Selective depletion of Vβ2+CD8+ T cells in peripheral blood from rheumatic heart disease patients

被引:10
作者
Carrión, F
Fernandez, M
Iruretagoyena, M
Andrade, LEC
Odete-Hilário, M
Figueroa, F
机构
[1] Univ Los Andes, Fac Med, Santiago, Chile
[2] Pontificia Univ Catolica Chile, Fac Med, Santiago, Chile
[3] Hosp Sao Paulo, Escola Paulista Med, Sao Paulo, Brazil
关键词
rheumatic heart disease; rheumatic fever; superantigens; T cells; T-cell receptor;
D O I
10.1016/S0896-8411(03)00002-7
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Acute rheumatic fever (ARF) and its chronic valvular sequelae are the delayed consequence of a pharyngeal infection with group A Streptococcus (GAS). Several GAS proteins have been shown to be superantigens, raising the possibility that the expansion or deletion of T cells expressing specific Vbeta regions might play a role in the pathogenesis of ARF or chronic rheumatic heart disease (RHD). We therefore analyzed by four-color flow cytometry, the V repertoire on CD3, CD4 and CD8 T cells from four ARF patients, 10 RHD patients and also nine healthy controls. A selective depletion of Vbeta2+ T cells was found only in the CD8 subset of chronic RHD patients. This is of interest since a number of GAS superantigens exert their effects on Vbeta2+ cells and because only CD8+ T cells from ARF and RHD patients undergo anergy in response to GAS superantigens. Our results suggests that an ongoing immune process is present in RHD patients and that CD8+ T cells may have an important immunoregulatory role in the pathogenesis of the disease. (C) 2003 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:183 / 190
页数:8
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