The Hematopoietic and Therapeutic Support (HATS) Service [formerly the Graft Engineering Laboratory (Gel)] provides support services to the Johns Hopkins Medical Institutions including peer reviewed, funded developmental core services to the bone marrow transplantation program. This expanded core service (of which the GEL remains an integral part) now includes several multidisciplinary services, facilities and personnel in the Johns Hopkins Departments of Oncology and Pathology. The ultimate goal of the HATS Service is to provide a common pathway to expedite the process of translating new therapies and protocols into clinical trials. This facility has become the sole Cancer Center resource for hematopoietic cell manipulation, therapeutic apheresis (including cytopheresis), cellular expansion, bone marrow and stem cell collection and regulatory oversight of cellular therapy protocols. Specifically, HATS' major functions are 1) to support, adapt develop and implement the clinical use of quality-controlled cellular products as required by all 5 projects and 2) to serve as a core resource for hematopoietic/lymphoid tissues essential to individual projects. The HATS Service itself does hot perform clinical or laboratory research. HATS contains equipment for investigational drugs/devices, bone marrow (BM) peripheral blood stem cell (PBSC), lymphoid and tumor cell collection, incubators for cell culture, programmed cryogenic freezing, liquid nitrogen storage, chemo-purging of BM and PBSC grafts and graft manipulation, lymphoid processing and expansion, cell procurement/manipulation for breast cancer and hematologic malignancies vaccine development and a broader scope of clinical applications of transplantation. One of the major challenges of this core function will be to ensure that the PO1 investigator's newly developed clinical trials involving somatic cell therapy are in compliance with the various regulatory agencies.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Program Projects (P01)
Project #
5P01CA015396-28
Application #
6592143
Study Section
Subcommittee E - Prevention &Control (NCI)
Project Start
2002-05-09
Project End
2003-02-28
Budget Start
Budget End
Support Year
28
Fiscal Year
2002
Total Cost
Indirect Cost
Name
Johns Hopkins University
Department
Type
DUNS #
045911138
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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