Research Article


DOI :10.26650/experimed.2019.19026   IUP :10.26650/experimed.2019.19026    Full Text (PDF)

B Cell Immunophenotyping and Expression Analysis of B Cell Specific Molecules of Patients with Benign Multiple Sclerosis

Melis ŞenEce AkbayırRecai TürkoğluErdem TüzünVuslat Yılmaz

Objective: Multiple Sclerosis (MS) is a progresive and an immune mediated inflammatory central nervous disease. The focus of this study was to determine the possible relationship between B cell immunophenotypes and related gene expressions in the benign MS (BMS) group with disease and cognitive processes.


Material and Method: Twenty BMS patients, 16 non-BMS and 28 healthy volunteers were included in the study. Gene expression was performed by real-time PCR (RT-PCR). Immunophenotyping of peripheral B cells was also evaluated by flow cytometry. The relationship between cognitive functions and gene expression levels and B cell subtypes was investigated.


Results: It was observed that naïve (CD19+ IgD+CD27- ) cells were higher in the BMS group compared to the healthy group (HC), and memory B cells showed opposite changes. Un-switched memory B cells(CD19+IgD+CD27+) were found to be higher in the benign group than in the HC. The expression of BANK and BLNK was found to be lower in both MS groups than in the HC. As a result of neuropsychological examinations and cognitive tests; it was observed that motor processes in BMS were better protected than Non-BMS.


Conclusion: These findings support that B cell functions may have molecular and cellular effects, and may lead to regression in inflammation and clinical progression. Molecules showing significant changes in our study may play a role as prognostic biomarkers in MS.

DOI :10.26650/experimed.2019.19026   IUP :10.26650/experimed.2019.19026    Full Text (PDF)

Benign MS Hastalarinin B Hücre İmmünfenotiplemesi ve B Hücresine Özgü Moleküllerin Ekspresyon Analizi

Melis ŞenEce AkbayırRecai TürkoğluErdem TüzünVuslat Yılmaz

Amaç: Multipl Skleroz (MS), aksonal dejenerasyona, demiyelinizasyona ve inflamasyona bağlı gelişen, merkezi sinir sistemini etkileyen progresif bir hastalıktır. Bu çalışmada benign MS (BMS) grubunda periferik kan B hücre immünofenotiplerinin ve B hücresi ile ilişkili gen ekspresyonlarının hastalık ve bilişsel süreçlerle ilişkisinin araştırılması hedeflenmiştir.


Gereç ve Yöntem: Yirmi BMS hastası, 16 benign olmayan MS (NonBMS) hastası ve 28 sağlıklı gönüllü çalışmaya dahil edildi. Daha önce periferik kan hücrelerinde yapılan gen mikroarray çalışması ile gruplar arasında ekspresyonu değişikliği gözlenen genlerin validasyonu gerçek zamanlı PZR ile yapıldı. Periferik B hücrelerinin immünofenotiplemesi akım sitometrisi ile değerlendirildi. Bilişsel fonksiyonlar ile gen ekspresyon seviyeleri ve B hücre alttipleri arasındaki olası ilişki araştırıldı.


Bulgular: Naif (CD19+ IgD+CD27- ) B hücrelerinin BMS grubunda sağlıklılara göre yüksek olduğu, hafıza B hücrelerinin zıt yönde değişiklik gösterdiği gözlendi. Dönüşmemiş hafıza B hücrelerinin (CD19+IgD+CD27+) ise benign grupta sağlıklılara göre yüksek olduğu belirlendi. BANK ve BLNK gen ekspresyonları her iki MS grubunda da sağlıklılardan düşük olarak belirlendi. Nöropsikolojik incelemeler ve kognitif testler sonucunda, BMS’te motor süreçlerin Non-BMS’ye göre korunduğu gözlendi.


Sonuç: Bu bulgular B hücresi işlevlerinin moleküler ve hücresel etkileri olabileceği ve inflamasyon ile klinik progresyonda gerilemeye yol açabileceği yönündeki görüşleri desteklemektedir. Değişiklik gösteren moleküllerin MS hastalığında prognostik biyobelirteç olarak rol oynaması da mümkündür.


