L-Selectinhi but not the L-selectinlo CD4+25+ T-regulatory cells are potent inhibitors of GVHD and BM graft rejection

被引:273
作者
Taylor, PA
Panoskaltsis-Mortari, A
Swedin, JM
Lucas, PJ
Gress, RE
Levine, BL
June, CH
Serody, JS
Blazar, BR [1 ]
机构
[1] Univ Minnesota, Ctr Canc, Minneapolis, MN 55455 USA
[2] Dept Pediat, Div BMT, Minneapolis, MN 55455 USA
[3] NCI, Expt Immunol Branch, NIH, Bethesda, MD 20892 USA
[4] Univ Penn, Abramson Family Canc Res Inst, Ctr Canc, Philadelphia, PA 19104 USA
[5] Univ N Carolina, Lineberger Comprehens Canc Ctr, Sch Med, Chapel Hill, NC 27599 USA
关键词
D O I
10.1182/blood-2004-05-1850
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Graft-versus-host disease (GVHD) is a major cause of morbidity and mortality after bone marrow transplantation (BMT). CD4(+)CD25(+) immune regulatory T cells (Tregs), long recognized for their critical role in induction and maintenance of self-tolerance and prevention of autoimmunity, are also important in the regulation of immune responses in allogeneic bone marrow (BM) and solid organ transplantation. Published data indicate that ex vivo activated and expanded donor Tregs result in significant inhibition of lethal nor- or host-type LSel(hi), but not LSeIlo, Tregs potently increased donor BM engraftment in sublethally irradiated mice, an event occurring independently of transforming growth factor beta signaling of host T cells. These data indicate that Treg cellular therapy warrants clinical consideration for the inhibition of GVHD and the promotion of alloengraftment.
引用
收藏
页码:3804 / 3812
页数:9
相关论文
共 24 条
[1]   Engraftment of severe combined immune deficient mice receiving allogeneic bone marrow via in utero or postnatal transfer [J].
Blazar, BR ;
Taylor, PA ;
McElmurry, R ;
Tian, L ;
Panoskaltsis-Mortari, A ;
Lam, S ;
Lees, C ;
Waldschmidt, T ;
Vallera, DA .
BLOOD, 1998, 92 (10) :3949-3959
[2]   TGF-β:: the missing link in CD4+CD25+ regulatory T cell-mediated immunosuppression [J].
Chen, WJ ;
Wahl, SM .
CYTOKINE & GROWTH FACTOR REVIEWS, 2003, 14 (02) :85-89
[3]   CD4+CD25+ immunoregulatory T cells:: New therapeutics for graft-versus-host disease [J].
Cohen, JL ;
Trenado, A ;
Vasey, D ;
Klatzmann, D ;
Salomon, BL .
JOURNAL OF EXPERIMENTAL MEDICINE, 2002, 196 (03) :401-406
[4]   CD4+CD25+ regulatory T cells preserve graft-versus-tumor activity while inhibiting graft-versus-host disease after bone marrow transplantation [J].
Edinger, M ;
Hoffmann, P ;
Ermann, J ;
Drago, K ;
Fathman, CG ;
Strober, S ;
Negrin, RS .
NATURE MEDICINE, 2003, 9 (09) :1144-1150
[5]   CD4+ CD25+ CD62+ T-regulatory cell subset has optimal suppressive and proliferative potential [J].
Fu, S ;
Yopp, AC ;
Mao, X ;
Chen, DM ;
Zhang, N ;
Chen, D ;
Mao, MW ;
Ding, YZ ;
Bromberg, JS .
AMERICAN JOURNAL OF TRANSPLANTATION, 2004, 4 (01) :65-78
[6]   In vitro-expanded human CD4+CD25+ T-regulatory cells can markedly inhibit allogeneic dendritic cell-stimulated MLR cultures [J].
Godfrey, WR ;
Ge, YG ;
Spoden, DJ ;
Levine, BL ;
June, CH ;
Blazar, BR ;
Porter, SB .
BLOOD, 2004, 104 (02) :453-461
[7]   CD4+CD25+ T regulatory cells control anti-islet CD8+ T cells through TGF-β-TGF-β receptor interactions in type 1 diabetes [J].
Green, EA ;
Gorelik, L ;
McGregor, CM ;
Tran, EH ;
Flavell, RA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (19) :10878-10883
[8]   Regulatory T cells induced by 1α,25-dihydroxyvitamin D3 and mycophenolate mofetil treatment mediate transplantation tolerance [J].
Gregori, S ;
Casorati, M ;
Amuchastegui, S ;
Smiroldo, S ;
Davalli, AM ;
Adorini, L .
JOURNAL OF IMMUNOLOGY, 2001, 167 (04) :1945-1953
[9]   IL-30 is required for regulatory T cells to mediate tolerance to alloantigens in vivo [J].
Hara, M ;
Kingsley, CI ;
Niimi, M ;
Read, S ;
Turvey, SE ;
Bushell, AR ;
Morris, PJ ;
Powrie, F ;
Wood, KJ .
JOURNAL OF IMMUNOLOGY, 2001, 166 (06) :3789-3796
[10]   Donor-type CD4+CD25+ regulatory T cells suppress lethal acute graft-versus-host disease after allogeneic bone marrow transplantation [J].
Hoffmann, P ;
Ermann, J ;
Edinger, M ;
Fathman, CG ;
Strober, S .
JOURNAL OF EXPERIMENTAL MEDICINE, 2002, 196 (03) :389-399