Abstract |
Psoriasis is associated with atherosclerosis, in which circulating microparticles play an important role. In severe psoriasis, there was an increase of endothelial- and platelet- microparticles which could be decreased by anti-TNFα. However, whether anti- IL-12/23 treatment would decrease the level of microparticles remains unknown. Our study showed that, despite the clinical improvement of psoriasis after IL-12/13 blockage, the increased levels of circulating CD41a and CD31 microparticles were unchanged after anti- IL-12/23. This result suggested that anti- IL12/23 treatment may not alter the development of cardiovascular disease in patients with psoriasis.
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Authors | Ji-Chen Ho, Chih-Hung Lee, Shang-Hung Lin |
Journal | BioMed research international
(Biomed Res Int)
Vol. 2016
Pg. 3242143
( 2016)
ISSN: 2314-6141 [Electronic] United States |
PMID | 27144162
(Publication Type: Clinical Trial, Journal Article)
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Chemical References |
- Interleukin-12 Subunit p40
- Ustekinumab
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Topics |
- Adult
- Aged
- Blood Platelets
(drug effects, immunology, pathology)
- Cell-Derived Microparticles
(drug effects, immunology, pathology)
- Endothelial Progenitor Cells
(drug effects, immunology, pathology)
- Female
- Humans
- Interleukin-12 Subunit p40
(immunology)
- Male
- Middle Aged
- Psoriasis
(blood, immunology, therapy)
- Treatment Outcome
- Ustekinumab
(administration & dosage, immunology)
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