Peripheral follicular cytotoxic T -like cells in Kawasaki disease with coronary artery aneurysms A case report

被引:3
作者
Xu, Meng [1 ]
Liu, Jinxiang [1 ]
Pan, Lu [1 ]
Yang, Sirui [1 ]
机构
[1] First Hosp Jilin Univ, Dept Pediat Rheumatol Immunol & Allergy, Changchun 130021, Peoples R China
关键词
coronary artery aneurysm; follicular cytotoxic T cells; Kawasaki disease;
D O I
10.1097/MD.0000000000023714
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction: Kawasaki disease (KD) is the leading cause of acquired heart abnormalities during childhood. The infiltration of CD8+ T cells plays an essential role in the formation of coronary aneurysms. Follicular cytotoxic T (Tfc) cells are a newly defined subset of CD8+ T cells that express CXC-chemokine receptor 5. The role of Tfc cells in KD is unclear. However, in this report, we present 2 KD children with sustained coronary artery aneurysms (CAA), and we found that their peripheral C-X-C Chemokine Receptor 5+ T cells contained quite amounts of CD4 negative cells. Importantly, these cells have never been reported in KD. Patients concerns: Case 1 was a 3-year-old boy with a complaint of continuous fever for 6 days and conjunctival injection for 3 days. Case 2 was a 6-month-old boy who was hospitalized because of persistent fever for 5 days, rashes and conjunctival injection for 1 day. Diagnosis: Case 1 was diagnosed with KD according to typical symptoms and signs including fever over 5 days, conjunctival injection, rashes, swelling cervical lymph nodes and a strawberry tongue. Case 2 had atypical symptoms including persistent fever for 5 days, rashes and conjunctival injection, and he was diagnosed with KD based on the echocardiographic findings. Intervention: Both the 2 patients received intravenous immunoglobulin and oral aspirin. Besides, case 1 was given the second infusion of intravenous immunoglobulin, intravenous prednisolone and low-molecular-weight heparin. Outcomes: The CAA of case 1 did not regress until the 12th month after disease onset. The CAA of patient 2 began to regress at the third month after disease onset. During the months from disease onset to the recent follow-up, no cardiovascular events had occurred. Conclusions: We speculate that Tfc cells may be associated with the formation of CAA. Further studies with larger sample size and functional analysis of these cells are needed.
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