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Associations between type I interferon and antiphospholipid antibody status differ between ancestral backgrounds

OBJECTIVE: The type I interferon pathway is activated in many patients with systemic lupus erythematosus (SLE), and anti-double-stranded DNA (dsDNA) and anti-RNA binding protein autoantibodies are correlated with high interferon-α (IFNα) activity. We studied whether antiphospholipid (APL) antibodies...

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Autores principales: Iwamoto, Taro, Dorschner, Jessica, Jolly, Meenakshi, Huang, Xiangyang, Niewold, Timothy B
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5786906/
https://www.ncbi.nlm.nih.gov/pubmed/29387437
http://dx.doi.org/10.1136/lupus-2017-000246
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author Iwamoto, Taro
Dorschner, Jessica
Jolly, Meenakshi
Huang, Xiangyang
Niewold, Timothy B
author_facet Iwamoto, Taro
Dorschner, Jessica
Jolly, Meenakshi
Huang, Xiangyang
Niewold, Timothy B
author_sort Iwamoto, Taro
collection PubMed
description OBJECTIVE: The type I interferon pathway is activated in many patients with systemic lupus erythematosus (SLE), and anti-double-stranded DNA (dsDNA) and anti-RNA binding protein autoantibodies are correlated with high interferon-α (IFNα) activity. We studied whether antiphospholipid (APL) antibodies, which should not stimulate Toll-like receptors, are also associated with high levels of IFNα activity. METHODS: Serum IFNα activity was measured in patients with SLE using the WISH cell bioassay. IgG APL, anti-RBP and anti-dsDNA antibodies were measured in the clinical laboratory, and standard clinical cut-offs were used to define the positive results. RESULTS: High IFNα activity was associated with anti-RBP and anti-dsDNA antibodies in all three ancestral backgrounds. Strikingly, African-American subjects with a positive APL antibody test had higher IFNα activity than those without IgG APL antibodies. This was not shared with other ancestral backgrounds. This finding was independent of other autoantibody profiles, and clinical features did not differ between IgG APL antibody positive versus negative African-American patients. CONCLUSION: The difference in association between IFNα activity and IgG APL status between ancestral backgrounds supports differences in molecular pathogenesis. This may suggest B cell hyperactivity in the setting of type I IFN in African-Americans and could suggest ways to individualise therapy.
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spelling pubmed-57869062018-01-31 Associations between type I interferon and antiphospholipid antibody status differ between ancestral backgrounds Iwamoto, Taro Dorschner, Jessica Jolly, Meenakshi Huang, Xiangyang Niewold, Timothy B Lupus Sci Med Brief Communication OBJECTIVE: The type I interferon pathway is activated in many patients with systemic lupus erythematosus (SLE), and anti-double-stranded DNA (dsDNA) and anti-RNA binding protein autoantibodies are correlated with high interferon-α (IFNα) activity. We studied whether antiphospholipid (APL) antibodies, which should not stimulate Toll-like receptors, are also associated with high levels of IFNα activity. METHODS: Serum IFNα activity was measured in patients with SLE using the WISH cell bioassay. IgG APL, anti-RBP and anti-dsDNA antibodies were measured in the clinical laboratory, and standard clinical cut-offs were used to define the positive results. RESULTS: High IFNα activity was associated with anti-RBP and anti-dsDNA antibodies in all three ancestral backgrounds. Strikingly, African-American subjects with a positive APL antibody test had higher IFNα activity than those without IgG APL antibodies. This was not shared with other ancestral backgrounds. This finding was independent of other autoantibody profiles, and clinical features did not differ between IgG APL antibody positive versus negative African-American patients. CONCLUSION: The difference in association between IFNα activity and IgG APL status between ancestral backgrounds supports differences in molecular pathogenesis. This may suggest B cell hyperactivity in the setting of type I IFN in African-Americans and could suggest ways to individualise therapy. BMJ Publishing Group 2018-01-13 /pmc/articles/PMC5786906/ /pubmed/29387437 http://dx.doi.org/10.1136/lupus-2017-000246 Text en © Article author(s) (or their employer(s) unless otherwise stated in the text of the article) 2018. All rights reserved. No commercial use is permitted unless otherwise expressly granted. This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/
spellingShingle Brief Communication
Iwamoto, Taro
Dorschner, Jessica
Jolly, Meenakshi
Huang, Xiangyang
Niewold, Timothy B
Associations between type I interferon and antiphospholipid antibody status differ between ancestral backgrounds
title Associations between type I interferon and antiphospholipid antibody status differ between ancestral backgrounds
title_full Associations between type I interferon and antiphospholipid antibody status differ between ancestral backgrounds
title_fullStr Associations between type I interferon and antiphospholipid antibody status differ between ancestral backgrounds
title_full_unstemmed Associations between type I interferon and antiphospholipid antibody status differ between ancestral backgrounds
title_short Associations between type I interferon and antiphospholipid antibody status differ between ancestral backgrounds
title_sort associations between type i interferon and antiphospholipid antibody status differ between ancestral backgrounds
topic Brief Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5786906/
https://www.ncbi.nlm.nih.gov/pubmed/29387437
http://dx.doi.org/10.1136/lupus-2017-000246
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