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Advanced glycation end products contribute to the immunogenicity of IFN-[beta] pharmaceuticals
Protein-derived AGEs are formed in both eukaryotic and prokaryotic cells. [...]we hypothesized that human IFN-β produced in either Chinese hamster ovary cells (IFN-β1a) or E coli (IFN-β1b) will accumulate AGEs. [...]experimental data support involvement of both innate6 and adaptive7 immune reacti...
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Published in: | Journal of allergy and clinical immunology 2012-03, Vol.129 (3), p.855 |
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container_title | Journal of allergy and clinical immunology |
container_volume | 129 |
creator | Bozhinov, Angelina Handzhiyski, Yordan Genov, Krasimir Daskalovska, Vera Niwa, Toshimitsu Ivan ov, Ivan Mironova, Roumyana |
description | Protein-derived AGEs are formed in both eukaryotic and prokaryotic cells. [...]we hypothesized that human IFN-β produced in either Chinese hamster ovary cells (IFN-β1a) or E coli (IFN-β1b) will accumulate AGEs. [...]experimental data support involvement of both innate6 and adaptive7 immune reactions against AGEs. |
doi_str_mv | 10.1016/j.jaci.2011.10.035 |
format | article |
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language | eng |
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source | Elsevier |
subjects | Age E coli Multiple sclerosis Patients Pharmaceuticals Proteins |
title | Advanced glycation end products contribute to the immunogenicity of IFN-[beta] pharmaceuticals |
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