKOÇ, T., İNANÇ, N., GENÇ, D., ZIBANDEH, N., DİRESKENELİ, H. (2022). IFN-γ stimulated dental follicle mesenchymal stem cells regulate activated lymphocyte response in rheumatoid arthritis patients in vitro. Turkish Journal of Medical Sciences, Cilt: 49 - Sayı: 6, 1779–1788. https://ajindex.com/articles/610032

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References (13)

  1. Burmester GR, Kivitz AJ, Kupper H, Arulmani U, Florentinus S, Goss SL, Rathmann SS, Fleischmann RM. Efficacy and safety of ascending methotrexate dose in combination with adalimumab: the randomised CONCERTO trial. Ann Rheum Dis 2015; 74: 1037-1044
  2. Furst DE, Emery P. Rheumatoid arthritis pathophysiology: update on emerging cytokine and cytokine-associated cell targets. Rheumatology (Oxford) 2014; 53: 1560-1569
  3. McInnes IB, Schett G. The pathogenesis of rheumatoid arthritis. N Engl J 2011; 365: 2205-2219
  4. Diarra D, Stolina M, Polzer K,, Zwerina J, Ominsky MS, Dwyer D, Korb A, Smolen J, Hoffmann M, Scheinecker C et al. Dickkopf-1 is a master regulator of joint remodeling. Nat Med 2007; 13: 156-163
  5. Aletaha D, Neogi T, Silman AJ, Funovits J, Felson DT, Bingham CO 3rd, Birnbaum NS, Burmester GR, Bykerk VP, Cohen MD. 2010 Rheumatoid arthritis classification criteria: an American College of Rheumatology/European league against rheumatism collaborative initiative. Arthritis Rheum 2010; 69: 1580-1588
  6. Smolen JS, Aletaha D, Bijlsma JW, Breedveld FC, Boumpas D, Burmester G, Combe B, Cutolo M, de Wit M, Dougados M. Treating rheumatoid arthritis to target: recommendations recommendations of an international task force. Ann Rheum Dis 2010; 69: 631-637
  7. Mewar D, Wilson AG. Treatment of rheumatoid arthritis with tumour necrosis factor inhibitors. Br J Pharmacol 2011; 162: 785-791
  8. Al-Nbaheen M, Vishnubalaji R, Ali D, Bouslimi A, Al-Jassir F, Megges M, Prigione A, Adjaye J, Kassem M, Aldahmash A. Human stromal (mesenchymal) stem cells from bone marrow, adipose tissue and skin exhibit differences in molecular phenotype and differentiation potential. Stem Cell Rev 2013; 9: 32-43
  9. Kim RH, Mehrazarin S, Kang MK. Therapeutic potential of mesenchymal stem cells for oral and systemic diseases. Dent Clin North Am 2012; 56: 651-675
  10. Bluestone JA. Regulatory T-cell therapy: is it ready for the clinic? Nat Rev Immunol 2005; 5: 343-349
  11. Ehrenstein MR, Evans JG, Singh A, Moore S, Warnes G, Isenberg DA, Mauri C. Compromised function of regulatory T cells in rheumatoid arthritis and reversal by anti-TNF therapy. J Exp Med 2004; 200: 277-285
  12. Esensten J, Wofsy D, Bluestone A. Regulatory T cells as therapeutic targets in rheumatoid arthritis. Nat Rev Rheumatol 2009; 5: 560-565
  13. Sugiyama H, Gyulai R, Toichi E, Garaczi E, Shimada S, Stevens SR, McCormick TS, Cooper KD. Dysfunctional blood and target tissue CD4CD25 high regulatory T cells in psor