Cytokine profiles show heterogeneity of interferon-β response in multiple sclerosis patients

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Standard

Cytokine profiles show heterogeneity of interferon-β response in multiple sclerosis patients. / Hegen, Harald; Adrianto, Indra; Lessard, Christopher J; Millonig, Alban; Bertolotto, Antonio; Comabella, Manuel; Giovannoni, Gavin; Guger, Michael; Hoelzl, Martina; Khalil, Michael; Fazekas, Franz; Killestein, Joep; Lindberg, Raija L P; Malucchi, Simona; Mehling, Matthias; Montalbán, Xavier; Rudzki, Dagmar; Schautzer, Franz; Sellebjerg, Finn; Sorensen, Per Soelberg; Deisenhammer, Florian; Steinman, Lawrence; Axtell, Robert C.

I: Neurology: Neuroimmunology & Neuroinflammation, Bind 3, Nr. 2, e202, 04.2016.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Hegen, H, Adrianto, I, Lessard, CJ, Millonig, A, Bertolotto, A, Comabella, M, Giovannoni, G, Guger, M, Hoelzl, M, Khalil, M, Fazekas, F, Killestein, J, Lindberg, RLP, Malucchi, S, Mehling, M, Montalbán, X, Rudzki, D, Schautzer, F, Sellebjerg, F, Sorensen, PS, Deisenhammer, F, Steinman, L & Axtell, RC 2016, 'Cytokine profiles show heterogeneity of interferon-β response in multiple sclerosis patients', Neurology: Neuroimmunology & Neuroinflammation, bind 3, nr. 2, e202. https://doi.org/10.1212/NXI.0000000000000202

APA

Hegen, H., Adrianto, I., Lessard, C. J., Millonig, A., Bertolotto, A., Comabella, M., Giovannoni, G., Guger, M., Hoelzl, M., Khalil, M., Fazekas, F., Killestein, J., Lindberg, R. L. P., Malucchi, S., Mehling, M., Montalbán, X., Rudzki, D., Schautzer, F., Sellebjerg, F., ... Axtell, R. C. (2016). Cytokine profiles show heterogeneity of interferon-β response in multiple sclerosis patients. Neurology: Neuroimmunology & Neuroinflammation, 3(2), [e202]. https://doi.org/10.1212/NXI.0000000000000202

Vancouver

Hegen H, Adrianto I, Lessard CJ, Millonig A, Bertolotto A, Comabella M o.a. Cytokine profiles show heterogeneity of interferon-β response in multiple sclerosis patients. Neurology: Neuroimmunology & Neuroinflammation. 2016 apr.;3(2). e202. https://doi.org/10.1212/NXI.0000000000000202

Author

Hegen, Harald ; Adrianto, Indra ; Lessard, Christopher J ; Millonig, Alban ; Bertolotto, Antonio ; Comabella, Manuel ; Giovannoni, Gavin ; Guger, Michael ; Hoelzl, Martina ; Khalil, Michael ; Fazekas, Franz ; Killestein, Joep ; Lindberg, Raija L P ; Malucchi, Simona ; Mehling, Matthias ; Montalbán, Xavier ; Rudzki, Dagmar ; Schautzer, Franz ; Sellebjerg, Finn ; Sorensen, Per Soelberg ; Deisenhammer, Florian ; Steinman, Lawrence ; Axtell, Robert C. / Cytokine profiles show heterogeneity of interferon-β response in multiple sclerosis patients. I: Neurology: Neuroimmunology & Neuroinflammation. 2016 ; Bind 3, Nr. 2.

Bibtex

@article{2b041c3dcbe04000bc24b251f2531fed,
title = "Cytokine profiles show heterogeneity of interferon-β response in multiple sclerosis patients",
abstract = "OBJECTIVE: To evaluate serum cytokine profiles for their utility to determine the heterogeneous responses to interferon (IFN)-β treatment in patients with multiple sclerosis (MS).METHODS: Patients with relapsing-remitting MS (RRMS) or clinically isolated syndrome receiving de novo IFN-β treatment were included in this prospective, observational study. Number of relapses and changes in disability were assessed 2 years prior to and 2 years after initiation of treatment. Sera were collected at baseline and after 3 months on therapy. Cytokine levels in sera were assessed by Luminex multiplex assays. Baseline cytokine profiles were grouped by hierarchical clustering analysis. Demographic features, changes in cytokines, and clinical outcome were then assessed in the clustered patient groups.RESULTS: A total of 157 patients were included in the study and clustered into 6 distinct subsets by baseline cytokine profiles. These subsets differed significantly in their clinical and biological response to IFN-β therapy. Two subsets were associated with patients who responded poorly to therapy. Two other subsets, associated with a good response to therapy, showed a significant reduction in relapse rates and no worsening of disability. Each subset also had differential changes in cytokine levels after 3 months of IFN-β treatment.CONCLUSIONS: There is heterogeneity in the immunologic pathways of the RRMS population, which correlates with IFN-β response.",
author = "Harald Hegen and Indra Adrianto and Lessard, {Christopher J} and Alban Millonig and Antonio Bertolotto and Manuel Comabella and Gavin Giovannoni and Michael Guger and Martina Hoelzl and Michael Khalil and Franz Fazekas and Joep Killestein and Lindberg, {Raija L P} and Simona Malucchi and Matthias Mehling and Xavier Montalb{\'a}n and Dagmar Rudzki and Franz Schautzer and Finn Sellebjerg and Sorensen, {Per Soelberg} and Florian Deisenhammer and Lawrence Steinman and Axtell, {Robert C}",
year = "2016",
month = apr,
doi = "10.1212/NXI.0000000000000202",
language = "English",
volume = "3",
journal = "Neurology: Neuroimmunology & Neuroinflammation",
issn = "2332-7812",
publisher = "AAN Publications",
number = "2",

