2017
DOI: 10.1186/s12896-017-0383-0
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Immobilisation of Delta-like 1 ligand for the scalable and controlled manufacture of hematopoietic progenitor cells in a stirred bioreactor

Abstract: BackgroundUmbilical cord blood provides a source of hematopoietic stem cells for transplantation with immunological and availability advantages over conventional bone marrow sources. Limited cell numbers and slower engraftment from umbilical cord blood units has led to the clinical development of immobilised Notch ligand Delta-Like 1 to promote ex vivo expansion of a rapidly engrafting cell population. However, current immobilisation methods are not simple to scale in a controlled manner.ResultsDelta-Like 1 wa… Show more

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Cited by 4 publications
(2 citation statements)
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References 45 publications
(43 reference statements)
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“…Usually, the immobilized surface is functionalized with either avidin or streptavidin, while biotin is coupled to the molecule of interest. In some instances, it is necessary to test GF immobilization efficiency depending on either the biotin-GF binding or the biotin-streptavidin binding occurring first (Moore et al, 2017). In most approaches, GF immobilization by biotin-streptavidin interactions involves the use of tetrameric streptavidin, which makes the biotinavidin/streptavidin interaction non-reversible.…”
Section: Biotin-streptavidin Interactionsmentioning
confidence: 99%
“…Usually, the immobilized surface is functionalized with either avidin or streptavidin, while biotin is coupled to the molecule of interest. In some instances, it is necessary to test GF immobilization efficiency depending on either the biotin-GF binding or the biotin-streptavidin binding occurring first (Moore et al, 2017). In most approaches, GF immobilization by biotin-streptavidin interactions involves the use of tetrameric streptavidin, which makes the biotinavidin/streptavidin interaction non-reversible.…”
Section: Biotin-streptavidin Interactionsmentioning
confidence: 99%
“…[ 97 ] The combination of these systems could enable the scaled‐up feeder‐ and xeno‐free expansion of HSPC, together with their differentiation towards T lineage, for adoptive cell therapies. [ 98 ]…”
Section: Thymus Tissue Engineeringmentioning
confidence: 99%