scholarly journals A type I interferon signature in monocytes is associated with poor response to interferon-β in multiple sclerosis

Brain ◽  
2009 ◽  
Vol 132 (12) ◽  
pp. 3353-3365 ◽  
Author(s):  
M. Comabella ◽  
J. D. Lünemann ◽  
J. Río ◽  
A. Sánchez ◽  
C. López ◽  
...  
2012 ◽  
Vol 313 (1-2) ◽  
pp. 48-53 ◽  
Author(s):  
Xuan Feng ◽  
Nicholas P. Reder ◽  
Mounica Yanamandala ◽  
Addie Hill ◽  
Beverly S. Franek ◽  
...  

2020 ◽  
Author(s):  
Patrick Ostkamp ◽  
Anke Salmen ◽  
Beatrice Pignolet ◽  
Dennis Goerlich ◽  
Till F. M. Andlauer ◽  
...  

Background: Multiple sclerosis (MS) disease risk is associated with reduced sun exposure. This study assessed the relationship between measures of sun-exposure (vitamin D (vitD), latitude) and MS disease severity, the mechanisms of action, and effect-modification by medication and sun-sensitivity associated MC1R variants. Methods: Two multi-center cohort studies (nNationMS=946, nBIONAT=991). Outcomes were the multiple sclerosis severity score (MSSS) and the number of Gd-enhancing lesion (GELs). RNAseq of four immune cell populations before and after UV-phototherapy of five MS patients. Results: High serum vitD was associated with reduced MSSS (PNationMS=0.021; PBIONAT=0.007) and reduced risk for disease aggravation (PNationMS=0.032). Low latitude was associated with higher vitD, lower MSSS (PNationMS=0.018), fewer GELs (PNationMS=0.030) and reduced risk for aggravation (PNationMS=0.044). The influence of latitude on disability seemed to be lacking in the subgroup of interferon-β treated patients (interaction-PBIONAT=0.042, interaction-PNationMS=0.053). In genetic analyses, carriers of MC1R:rs1805008(T), who reported increased sensitivity towards sunlight (PNationMS=0.038), the relationship between latitude und the number of GELs was inversed (PNationMS=0.001). Phototherapy induced a vitD and type I interferon signature that was most apparent in the transcriptome of monocytes (P=1x10-6). Conclusion: VitD is associated with reduced MS severity and disease aggravation. This is likely driven by sun-exposure, as latitude also correlated with disability and serum vitD. However, sun-exposure might be detrimental for sun-sensitive patients. A direct induction of type I interferons through sun-exposure could explain a reduced effect of latitude in interferon-β treated patients. This could also explain opposite effects of sun-exposure in MS and the type I interferon and sun-sensitivity-associated disease Lupus.


2014 ◽  
Vol 2 (1) ◽  
pp. e55 ◽  
Author(s):  
Elisabeth Schuh ◽  
Birgit Ertl-Wagner ◽  
Peter Lohse ◽  
Waltraud Wolf ◽  
Johannes F. Mann ◽  
...  

2021 ◽  
pp. 0
Author(s):  
K Souaid ◽  
B Oulès ◽  
P Sohier ◽  
L Deschamps ◽  
S Aractingi ◽  
...  

Diagnostics ◽  
2019 ◽  
Vol 9 (3) ◽  
pp. 113 ◽  
Author(s):  
Alessia Pin ◽  
Lorenzo Monasta ◽  
Andrea Taddio ◽  
Elisa Piscianz ◽  
Alberto Tommasini ◽  
...  

Interferon-stimulated genes (ISGs) are a set of genes whose transcription is induced by interferon (IFN). The measure of the expression of ISGs enables calculating an IFN score, which gives an indirect estimate of the exposition of cells to IFN-mediated inflammation. The measure of the IFN score is proposed for the screening of monogenic interferonopathies, like the Aicardi-Goutières syndrome, or to stratify subjects with systemic lupus erythematosus to receive IFN-targeted treatments. Apart from these scenarios, there is no agreement on the diagnostic value of the score in distinguishing IFN-related disorders from diseases dominated by other types of cytokines. Since the IFN score is currently measured in several research hospitals, merging experiences could help define the potential of scoring IFN inflammation in clinical practice. However, the IFN score calculated at different laboratories may be hardly comparable due to the distinct sets of IFN-stimulated genes assessed and to different controls used for data normalization. We developed a reliable approach to minimize the inter-laboratory variability, thereby providing shared strategies for the IFN signature analysis and allowing different centers to compare data and merge their experiences.


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