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Boyko A.N.

Pirogov Russian National Research Medical University;
Federal Center of Brain Research and Neurotechnologies of the Federal Medical Biological Agency

Smirnova N.F.

Pirogov Russian National Research Medical University;
Federal Center for Brain and Neurotechnology of the FMBA

Shchukin I.A.

Pirogov Russian National Research Medical University;
Federal Center of Brain and Neurotechnologies of the Federal Medical and Biological Agency of Russia;
Pirogov City Clinical Hospital No. 1

Guseva M.E.

Pirogov Russian National Research Medical University

Volkov A.I.

Federal Center of Brain and Neurotechnology of Federal Medical-Biological Agency of Russia

Ofatumumab — a new drug for the treatment of multiple sclerosis

Authors:

Boyko A.N., Smirnova N.F., Shchukin I.A., Guseva M.E., Volkov A.I.

More about the authors

Read: 10680 times


To cite this article:

Boyko AN, Smirnova NF, Shchukin IA, Guseva ME, Volkov AI. Ofatumumab — a new drug for the treatment of multiple sclerosis. S.S. Korsakov Journal of Neurology and Psychiatry. 2021;121(7‑2):37‑43. (In Russ.)
https://doi.org/10.17116/jnevro202112107237

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References:

  1. Li R, Patterson KR, Bar-Or A. Reassessing B cell contributions in multiple sclerosis. Nat Immunol. 2018;19:696-707.  https://doi.org/10.1038/s41590-018-0135-x
  2. Blauth K, Owens GP, Bennett JL. The ins and outs of B cells in multiple sclerosis. Front Immunol. 2015;6:565.  https://doi.org/10.3389/fimmu.2015.00565
  3. Brändle SM, Obermeier B, Senel M, et al. Distinct oligoclonal band antibodies in multiple sclerosis recognize ubiquitous self-proteins. Proc Natl Acad Sci USA. 2016;113:7864-7869. https://doi.org/10.1073/pnas.1522730113
  4. Rodríguez-Pinto D. B cells as antigen presenting cells. Cell Immunol. 2005;238:67-75.  https://doi.org/10.1016/j.cellimm.2006.02.005
  5. Genç K, Dona DL, Reder AT. Increased CD80(+) B cells in active multiple sclerosis and reversal by interferon beta-1b therapy. J Clin Invest. 2007;99:2664-2671. https://doi.org/10.1172/JCI119455
  6. Staun-Ram E, Miller A. Effector and regulatory B cells in multiple sclerosis. Clin Immunol. 2017;184:11-25.  https://doi.org/10.1016/j.clim.2017.04.014
  7. Magliozzi R, Howell O, Vora A, et al. Meningeal B-cell follicles in secondary progressive multiple sclerosis associate with early onset of disease and severe cortical pathology. Brain. 2007;130:1089-1104. https://doi.org/10.1093/brain/awm038
  8. Lucchinetti CF, Popescu BF, Bunyan RF, et al. Inflammatory cortical demyelination in early multiple sclerosis. N Engl J Med. 2011;365:2188-2197. https://doi.org/10.1056/NEJMoa1100648
  9. Frischer JM, Bramow S, Dal-Bianco A, et al. The relation between inflammation and neurodegeneration in multiple sclerosis brains. Brain. 2009;132:1175-1189. https://doi.org/10.1093/brain/awp070
  10. Bharadia T, Kesselring J, Boyko A, et al. Systematic mapping of the global educational offerings for multiple sclerosis patients on the topic of disease progression. Multiple Sclerosis Journal. 2019;25(S2):384.  https://doi.org/10.2147/PPA.S268829
  11. Lisak RP, Benjamins JA, Nedelkoska L, et al. Secretory products of multiple sclerosis B cells are cytotoxic to oligodendroglia in vitro. J Neuroimmunol. 2012;246:85-95.  https://doi.org/10.1016/j.jneuroim.2012.02.015
  12. Benjamins JA, Nedelkoska L, Touil H, et al. Exosome-enriched fractions from MS B cells induce oligodendrocyte death. Neurol Neuroimmunol Neuroinflamm. 2019;6(3):e550. https://doi.org/10.1212/NXI.0000000000000550
  13. Lisak RP, Nedelkoska L, Benjamins JA, et al. B cells from patients with multiple sclerosis induce cell death via apoptosis in neurons in vitro. J Neuroimmunol. 2017;309:88-99.  https://doi.org/10.1016/j.jneuroim.2017.05.004
  14. Teeling JL, Mackus WJ, Wiegman LJ, et al. The biological activity of human CD20 monoclonal antibodies is linked to unique epitopes on CD20. J ImmunoI. 2006;177:362-371.  https://doi.org/10.4049/jimmunol.177.1.362
  15. Hauser SL, Bar-Or A, Comi G, et al. OPERA I and OPERA II Clinical Investigators. Ocrelizumab versus Interferon Beta-1a in Relapsing Multiple Sclerosis. N Engl J Med. 2017;376(3):221-234.  https://doi.org/10.1056/NEJMoa1601277
  16. Montalban X, Hauser SL, Kappos L, et al. ORATORIO Clinical Investigators. Ocrelizumab versus Placebo in Primary Progressive Multiple Sclerosis. N Engl J Med. 2017;376(3):209-220.  https://doi.org/10.1056/NEJMoa1606468
  17. Boyko AN, Davydovskaya MV, Khachanova NV, et al. Clinical recommendations for the use of ocrelizumab in patients with multiple sclerosis. Neurology, Neuropsychiatry, Psychosomatics. 2019;11(3):16-25. (In Russ.). https://doi.org/10.14412/2074-2711-2019-3-16-25
  18. Kurrasch R, Brown JC, Chu M, et al. Subcutaneously administered ofatumumab in rheumatoid arthritis: a phase I/II study of safety, tolerability, pharmacokinetics, and pharmacodynamics. J Rheumatol. 2013;40:1089-1096. https://doi.org/10.3899/jrheum.121118
  19. Hauser SL, Bar-Or A, Cohen JA, et al. ASCLEPIOS I and ASCLEPIOS II Trial Groups. Ofatumumab versus Teriflunomide in Multiple Sclerosis. N Engl J Med. 2020;383(6):546-557.  https://doi.org/10.1056/NEJMoa1917246
  20. Bar-Or A, Grove RA, Austin DJ, et al. Subcutaneous ofatumumab in patients with relapsing-remitting multiple sclerosis: The MIRROR study. Neurology. 2018;90:1805-1814. https://doi.org/10.1212/WNL.0000000000005516
  21. Florou D, Katsara M, Feehan J, et al. Anti-CD20 Agents for Multiple Sclerosis: Spotlight on Ocrelizumab and Ofatumumab. Brain Sci. 2020;10(10):758.  https://doi.org/10.3390/brainsci10100758
  22. Sanford M, McCormack PL. Ofatumumab Drugs. 2010;70(8):1013-1019. https://doi.org/10.2165/11203850-000000000-00000
  23. Boyko AN. Additional study of efficacy and safety of therapy in Russian population of MS patients, participated in phase III international multicentral clinical trials: data from alemtuzumab trials. Zhurnal Nevrologii i Psihiatrii im. S.S. Korsakova. 2019;119:10(2):148-153. (In Russ.). https://doi.org/10.17116/jnevro2019119102148
  24. Samjoo IA, Worthington E, Drudge C, et al. Comparison of ofatumumab and other disease-modifying therapies for relapsing multiple sclerosis: a network meta-analysis. Comp Eff Res. 2020;(18):1255-1274. https://doi.org/10.2217/cer-2020-0122

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