Increased Th17 response to myelin peptides in pediatric MS

被引:22
|
作者
Vargas-Lowy, David [1 ]
Kivisaekk, Pia [1 ]
Gandhi, Roopali [1 ]
Raddassi, Khadir [1 ]
Soltany, Pejvak [1 ]
Gorman, Mark P. [2 ,3 ]
Khoury, Samia J. [1 ]
Chitnis, Tanuja [1 ,3 ]
机构
[1] Brigham & Womens Hosp, Ctr Neurol Dis, Boston, MA 02115 USA
[2] Childrens Hosp, Dept Neurol, Boston, MA USA
[3] Massachusetts Gen Hosp Children, Partners Pediat MS Ctr, Boston, MA USA
关键词
Multiple sclerosis; Th17; Pediatric; Myelin; T cell; T-CELL SUBSETS; MULTIPLE-SCLEROSIS; INTERLEUKIN-7; RECEPTOR; DIAGNOSTIC-CRITERIA; CENTRAL MEMORY; CHILDHOOD; ONSET; DISEASE; RISK; EXPRESSION;
D O I
10.1016/j.clim.2012.12.008
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Studies of the underlying immune mechanisms of multiple sclerosis (MS) in children may shed light on the initial events of MS pathogenesis. We studied T cell responses to myelin peptides in 10 pediatric MS patients (PMS), 10 pediatric healthy controls (PHC), 10 adult MS patients (AMS) and 10 adult healthy controls (AHC). A significantly higher proportion of divided CD4+ T cell responses in response to myelin peptides by the CFSE assay in PMS compared to PHC at both concentrations of myelin peptide tested (t test, 95% CI, p = 0.0067 for MP1; p = 0.0086 for MP10), and between PMS and AMS (p = 0.0012 at 1 mu g/mL of myelin peptides, p<0.0001 at 10 mu g/mL) was found. In addition, T cells with a central memory phenotype producing IL-17 were increased in PMS compared to PHC (p<0.05). IL-7 levels in culture supernatants were elevated in PMS compared to PHC and AMS (t test<0.01). (C) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:176 / 184
页数:9
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