S. Gurkan, Immune reconstitution following rabbit antithymocyte globulin, Am J Transplant, vol.10, issue.9, pp.2132-2141, 2010.

A. Sener, A. L. Tang, and D. L. Farber, Memory T-cell predominance following T-cell depletional therapy derives from homeostatic expansion of naive T cells, Am J Transplant, vol.9, issue.11, pp.2615-2623, 2009.

J. C. Engram, Lineage-specific T-cell reconstitution following in vivo CD4+ and CD8+ lymphocyte depletion in nonhuman primates, Blood, vol.116, issue.5, pp.748-758, 2010.

Z. Wu, Homeostatic proliferation is a barrier to transplantation tolerance, Nat Med, vol.10, issue.1, pp.87-92, 2004.

D. C. Neujahr, Accelerated memory cell homeostasis during T cell depletion and approaches to overcome it, J Immunol, vol.176, issue.8, pp.4632-4639, 2006.

A. D. Kirk, Results from a human renal allograft tolerance trial evaluating the humanized CD52-specific monoclonal antibody alemtuzumab (CAM-PATH-1H), Transplantation, vol.76, issue.1, pp.120-129, 2003.

J. P. Pearl, Immunocompetent T-cells with a memory-like phenotype are the dominant cell type following antibody-mediated T-cell depletion, Am J Transplant, vol.5, issue.3, pp.465-474, 2005.

K. M. Williams, F. T. Hakim, and R. E. Gress, T cell immune reconstitution following lymphodepletion, Semin Immunol, vol.19, issue.5, pp.318-330, 2007.

N. K. Tchao and L. A. Turka, Lymphodepletion and homeostatic proliferation: implications for transplantation, Am J Transplant, vol.12, issue.5, pp.1079-1090, 2012.

Y. Rochman, R. Spolski, and W. J. Leonard, New insights into the regulation of T cells by gamma(c) family cytokines, Nat Rev Immunol, vol.9, issue.7, pp.480-490, 2009.

U. Von-freeden-jeffry, P. Vieira, L. A. Lucian, T. Mcneil, S. E. Burdach et al., Lymphopenia in interleukin (IL)-7 gene-deleted mice identifies IL-7 as a nonredundant cytokine, J Exp Med, vol.181, issue.4, pp.1519-1526, 1995.

J. J. Peschon, Early lymphocyte expansion is severely impaired in interleukin 7 receptor-deficient mice, J Exp Med, vol.180, issue.5, pp.1955-1960, 1994.

S. Giliani, Analysis of clinical, immunological, and molecular features in 16 novel patients, Immunol Rev, vol.203, pp.110-126, 2005.

K. S. Schluns, W. C. Kieper, S. C. Jameson, and L. Lefrancois, Interleukin-7 mediates the homeostasis of naive and memory CD8 T cells in vivo, Nat Immunol, vol.1, issue.5, pp.426-432, 2000.

J. T. Tan, IL-7 is critical for homeostatic proliferation and survival of naive T cells, Proc Natl Acad Sci U S A, vol.98, issue.15, pp.8732-8737, 2001.

R. M. Kondrack, J. Harbertson, J. T. Tan, M. E. Mcbreen, C. D. Surh et al., Interleukin 7 regulates the survival and generation of memory CD4 cells, J Exp Med, vol.198, issue.12, pp.1797-1806, 2003.

B. Seddon, P. Tomlinson, and R. Zamoyska, Interleukin 7 and T cell receptor signals regulate homeostasis of CD4 memory cells, Nat Immunol, vol.4, issue.7, pp.680-686, 2003.

J. Sprent and C. D. Surh, Normal T cell homeostasis: the conversion of naive cells into memory-phenotype cells, Nat Immunol, vol.12, issue.6, pp.478-484, 2011.

M. Racape, B. Vanhove, J. P. Soulillou, and S. Brouard, Interleukin 7 receptor alpha as a potential therapeutic target in transplantation, Arch Immunol Ther Exp (Warsz), vol.57, issue.4, pp.253-261, 2009.

T. Sudo, S. Nishikawa, N. Ohno, N. Akiyama, M. Tamakoshi et al., Expression and function of the interleukin 7 receptor in murine lymphocytes, Proc Natl Acad Sci, vol.90, pp.9125-9129, 1993.

C. Penaranda, IL-7 receptor blockade reverses autoimmune diabetes by promoting inhibition of effector/memory T cells, Proc Natl Acad Sci U S A, vol.109, issue.31, pp.12668-12673, 2012.

L. F. Lee, Anti-IL-7 receptor-? reverses established type 1 diabetes in nonobese diabetic mice by modulating effector T-cell function, Proc Natl Acad Sci, vol.109, issue.31, pp.12674-12679, 2012.

K. K. Hoyer, K. Wolslegel, H. Dooms, and A. K. Abbas, Targeting T cell-specific costimulators and growth factors in a model of autoimmune hemolytic anemia, J Immunol, vol.179, issue.5, pp.2844-2850, 2007.

