Volume 57, Issue 5 pp. 1115-1121
HOW DO I…?

How do i participate in T-cell immunotherapy?

Megan M. Suhoski Davis

Megan M. Suhoski Davis

Department of Pathology and Laboratory Medicine and the Center for Cellular Immunotherapies, University of Pennsylvania, Philadelphia, Pennsylvania

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David H. McKenna

Corresponding Author

David H. McKenna

Division of Minnesota Molecular and Cellular Therapeutics Facility, University of Minnesota, Saint Paul, Minnesota

Address reprint requests to: David H. McKenna, MD, Molecular & Cellular Therapeutics, University of Minnesota, 1900 Fitch Avenue, Saint Paul, MN 55108; e-mail: [email protected].Search for more papers by this author
Philip J. Norris

Philip J. Norris

Blood Systems Research Institute

Departments of Laboratory Medicine and Medicine, University of California, San Francisco, California

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First published: 05 April 2017
Citations: 3

Abstract

T cells play a key role in the adaptive immune response, and the ability to manipulate T cells for therapeutic uses has advanced in the past decade. Infusion of expanded or engineered T cells can potentially be used to treat cancer, viral infections, graft-versus-host disease, and organ transplant rejection. The role that blood banks play in the manufacture and distribution of T-cell therapeutics is still being defined. Given the regulatory framework of blood banks, they are well positioned to collect raw material for manufacture of T-cell therapies and to distribute finished product to hospitals in support of clinical trials or eventually for licensed products.

A deeper level of involvement in manufacture of T-cell therapeutics is also possible, although that requires more substantial investment in physical facilities and personnel with the regulatory and scientific expertise to prepare and produce cellular therapy products. Examples of physical infrastructure needed would be a laboratory with a clean room for culture of T cells, specialized equipment for expansion of the cells, and adequate administrative and storage support space. Processes that would need to be developed to produce T-cell therapeutics would include development of standard operating procedures and an appropriate quality assurance program. As blood banks consider supporting this novel class of therapies, they will need to weigh capital and expertise requirements with the benefits of providing a novel therapy and the potential of growth for their operations.

The full text of this article hosted at iucr.org is unavailable due to technical difficulties.