Division of Allergy, Immunology and Rheumatology, Taichung Veterans General Hospital and Faculty of Medicine, National Yang-Ming University, Taiwan.
Clin Chim Acta. 2012 May 18;413(9-10):855-60. doi: 10.1016/j.cca.2012.01.027. Epub 2012 Jan 27.
Human parvovirus B19 (B19) infection has been reported as a possible cause of autoimmune diseases. The association of B19 infection with adult-onset Still's diseases (AOSD) remains unclear.
IgM and IgG against B19-VP1/2 were determined using ELISA in 86 patients with AOSD, 58 patients with systemic lupus erythematosus (SLE) and 64 healthy controls. Anti-B19-VP1-unique region (VP1u) and anti-B19-nonstructural protein-1(NS1) antibodies were assessed by Western blot. B19 DNA was detected by nested PCR.
Forty-three (50.0%) of 86 AOSD patients, 27 (46.6%) of 58 SLE patients and 30 (46.9%) of 64 controls had positivity for anti-B19-VP1/2-IgG in the absence of anti-B19-VP1/2-IgM, indicating past infection. None of enrolled subjects had detectable circulating B19 DNA. Significantly higher positivity rates for anti-B19-VP1u and anti-B19-NS1 IgG were observed in AOSD patients (39.5% and 46.5% respectively) and SLE patients (34.5% and 36.2% respectively) than in healthy controls (14.1%, p<0.005 for AOSD and p<0.05 for SLE, and 15.6%, p<0.001 for AOSD and p<0.05 for SLE; respectively). AOSD patients and SLE patients with seropositive results for anti-B19-VP1/2 IgG, anti-B19-VP1u or anti-B19-NS1 antibodies had a higher frequency of leucopenia and thrombocytopenia when compared to those with seronegative results. AOSD patients with anti-B19-VP1u or anti-B19-NS1 antibodies were more likely to have arthritis in comparison with those without these antibodies.
Higher seroreactivity for anti-B19-VP1u and anti-B19-NS1 IgG were associated with cytopenia in both AOSD and SLE patients with unique correlation to arthritis in the AOSD. Further studies are necessary to determine if these responses correlate with a common genetic risk in patients with AOSD and SLE.
人类细小病毒 B19(B19)感染已被报道为自身免疫性疾病的可能病因。B19 感染与成人斯蒂尔病(AOSD)的关联尚不清楚。
采用酶联免疫吸附试验(ELISA)检测 86 例 AOSD 患者、58 例系统性红斑狼疮(SLE)患者和 64 名健康对照者的 B19-VP1/2 抗体 IgM 和 IgG。采用 Western blot 检测抗 B19-VP1 独特区(VP1u)和抗 B19-非结构蛋白-1(NS1)抗体。采用巢式 PCR 检测 B19 DNA。
86 例 AOSD 患者中有 43 例(50.0%)、58 例 SLE 患者中有 27 例(46.6%)和 64 例对照者中有 30 例(46.9%)抗 B19-VP1/2-IgG 阳性而无抗 B19-VP1/2-IgM,表明既往感染。所有纳入的研究对象均未检测到循环 B19 DNA。AOSD 患者(分别为 39.5%和 46.5%)和 SLE 患者(分别为 34.5%和 36.2%)抗 B19-VP1u 和抗 B19-NS1 IgG 阳性率显著高于健康对照者(分别为 14.1%,p<0.005 对于 AOSD 和 p<0.05 对于 SLE,以及 15.6%,p<0.001 对于 AOSD 和 p<0.05 对于 SLE;分别)。与抗 B19-VP1/2 IgG 血清阴性结果相比,抗 B19-VP1/2 IgG、抗 B19-VP1u 或抗 B19-NS1 抗体血清阳性的 AOSD 患者和 SLE 患者白细胞减少症和血小板减少症的发生率更高。与无这些抗体的患者相比,抗 B19-VP1u 或抗 B19-NS1 抗体的 AOSD 患者更有可能发生关节炎。
在 AOSD 和 SLE 患者中,抗 B19-VP1u 和抗 B19-NS1 IgG 的血清反应性更高与血细胞减少症相关,且与 AOSD 关节炎具有独特相关性。需要进一步研究以确定这些反应是否与 AOSD 和 SLE 患者的共同遗传风险相关。