2005
DOI: 10.1016/j.humimm.2005.01.007
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The Single Antigen expressing Lines (SALs) Concept: An Excellent Tool for Screening for HLA-Specific Antibodies

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Cited by 38 publications
(33 citation statements)
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“…This was confirmed by a study of Van den BergLoonen et al [11], who showed, in a retrospective study, that in patients undergoing transplantation in the acceptable mismatch program on basis of a negative CDC crossmatch, the presence of donor-specific antibodies detectable in Luminex was not associated with a poorer graft survival compared with patients without donor specific antibodies in Luminex. The presence of donor specific antibodies in Luminex was associated with a higher incidence of acute rejection in the first 6 months but this did not affect graft survival at the long term.…”
Section: Acceptable Mismatch Programmentioning
confidence: 63%
“…This was confirmed by a study of Van den BergLoonen et al [11], who showed, in a retrospective study, that in patients undergoing transplantation in the acceptable mismatch program on basis of a negative CDC crossmatch, the presence of donor-specific antibodies detectable in Luminex was not associated with a poorer graft survival compared with patients without donor specific antibodies in Luminex. The presence of donor specific antibodies in Luminex was associated with a higher incidence of acute rejection in the first 6 months but this did not affect graft survival at the long term.…”
Section: Acceptable Mismatch Programmentioning
confidence: 63%
“…In essence these solid SPAs are based on the solubilization of the molecules from the cell surface of either EpsteinBarr virus (EBV) cell lines or lines expressing a single HLA molecule after transfection with the respective sequence [9]. The molecules are bound on the surface of the assay in question.…”
Section: Methodsmentioning
confidence: 99%
“…K562 and EBV-LCLs expressing single allo-HLA molecules were generated by transduction with retroviral vectors encoding for the allo-HLA molecules or by transfection of allo-HLA molecules. 27,28 For the isolation of T cells, B cells, and monocytes, peripheral blood mononuclear cells of healthy donors were stained with either anti-CD3, anti-CD19, or anti-CD14 magnetic-activated cell sorting beads (Miltenyi Biotec), respectively, and isolated according to the manufacturer's instructions. CD40 ligand (CD40L)-activated B cells were generated by culturing the CD19 ϩ fraction for 3 days on CD40L-transduced murine fibroblasts 29 in medium containing CpG (10 g/mL) and IL-4 (500 IU/mL; Schering-Plough).…”
Section: Cell Collection and Preparationmentioning
confidence: 99%