Breakthrough disease during interferon-[beta] therapy in MS: No signs of impaired biologic response
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Breakthrough disease during interferon-[beta] therapy in MS: No signs of impaired biologic response. / Hesse, D; Krakauer, M; Lund, H; Søndergaard, H B; Langkilde, A; Ryder, L P; Sørensen, Per Soelberg; Sellebjerg, F; Langkilde, Annika.
I: Neurology, Bind 74, Nr. 18, 04.05.2010, s. 1455-62.Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
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TY - JOUR
T1 - Breakthrough disease during interferon-[beta] therapy in MS: No signs of impaired biologic response
AU - Hesse, D
AU - Krakauer, M
AU - Lund, H
AU - Søndergaard, H B
AU - Langkilde, A
AU - Ryder, L P
AU - Sørensen, Per Soelberg
AU - Sellebjerg, F
AU - Langkilde, Annika
PY - 2010/5/4
Y1 - 2010/5/4
N2 - Disease activity is highly variable in patients with multiple sclerosis (MS), both untreated and during interferon (IFN)-beta therapy. Breakthrough disease is often regarded as treatment failure; however, apart from neutralizing antibodies (NAbs), no blood biomarkers have been established as reliable indicators of treatment response, despite substantial, biologically measurable effects. We studied the biologic response to treatment in a cohort of NAb-negative patients to test whether difference in responsiveness could segregate patients with and without breakthrough disease during therapy.
AB - Disease activity is highly variable in patients with multiple sclerosis (MS), both untreated and during interferon (IFN)-beta therapy. Breakthrough disease is often regarded as treatment failure; however, apart from neutralizing antibodies (NAbs), no blood biomarkers have been established as reliable indicators of treatment response, despite substantial, biologically measurable effects. We studied the biologic response to treatment in a cohort of NAb-negative patients to test whether difference in responsiveness could segregate patients with and without breakthrough disease during therapy.
U2 - http://dx.doi.org/10.1212/WNL.0b013e3181dc1a94
DO - http://dx.doi.org/10.1212/WNL.0b013e3181dc1a94
M3 - Journal article
VL - 74
SP - 1455
EP - 1462
JO - Neurology
JF - Neurology
SN - 0028-3878
IS - 18
ER -
ID: 34078810