Rheumatology Division, Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo (USP), São Paulo, Brazil.
Rheumatol Int. 2013 May;33(5):1149-57. doi: 10.1007/s00296-012-2504-3. Epub 2012 Sep 6.
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.
抗 EB 病毒早期抗原弥散抗体(抗-EA-D)与病毒复制有关。然而,它们与原发性干燥综合征(pSS)的临床/治疗特征的可能关联尚未确定。我们评估了 100 例 pSS 患者(欧洲美国风湿病学会标准)和 89 名年龄、性别、种族相匹配的健康对照者。疾病活动度采用 EULAR 干燥综合征疾病活动指数(ESSDAI)进行评估。通过酶联免疫吸附试验(ELISA)检测抗 EBV(抗-VCA IgG/IgM、抗-EBNA-1 IgG、抗-EA-D IgG)。患者和对照组的抗-VCA IgG 频率和平均水平相当(90%对 86.5%,p=0.501;2.6±1.1 对 2.5±1.1 AU/mL,p=0.737)和抗-EBNA-1 IgG(92%对 94.4%,p=0.576;141.3±69.8 对 135.6±67.5 RU/mL,p=0.464)。所有病例的抗-VCA IgM 均为阴性。值得注意的是,与对照组相比,患者的抗-EA-D 频率更高,平均水平也更高(36%对 4.5%,p<0.0001;38.6±57.4 对 7.9±26.3 RU/mL,p<0.0001)。对有(n=36)和无(n=64)抗-EA-D 的患者进行进一步分析,发现年龄、性别、种族(p≥0.551)、当前泼尼松剂量(4.8±6.9 对 5.1±10.4 mg/天,p=0.319)和当前使用泼尼松(52.8%对 37.5%,p=0.148)和免疫抑制剂(44.4%对 31.3%,p=0.201)相当。 ESSDAI 值相当(p=0.102),但抗-EA-D 阳性患者的关节活动更频繁(25%对 9.4%,p=0.045)。抗-EA-D 抗体与抗 Ro/SSA(p=1.000)、抗-La/SSB(p=0.652)、类风湿因子(p=1.000)、抗-α-原纤维(p=0.390)或抗磷脂抗体(p=0.573)无关,这表明不存在交叉反应。与关节活动相关的抗-EA-D 频率升高提示亚临床 EBV 再激活可能引发或持续 pSS 的关节受累。