Generation of anergic and potentially immunoregulatory CD25+CD4 T cells in vivo after induction of peripheral tolerance with intravenous or oral antigen

被引:354
作者
Thorstenson, KM [1 ]
Khoruts, A [1 ]
机构
[1] Univ Minnesota, Ctr Immunol, Div Gastroenterol, Dept Med, Minneapolis, MN 55455 USA
关键词
D O I
10.4049/jimmunol.167.1.188
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Immunoregulatory CD25(+)CD4 T cells are thought to arise from the thymus as a distinct lineage of CD4 T cells specific for self Ags. We used the DO11.10 TCR transgenic adoptive transfer system to show that cells of similar phenotype may also arise in the course of peripheral tolerance induction. Such cells emerged within 1 wk following Ag exposure and correlated negatively with the number of initial cell divisions. Limiting i.v. Ag dose or using an oral tolerance protocol yielded the greatest numbers of Ag-specific CD25(+)CD4 T cells. In contrast, immunogenic Ag exposure in the presence of an adjuvant did not lead to emergence of CD25(+)CD4 T cells. The profound anergic phenotype of these cells and their potential immunoregulatory properties make them an especially desirable population to induce in the course of immunotherapy in numerous clinical settings. This experimental system may be useful in future studies designed to optimize immunologic tolerance induction.
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收藏
页码:188 / 195
页数:8
相关论文
共 33 条
[11]   A natural immunological adjuvant enhances T cell clonal expansion through a CD28-dependent, interleukin (IL)-2-independent mechanism [J].
Khoruts, A ;
Mondino, A ;
Pape, KA ;
Reiner, SL ;
Jenkins, MK .
JOURNAL OF EXPERIMENTAL MEDICINE, 1998, 187 (02) :225-236
[12]   GENETIC SUSCEPTIBILITY TO POST-THYMECTOMY AUTOIMMUNE-DISEASES IN MICE [J].
KOJIMA, A ;
PREHN, RT .
IMMUNOGENETICS, 1981, 14 (1-2) :15-27
[13]   Naturally anergic and suppressive CD25+CD4+ T cells as a functionally and phenotypically distinct immunoregulatory T cell subpopulation [J].
Kuniyasu, Y ;
Takahashi, T ;
Itoh, M ;
Shimizu, J ;
Toda, G ;
Sakaguchi, S .
INTERNATIONAL IMMUNOLOGY, 2000, 12 (08) :1145-1155
[14]   DETERMINATION OF LYMPHOCYTE DIVISION BY FLOW-CYTOMETRY [J].
LYONS, AB ;
PARISH, CR .
JOURNAL OF IMMUNOLOGICAL METHODS, 1994, 171 (01) :131-137
[15]   Antigen-experienced CD4 T cells display a reduced capacity for clonal expansion in vivo that is imposed by factors present in the immune host [J].
Merica, R ;
Khoruts, A ;
Pape, KA ;
Reinhardt, RL ;
Jenkins, MK .
JOURNAL OF IMMUNOLOGY, 2000, 164 (09) :4551-4557
[16]   THE REGULATION OF IMMUNE-RESPONSES TO DIETARY-PROTEIN ANTIGENS [J].
MOWAT, AM .
IMMUNOLOGY TODAY, 1987, 8 (03) :93-98
[17]   INDUCTION BY ANTIGEN OF INTRATHYMIC APOPTOSIS OF CD4+CD8+TCRLO THYMOCYTES INVIVO [J].
MURPHY, KM ;
HEIMBERGER, AB ;
LOH, DY .
SCIENCE, 1990, 250 (4988) :1720-1723
[18]  
Pape KA, 1997, J IMMUNOL, V159, P591
[19]  
Pape KA, 1998, J IMMUNOL, V160, P4719
[20]   Cytotoxic T lymphocyte-associated antigen 4 plays an essential role in the function of CD25+CD4+ regulatory cells that control intestinal inflammation [J].
Read, S ;
Malmström, V ;
Powrie, F .
JOURNAL OF EXPERIMENTAL MEDICINE, 2000, 192 (02) :295-302