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

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 wer...

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Veröffentlicht in:Neurology : neuroimmunology & neuroinflammation 2016-04, Vol.3 (2), p.e202-e202
Hauptverfasser: 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, Montalban, Xavier, Rudzki, Dagmar, Schautzer, Franz, Sellebjerg, Finn, Sorensen, Per Soelberg, Deisenhammer, Florian, Steinman, Lawrence, Axtell, Robert C
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container_issue 2
container_start_page e202
container_title Neurology : neuroimmunology & neuroinflammation
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creator 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
Montalban, Xavier
Rudzki, Dagmar
Schautzer, Franz
Sellebjerg, Finn
Sorensen, Per Soelberg
Deisenhammer, Florian
Steinman, Lawrence
Axtell, Robert C
description 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.
doi_str_mv 10.1212/NXI.0000000000000202
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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. 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neuroinflammation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hegen, Harald</au><au>Adrianto, Indra</au><au>Lessard, Christopher J</au><au>Millonig, Alban</au><au>Bertolotto, Antonio</au><au>Comabella, Manuel</au><au>Giovannoni, Gavin</au><au>Guger, Michael</au><au>Hoelzl, Martina</au><au>Khalil, Michael</au><au>Fazekas, Franz</au><au>Killestein, Joep</au><au>Lindberg, Raija L.P</au><au>Malucchi, Simona</au><au>Mehling, Matthias</au><au>Montalban, Xavier</au><au>Rudzki, Dagmar</au><au>Schautzer, Franz</au><au>Sellebjerg, Finn</au><au>Sorensen, Per Soelberg</au><au>Deisenhammer, Florian</au><au>Steinman, Lawrence</au><au>Axtell, Robert C</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cytokine profiles show heterogeneity of interferon-β response in multiple sclerosis patients</atitle><jtitle>Neurology : neuroimmunology &amp; neuroinflammation</jtitle><addtitle>Neurol Neuroimmunol Neuroinflamm</addtitle><date>2016-04</date><risdate>2016</risdate><volume>3</volume><issue>2</issue><spage>e202</spage><epage>e202</epage><pages>e202-e202</pages><issn>2332-7812</issn><eissn>2332-7812</eissn><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. 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title Cytokine profiles show heterogeneity of interferon-β response in multiple sclerosis patients
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