Department of Ophthalmology, Scheie Eye Institute, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA.
Department of Rheumatology, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA.
Cornea. 2019 Dec;38(12):1500-1505. doi: 10.1097/ICO.0000000000002147.
To evaluate the prevalence of novel candidate autoantibodies associated with Sjögren syndrome (SS) and their ability to identify those with SS among participants with dry eye enrolled in the Sjögren's International Collaborative Clinical Alliance (SICCA) study at the University of Pennsylvania (Penn).
All participants previously underwent a full ocular and systemic evaluation for possible SS as part of the SICCA study. An enzyme-linked immunosorbent assay was used to detect IgG, IgA, and IgM autoantibodies to salivary protein 1 (SP-1), parotid secretory protein (PSP), and carbonic anhydrase 6 from previously banked baseline serum samples from SICCA study participants enrolled at Penn. The prevalence rate of each autoantibody, calculated by considering the presence of any isotype as antibody positive, was compared between participants with dry eye with SS (n = 81) or without SS (n = 129) using the Fisher exact test.
The prevalence of SP-1 IgM autoantibodies was higher in those with SS compared with those without SS (14% vs. 5%; P = 0.03). Similarly, the prevalence of PSP IgA autoantibodies was higher in those with SS compared with non-SS dry eye participants (21% vs. 11%; P = 0.048). There was no statistically significant difference in the prevalence of carbonic anhydrase 6 autoantibodies between those with or without SS (15% vs. 20%; P = 0.36).
In the Penn SICCA cohort, SP-1 IgM and PSP IgA autoantibodies were more prevalent in the serum of SS-related dry eye participants compared with those without SS. Further longitudinal studies are needed to determine the clinical significance of these findings.
评估与干燥综合征(SS)相关的新型候选自身抗体的流行情况及其在宾夕法尼亚大学(Penn)Sjögren 国际合作临床联盟(SICCA)研究中招募的干眼症参与者中识别 SS 患者的能力。
所有参与者先前都接受了全面的眼部和全身评估,以确定是否可能患有 SS,这是 SICCA 研究的一部分。采用酶联免疫吸附试验检测先前从 SICCA 研究参与者的基线血清样本中储存的唾液蛋白 1(SP-1)、腮腺分泌蛋白(PSP)和碳酸酐酶 6 的 IgG、IgA 和 IgM 自身抗体。通过考虑任何同种型作为抗体阳性,计算每种自身抗体的患病率,并使用 Fisher 确切检验比较 SS(n = 81)或非 SS(n = 129)干眼症参与者之间的患病率。
与非 SS 干眼症参与者相比,SS 患者的 SP-1 IgM 自身抗体患病率更高(14%比 5%;P = 0.03)。同样,SS 患者的 PSP IgA 自身抗体患病率也高于非 SS 干眼症参与者(21%比 11%;P = 0.048)。SS 患者与非 SS 患者之间,碳酸酐酶 6 自身抗体的患病率没有统计学差异(15%比 20%;P = 0.36)。
在 Penn SICCA 队列中,与非 SS 患者相比,SS 相关干眼症患者的血清中 SP-1 IgM 和 PSP IgA 自身抗体更为常见。需要进一步的纵向研究来确定这些发现的临床意义。