Status
Conditions
About
Background:
Objectives:
Eligibility:
Design:
Full description
Bone marrow stromal cells (BMSCs) can be grown from bone marrow aspirates and biopsies, and are being used to treat a number of disorders including: graft-versus-host disease (GVHD), ischemic heart disease, peripheral vascular disease and autoimmune diseases. The purpose of this protocol is to collect bone marrow aspirates and biopsies from healthy volunteers to produce clinical grade BMSCs to treat Clinical Center patients and to develop new methods for producing and assessing the quality of BMSCs. In some cases, the donors will be the recipients of the ex vivo expanded cells (autologous transplantation). In other cases, no matching of HLA or other antigens is required between the marrow donor and the BMSC recipient, so the donors will be required to meet the same healthy history and infectious disease marker screening criteria as volunteer blood donors. The BMSCs will be produced in the GMP Clinical Cell Processing Laboratory, located in the Cell Processing Section (CPS), Department of Transfusion Medicine (DTM), Clinical Center. After the BMSCs are produced by the Cell Processing Laboratory, they will be infused directly into Clinical Center patients on protocol, or cryopreserved and stored, and used as they are needed to treat Clinical Center patients. Up to 250 subjects will be enrolled in this study. This protocol will provide a mechanism for banking fresh and frozen BMSC products that can be used for patient care and research. This is not a treatment protocol. Subjects receiving these BMSC products will be enrolled in specific BMSC treatment protocols.
Enrollment
Sex
Ages
Volunteers
Inclusion and exclusion criteria
INCLUSION CRITERIA RELATED OR THIRD PARTY DONORS (ALLOGENEIC CELLS):
Age greater than or equal to 18 years old
Ability to give informed consent
Adequate clinical parameters (all of the following):
Females of child-bearing potential must have a negative pregnancy test and one of the following:
Use (by ensuring her male partner(s) use(s) barrier contraception (condom) as birth control
INCLUSION CRITERIA AUTOLOGOUS DONORS
Age greater than or equal to 18 years old
Ability to give informed consent
Females of child-bearing potential must have a negative pregnancy test and one of the following:
EXCLUSION CRITERIA RELATED OR THIRD PARTY DONORS (ALLOGENEIC CELLS)
Medical history that includes any of the following:
If female, pregnant within the past 6 weeks
Febrile (temperature greater than 38 (Infinite) C)
Systolic blood pressure less than 100 or greater than 180 mmHg
Diastolic blood pressure less than 50 or greater than 100 mmHg
Heart rate less than 40 or greater than 100 beats/minute
Anemia, thrombocytopenia, or leukopenia
Hemoglobin level
African American women < 11.5 grams/dL
Other women < 12.0 grams/dL
Men < 12.5 grams/dL
HCT
African American women < 34%
Other women < 36%
Men < 38%
Platelets less than 150 x 10(3)/microL
Absolute neutrophil count less than 1.0 x 10(3)/microL
Prolonged coagulation assays
Positive tests for blood borne pathogens (as required by the Standards for Blood Banks and Transfusion Services, American Association of Blood Banks. The currently required tests include anti-HIV1/2, anti-HCV, Anti-HTVLI/II, anti-T. Cruzi, HBsAg, syphilis, and molecular testing for West Nile virus, HCV and HIV).
Experiencing fever, malaise, anorexia, weight loss or night sweats consistent with active tuberculosis infection
EXCLUSION CRITERIA AUTOLOGOUS DONORS
-Medical history that includes any of the following:
65 participants in 2 patient groups
Loading...
Data sourced from clinicaltrials.gov
Clinical trials
Research sites
Resources
Legal