| Literature DB >> 20493393 |
Agnieszka Czechowicz1, Irving L Weissman.
Abstract
Replacement of disease-causing stem cells with healthy ones has been achieved clinically via hematopoietic cell transplantation (HCT) for the last 40 years, as a treatment modality for a variety of cancers and immunodeficiencies with moderate, but increasing, success. This procedure has traditionally included transplantation of mixed hematopoietic populations that include hematopoietic stem cells (HSC) and other cells, such as T cells. This article explores and delineates the potential expansion of this technique to treat a variety of inherited diseases of immune function, the current barriers in HCT and pure HSC transplantation, and the up-and-coming strategies to combat these obstacles. Copyright (c) 2010 Elsevier Inc. All rights reserved.Entities:
Mesh:
Year: 2010 PMID: 20493393 PMCID: PMC3071240 DOI: 10.1016/j.iac.2010.03.003
Source DB: PubMed Journal: Immunol Allergy Clin North Am ISSN: 0889-8561 Impact factor: 3.479