IL-2, IL-6 and chitinase 3-like 2 might predict early relapse activity in multiple sclerosis
The possibility to better predict the severity of the disease in a patient newly diagnosed with multiple sclerosis would allow the treatment strategy to be personalized and lead to better clinical outcomes. Prognostic biomarkers are highly needed. To assess the prognostic value of intrathecal IgM sy...
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Published in | PloS one Vol. 17; no. 6; p. e0270607 |
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Main Authors | , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
San Francisco
Public Library of Science
27.06.2022
Public Library of Science (PLoS) |
Subjects | |
Online Access | Get full text |
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Summary: | The possibility to better predict the severity of the disease in a patient newly diagnosed with multiple sclerosis would allow the treatment strategy to be personalized and lead to better clinical outcomes. Prognostic biomarkers are highly needed. To assess the prognostic value of intrathecal IgM synthesis, cerebrospinal fluid and serum IL-2, IL-6, IL-10, chitinase 3-like 2 and neurofilament heavy chains obtained early after the onset of the disease. 58 patients after the first manifestation of multiple sclerosis were included. After the initial diagnostic assessment including serum and cerebrospinal fluid biomarkers, all patients initiated therapy with either glatiramer acetate, teriflunomide, or interferon beta. To assess the evolution of the disease, we followed the patients clinically and with MRI for two years. The IL-2:IL-6 ratio (both in cerebrospinal fluid) <0.48 (p = 0.0028), IL-2 in cerebrospinal fluid [greater than or equal to]1.23pg/ml (p = 0.026), and chitinase 3-like 2 in cerebrospinal fluid [greater than or equal to]7900pg/ml (p = 0.033), as well as baseline EDSS [greater than or equal to]1.5 (p = 0.0481) and age <22 (p = 0.0312), proved to be independent markers associated with shorter relapse free intervals. The IL-2:IL-6 ratio, IL-2, and chitinase 3-like 2 (all in cerebrospinal fluid) might be of value as prognostic biomarkers in early phases of multiple sclerosis. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Competing Interests: I have read the journal’s policy and the authors of this manuscript have the following competing interests: MP received publication honorarium and compensations for travel and conference registration fees from Novartis, Merck Serono and Sanofi Genzyme; all outside the submitted work. EM received speaker honoraria and consultant fees from Novartis, Merck Serono, Sanofi Genzyme, Roche, Biogen Idec and Teva; all outside the submitted work. JL received compensations for travel, speaker honoraria and consultant fees from Novartis, Merck Serono, Sanofi-Genzyme, Roche, Biogen Idec, Teva and Bayer Healthcare; all outside the submitted work. HM received compensations for travel and conference registration fees from Novartis, Merck Serono, Sanofi Genzyme and Roche; all outside the submitted work. ME received publication honorarium, speaker honoraria and compensations for travel and conference registration fees from Novartis, Merck Serono, Roche, Teva and UCB; all outside the submitted work. JH, PR, SK, JŠ, OS, and PM declare that they have no competing interests. These authors also contributed equally to this work. |
ISSN: | 1932-6203 1932-6203 |
DOI: | 10.1371/journal.pone.0270607 |