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Immunoengineering can overcome the glycocalyx armour of cancer cells

  • Sangwoo Park
  • , Marshall J. Colville
  • , Justin H. Paek
  • , Carolyn R. Shurer
  • , Arun Singh
  • , Erica J. Secor
  • , Cooper J. Sailer
  • , Ling Ting Huang
  • , Joe Chin Hun Kuo
  • , Marc C. Goudge
  • , Jin Su
  • , Minsoo Kim
  • , Matthew P. DeLisa
  • , Sriram Neelamegham
  • , Jan Lammerding
  • , Warren R. Zipfel
  • , Claudia Fischbach
  • , Heidi L. Reesink
  • , Matthew J. Paszek
  • Cornell University
  • SUNY Buffalo
  • Cornell University College of Veterinary Medicine
  • University of Rochester

Research output: Contribution to journalArticlepeer-review

34 Scopus citations

Abstract

Cancer cell glycocalyx is a major line of defence against immune surveillance. However, how specific physical properties of the glycocalyx are regulated on a molecular level, contribute to immune evasion and may be overcome through immunoengineering must be resolved. Here we report how cancer-associated mucins and their glycosylation contribute to the nanoscale material thickness of the glycocalyx and consequently modulate the functional interactions with cytotoxic immune cells. Natural-killer-cell-mediated cytotoxicity is inversely correlated with the glycocalyx thickness of the target cells. Changes in glycocalyx thickness of approximately 10 nm can alter the susceptibility to immune cell attack. Enhanced stimulation of natural killer and T cells through equipment with chimeric antigen receptors can improve the cytotoxicity against mucin-bearing target cells. Alternatively, cytotoxicity can be enhanced through engineering effector cells to display glycocalyx-editing enzymes, including mucinases and sialidases. Together, our results motivate the development of immunoengineering strategies that overcome the glycocalyx armour of cancer cells.

Original languageEnglish
Pages (from-to)429-438
Number of pages10
JournalNature Materials
Volume23
Issue number3
DOIs
StatePublished - Mar 2024

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