Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 1995 Oct 24;92(22):10119-22.
doi: 10.1073/pnas.92.22.10119.

Processing and cryopreservation of placental/umbilical cord blood for unrelated bone marrow reconstitution

Affiliations

Processing and cryopreservation of placental/umbilical cord blood for unrelated bone marrow reconstitution

P Rubinstein et al. Proc Natl Acad Sci U S A. .

Abstract

Clinical evidence of hematopoietic restoration with placental/umbilical cord blood (PCB) grafts indicates that PCB can be a useful source of hematopoietic stem cells for routine bone marrow reconstitution. In the unrelated setting, human leukocyte antigen (HLA)-matched donors must be obtained for candidate patients and, hence, large panels of frozen HLA-typed PCB units must be established. The large volume of unprocessed units, consisting mostly of red blood cells, plasma, and cryopreservation medium, poses a serious difficulty in this effort because storage space in liquid nitrogen is limited and costly. We report here that almost all the hematopoietic colony-forming cells present in PCB units can be recovered in a uniform volume of 20 ml by using rouleaux formation induced by hydroxyethyl starch and centrifugation to reduce the bulk of erythrocytes and plasma and, thus, concentrate leukocytes. This method multiples the number of units that can be stored in the same freezer space as much as 10-fold depending on the format of the storage system. We have also investigated the proportion of functional stem/progenitor cells initially present that are actually available to the recipient when thawed cryopreserved PCB units are infused. Progenitor cell viability is measurably decreased when thawed cells, still suspended in hypertonic cryopreservative solutions, are rapidly mixed with large volumes of isotonic solutions or plasma. The osmotic damage inflicted by the severe solute concentration gradient, however, can be averted by a simple 2-fold dilution after thawing, providing almost total recovery of viable hematopoietic progenitor cells.

PubMed Disclaimer

Similar articles

Cited by

References

    1. N Engl J Med. 1989 Oct 26;321(17):1174-8 - PubMed
    1. Proc Natl Acad Sci U S A. 1989 May;86(10):3828-32 - PubMed
    1. J Hematother. 1993 Summer;2(2):233-4 - PubMed
    1. Blood Cells. 1994;20(2-3):275-83; discussion 284 - PubMed
    1. Blood Cells. 1994;20(2-3):587-96; discussion 596-600 - PubMed

Publication types