The studies proposed in Project II focus on the problem of post-HCT disease relapse of B-lineage acute? lymphoblastic leukemia (ALL). We hypothesize that the incidence of treatment failure due to relapse? following allogeneic HCT can be reduced by targeting post-transplant minimal residual disease (MRD) with? adoptively transferred donor-derived leukemia-specific T-cells. As a strategy to reproducibly generate? effector cells for adoptive therapy, we have designed a chimeric antigen receptor (CAR) that re-directs the? antigen specificity of T-cells to the B-cell lineage-restricted cell-surface molecule CD19. Genetically-modified? CD19-CAR* CTL's lyse B-cell lymphoma and leukemia target cells and are activated for TC1 cytokine? production in a CAR-regulated manner. T-cell isolation, genetic modification, ;and expansion Standard? Operating Procedures are in place at City of Hope to manufacture clinical cell doses in accordance with? quality control/assurance standards mandated by the FDA. The studies proposed in Specific Aim #1 will? evaluate the feasibility and safety of adoptive therapy using three escalating doses (10[8]/m -10[10]/m2) of donorderived? CD19R+HyTK+ CTL clones versus oligoclonal/ polyclonal T-cell lines, shortly following related-donor? allogeneic HCT for high-risk CD19+ ALL. In addition to reducing the incidence of GVHD requiring iatrogenic? immunosuppression, we hypothesize that donor HCT T-cell depletion (TCD), in combination with a? lymphodepleting preparative regimen consisting of TBI, thiotepa, and fludarabine, will promote homeostatic? proliferation of transferred T-cells, as well as, limit anti-transgene rejection responses. The correlative studies? in Specific Aim #2 focus on delineating the magnitude and duration of persistence of transferred clones? versus lines at the three prescribed T-cell dose levels using vector-specific Q-PCR and TCR spectratyping? analyses on serially acquired PBMC specimens. We will also evaluate the utility of administering? recombinant human IL-2 for enhancing the expansion of transferred T-cells in vivo. The correlative studies? proposed in Specific Aim 3 seek to evaluate the bone marrow trafficking of transferred clones versus lines,? and, the functional status of transferred T-cells in this anatomic site of ALL minimal residual disease. In? aggregate, the results of the studies proposed in Project II will facilitate the evolution of targeting post-HCT? MRD with CD19-specific T-cells for enhanced disease-free survival of patients with B-lineage ALL, and? substantiate the rationale to expand this approach to a broader array of CD19+ malignancies treated by HCT.
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