PDF View

References

  • 1. Garg N, Smith TW. An update on immunopathogenesis, diagnosis and treatment of multiple sclerosis. Brain Behav 2015; 5: 1-13. [CrossRef] google scholar
  • 2. Samkoff LM, Goodman AD. Multiple Sclerosis and CNS İnflammatory Disorders,Wiley-Blackwell; 2014. [CrossRef] google scholar
  • 3. Lublin FD, Reingold SC. Defining the clinical course of multiple sclerosis: Results of an international survey. Neurology 1996; 46: 907-11. [CrossRef] google scholar
  • 4. Hawkins SA, McDonell GV. Benign multiple sclerosis? Clinical course, long term follow up, and assessment of prognostic factors. J Neurol Neurosurg Psychiatry 1999; 67: 148-52. [CrossRef] google scholar
  • 5. Ozakbas S, Turkoglu R, Tamam Y, Terzi M, Taskapilioglu O, Yucesan C, et al N. Prevalence of and risk factors for cognitive impairment in patients with relapsing-remitting multiple sclerosis: Multi-center, controlled trial. Mult Scler Relat Disord 2018; 22: 70-6. [CrossRef] google scholar
  • 6. Tuzun E. Multipl skleroz patogenezinde B hücrelerinin rolü ve B hücre karşıtı monoklonal antikor tedavileri. Nöropsikiyatri Arşivi 2011; 48: 73-8. [CrossRef] google scholar
  • 7. Sospedra M, Martin R. Immunology of multiple sclerosis. Annu Rev Immunol 2005; 23: 683-747. [CrossRef] google scholar
  • 8. Naegelin Y, Naegelin P, von Felten S, Lorscheider J, Sonder J, Uitdehaag BMJ, et al. Association of Rituximab Treatment With Disability Progression Among Patients With Secondary Progressive Multiple Sclerosis JAMA Neurol 2019; 76: 274-81. [CrossRef] google scholar
  • 9. Yamout BI, El-Ayoubi NK, Nicolas J, El Kouzi Y, Khoury SJ, Zeineddine MM.Safety and Efficacy of Rituximab in Multiple Sclerosis: A Retrospective Observational Study. J Immunol Res 2018; 2018: doi: 10.1155/2018/9084759. [CrossRef] google scholar
  • 10. Achiron A, Feldman A, Magalashvili D, Dolev M, Gurevich M. Suppressed RNA-polymerase 1 pathway is associated with benign multiple sclerosis. PLoS One 2012; 7: doi: 10.1371/journal.pone.0046871. [CrossRef] google scholar
  • 11. Yang J, Ren J, Yang Y, Sun J, Zhou X, Zheng S, et al. BANK1 alters B cell responses and influences the interactions between B cells and induced T regulatory cells in mice with collagen-induced arthritis. Arthritis Res Ther 2018; 20: 9. doi: 10.1186/s13075-017-1503-x. [CrossRef] google scholar
  • 12. Kurtzke, J.F., A reassessment of the distribution of multiple sclerosis. Acta Neurologica Scandinavica 1975; 51: 110-36. [CrossRef] google scholar
  • 13. Willer CJ, Dyment DA, Sadovnick AD, Ebers GC. Maternal-offspring HLA-DRB1 compatibility in multiple sclerosis. Tissue Antigens 2005; 66: 44-7. [CrossRef] google scholar
  • 14. Düzgün N. İmmün Sistemin Tanıtımı. s: 97-122. Available from: URL: http://ichastaliklariromatoloji.medicine.ankara.edu.tr/files/2014/02/%C4%B0mm%C3%BCn-Sistemin-Tan%C4%B1t%C4%B1m%C4%B1.pdf google scholar
  • 15. O’Connor BP, Raman VS, Erickson LD, Cook WJ, Weaver LK, Ahonen C, et al. BCMA is essential for the survival of long-lived bone marrow plasma cells. J Exp Med 2004; 199: 91-8. [CrossRef] google scholar
  • 16. Aktura ŞD, Yılmaz V, Özkan-Yaşargün D, Ulusoy C, Tüzün E, Türkoğlu R. Peripheral blood memory B cell frequency predicts conversion from clinically isolated syndrome to multiple sclerosis. Mult Scler Relat Disord 2018; 23: 9-14. [CrossRef] google scholar
  • 17. Komai T, Inoue M, Okamura T, Morita K, Iwasaki Y, Sumitomo S, et al. Transforming growth factor-β and interleukin-10 synergistically regulate humoral immunity via modulating metabolic signals. Front Immunol 2018; 9: 1364. doi: 10.3389/fimmu.2018.01364. [CrossRef] google scholar
  • 18. Molnarfi N, Bjarnadóttir K, Benkhoucha M, Juillard C, Lalive PH. Activation of human B cells negatively regulates TGF-β1 production. J Neuroinflammation 2017; 14: 13. doi: 10.1186/s12974-017-0798-5. [CrossRef] google scholar

