Contrasting CD25hiCD4+T cells/FOXP3 patterns in chronic rejection and operational drug-free tolerance

被引:234
作者
Louis, S
Braudeau, C
Giral, M
Dupont, A
Moizant, F
Robillard, N
Moreau, A
Soulillou, JP [1 ]
Brouard, S
机构
[1] Univ Nantes, U643, INSERM, 30 Bd Jean Monnet, F-44093 Nantes 01, France
[2] Univ Hosp Nantes, ITERT, Nantes, France
[3] Univ Hosp Nantes, Hematol Lab, Nantes, France
[4] Ctr Hosp Univ Nantes, Hotel Dieu, Serv Anatomopathol, Nantes, France
关键词
chronic rejection; kidney; tolerance; phenotype;
D O I
10.1097/01.tp.0000203166.44968.86
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. Although immunosuppression withdrawal in kidney recipients usually leads to rejection, in some patients it does not, leading to a state of clinical operational tolerance. Methods. We compared these highly contrasted situations by analyzing blood cell phenotype and transcriptional patterns in drug-free spontaneously tolerant kidney recipients, recipients with chronic rejection, recipients with stable graft function under standard or minimal immunosuppression and healthy individuals Results. The blood cell phenotype of clinically tolerant patients did not differ from that of healthy individuals. In contrast, recipients with chronic rejection had significantly less CD25(hi)CD4(+) T cells and lower levels of FOXP3 transcripts compared with clinically tolerant recipients. Patients with chronic rejection also displayed CD25 CD4 T+ cells expressing NKG2D(+) CD94(+) and CD57(+) CD27(-) CD28(-) cytotoxic-associated markers (P < 0.05). Conclusion. These data show that whereas clinically tolerant recipients displayed normal levels of CD25(hi)CD4(+) T cells and FOXP3 transcripts, chronic rejection is associated with a decrease in CD25(hi)CD4(+) T cells and FOXP3 transcripts, suggesting that clinically "operational tolerance" may be due to a maintained phenomenon of natural tolerance that is lacking in patients with chronic rejection.
引用
收藏
页码:398 / 407
页数:10
相关论文
共 54 条
[11]   The concept of "partial" clinical tolerance [J].
Cortesini, R ;
Suciu-Foca, N .
TRANSPLANT IMMUNOLOGY, 2004, 13 (02) :101-104
[12]   Tailoring of immunosuppression in renal and liver allograft recipients displaying donor specific T-suppressor cells [J].
Cortesini, R ;
Renna-Molajoni, E ;
Cinti, P ;
Pretagostini, R ;
Ho, E ;
Rossi, P ;
Cortesini, NSF .
HUMAN IMMUNOLOGY, 2002, 63 (11) :1010-1018
[13]   Effect of long-term immunosuppression in kidney-graft recipients on cancer incidence: randomised comparison of two cyclosporin regimens [J].
Dantal, J ;
Hourmant, M ;
Cantarovich, D ;
Giral, M ;
Blancho, G ;
Dreno, B ;
Soulillou, JP .
LANCET, 1998, 351 (9103) :623-628
[14]   Ex vivo isolation and characterization of CD4+CD25+ T cells with regulatory properties from human blood [J].
Dieckmann, D ;
Plottner, H ;
Berchtold, S ;
Berger, T ;
Schuler, G .
JOURNAL OF EXPERIMENTAL MEDICINE, 2001, 193 (11) :1303-1310
[15]   Phenotypic and functional separation of memory and effector human CD8(+) T cells [J].
Hamann, D ;
Baars, P ;
Rep, MHG ;
Hooibrink, B ;
KerkhofGarde, SR ;
Klein, MR ;
vanLier, RAW .
JOURNAL OF EXPERIMENTAL MEDICINE, 1997, 186 (09) :1407-1418
[16]   Improved graft survival after renal transplantation in the United States, 1988 to 1996. [J].
Hariharan, S ;
Johnson, CP ;
Bresnahan, BA ;
Taranto, SE ;
McIntosh, MJ ;
Stablein, D .
NEW ENGLAND JOURNAL OF MEDICINE, 2000, 342 (09) :605-612
[17]   Cyclosporine induces cancer progression by a cell-autonomous mechanism [J].
Hojo, M ;
Morimoto, T ;
Maluccio, M ;
Asano, T ;
Morimoto, K ;
Lagman, M ;
Shimbo, T ;
Suthanthiran, M .
NATURE, 1999, 397 (6719) :530-534
[18]   Control of regulatory T cell development by the transcription factor Foxp3 [J].
Hori, S ;
Nomura, T ;
Sakaguchi, S .
SCIENCE, 2003, 299 (5609) :1057-1061
[19]   Frequency and clinical implications of development of donor-specific and non-donor-specific HLA antibodies after kidney transplantation [J].
Hourmant, M ;
Cesbron-Gautier, A ;
Terasaki, PI ;
Mizutani, K ;
Moreau, A ;
Meurette, A ;
Dantal, J ;
Giral, M ;
Blancho, G ;
Cantarovich, D ;
Karam, G ;
Follea, G ;
Soulillou, JP ;
Bignon, JD .
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2005, 16 (09) :2804-2812
[20]   Unique chemotactic response profile and specific expression of chemokine receptors CCR4 and CCR8 by CD4+CD25+ regulatory T cells [J].
Iellem, A ;
Mariani, M ;
Lang, R ;
Recalde, H ;
Panina-Bordignon, P ;
Simigaglia, F ;
D'Ambrosio, D .
JOURNAL OF EXPERIMENTAL MEDICINE, 2001, 194 (06) :847-853