Identification of Streptococcal M-Protein Cardiopathogenic Epitopes in Experimental Autoimmune Valvulitis

被引:36
|
作者
Kirvan, Christine A. [1 ]
Galvin, Jeffrey E. [2 ]
Hilt, Silvia [1 ]
Kosanke, Stanley [3 ]
Cunningham, Madeleine W. [4 ]
机构
[1] Calif State Univ Sacramento, Dept Biol Sci, Sacramento, CA 95819 USA
[2] Zoetis, Lincoln, NE USA
[3] Univ Oklahoma, HSC, Dept Pathol, Oklahoma City, OK 73104 USA
[4] Univ Oklahoma, Biomed Res Ctr, HSC, Dept Microbiol & Immunol, Oklahoma City, OK 73104 USA
关键词
Autoimmunity; Rheumatic heart disease; T cells; M protein; RHEUMATIC HEART-DISEASE; T-CELL-CLONES; INTERMOUNTAIN AREA; MOLECULAR ANALYSIS; FEVER; MIMICRY; MYOSIN; INDUCTION; PATHOGENESIS; RECOGNITION;
D O I
10.1007/s12265-013-9526-4
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The M protein of rheumatogenic group A streptococci induces carditis and valvulitis in Lewis rats and may play a role in pathogenesis of rheumatic heart disease. To identify the epitopes of M5 protein that produce valvulitis, synthetic peptides spanning A, B, and C repeat regions contained within the extracellular domain of the streptococcal M5 protein were investigated. A repeat region peptides NT4, NT5/6, and NT7 induced valvulitis similar to the intact pepsin fragment of M5 protein. T cell lines from rats with valvulitis recognized M5 peptides NT5/6 and NT6. Passive transfer of an NT5/6-specific T cell line into na < ve rats produced valvulitis characterized by infiltration of CD4+ cells and upregulation of VCAM-1, while an NT6-specific T cell line did not target the valve. Our new data suggests that M protein-specific T cells may be important mediators of valvulitis in the Lewis rat model of rheumatic carditis.
引用
收藏
页码:172 / 181
页数:10
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