Immunocompetent T-cells with a memory-like phenotype are the dominant cell type following antibody-mediated T-cell depletion

被引:388
作者
Pearl, JP
Parris, J
Hale, DA
Hoffmann, SC
Bernstein, WB
McCoy, KL
Swanson, SJ
Mannon, RB
Roederer, M
Kirk, AD [1 ]
机构
[1] NIDDKD, Transplant Branch, NIH, Dept Hlth & Human Serv, Bethesda, MD 20892 USA
[2] Natl Naval Med Res Inst, Dept Surg, Bethesda, MD USA
[3] Walter Reed Army Med Ctr, Organ Transplant Serv, Washington, DC 20307 USA
[4] Walter Reed Army Inst Res, Div Retrovirol, Rockville, MD USA
[5] NIAID, Immunotechnol Sect, Vaccine Res Ctr, NIH,Dept Hlth & Human Serv, Bethesda, MD 20892 USA
关键词
depletion; immunosuppression; T cell; transplantation;
D O I
10.1111/j.1600-6143.2005.00759.x
中图分类号
R61 [外科手术学];
学科分类号
摘要
cell depletion facilitates reduced immunosuppression following organ transplantation and has been suggested to be pro-tolerant. However, the characteristics of post-depletional T cells have not been evaluated as they relate to tolerance induction. We therefore studied patients undergoing profound T-cell depletion with alemtuzumab or rabbit anti-thymocyte globulin following renal transplantation, evaluating the phenotype and functional characteristics of their residual cells. Naive T cells and T cells with potential regulatory function (CD4+CD25+) were not prevalent following aggressive depletion. Rather, post-depletion T cells were of a single phenotype (CD3+CD4+CD45RA-CD62L- CCR7-) consistent with depletion-resistant effector memory T cells that expanded in the first month and were uniquely prevalent at the time of rejection. These cells were resistant to steroids, deoxyspergualin or sirolimus in vitro, but were calcineurin-inhibitor sensitive. These data demonstrate that therapeutic depletion begets a limited population of functional memory-like T cells that are easily suppressed with certain immunosuppressants, but cannot be considered uniquely pro-tolerant.
引用
收藏
页码:465 / 474
页数:10
相关论文
共 47 条
[1]   Heterologous immunity provides a potent barrier to transplantation tolerance [J].
Adams, AB ;
Williams, MA ;
Jones, TR ;
Shirasugi, N ;
Durham, MM ;
Kaech, SM ;
Wherry, EJ ;
Onami, T ;
Lanier, JG ;
Kokko, KE ;
Pearson, TC ;
Ahmed, R ;
Larsen, CP .
JOURNAL OF CLINICAL INVESTIGATION, 2003, 111 (12) :1887-1895
[2]  
Arden Bernhard, 1995, Immunogenetics, V42, P455
[3]   Immune reconstitution following autologous transfers of CD3/CD28 stimulated CD4+ T cells to HIV-infected persons [J].
Bernstein, WB ;
Cox, JH ;
Aronson, NE ;
Tracy, LR ;
Schlienger, K ;
Ratto-Kim, S ;
Garner, R ;
Cotte, J ;
Zheng, ZH ;
Winestone, L ;
Liebig, C ;
Galley, LM ;
Connors, M ;
Birx, DL ;
Carroll, RG ;
Levine, BL .
CLINICAL IMMUNOLOGY, 2004, 111 (03) :262-274
[4]   T cell immunodominance and maintenance of memory regulated by unexpectedly cross-reactive pathogens [J].
Brehm, MA ;
Pinto, AK ;
Daniels, KA ;
Schneck, JP ;
Welsh, RM ;
Selin, LK .
NATURE IMMUNOLOGY, 2002, 3 (07) :627-634
[5]  
BUNNAPRADIST S, 2003, CLIN TRANSPLANTS 200, P351
[6]   Campath 1H allows low-dose cyclosporine monotherapy in 31 cadaveric renal allograft recipients [J].
Calne, R ;
Moffatt, SD ;
Friend, PJ ;
Jamieson, NV ;
Bradley, JA ;
Hale, G ;
Firth, J ;
Bradley, J ;
Smith, KGC ;
Waldmann, M .
TRANSPLANTATION, 1999, 68 (10) :1613-1616
[7]   Prope tolerance, perioperative campath 1H, and low-dose cyclosporin monotherapy in renal allograft recipients [J].
Calne, R ;
Friend, P ;
Moffatt, S ;
Bradley, A ;
Hale, G ;
Firth, J ;
Bradley, J ;
Smith, K ;
Waldmann, H .
LANCET, 1998, 351 (9117) :1701-1702
[8]   Recall and propagation of allospecific memory T cells independent of secondary lymphoid organs [J].
Chalasani, G ;
Dai, ZH ;
Konieczny, BT ;
Baddoura, FK ;
Lakkis, FG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (09) :6175-6180
[9]   TOLERANCE IN THE MOUSE TO MAJOR HISTOCOMPATIBILITY COMPLEX-MISMATCHED HEART ALLOGRAFTS, AND TO RAT-HEART XENOGRAFTS, USING MONOCLONAL-ANTIBODIES TO CD4 AND CD8 [J].
CHEN, ZH ;
COBBOLD, S ;
METCALFE, S ;
WALDMANN, H .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1992, 22 (03) :805-810
[10]   INTERACTION OF STAPHYLOCOCCUS-AUREUS TOXIN SUPERANTIGENS WITH HUMAN T-CELLS [J].
CHOI, YW ;
KOTZIN, B ;
HERRON, L ;
CALLAHAN, J ;
MARRACK, P ;
KAPPLER, J .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (22) :8941-8945