Immunogenicity of human interferon-beta-containing pharmaceuticals


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Resumo

Multiple sclerosis is a severe autoimmune disease with inflammatory component that continues to be resistant to treatment. One of the approaches retarding its progression is based on using nonspecific therapy with human interferon-beta (IFN-β)-containing pharmaceuticals. Neutralizing antibodies (NAbs) against genetically engineered pharmaceuticals developed by the patient’s immune system, which reduce their therapeutic and biological activity, pose a serious problem. Cell lines sensitive to IFN-β activity also quantifying NAb level are applied because direct measurement of IFN-β antiviral activity is complicated. This study was aimed at standardization and validation of a reporter cell system for measuring antihuman IFN-β NAb titers, and evaluation data were obtained with samples from 33 patients with multiple sclerosis.

Sobre autores

V. Nazarov

Center for Molecular Medicine

Autor responsável pela correspondência
Email: Nazarov19932@mail.ru
Rússia, St. Petersburg, 197022

S. Lapin

Center for Molecular Medicine

Email: Nazarov19932@mail.ru
Rússia, St. Petersburg, 197022

A. Mazing

Center for Molecular Medicine

Email: Nazarov19932@mail.ru
Rússia, St. Petersburg, 197022

E. Evdoshenko

Saint-Petersburg Center of Multiple Sclerosis and Autoimmune Diseases Clinical Hospital No. 31

Email: Nazarov19932@mail.ru
Rússia, St. Petersburg, 197110

A. Totolian

Center for Molecular Medicine; Saint Petersburg Pasteur Research Institute of Epidemiology and Microbiology (St. Petersburg Pasteur Institute)

Email: Nazarov19932@mail.ru
Rússia, St. Petersburg, 197022; St. Petersburg, 197101


Declaração de direitos autorais © Pleiades Publishing, Ltd., 2016

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