Peripheral CD8+CD25+ T lymphocytes from MHC class II-deficient mice exhibit regulatory activity

被引:85
作者
Bienvenu, B
Martin, B
Auffray, C
Cordier, C
Bécourt, C
Lucas, B
机构
[1] Hop St Vincent de Paul, INSERM, U561, F-75014 Paris, France
[2] Inst Federatif Rech 94, Fac Necker, Paris, France
关键词
D O I
10.4049/jimmunol.175.1.246
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
We characterized CD8(+) T cells constitutively expressing CD25 in mice lacking the expression of MHC class II molecules. We showed that these cells are present not only in the periphery but also in the thymus. Like CD4(+)CD25(+) T cells, CD8(+)CD25(+) T cells appear late in the periphery during ontogeny. Peripheral CD8(+)CD25(+) T cells from MHC class II-deficient mice also share phenotypic and functional features with regulatory CD4(+)CD25(+) T cells: in particular, they strongly express glucocorticoid-induced TNFR family-related gene, CTLA-4 and Foxp3, produce IL-10, and inhibit CD25(-) T cell responses to anti-CD3 stimulation through cell contacts with similar efficiency to CD4(+)CD25(+) T cells. However, unlike CD4(+)CD25(+) T cells CD8(+)CD25(+) T cells from MHC class II-deficient mice strongly proliferate and produce IFN-gamma in vitro in response to stimulation in the absence of exogenous IL-2.
引用
收藏
页码:246 / 253
页数:8
相关论文
共 41 条
[1]   Origin of regulatory T cells with known specificity for antigen [J].
Apostolou, I ;
Sarukhan, A ;
Klein, L ;
von Boehmer, H .
NATURE IMMUNOLOGY, 2002, 3 (08) :756-763
[2]   Autoimmune disease as a consequence of developmental abnormality of a T cell subpopulation [J].
Asano, M ;
Toda, M ;
Sakaguchi, N ;
Sakaguchi, S .
JOURNAL OF EXPERIMENTAL MEDICINE, 1996, 184 (02) :387-396
[3]   An essential role for interleukin 10 in the function of regulatory T cells that inhibit intestinal inflammation [J].
Asseman, C ;
Mauze, S ;
Leach, MW ;
Coffman, RL ;
Powrie, F .
JOURNAL OF EXPERIMENTAL MEDICINE, 1999, 190 (07) :995-1003
[4]   CD25+CD4+ T cells compete with naive CD4+ T cells for IL-2 and exploit it for the induction of IL-10 production [J].
Barthlott, T ;
Moncrieffe, H ;
Veldhoen, M ;
Atkins, CJ ;
Christensen, J ;
O'Garra, A ;
Stockinger, B .
INTERNATIONAL IMMUNOLOGY, 2005, 17 (03) :279-288
[5]   Major histocompatibility complex class II-positive cortical epithelium mediates the selection of CD4+25+ immunoregulatory T cells [J].
Bensinger, SJ ;
Bandeira, A ;
Jordan, MS ;
Caton, AJ ;
Laufer, TM .
JOURNAL OF EXPERIMENTAL MEDICINE, 2001, 194 (04) :427-438
[6]   Human CD8+CD25+ thymocytes share phenotypic and functional features with CD4+CD25+ re latory thyrnocytes [J].
Cosmi, L ;
Liotta, F ;
Lazzeri, E ;
Francalanci, M ;
Angeli, R ;
Mazzinghi, B ;
Santarlasci, V ;
Manetti, R ;
Vanini, V ;
Romagnani, P ;
Maggi, E ;
Romagnani, S ;
Annunziato, F .
BLOOD, 2003, 102 (12) :4107-4114
[7]  
Filaci Gilberto, 2002, Autoimmunity Reviews, V1, P279, DOI 10.1016/S1568-9972(02)00065-4
[8]   Foxp3 Programs the Development and Function of CD4+CD25+ Regulatory T Cells (Reprinted from vol 4, pg 330-336, 2003) [J].
Fontenot, Jason D. ;
Gavin, Marc A. ;
Rudensky, Alexander Y. .
JOURNAL OF IMMUNOLOGY, 2017, 198 (03) :986-992
[9]   REQUIREMENT FOR CD8+ CELLS IN T-CELL RECEPTOR PEPTIDE-INDUCED CLONAL UNRESPONSIVENESS [J].
GAUR, A ;
HASPEL, R ;
MAYER, JP ;
FATHMAN, CG .
SCIENCE, 1993, 259 (5091) :91-94
[10]  
GERSHON RK, 1975, TRANSPLANT REV-DENMA, V26, P170