Effector memory CD4+ T cells mediate graft-versus-leukemia without inducing graft-versus-host disease.

Much of the efficacy of allogeneic hematopoietic stem cell transplantation (alloSCT) in curing hematologic malignancies is due to a graft-versus-leukemia (GVL) effect mediated by donor T cells that recognize recipient alloantigens on leukemic cells. Donor T cells are also important for reconstituting immunity in the recipient. Unfortunately, donor T cells can attack nonmalignant host tissues and cause graft-versus-host disease (GVHD). We previously reported that donor CD4(+) effector memory T cells (T(EMs)) do not cause GVHD but transfer functional T-cell memory. In the present work, we demonstrate in an MHC-mismatched model that CD4(+) T(EMs) (unprimed to recipient antigens) mediate GVL against clinically relevant mouse models of chronic phase and blast crisis chronic myelogenous leukemia, without causing GVHD. By creating gene-deficient leukemias and using perforin-deficient T cells, we demonstrate that direct cytolytic function is essential for T(EM)-mediated GVL, but that GVL is retained when killing via FasL, TNF-alpha, TRAIL, and perforin is individually impaired. However, T(EM)-mediated GVL was diminished when both FasL and perforin pathways were blocked. Taken together, our studies identify T(EMs) as a clinically applicable cell therapy for promoting GVL and immune reconstitution, particularly in MHC-mismatched haploidentical alloSCTs in which T cell-depleted allografts are commonly used to minimize GVHD.

[1]  John M. Ashton,et al.  Leukemia stem cells in a genetically defined murine model of blast-crisis CML. , 2007, Blood.

[2]  C. Bordignon,et al.  Antitumor effects of HSV-TK-engineered donor lymphocytes after allogeneic stem-cell transplantation. , 2007, Blood.

[3]  Mark J. Smyth,et al.  Perforin-mediated target-cell death and immune homeostasis , 2006, Nature Reviews Immunology.

[4]  T. George,et al.  Allosensitized Memory CD4 T Cells Induce Chronic Graft Versus Host Disease. , 2006 .

[5]  W. Shlomchik,et al.  Leukemia-Specific Antigens Alone Are Insufficient for GVL in MHC-Matched Allogeneic Stem Cell Transplantation: An Essential Role for Minor H Antigens. , 2006 .

[6]  Lieping Chen,et al.  Mechanisms of GVL Against a Murine Blast Crisis CML. , 2006 .

[7]  Charles P. Lin,et al.  An inflammatory checkpoint regulates recruitment of graft-versus-host reactive T cells to peripheral tissues , 2006, The Journal of experimental medicine.

[8]  R. Bronson,et al.  Expression of chemokines in GVHD target organs is influenced by conditioning and genetic factors and amplified by GVHR. , 2006, Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation.

[9]  C. Contag,et al.  Prevention of acute graft-versus-host disease despite compensatory function of lymphoid organs in vivo , 2006 .

[10]  T. George,et al.  L-selectin and beta7 integrin on donor CD4 T cells are required for the early migration to host mesenteric lymph nodes and acute colitis of graft-versus-host disease. , 2005, Blood.

[11]  M. Shlomchik,et al.  The Influence of Migration, Alloreactive Repertoire and Memory Subset on the Differential Ability of Naive and Memory T Cells To Induce GVHD. , 2005 .

[12]  T. George,et al.  Memory CD4 T Cells Induce Graft Versus Host Disease. , 2005 .

[13]  C. Halin,et al.  In vivo imaging of lymphocyte trafficking. , 2005, Annual review of cell and developmental biology.

[14]  M. Starnbach,et al.  Activation of bone marrow–resident memory T cells by circulating, antigen-bearing dendritic cells , 2005, Nature Immunology.

[15]  C. Contag,et al.  In vivo analyses of early events in acute graft-versus-host disease reveal sequential infiltration of T-cell subsets. , 2005, Blood.

[16]  J. Serody,et al.  Leukocyte migration and graft-versus-host disease. , 2005, Blood.

[17]  D. Jain,et al.  Donor APCs are required for maximal GVHD but not for GVL , 2004, Nature Medicine.

[18]  W. Pear,et al.  Graft-versus-leukemia in a retrovirally induced murine CML model: mechanisms of T-cell killing. , 2004, Blood.

[19]  B. Levine,et al.  Dendritic cell-activated CD44hiCD8+ T cells are defective in mediating acute graft-versus-host disease but retain graft-versus-leukemia activity. , 2004, Blood.

[20]  N. Chao,et al.  Transfer of allogeneic CD62L- memory T cells without graft-versus-host disease. , 2004, Blood.

[21]  M. Shlomchik,et al.  Memory CD4+ T cells do not induce graft-versus-host disease. , 2003, The Journal of clinical investigation.

[22]  S. Trocciola,et al.  Donor immunization with pneumococcal conjugate vaccine and early protective antibody responses following allogeneic hematopoietic cell transplantation. , 2003, Blood.

[23]  J. Crawford,et al.  T cells require TRAIL for optimal graft-versus-tumor activity , 2002, Nature Medicine.

[24]  D. Housman,et al.  A murine model of CML blast crisis induced by cooperation between BCR/ABL and NUP98/HOXA9 , 2002, Proceedings of the National Academy of Sciences of the United States of America.