}

RIS

TY - JOUR

T1 - Cytokine profiles show heterogeneity of interferon-β response in multiple sclerosis patients

AU - Hegen, Harald

AU - Adrianto, Indra

AU - Lessard, Christopher J

AU - Millonig, Alban

AU - Bertolotto, Antonio

AU - Comabella, Manuel

AU - Giovannoni, Gavin

AU - Guger, Michael

AU - Hoelzl, Martina

AU - Khalil, Michael

AU - Fazekas, Franz

AU - Killestein, Joep

AU - Lindberg, Raija L P

AU - Malucchi, Simona

AU - Mehling, Matthias

AU - Montalbán, Xavier

AU - Rudzki, Dagmar

AU - Schautzer, Franz

AU - Sellebjerg, Finn

AU - Sorensen, Per Soelberg

AU - Deisenhammer, Florian

AU - Steinman, Lawrence

AU - Axtell, Robert C

PY - 2016/4

Y1 - 2016/4

N2 - OBJECTIVE: To evaluate serum cytokine profiles for their utility to determine the heterogeneous responses to interferon (IFN)-β treatment in patients with multiple sclerosis (MS).METHODS: Patients with relapsing-remitting MS (RRMS) or clinically isolated syndrome receiving de novo IFN-β treatment were included in this prospective, observational study. Number of relapses and changes in disability were assessed 2 years prior to and 2 years after initiation of treatment. Sera were collected at baseline and after 3 months on therapy. Cytokine levels in sera were assessed by Luminex multiplex assays. Baseline cytokine profiles were grouped by hierarchical clustering analysis. Demographic features, changes in cytokines, and clinical outcome were then assessed in the clustered patient groups.RESULTS: A total of 157 patients were included in the study and clustered into 6 distinct subsets by baseline cytokine profiles. These subsets differed significantly in their clinical and biological response to IFN-β therapy. Two subsets were associated with patients who responded poorly to therapy. Two other subsets, associated with a good response to therapy, showed a significant reduction in relapse rates and no worsening of disability. Each subset also had differential changes in cytokine levels after 3 months of IFN-β treatment.CONCLUSIONS: There is heterogeneity in the immunologic pathways of the RRMS population, which correlates with IFN-β response.

AB - OBJECTIVE: To evaluate serum cytokine profiles for their utility to determine the heterogeneous responses to interferon (IFN)-β treatment in patients with multiple sclerosis (MS).METHODS: Patients with relapsing-remitting MS (RRMS) or clinically isolated syndrome receiving de novo IFN-β treatment were included in this prospective, observational study. Number of relapses and changes in disability were assessed 2 years prior to and 2 years after initiation of treatment. Sera were collected at baseline and after 3 months on therapy. Cytokine levels in sera were assessed by Luminex multiplex assays. Baseline cytokine profiles were grouped by hierarchical clustering analysis. Demographic features, changes in cytokines, and clinical outcome were then assessed in the clustered patient groups.RESULTS: A total of 157 patients were included in the study and clustered into 6 distinct subsets by baseline cytokine profiles. These subsets differed significantly in their clinical and biological response to IFN-β therapy. Two subsets were associated with patients who responded poorly to therapy. Two other subsets, associated with a good response to therapy, showed a significant reduction in relapse rates and no worsening of disability. Each subset also had differential changes in cytokine levels after 3 months of IFN-β treatment.CONCLUSIONS: There is heterogeneity in the immunologic pathways of the RRMS population, which correlates with IFN-β response.

U2 - 10.1212/NXI.0000000000000202

DO - 10.1212/NXI.0000000000000202

M3 - Journal article

C2 - 26894205

VL - 3

JO - Neurology: Neuroimmunology & Neuroinflammation

JF - Neurology: Neuroimmunology & Neuroinflammation

SN - 2332-7812

IS - 2

M1 - e202

ER -

ID: 180853932