EBV reactivation serological profile in primary Sjögren’s syndrome: an underlying trigger of active articular involvement?
Antibody to Epstein–Barr virus (EBV) early antigen diffuse (anti-EA-D) is associated with viral replication. However, their possible associations with clinical/therapeutic features in primary Sjögren’s syndrome (pSS) were not established. We evaluated 100 pSS patients (American–European Criteria) an...
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Published in | Rheumatology international Vol. 33; no. 5; pp. 1149 - 1157 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Berlin/Heidelberg
Springer-Verlag
01.05.2013
Springer Nature B.V |
Subjects | |
Online Access | Get full text |
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Summary: | Antibody to Epstein–Barr virus (EBV) early antigen diffuse (anti-EA-D) is associated with viral replication. However, their possible associations with clinical/therapeutic features in primary Sjögren’s syndrome (pSS) were not established. We evaluated 100 pSS patients (American–European Criteria) and 89 age/gender/ethnicity-matched healthy controls. Disease activity was measured by EULAR Sjögren’s Syndrome Disease Activity Index (ESSDAI). Antibodies to EBV (anti-VCA IgG/IgM, anti-EBNA-1 IgG, anti-EA-D IgG) were determined by ELISA. Patients and controls had comparable frequencies and mean levels of anti-VCA IgG (90 vs. 86.5 %,
p
= 0.501; 2.6 ± 1.1 vs. 2.5 ± 1.1 AU/mL,
p
= 0.737) and anti-EBNA-1 IgG (92 vs. 94.4 %,
p
= 0.576; 141.3 ± 69.8 vs. 135.6 ± 67.5 RU/mL,
p
= 0.464). Anti-VCA IgM was negative in all cases. Noteworthy, higher frequency and increased mean levels of anti-EA-D were observed in patients than controls (36 vs. 4.5 %,
p
< 0.0001; 38.6 ± 57.4 vs. 7.9 ± 26.3 RU/mL,
p
< 0.0001). Further analysis of patients with (
n
= 36) and without (
n
= 64) anti-EA-D revealed comparable age/gender/ethnicity (
p
≥ 0.551), current prednisone dose (4.8 ± 6.9 vs. 5.1 ± 10.4 mg/day,
p
= 0.319), and current uses of prednisone (52.8 vs. 37.5 %,
p
= 0.148) and immunosuppressants (44.4 vs. 31.3 %,
p
= 0.201). ESSDAI values were comparable (
p
= 0.102), but joint activity was more frequent (25 vs. 9.4 %,
p
= 0.045) in anti-EA-D positive patients. Anti-EA-D antibodies were not associated with anti-Ro/SSA (
p
= 1.000), anti-La/SSB (
p
= 0.652), rheumatoid factor (
p
= 1.000), anti-α-fodrin (
p
= 0.390) or antiphospholipid antibodies (
p
= 0.573), not suggesting cross-reactivity. The higher anti-EA-D frequency associated with joint activity raises the possibility that a subclinical EBV reactivation may trigger or perpetuate the articular involvement in pSS. |
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ISSN: | 0172-8172 1437-160X |
DOI: | 10.1007/s00296-012-2504-3 |