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A Humanized Mouse Model Generated Using Surplus Neonatal Tissue

Authors :
Timothy J. Kamp
Jeremy A. Sullivan
Ying Zhou
Mitch Biermann
Brian E. McIntosh
James A. Thomson
William J. Burlingham
Petros V. Anagnostopoulos
Hannah E. Lou
Ian G. Norman
Matthew E. Brown
Source :
Stem Cell Reports, Stem Cell Reports, Vol 10, Iss 4, Pp 1175-1183 (2018)
Publication Year :
2017

Abstract

Summary Here, we describe the NeoThy humanized mouse model created using non-fetal human tissue sources, cryopreserved neonatal thymus and umbilical cord blood hematopoietic stem cells (HSCs). Conventional humanized mouse models are made by engrafting human fetal thymus and HSCs into immunocompromised mice. These mice harbor functional human T cells that have matured in the presence of human self-peptides and human leukocyte antigen molecules. Neonatal thymus tissue is more abundant and developmentally mature and allows for creation of up to ∼50-fold more mice per donor compared with fetal tissue models. The NeoThy has equivalent frequencies of engrafted human immune cells compared with fetal tissue humanized mice and exhibits T cell function in assays of ex vivo cell proliferation, interferon γ secretion, and in vivo graft infiltration. The NeoThy model may provide significant advantages for induced pluripotent stem cell immunogenicity studies, while bypassing the requirement for fetal tissue.<br />Highlights • Neonatal tissue is a viable alternative to fetal for mouse humanization • Over 1,000 NeoThy mice can be made from one neonatal thymus donor • The NeoThy enables robust pre-clinical immunogenicity studies of iPSC therapies<br />Corresponding author William Burlingham and colleagues created a humanized mouse model called the NeoThy. The NeoThy uses human neonatal, rather than fetal, tissue sources for generating a human immune system within immunocompromised mouse hosts. NeoThy mice are an attractive alternative to conventional humanized mouse models, as they enable robust and reproducible iPSC immunogenicity experiments in vivo.

Details

ISSN :
22136711
Volume :
10
Issue :
4
Database :
OpenAIRE
Journal :
Stem cell reports
Accession number :
edsair.doi.dedup.....44589f90cc93f5799ccb57f657f0b904