4.8 Article

Inclusion of Strep-tag II in design of antigen receptors for T-cell immunotherapy

Journal

NATURE BIOTECHNOLOGY
Volume 34, Issue 4, Pages 430-+

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/nbt.3461

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Funding

  1. Walker Immunotherapy Fellowship
  2. Fred Hutchinson Cancer Research Center (FHCRC) Synergy Technology Fund
  3. National Institute of Health (NIH) grants [CA136551, CA114536, P50 CA138293]

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Adoptive immunotherapy with genetically engineered T cells has the potential to treat cancer and other diseases. The introduction of Strep-tag II sequences into specific sites in synthetic chimeric antigen receptors or natural T-cell receptors of diverse specificities provides engineered T cells with a marker for identification and rapid purification, a method for tailoring spacer length of chimeric receptors for optimal function, and a functional element for selective antibodycoated, microbead-driven, large-scale expansion. These receptor designs facilitate cGMP manufacturing of pure populations of engineered T cells for adoptive T-cell therapies and enable in vivo tracking and retrieval of transferred cells for downstream research applications.

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