Improving the outcome of cord blood transplantation: use of mobilized HSC and other cells from third party donors
- PMID: 19796265
- DOI: 10.1111/j.1365-2141.2009.07766.x
Improving the outcome of cord blood transplantation: use of mobilized HSC and other cells from third party donors
Abstract
We developed the strategy of umbilical cord blood transplants (UCBT) with co-infusion of a limited number of highly purified mobilized haematopoietic stem cells (MHSC) from a human leucocyte antigen (HLA) unrestricted third party donor (TPD). Short post-transplant periods of neutropenia were usually observed in adults with haematological neoplasms receiving UCBT with a relatively low cell content and 0-3 HLA mismatches after myeloablative conditioning. This resulted from an early and initially predominant engraftment of the TPD-MHSC. After a variable period of double complete TPD + UCB chimerism, final full UCB chimerism was achieved (cumulative incidence >90%) within 100 d. Early recovery of the circulating neutrophils resulting from the 'bridge transplant' of the TPD-MHSC reduced the incidence of serious neutropenia-related infections, also facilitating the use of drugs with myelosuppressive side effects to combat other infections. The observed incidence of graft-versus-host disease and relapses was low, with overall and disease-free survival curves comparable to those of HLA identical sibling transplants. Post-transplant recovery of natural killer cells occurred soon after the transplant and B cells recovered around 6 months, but T-cell recovery took more than 1 year. Available data show that T cell recovery derives from UCB-HSC through thymic differentiation and that cytomegalovirus (CMV)-specific lymphocytes develop following CMV reactivations.
Comment in
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Long-term dual donor derived haematopoietic reconstitution following double unrelated cord blood transplantation--single unit dominance is not always the case.Br J Haematol. 2010 Apr;149(2):298-9. doi: 10.1111/j.1365-2141.2009.08045.x. Epub 2010 Jan 13. Br J Haematol. 2010. PMID: 20067567 No abstract available.
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