PMID- 17884641 OWN - NLM STAT- MEDLINE DCOM- 20080226 LR - 20181113 IS - 1079-9796 (Print) IS - 1096-0961 (Electronic) IS - 1079-9796 (Linking) VI - 40 IP - 1 DP - 2008 Jan-Feb TI - Nonmyeloablative allogeneic hematopoietic stem cell transplant using mismatched/haploidentical donors: a review. PG - 20-4 AB - Haploidentical hematopoietic stem cell transplantation (HSCT) provides an opportunity for patients to benefit from HCT when a human leukocyte antigen (HLA) genotypically matched sibling is not available. Initial results with the use of mismatched allograft has been disappointing due to the high incidence of graft-versus-host disease (GVHD) and infectious complications resulting in an unacceptable treatment-related morbidity and mortality. Recent advances with effective T-cell depletion, the use of 'megadose' of stem cells and reduced intensity conditioning has significantly decreased the early transplant related mortality and GvHD, while enabling robust and prompt engraftment, and hence enhancing the therapeutic benefits of haploidentical transplantation. However, the cardinal problems related to delayed immune reconstitution causing posttransplant infectious complications and relapse remain, limiting the efficacy of haploidentical transplant. Preliminary data have demonstrated the great potential in the use of adoptive cellular immunity and selective allodepletion in rapidly reconstituting immunity without GvHD. The encouraging reports from haploidentical transplant using noninherited maternal antigen (NIMA)-mismatched donors or natural killer alloreactive donors may greatly increase the donor availability and open a way to more appropriate donor selection in HLA-haploidentical HSCT. Future challenges remain in determining the safest approach for haploidentical transplant to be performed with minimal risk of GvHD, while preserving effective graft-versus-leukemia activity and promoting prompt immune reconstitution. FAU - Koh, Liang-Piu AU - Koh LP AD - Adult Bone Marrow and Stem Cell Transplantation Program, Duke University Medical Center, Durham, NC, USA. FAU - Chao, Nelson J AU - Chao NJ LA - eng GR - P01 CA047741/CA/NCI NIH HHS/United States GR - P01 CA047741-15/CA/NCI NIH HHS/United States PT - Journal Article PT - Review DEP - 20070919 PL - United States TA - Blood Cells Mol Dis JT - Blood cells, molecules & diseases JID - 9509932 SB - IM MH - *Haplotypes MH - Hematopoietic Stem Cell Transplantation/*methods MH - *Histocompatibility MH - Humans MH - Transplantation Conditioning/*methods MH - Treatment Outcome PMC - PMC2330277 MID - NIHMS37098 EDAT- 2007/09/22 09:00 MHDA- 2008/02/27 09:00 PMCR- 2009/01/01 CRDT- 2007/09/22 09:00 PHST- 2007/06/25 00:00 [received] PHST- 2007/06/30 00:00 [revised] PHST- 2007/06/30 00:00 [accepted] PHST- 2007/09/22 09:00 [pubmed] PHST- 2008/02/27 09:00 [medline] PHST- 2007/09/22 09:00 [entrez] PHST- 2009/01/01 00:00 [pmc-release] AID - S1079-9796(07)00135-0 [pii] AID - 10.1016/j.bcmd.2007.06.017 [doi] PST - ppublish SO - Blood Cells Mol Dis. 2008 Jan-Feb;40(1):20-4. doi: 10.1016/j.bcmd.2007.06.017. Epub 2007 Sep 19.