Kawasaki disease: A maturational defect in immune responsiveness

被引:46
作者
Kuijpers, TW
Wiegman, A
van Lier, RAW
Roos, MTL
Wertheim-van Dillen, PME
Pinedo, S
Ottenkamp, J
机构
[1] Emma Childrens Hosp, Acad Med Ctr, NL-1105 AZ Amsterdam, Netherlands
[2] Acad Med Ctr, Dept Virol, NL-1105 AZ Amsterdam, Netherlands
[3] Netherlands Red Cross, Blood Transfus Serv, Cent Lab, Dept Clin Viroimmunol, Amsterdam, Netherlands
关键词
D O I
10.1086/315111
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Kawasaki disease (KD), an acute febrile disease in children of unknown etiology, is characterized by a vasculitis that may result in coronary artery aneurysms (CAAs). In new patients with KD, a selective and prolonged T cell unresponsiveness to activation via the T cell antigen receptor CD3 was observed, whereas proliferation to other stimuli was intact. This "split T cell anergy" delineated KD from other pediatric infections and autoimmune diseases and correlated with CAA formation (P < .001), A transient immune dysfunction was also suggested by an incomplete responsiveness to measles-mumps-rubella (MMR) vaccination in patients with KD versus controls (P < .0001; odds ratio, 15.6; 95% confidence interval, 4.8-51.1), which was overcome by revaccination(s), The reduced responsiveness to MMR in patients with KD suggests a subtle and predetermining immune dysfunction, An inherent immaturity to dear certain antigens may be an important cause that precipitates KD and the immune dysregulation during acute disease.
引用
收藏
页码:1869 / 1877
页数:9
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