[25]  S. Burakoff,et al.  Cytolytic pathways in haematopoietic stem-cell transplantation , 2002, Nature Reviews Immunology.

[26]  Katia Perruccio,et al.  Effectiveness of Donor Natural Killer Cell Alloreactivity in Mismatched Hematopoietic Transplants , 2002, Science.

[27]  M. Baccarani,et al.  Hematologic and cytogenetic responses to imatinib mesylate in chronic myelogenous leukemia. , 2002, The New England journal of medicine.

[28]  M. Shlomchik,et al.  Selective T-cell subset ablation demonstrates a role for T1 and T2 cells in ongoing acute graft-versus-host disease: a model system for the reversal of disease. , 2001, Blood.

[29]  C. Craddock,et al.  Direct visualization of cytomegalovirus-specific T-cell reconstitution after allogeneic stem cell transplantation. , 2001, Blood.

[30]  T. Kitamura,et al.  Plat-E: an efficient and stable system for transient packaging of retroviruses , 2000, Gene Therapy.

[31]  G. Hill,et al.  The p55 TNF-α Receptor Plays a Critical Role in T Cell Alloreactivity1 , 2000, The Journal of Immunology.

[32]  J. Connors,et al.  Long-term follow-up of patients who achieved complete remission after donor leukocyte infusions. , 1999, Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation.

[33]  M. Shlomchik,et al.  Prevention of graft versus host disease by inactivation of host antigen-presenting cells. , 1999, Science.

[34]  George Q. Daley,et al.  The P190, P210, and P230 Forms of the BCR/ABL Oncogene Induce a Similar Chronic Myeloid Leukemia–like Syndrome in Mice but Have Different Lymphoid Leukemogenic Activity , 1999, The Journal of experimental medicine.

[35]  R G Miller,et al.  A role for perforin in activation-induced T cell death in vivo: increased expansion of allogeneic perforin-deficient T cells in SCID mice. , 1999, Journal of immunology.

[36]  Jon C. Aster,et al.  Efficient and Rapid Induction of a Chronic Myelogenous Leukemia-Like Myeloproliferative Disease in Mice Receiving P210 bcr/abl-Transduced Bone Marrow , 1998 .

[37]  M. Martelli,et al.  Treatment of high-risk acute leukemia with T-cell-depleted stem cells from related donors with one fully mismatched HLA haplotype. , 1998, The New England journal of medicine.

[38]  G. Hill,et al.  Cytokine cascades in acute graft-versus-host disease. , 1997, Transplantation.

[39]  C. Mackall,et al.  Pathways of T‐cell regeneration in mice and humans: implications for bone marrow transplantation and immmunotherapy , 1997, Immunological reviews.

[40]  Robert H. Collins,et al.  Donor leukocyte infusions in 140 patients with relapsed malignancy after allogeneic bone marrow transplantation. , 1997, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[41]  A. Lanzavecchia,et al.  Restricted TCR repertoire and long-term persistence of donor-derived antigen-experienced CD4+ T cells in allogeneic bone marrow transplantation recipients. , 1996, Journal of immunology.

[42]  S. Parsons,et al.  Haemophilus influenzae type b (HIB)-conjugate immunization before bone marrow harvest in autologous bone marrow transplantation. , 1996, Bone marrow transplantation.

[43]  A Ferrant,et al.  Graft-versus-leukemia effect of donor lymphocyte transfusions in marrow grafted patients. , 1995, Blood.

[44]  S. Ju,et al.  Fas(CD95)/FasL interactions required for programmed cell death after T-cell activation , 1995, Nature.

[45]  M. Ladanyi,et al.  Infusions of donor leukocytes to treat Epstein-Barr virus-associated lymphoproliferative disorders after allogeneic bone marrow transplantation. , 1994, The New England journal of medicine.

[46]  MJ Grusby,et al.  Depletion of CD4+ T cells in major histocompatibility complex class II-deficient mice , 1991, Science.

[47]  L. Picker,et al.  Differential expression of homing-associated adhesion molecules by T cell subsets in man. , 1990, Journal of immunology.

[48]  H. Nakamura [Graft-versus-leukemia effect (GVL effect): pathophysiological and clinical aspects]. , 1990, Nihon rinsho. Japanese journal of clinical medicine.

[49]  G. Daley,et al.  Induction of chronic myelogenous leukemia in mice by the P210bcr/abl gene of the Philadelphia chromosome. , 1990, Science.

[50]  A. Rimm,et al.  Graft-versus-leukemia reactions after bone marrow transplantation. , 1990, Blood.

[51]  N. Letvin,et al.  The isolation and characterization of the human suppressor inducer T cell subset. , 1985, Journal of immunology.

[52]  L. Lenz,et al.  TRAIL-R as a negative regulator of innate immune cell responses. , 2004, Immunity.

[53]  J. Ferrara,et al.  Acute graft-versus-host disease does not require alloantigen expression on host epithelium , 2002, Nature Medicine.

[54]  G. Hill,et al.  The p55 TNF-alpha receptor plays a critical role in T cell alloreactivity. , 2000, Journal of immunology.

[55]  S. Woo,et al.  Graft-vs.-host disease. , 1997, Critical reviews in oral biology and medicine : an official publication of the American Association of Oral Biologists.

[56]  G. Nolan,et al.  Production of high-titer helper-free retroviruses by transient transfection. , 1993, Proceedings of the National Academy of Sciences of the United States of America.