HLA restriction patterns of gliadin- and astrovirus-specific CD4+ T cells isolated in parallel from the small intestine of celiac disease patients

被引:20
作者
Molberg, O [1 ]
Lundin, KEA
Nilsen, EM
Scott, H
Kett, K
Brandtzaeg, P
Thorsby, E
Sollid, LM
机构
[1] Univ Oslo, Natl Hosp Norway, Inst Transplantat Immunol, N-0027 Oslo, Norway
[2] Univ Oslo, Ullevaal Hosp, Dept Gastroenterol, N-0407 Oslo, Norway
[3] Univ Oslo, Natl Hosp Norway, Inst Pathol, Lab Immunohistochem & Immunopathol, N-0027 Oslo, Norway
[4] Univ Oslo, Natl Hosp Norway, Dept Med A, Gastroenterol Unit, N-0027 Oslo, Norway
来源
TISSUE ANTIGENS | 1998年 / 52卷 / 05期
关键词
astrovirus; celiac disease; gliadin; immunity; mucosa; T lymphocyte;
D O I
10.1111/j.1399-0039.1998.tb03066.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Celiac disease is a common HLA-DQ2-associated enteropathy caused by an abnormal T-cell-mediated immune response to ingested wheat gliadin proteins. We have previously isolated in situ activated mucosal T cells from celiac disease patients and demonstrated that these T cells were gliadin specific and predominantly DQ2 restricted. In contrast to this, gliadin-specific T cells isolated from peripheral blood display a variable HLA restriction pattern, thereby indicating that the skewed DQ restriction of T cells resident in the celiac lesions could be dictated by a preference for DQ-mediated antigen presentation in the mucosa of CD patients. To address this, we analyzed the HLA restriction of T cells recognizing astrovirus, a common gastroentetitis virus, isolated from intestinal mucosa of six celiac disease patients. As an internal control, gliadin-specific T cells were isolated and analyzed in parallel. The gliadin-specific mucosal T cells were marked in their DQ2 restriction, whereas the parallel astrovirus-specific T cells were predominantly restricted by DR molecules, Our data indicate that the repertoire of T cells present in celiac lesions is determined by the priming antigen(s) and not by a skewing in the expression of functional HLA class II isotypes in the disease affected small intestinal mucosa.
引用
收藏
页码:407 / 415
页数:9
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