Citations

Copy and paste a formatted citation or use one of the options to export in your chosen format


EXPORT



APA

Şen, M., Akbayır, E., Türkoğlu, R., Tüzün, E., & Yılmaz, V. (2019). B Cell Immunophenotyping and Expression Analysis of B Cell Specific Molecules of Patients with Benign Multiple Sclerosis. Experimed, 9(3), 105-112. https://doi.org/10.26650/experimed.2019.19026


AMA

Şen M, Akbayır E, Türkoğlu R, Tüzün E, Yılmaz V. B Cell Immunophenotyping and Expression Analysis of B Cell Specific Molecules of Patients with Benign Multiple Sclerosis. Experimed. 2019;9(3):105-112. https://doi.org/10.26650/experimed.2019.19026


ABNT

Şen, M.; Akbayır, E.; Türkoğlu, R.; Tüzün, E.; Yılmaz, V. B Cell Immunophenotyping and Expression Analysis of B Cell Specific Molecules of Patients with Benign Multiple Sclerosis. Experimed, [Publisher Location], v. 9, n. 3, p. 105-112, 2019.


Chicago: Author-Date Style

Şen, Melis, and Ece Akbayır and Recai Türkoğlu and Erdem Tüzün and Vuslat Yılmaz. 2019. “B Cell Immunophenotyping and Expression Analysis of B Cell Specific Molecules of Patients with Benign Multiple Sclerosis.” Experimed 9, no. 3: 105-112. https://doi.org/10.26650/experimed.2019.19026


Chicago: Humanities Style

Şen, Melis, and Ece Akbayır and Recai Türkoğlu and Erdem Tüzün and Vuslat Yılmaz. B Cell Immunophenotyping and Expression Analysis of B Cell Specific Molecules of Patients with Benign Multiple Sclerosis.” Experimed 9, no. 3 (Apr. 2024): 105-112. https://doi.org/10.26650/experimed.2019.19026


Harvard: Australian Style

Şen, M & Akbayır, E & Türkoğlu, R & Tüzün, E & Yılmaz, V 2019, 'B Cell Immunophenotyping and Expression Analysis of B Cell Specific Molecules of Patients with Benign Multiple Sclerosis', Experimed, vol. 9, no. 3, pp. 105-112, viewed 23 Apr. 2024, https://doi.org/10.26650/experimed.2019.19026


Harvard: Author-Date Style

Şen, M. and Akbayır, E. and Türkoğlu, R. and Tüzün, E. and Yılmaz, V. (2019) ‘B Cell Immunophenotyping and Expression Analysis of B Cell Specific Molecules of Patients with Benign Multiple Sclerosis’, Experimed, 9(3), pp. 105-112. https://doi.org/10.26650/experimed.2019.19026 (23 Apr. 2024).


MLA

Şen, Melis, and Ece Akbayır and Recai Türkoğlu and Erdem Tüzün and Vuslat Yılmaz. B Cell Immunophenotyping and Expression Analysis of B Cell Specific Molecules of Patients with Benign Multiple Sclerosis.” Experimed, vol. 9, no. 3, 2019, pp. 105-112. [Database Container], https://doi.org/10.26650/experimed.2019.19026


Vancouver

Şen M, Akbayır E, Türkoğlu R, Tüzün E, Yılmaz V. B Cell Immunophenotyping and Expression Analysis of B Cell Specific Molecules of Patients with Benign Multiple Sclerosis. Experimed [Internet]. 23 Apr. 2024 [cited 23 Apr. 2024];9(3):105-112. Available from: https://doi.org/10.26650/experimed.2019.19026 doi: 10.26650/experimed.2019.19026


ISNAD

Şen, Melis - Akbayır, Ece - Türkoğlu, Recai - Tüzün, Erdem - Yılmaz, Vuslat. B Cell Immunophenotyping and Expression Analysis of B Cell Specific Molecules of Patients with Benign Multiple Sclerosis”. Experimed 9/3 (Apr. 2024): 105-112. https://doi.org/10.26650/experimed.2019.19026



TIMELINE


Accepted27.11.2019

LICENCE


Attribution-NonCommercial (CC BY-NC)

This license lets others remix, tweak, and build upon your work non-commercially, and although their new works must also acknowledge you and be non-commercial, they don’t have to license their derivative works on the same terms.


SHARE




Istanbul University Press aims to contribute to the dissemination of ever growing scientific knowledge through publication of high quality scientific journals and books in accordance with the international publishing standards and ethics. Istanbul University Press follows an open access, non-commercial, scholarly publishing.