Allogeneic blood or marrow transplantation, or alloBMT, is a potentially curative therapy for a wide variety ofchemotherapy-incurable hematologic malignancies. However, the overall success of alloBMT remainsconstrained by procedure-related toxicity, which limits eligibility to relatively young patients withhistocompatible donors, and by lack of efficacy, manifested as post-transplantation progression of theunderlying disease. In the previous funding period, we had conducted clinical trials of post-transplantation,high dose cyclophosphamide (Cy) to reduce toxicity by promoting bi-directional transplantation tolerancewhile sparing stem cells and preserving immune responses to infection. A major goal of Aim 1 of the currentproposal is to characterize in detail the mechanisms of Cy-induced tolerance and the effect of post-transplantation Cy on regulatory T cells, antigen-presenting cells, and antigen-specific T cells. To increasethe anti-tumor efficacy of allogeneic T cell infusions, we will focus on inducing tumor-specific immunity by twodistinct approaches. The first approach is to administer cell-based tumor vaccines, with or without donorlymphocyte infusion, after nonmyeloablative allogeneic stem cell transplantation (Aim 2). The secondapproach will be to treat non-BMT candidates with Cy followed by transiently engrafting allogeneiclymphocytes so as to induce an 'allogeneic effect' that breaks tolerance in the patient's tumor-specific T cells(Aim 3). We will also study the capacity of tumor-targeted therapies to augment the effect of administeringallogeneic lymphocytes in this context (Aim 4). The ultimate goals of this project are to establish post-transplantation Cy as the gold standard of GVHD prophylaxis and to extend the application of adoptivecellular immunotherapy with allogeneic T cells outside of the context of alloBMT.Cancer is now the leading killer of Americans under the age of 85. Transfusions of white blood cells from ahealthy donor can actually make a cancer shrink, but this is a dangerous treatment that doesn't always work.The goal of this project is to find ways to make white blood cell transfusions safer and more effective in thetreatment of cancer.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Program Projects (P01)
Project #
2P01CA015396-32A1
Application #
7271669
Study Section
Special Emphasis Panel (ZCA1-RPRB-M (J1))
Project Start
2007-04-01
Project End
2012-02-28
Budget Start
2007-04-05
Budget End
2008-02-29
Support Year
32
Fiscal Year
2007
Total Cost
$319,530
Indirect Cost
Name
Johns Hopkins University
Department
Type
DUNS #
001910777
City
Baltimore
State
MD
Country
United States
Zip Code
21218
Schoch, Laura K; Cooke, Kenneth R; Wagner-Johnston, Nina D et al. (2018) Immune checkpoint inhibitors as a bridge to allogeneic transplantation with posttransplant cyclophosphamide. Blood Adv 2:2226-2229
Kasamon, Yvette L; Fuchs, Ephraim J; Zahurak, Marianna et al. (2018) Shortened-Duration Tacrolimus after Nonmyeloablative, HLA-Haploidentical Bone Marrow Transplantation. Biol Blood Marrow Transplant 24:1022-1028
Robinson, Tara M; Prince, Gabrielle T; Thoburn, Chris et al. (2018) Pilot trial of K562/GM-CSF whole-cell vaccination in MDS patients. Leuk Lymphoma 59:2801-2811
Grant, Melanie L; Bollard, Catherine M (2018) Cell therapies for hematological malignancies: don't forget non-gene-modified t cells! Blood Rev 32:203-224
Ghosh, Nilanjan; Ye, Xiaobu; Tsai, Hua-Ling et al. (2017) Allogeneic Blood or Marrow Transplantation with Post-Transplantation Cyclophosphamide as Graft-versus-Host Disease Prophylaxis in Multiple Myeloma. Biol Blood Marrow Transplant 23:1903-1909
Majzner, Robbie G; Mogri, Huzefa; Varadhan, Ravi et al. (2017) Post-Transplantation Cyclophosphamide after Bone Marrow Transplantation Is Not Associated with an Increased Risk of Donor-Derived Malignancy. Biol Blood Marrow Transplant 23:612-617
Alonso, Salvador; Jones, Richard J; Ghiaur, Gabriel (2017) Retinoic acid, CYP26, and drug resistance in the stem cell niche. Exp Hematol 54:17-25
Cruz, Conrad R Y; Bollard, Catherine M (2017) Adoptive Immunotherapy For Leukemia With Ex vivo Expanded T Cells. Curr Drug Targets 18:271-280
Fuchs, Ephraim Joseph (2017) Related haploidentical donors are a better choice than matched unrelated donors: Point. Blood Adv 1:397-400
Kanakry, Christopher G; BolaƱos-Meade, Javier; Kasamon, Yvette L et al. (2017) Low immunosuppressive burden after HLA-matched related or unrelated BMT using posttransplantation cyclophosphamide. Blood 129:1389-1393

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