Literature DB >> 16010652

The Minnesota Molecular and Cellular Therapeutics Facility: a state-of-the-art biotherapeutics engineering laboratory.

David H McKenna1, Diane M Kadidlo, Jeffrey S Miller, Paul J Orchard, John E Wagner, Jeffrey McCullough.   

Abstract

Molecular-, gene-, cellular-, and tissue-based therapies have become increasingly acceptable modes of clinical therapy. Regulatory requirements and oversight have increased, and the need for facilities suited for production of such therapies has become more apparent. The Minnesota Molecular and Cellular Therapeutics Facility is a state-of-the-art laboratory at the University of Minnesota, Saint Paul, Minn, that was designed to support production of biologic products for use in clinical trials. A talented staff experienced in the medical, scientific, technical, and regulatory aspects of the development, production, and administration of such products complements the special design and construction of the facility. Hematopoietic stem cells (HSCs) are manipulated for transplant, and current clinical trials involving novel therapies include the use of allogeneic natural killer (NK) cells and tumor vaccines for the treatment of various malignancies and suicide gene-transduced T cells for the prevention of graft-vs-host disease (GVHD) after bone marrow transplantation. Other therapies, including marrow-derived multipotent adult progenitor cells (MAPCs), umbilical cord blood (UCB) stem cells, regulatory T cells, skeletal myoblasts, and monoclonal antibodies, will be used to treat a spectrum of disease and are in various phases of development. Here we provide an overview of the Minnesota Molecular and Cellular Therapeutics (MMCT) Facility, detailing our approach to the manufacture of novel therapeutics and highlighting current and future activities.

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Year:  2005        PMID: 16010652     DOI: 10.1016/j.tmrv.2005.02.007

Source DB:  PubMed          Journal:  Transfus Med Rev        ISSN: 0887-7963


  7 in total

1.  Allogeneic natural killer cells for refractory lymphoma.

Authors:  Veronika Bachanova; Linda J Burns; David H McKenna; Julie Curtsinger; Angela Panoskaltsis-Mortari; Bruce R Lindgren; Sarah Cooley; Daniel Weisdorf; Jeffrey S Miller
Journal:  Cancer Immunol Immunother       Date:  2010-08-03       Impact factor: 6.968

2.  Clinical-scale production of cGMP compliant CD3/CD19 cell-depleted NK cells in the evolution of NK cell immunotherapy at a single institution.

Authors:  Shelly M Williams; Darin Sumstad; Diane Kadidlo; Julie Curtsinger; Xianghua Luo; Jeffrey S Miller; David H McKenna
Journal:  Transfusion       Date:  2018-03-12       Impact factor: 3.157

3.  Clearance of acute myeloid leukemia by haploidentical natural killer cells is improved using IL-2 diphtheria toxin fusion protein.

Authors:  Veronika Bachanova; Sarah Cooley; Todd E Defor; Michael R Verneris; Bin Zhang; David H McKenna; Julie Curtsinger; Angela Panoskaltsis-Mortari; Dixie Lewis; Keli Hippen; Philip McGlave; Daniel J Weisdorf; Bruce R Blazar; Jeffrey S Miller
Journal:  Blood       Date:  2014-04-09       Impact factor: 22.113

4.  Haploidentical natural killer cells induce remissions in non-Hodgkin lymphoma patients with low levels of immune-suppressor cells.

Authors:  Veronika Bachanova; Dhifaf Sarhan; Todd E DeFor; Sarah Cooley; Angela Panoskaltsis-Mortari; Bruce R Blazar; Julie M Curtsinger; Linda Burns; Daniel J Weisdorf; Jeffrey S Miller
Journal:  Cancer Immunol Immunother       Date:  2017-12-07       Impact factor: 6.968

Review 5.  Institutional shared resources and translational cancer research.

Authors:  Paolo De Paoli
Journal:  J Transl Med       Date:  2009-06-29       Impact factor: 5.531

Review 6.  Umbilical cord blood: current status & promise for the future.

Authors:  David McKenna; Jayesh Sheth
Journal:  Indian J Med Res       Date:  2011-09       Impact factor: 2.375

7.  Infusion reactions in natural killer cell immunotherapy: a retrospective review.

Authors:  Tewodros Mamo; Shelly M Williams; Stephanie Kinney; Katelyn M Tessier; Todd E DeFor; Sarah Cooley; Jeffrey S Miller; David H McKenna
Journal:  Cytotherapy       Date:  2021-05-09       Impact factor: 6.196

  7 in total

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