Abstract
Beta-interferons are still among the most commonly used drugs to treat Multiple Sclerosis (MS). The use of beta-interferons is limited by the development of anti-drug antibodies (ADA), which may abrogate the treatment effect of the drug. Although the antibody response has been well studied, little is known about the T cell response to interferon-beta (IFN-beta). We investigated T cell responses in four treatment naive MS patients and twenty-three patients treated with IFN-beta who had or had not developed ADA to IFN-beta. T cell responses were determined by split-well and primary proliferation assays against different IFN-beta protein preparations and a set of overlapping peptides covering the full sequence of IFN-beta. T cell responses to IFN-beta were observed in all donors. ADA positive patients showed higher T cell responses to IFN-beta protein than ADA negative patients and untreated controls. We identified two immunodominant regions;T cell responses to IFN-beta(1-40) were observed in all patients independent of ADA status, while T cell responses to IFN-beta(125-159) were stronger in ADA positive than ADA negative patients. IFN-beta specific T cell responses were HLA class II restricted and in ADA positive patients skewed towards a Th2 phenotype. In IFN-beta treated patients we observed a correlation between IFN-beta specific T cell responses, serum ADA titer and loss of biological activity of IFN-beta treatment. Our studies demonstrate the occurrence of an antigen specific HLA class II restricted Th2 T cell response associated with the development of ADA in IFN-beta treated patients.
Dokumententyp: | Zeitschriftenartikel |
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Fakultät: | Medizin > Munich Cluster for Systems Neurology (SyNergy) |
Themengebiete: | 600 Technik, Medizin, angewandte Wissenschaften > 610 Medizin und Gesundheit |
ISSN: | 0896-8411 |
Sprache: | Englisch |
Dokumenten ID: | 63027 |
Datum der Veröffentlichung auf Open Access LMU: | 19. Jul. 2019, 12:12 |
Letzte Änderungen: | 06. Jun. 2024, 13:04 |
DFG: | Gefördert durch die Deutsche Forschungsgemeinschaft (DFG) - 390857198 |