Efficient generation of human T cells from a tissue-engineered thymic organoid

被引:0
作者
Mark C. Poznansky
Richard H. Evans
Russell B. Foxall
Ivona T. Olszak
Anita H. Piascik
Kelly E. Hartman
Christian Brander
Thomas H. Meyer
Mark J. Pykett
Karissa T. Chabner
Spyros A. Kalams
Michael Rosenzweig
David T. Scadden
机构
[1] AIDS Research Center and MGH Cancer Center,Division of Infectious Diseases
[2] Massachusetts General Hospital,undefined
[3] Harvard Medical School,undefined
[4] AIDS Research Center,undefined
[5] Massachusetts General Hospital,undefined
[6] Harvard Medical School,undefined
[7] Cytomatrix,undefined
来源
Nature Biotechnology | 2000年 / 18卷
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摘要
Biocompatible inorganic matrices have been used to enhance bone repair by integrating with endogenous bone architecture. Hypothesizing that a three-dimensional framework might support reconstruction of other tissues as well, we assessed the capacity of a tantalum-coated carbon matrix to support reconstitution of functioning thymic tissue. We engineered a thymic organoid by seeding matrices with murine thymic stroma. Co-culture of human bone marrow-derived hematopoietic progenitor cells within this xenogeneic environment generated mature functional T cells within 14 days. The proportionate T-cell yield from this system was highly reproducible, generating over 70% CD3+ T cells from either AC133+ or CD34+ progenitor cells. Cultured T cells expressed a high level of T-cell receptor excision circles (TREC), demonstrating de novo T lymphopoiesis, and function of fully mature T cells. This system not only facilitates analysis of the T-lymphopoietic potential of progenitor cell populations; it also permits ex vivo genesis of T cells for possible applications in treatment of immunodeficiency.
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页码:729 / 734
页数:5
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