B. H. Koehn, PD-1-dependent mechanisms maintain peripheral tolerance of donor-reactive CD8+ T cells to transplanted tissue, J Immunol, vol.181, issue.8, pp.5313-5322, 2008.

Q. Shi, J. R. Lees, D. W. Scott, D. L. Farber, and S. T. Bartlett, Endogenous expansion of regulatory T cells leads to long-term islet graft survival in diabetic NOD mice, Am J Transplant, vol.12, issue.5, pp.1124-1132, 2012.

L. V. Riella, A. M. Paterson, A. H. Sharpe, and A. Chandraker, Role of the PD-1 pathway in the immune response, Am J Transplant, vol.12, issue.10, pp.2575-2587, 2012.

H. Ji, X. D. Shen, F. Gao, R. W. Busuttil, Y. Zhai et al., Alloreactive CD8 T-cell primed/ memory responses and accelerated graft rejection in B-cell-deficient sensitized mice, Transplantation, vol.91, issue.10, pp.1075-1081, 2011.

D. P. Al-adra and C. C. Anderson, Mixed chimerism and split tolerance: mechanisms and clinical correlations, Chimerism, vol.2, issue.4, pp.89-101, 2011.

S. Takeuchi and S. I. Katz, Use of interleukin 7 receptor-? knockout donor cells demonstrates the lymphoid independence of dendritic cells, Blood, vol.107, issue.1, pp.184-186, 2006.

X. Liu, Crucial role of interleukin-7 in T helper type 17 survival and expansion in autoimmune disease, Nat Med, vol.16, issue.2, pp.191-197, 2010.

R. Gonzalez-quintial, Systemic autoimmunity and lymphoproliferation are associated with excess IL-7 and inhibited by IL-7Ralpha blockade, PLoS One, vol.6, issue.11, p.27528, 2011.

M. Yamazaki, Mucosal T cells expressing high levels of IL-7 receptor are potential targets for treatment of chronic colitis, J Immunol, vol.171, issue.3, pp.1556-1563, 2003.

B. Chung, E. P. Dudl, D. Min, L. Barsky, N. Smiley et al., Prevention of graft-versus-host disease by anti IL-7Ralpha antibody, Blood, vol.110, issue.8, pp.2803-2810, 2007.

Y. Wang, H. Dai, Z. Liu, X. Cheng, G. Tellides et al., Neutralizing IL-7 promotes long-term allograft survival induced by CD40/CD40L costimulatory blockade, Am J Transplant, vol.6, issue.12, pp.2851-2860, 2006.

Y. D. Muller, Immunosuppressive effects of streptozotocin-induced diabetes result in absolute lymphopenia and a relative increase of T regulatory cells, Diabetes, vol.60, issue.9, pp.2331-2340, 2011.

C. A. London, M. P. Lodge, and A. K. Abbas, Functional responses and costimulator dependence of memory CD4+ T cells, J Immunol, vol.164, issue.1, pp.265-272, 2000.

M. Croft, L. M. Bradley, and S. L. Swain, Naive versus memory CD4 T cell response to antigen. Memory cells are less dependent on accessory cell costimulation and can respond to many antigen-presenting cell types including resting B cells, J Immunol, vol.152, issue.6, pp.2675-2685, 1994.

I. Den-braber, Maintenance of peripheral naive T cells is sustained by thymus output in mice but not humans, Immunity, vol.36, issue.2, pp.288-297, 2012.

J. C. Rice and R. P. Bucy, Differences in the degree of depletion, rate of recovery, and the preferential elimination of naive CD4+ T cells by anti-CD4 monoclonal antibody (GK1.5) in young and aged mice, J Immunol, vol.154, issue.12, pp.6644-6654, 1995.

M. J. Hanaway, Alemtuzumab induction in renal transplantation, N Engl J Med, vol.364, issue.20, pp.1909-1919, 2011.

S. Louis, Long-term cell monitoring of kidney recipients after an antilymphocyte globulin induction with and without steroids, Transplantation, vol.83, issue.6, pp.712-721, 2007.

C. P. Larsen, Long-term acceptance of skin and cardiac allografts after blocking CD40 and CD28 pathways, Nature, vol.381, issue.6581, pp.434-438, 1996.

C. R. Gilson, Anti-CD40 monoclonal antibody synergizes with CTLA4-Ig in promoting long-term graft survival in murine models of transplantation, J Immunol, vol.183, issue.3, pp.1625-1635, 2009.

N. M. Reisman, T. L. Floyd, M. E. Wagener, A. D. Kirk, C. P. Larsen et al., LFA-1 blockade induces effector and regulatory T-cell enrichment in lymph nodes and synergizes with CTLA-4Ig to inhibit effector function, Blood, vol.118, issue.22, pp.5851-5861, 2011.

V. G. Tusher, R. Tibshirani, and G. Chu, Significance analysis of microarrays applied to the ionizing radiation response, Proc Natl Acad Sci U S A, vol.98, issue.9, pp.5116-5121, 2001.

A. I. Saeed, TM4: a free, open-source system for microarray data management and analysis, Biotechniques, vol.34, issue.2, pp.374-378, 2003.