Serum type I interferon activity is dependent on maternal diagnosis in anti-SSA/Ro-positive mothers of children with neonatal lupus

被引:66
作者
Niewold, Timothy R. [1 ,2 ]
Rivera, Tania L. [3 ]
Buyon, Jill P. [3 ]
Crow, Mary K. [2 ]
机构
[1] Univ Chicago, Rheumatol Sect, Chicago, IL 60637 USA
[2] Hosp Special Surg, New York, NY 10021 USA
[3] Hosp Joint Dis & Med Ctr, New York, NY USA
来源
ARTHRITIS AND RHEUMATISM | 2008年 / 58卷 / 02期
关键词
D O I
10.1002/art.23191
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective. The type I interferon (IFN) pathway is activated in many patients with systemic lupus erythematosus (SLE), and high serum levels of IFN are associated with anti-SSA/Ro autoantibodies. To investigate the clinical features associated with type I IFN production in vivo, we compared serum IFN activity in individuals with anti-SSA/Ro antibodies who were asymptomatic with that in individuals with clinical manifestations of SLE or Sjogren's syndrome (SS). Methods. Antibody-positive sera from 84 mothers of children with manifestations of neonatal lupus were studied for type I IFN activity, using a functional reporter cell assay. Maternal health status was characterized as asymptomatic, SS, SLE, pauci-SLE, or pauci-SS, based on a screening questionnaire, telephone interview, and review of medical records. The prefix "pauci-" indicates symptoms insufficient for a formal classification of the disease. Results. Only 4% of asymptomatic mothers had high serum type I IFN activity, compared with 73% with pauci-SLE (P = 5.7 X 10(-5)) 35% with SLE (P = 0.011), and 32% of patients with SS (P = 0.032). One of the 4 patients with pauci-SS had high levels of IFN. The majority of patients for whom longitudinal data were available had stable type I IFN activity over time, and changes in IFN activity were not clearly accompanied by changes in the clinical diagnosis. Conclusion. Patients with SLE, patients with pauci-SLE, and patients with SS are more likely to have high serum IFN activity than asymptomatic individuals with SSA/Ro autoantibodies, suggesting that these autoantibodies are insufficient for activation of the type I IFN pathway, and that disease-specific factors are important for type I IFN generation in vivo.
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页码:541 / 546
页数:6
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