Allogeneic blood or marrow transplantation, or alloBMT, is a potentially curative therapy for a wide variety of chemotherapy-incurable hematologic malignancies. However, the overall success of alloBMT remains constrained by procedure-related toxicity, which limits eligibility to relatively young patients with histocompatible donors, and by lack of efficacy, manifested as post-transplantation progression of the underlying 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 tolerance while sparing stem cells and preserving immune responses to infection. A major goal of Aim 1 of the current proposal 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 increase the anti-tumor efficacy of allogeneic T cell infusions, we will focus on inducing tumor-specific immunity by two distinct approaches. The first approach is to administer cell-based tumor vaccines, with or without donor lymphocyte infusion, after nonmyeloablative allogeneic stem cell transplantation (Aim 2). The second approach will be to treat non-BMT candidates with Cy followed by transiently engrafting allogeneic lymphocytes 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 administering allogeneic 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 adoptive cellular 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 a healthy 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 the treatment of cancer.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Program Projects (P01)
Project #
5P01CA015396-34
Application #
7778273
Study Section
Special Emphasis Panel (ZCA1)
Project Start
Project End
Budget Start
2009-03-01
Budget End
2010-02-28
Support Year
34
Fiscal Year
2009
Total Cost
$348,785
Indirect Cost
Name
Johns Hopkins University
Department
Type
DUNS #
001910777
City
Baltimore
State
MD
Country
United States
Zip Code
21218
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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
Kasamon, Yvette L; Ambinder, Richard F; Fuchs, Ephraim J et al. (2017) Prospective study of nonmyeloablative, HLA-mismatched unrelated BMT with high-dose posttransplantation cyclophosphamide. Blood Adv 1:288-292
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McCurdy, Shannon R; Kasamon, Yvette L; Kanakry, Christopher G et al. (2017) Comparable composite endpoints after HLA-matched and HLA-haploidentical transplantation with post-transplantation cyclophosphamide. Haematologica 102:391-400
Gladstone, D E; Petri, M; BolaƱos-Meade, J et al. (2017) Long-term systemic lupus erythematosus disease control after allogeneic bone marrow transplantation. Lupus 26:773-776
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

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