Titlebook: Bone Marrow and Stem Cell Transplantation; Meral Beksa? Book 2014Latest edition Springer Science+Business Media, New York 2014 HLA.Hematop

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https://doi.org/10.1007/978-3-031-40556-3 (digoxigenin–CSPD)-, or fluorescence (FITC, PE)-based detection systems. To achieve a faster, reliable, automated typing technique microbead and fluorescence detection technology have been combined and introduced to this field (XMAP? technology). For each locus, a series of microspheres, which are

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https://doi.org/10.1007/978-3-031-40556-3 involved minor H antigens, the immune response may either cause graft-versus-host disease and a graft-versus-tumor effect or lead to only a graft-versus-leukemia effect. Thus, identification of recipient–donor pairs with minor H antigen mismatches has clinical importance. This chapter describes mol

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https://doi.org/10.1057/9780230615595mia, myelodysplastic syndromes, advanced myeloproliferative disorders, high-risk lymphomas, and multiple myeloma) and is currently applied in more than 15,000 patients per year in Europe. Following HSCT, patients experience a period of reconstitution of the immune system, which seems to be highly de

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https://doi.org/10.1057/9780230615595gous transplantation. The detection of MRD helps to identify patients who are at high risk for leukemic relapse after transplantation. The most commonly used techniques for MRD detection are qualitative and quantitative PCR methods, fluorescence in situ hybridization (FISH), fluorescence-activated c

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https://doi.org/10.1057/9780230339583 reconstitution period after transplantation, HSCT recipients are most likely to have bacterial or fungal infections. Invasive fungal infections (IFIs) and mycobacterial infections (MBIs) are among the complications of HSCT, with high morbidity and mortality rates. Early diagnosis of both is crucial

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