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  •   Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
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  •   Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
  • Επιστημονικές Δημοσιεύσεις Μελών ΠΘ (ΕΔΠΘ)
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Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
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Increased immunoreactivity against human cytomegalovirus UL83 in systemic sclerosis

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Συγγραφέας
Marou E., Liaskos C., Efthymiou G., Dardiotis E., Daponte A., Scheper T., Meyer W., Hadjigeorgiou G., Bogdanos D.P., Sakkas L.I.
Ημερομηνία
2017
Γλώσσα
en
Λέξη-κλειδί
autoantibody
centromere protein A
centromere protein B
Cytomegalovirus antibody
DNA directed RNA polymerase III
fibrillarin
immunoglobulin G antibody
Ku antigen
platelet derived growth factor receptor
protein NOR90
protein PM Scl100
protein PM Scl75
protein Ro52
protein RP11
protein RP155
scl 70 antibody
unclassified drug
autoantibody
cytomegalovirus matrix protein 65kDa
matrix protein
phosphoprotein
adult
age distribution
aged
antibody detection
Article
clinical feature
controlled study
female
human
Human cytomegalovirus
immunoassay
immunoreactivity
lung fibrosis
major clinical study
male
multiple sclerosis
priority journal
protein expression
sex difference
systemic sclerosis
very elderly
Western blotting
blood
immunology
middle aged
multiple sclerosis
systemic sclerosis
Adult
Aged
Aged, 80 and over
Autoantibodies
Female
Humans
Male
Middle Aged
Multiple Sclerosis
Phosphoproteins
Scleroderma, Systemic
Viral Matrix Proteins
Clinical and Experimental Rheumatology S.A.S.
Εμφάνιση Μεταδεδομένων
Επιτομή
Objective. To study immunoreactivity against human cytomegalovirus (HCMV) in systemic sclerosis (SSc), since HCMV has been put forward as a candidate infectious cause. Methods. Eighty four patients with SSc (67 females; median age 60 years, range 25-81), 30 patients with multiple sclerosis (MS) (23 females; median age 44, range 20-69 years) and 28 healthy controls (NCs), all pre-tested positive for IgG anti-HCMV antibodies, were studied. IgG anti-UL83 HCMV antibodies were tested by western immunoblotting and expressed in arbitrary units (AUs). Reactivity to UL83 HCMV was assessed in relation to clinical manifestations and SSc-related autoantibodies (autoAbs), tested by an IgG SSc autoantibody profile line immunoassay (Euroimmun) that detects autoAbs against Scl-70, CENPA, CENPB, RNA polymerase III subunit 11 (RP11), RP155, fibrillarin, NOR90, Th/To, PM-Scl100, PM-Scl75, Ku, PDGFR and Ro-52. Results. Fifty patients (59.5%) were anti-UL83 clear positive (UL83+), including 21/40 (52.5%) lcSSc and 29/44 (65.6%) dcSSc, compared to 15/30 (50%) patients with MS (SSc vs MS, p=ns and 11/28 (39.29%) of NCs (SSc vs NC, p=ns MS vs NC, p=ns). Anti- UL83 antibody AU levels (mean±SD) were higher in SSc (64.3 ± 26) compared to MS (49.1±21.6, p=0.05) or NCs (40.4±13.7, p < 0.001; MS vs NCs, p=ns) and were associated with pulmonary fibrosis. Conclusion. Immunoreactivity to UL83 HCMV is frequent and strong in patients with SSc, implying a possible pathogenic role for this disease. © Clinical and Experimental Rheumatology 2017.
URI
http://hdl.handle.net/11615/76392
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  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ. [19735]

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