Dietary gluten triggers concomitant activation of CD4+ and CD8+ αβ T cells and γδ T cells in celiac disease

被引:156
作者
Han, Arnold [1 ,2 ]
Newell, Evan W. [2 ,3 ]
Glanville, Jacob [4 ]
Fernandez-Becker, Nielsen [1 ]
Khosla, Chaitan [5 ,6 ]
Chien, Yueh-hsiu [2 ,4 ]
Davis, Mark M. [2 ,4 ,7 ]
机构
[1] Agcy Sci Technol & Res, Dept Med, Div Gastroenterol, Singapore 138648, Singapore
[2] Agcy Sci Technol & Res, Dept Microbiol & Immunol, Singapore 138648, Singapore
[3] Agcy Sci Technol & Res, Singapore Immunol Network, Singapore 138648, Singapore
[4] Stanford Univ, Sch Med, Inst Immun Transplantat & Infect, Stanford, CA 94305 USA
[5] Stanford Univ, Sch Med, Dept Chem, Stanford, CA 94305 USA
[6] Stanford Univ, Sch Med, Dept Chem Engn, Stanford, CA 94305 USA
[7] Stanford Univ, Sch Med, Howard Hughes Med Inst, Stanford, CA 94305 USA
基金
美国国家卫生研究院;
关键词
autoimmunity; mucosal immunity; INTRAEPITHELIAL LYMPHOCYTES; TISSUE TRANSGLUTAMINASE; INTESTINAL-MUCOSA; CD8-T-CELL MEMORY; CD4-T-CELL HELP; INFLUENZA-VIRUS; RECEPTOR; GLIADIN; MICE; EXPRESSION;
D O I
10.1073/pnas.1311861110
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Celiac disease is an intestinal autoimmune disease driven by dietary gluten and gluten-specific CD4(+) T-cell responses. In celiac patients on a gluten-free diet, exposure to gluten induces the appearance of gluten-specific CD4(+) T cells with gut-homing potential in the peripheral blood. Here we show that gluten exposure also induces the appearance of activated, gut-homing CD8(+) alpha beta and gamma delta T cells in the peripheral blood. Single-cell T-cell receptor sequence analysis indicates that both of these cell populations have highly focused T-cell receptor repertoires, indicating that their induction is antigen-driven. These results reveal a previously unappreciated role of antigen in the induction of CD8(+) alpha beta and gamma delta T cells in celiac disease and demonstrate a coordinated response by all three of the major types of T cells. More broadly, these responses may parallel adaptive immune responses to viral pathogens and other systemic autoimmune diseases.
引用
收藏
页码:13073 / 13078
页数:6
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