Unknown

Dataset Information

0

Efficient transplantation via antibody-based clearance of hematopoietic stem cell niches.


ABSTRACT: Upon intravenous transplantation, hematopoietic stem cells (HSCs) can home to specialized niches, yet most HSCs fail to engraft unless recipients are subjected to toxic preconditioning. We provide evidence that, aside from immune barriers, donor HSC engraftment is restricted by occupancy of appropriate niches by host HSCs. Administration of ACK2, an antibody that blocks c-kit function, led to the transient removal of >98% of endogenous HSCs in immunodeficient mice. Subsequent transplantation of these mice with donor HSCs led to chimerism levels of up to 90%. Extrapolation of these methods to humans may enable mild but effective conditioning regimens for transplantation.

SUBMITTER: Czechowicz A 

PROVIDER: S-EPMC2527021 | biostudies-literature | 2007 Nov

REPOSITORIES: biostudies-literature

altmetric image

Publications

Efficient transplantation via antibody-based clearance of hematopoietic stem cell niches.

Czechowicz Agnieszka A   Kraft Daniel D   Weissman Irving L IL   Bhattacharya Deepta D  

Science (New York, N.Y.) 20071101 5854


Upon intravenous transplantation, hematopoietic stem cells (HSCs) can home to specialized niches, yet most HSCs fail to engraft unless recipients are subjected to toxic preconditioning. We provide evidence that, aside from immune barriers, donor HSC engraftment is restricted by occupancy of appropriate niches by host HSCs. Administration of ACK2, an antibody that blocks c-kit function, led to the transient removal of >98% of endogenous HSCs in immunodeficient mice. Subsequent transplantation of  ...[more]

Similar Datasets

| S-EPMC9632731 | biostudies-literature
| S-EPMC3268766 | biostudies-literature
| S-EPMC6781287 | biostudies-literature
| S-EPMC4706788 | biostudies-literature
| S-EPMC2902161 | biostudies-literature
| S-EPMC4928522 | biostudies-literature
| S-EPMC9011370 | biostudies-literature
| S-EPMC4716886 | biostudies-literature
| S-EPMC3219875 | biostudies-literature
| S-EPMC4731181 | biostudies-literature