Successful haploidentical bone marrow transplantation in Fanconi anemia

14Citations
Citations of this article
16Readers
Mendeley users who have this article in their library.
Get full text

Abstract

A 10-year-old girl with Fanconi anemia and severe aplastic anemia underwent a haploidentical BMT from her mother due to lack of a matched family donor. T cell depletion was done by positive selection of CD34 cells with immunomagnetic beads. Due to graft rejection a second haploidentical BMT from the father was successfully undertaken. No immunosuppression was given after the transplant. Immunological reconstitution took approximately 6 months, with no GVHD or severe infections. Such a transplant, containing a large purified CD34 cell fraction with a minimal number of added T cells, should be considered as the treatment of choice for patients with Fanconi anemia if no HLA matched donor is available.

Cite

CITATION STYLE

APA

Elhasid, R., Ben Arush, M. W., Katz, T., Gan, Y., Shechter, Y., Sami, I., … Rowe, J. M. (2000). Successful haploidentical bone marrow transplantation in Fanconi anemia. Bone Marrow Transplantation, 26(11), 1221–1223. https://doi.org/10.1038/sj.bmt.1702701

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free